1. In adults with clinical suspicion of hip fracture but adequate quality negative standard X-rays (anteroposterior pelvis and lateral hip), cross-sectional imaging should be performed. Specifically:
1.1. Magnetic resonance imaging (MRI) is the preferred modality due to higher diagnostic sensitivity and specificity for occult hip fractures. (Strong recommendation, Moderate quality evidence)
1.2. Computed tomography (CT) should be considered when MRI is unavailable within 24 hours, contraindicated, or impractical. (Conditional Recommendation, Moderate quality evidence)
1.3. If CT is used first and is negative despite ongoing clinical suspicion, MRI should subsequently be obtained to rule out occult fracture (unless contraindicated). (Strong Recommendation, Moderate quality evidence)
When to Offer MRI
Clinical scenarios warranting MRI:
Rationale:
When to Offer CT
Appropriate scenarios:
Role of CT:
Meta-Analysis and Systematic Evidence
Observational Comparisons
Table 2: Diagnostic Accuracy of MRI versus CT for Occult Hip Fracture 9
|
Parameter |
MRI |
CT |
|
Pooled Sensitivity (Meta-analysis) |
0.94 (95% CI: 0.80–0.99) |
0.92 (95% CI: 0.81–0.96) |
|
Pooled Specificity (Meta-analysis) |
0.98 (95% CI: 0.94–1.00) |
0.94 (95% CI: 0.87–0.97) |
|
Positive LR |
8.14 (95% CI: 5.70–108.04) |
7.60 (95% CI: 5.07–34.44) |
|
Negative LR |
0.06 (95% CI: 0.01–0.22) |
0.09 (95% CI: 0.04–0.21) |
|
Area Under the ROC |
~0.99 (excellent) |
~0.98 (excellent) |
|
Summary |
High diagnostic accuracy; slightly superior to CT overall |
Very good accuracy but slightly lower than MRI |
Table 3: GRADE Assessment – Diagnostic Accuracy 9
|
Outcome |
MRI |
CT |
|
Overall Quality of Evidence |
Moderate – multiple studies with QUADAS-2 assessment; consistency in pooled diagnostic performance. |
Moderate (lower than MRI) – similar meta-analytic data but a trend toward slightly lower sensitivity; some studies highlight false negatives. |
|
Risk of Bias |
Generally low in meta-analysis; QUADAS-2 showed minimal concerns. |
Similar quality in QUADAS-2, but clinical follow-up in some cohorts showed missed fractures. |
|
Indirectness |
Directly applicable to patients with suspected occult hip fracture after negative radiographs. |
Same applicability. |
|
Imprecision |
Moderate (CI ranges reflect some uncertainty). |
Moderate (similar CI uncertainty). |
|
Publication Bias |
Not statistically significant in meta-analyses. |
Not statistically significant. |
We advise against the routine use of preoperative traction for patients with a hip fracture. (Conditional recommendation, High quality evidence)
Complications, comfort, and pain are important outcomes related to hip fracture. Not using preoperative traction ease the patient’s comfort in bed, decreases pain and lowers the incidence of possible bedridden complications.
Overall, there were two high quality13,14 and six moderate studies15-20 addressing preoperative traction. Since 2012, one high13 and one moderate quality study19 investigated preoperative traction. Tosun19 (2018) found that a position splint resulted in significant difference in immobilization comfort score (30.1/100) and pain compared to traction, whereas Endo13 found no differences in pain. Tosun also found that preoperative traction resulted in more pre-operative complications (constipation, pressure ulcers, adhesive plaster allergy, urinary tract infections, pulmonary complications, bleeding in the fractured joint) than a position splint applied for 1 day preoperatively, whereas Endo found no significant differences in complications between traction and no traction. These results are consistent with prior evidence and strengthen the body of evidence indicating that there are no benefits of preoperative traction. The recommendation reflects that there are some instances in which traction may be required (e.g., specific cases with peri-trochanteric fractures), however, in most cases pre- operative traction should not be used.
There are no known harms of implementing this recommendation. Use of alternatives to preoperative traction appeared to be acceptable to patients like positioning with pillows.
Perform hip fracture surgery on the day of, or the day after admission to hospital (within 48 hours); taking into consideration the patient optimization for surgery. (Conditional recommendation, Moderate quality evidence)
Traditionally, hip fracture patients have not always been considered a priority group in accessing theatres and the injury itself is rarely life threatening. However, older people with a hip fracture frequently have multiple co-morbidities, limited physiological reserve and are prone to an increase in complications from prolonged bed rest. Hospitals must therefore be organised in such a way that facilitates timely and planned surgery without delays, meaning not only adequate theatre capacity for trauma surgery and availability of anaesthetists and surgeons, but also a means of rapidly assessing and optimising frail, elderly patients with multiple co-morbidities.
Systematic reviews suggested that delay past 48hr increased one-year mortality by 32%. Recent studies, however, have suggested mortality reductions by reducing time to theatre to 24hr and even 12hr from admission21-24
Moderate evidence supports that hip fracture surgery within 48 hours of admission is
associated with better outcomes, less hospital stay and is more cost effective. Taking into consideration resource availability, the panel decided to downgrade the recommendation from strong to conditional, provided that reasons for any delay are clearly documented in the patients notes.
On admission, confirm the antithrombotic agent(s), last dose time, renal function and indication (VTE prophylaxis vs therapeutic anticoagulation) before committing to neuraxial or deep regional techniques. (Strong recommendation, Low quality evidence)
Document last known dose time from a reliable source (medication list, family, pharmacy, or electronic record). If timing is uncertain, manage as 'dose within the minimum interruption interval'.
The strong recommendation is based on low-certainty evidence derived from international consensus guidelines, primarily the American Society of Regional Anesthesia and Pain Medicine (ASRA) Fifth Edition Guidelines25 and the Joint ESAIC/ESRA Guideline26. These guidelines emphasize that the cornerstone of safe regional anesthesia in anticoagulated patients is an accurate, timely medication history. The evidence supporting this is largely indirect, stemming from case series and root-cause analyses of catastrophic complications like spinal hematoma, where a common contributing factor was inadequate documentation or verification of anticoagulant timing. The guidelines explicitly state that agent-specific interruption intervals cannot be applied safely without knowing the exact drug, dose, last administration time, and renal function (critical for DOAC and LMWH clearance). This operational step is considered a fundamental patient safety requirement in all perioperative pathways.
Timely, accurate drug history avoids unnecessary delays and reduces the risk of neuraxial or deep block hematoma from inadvertently performing a procedure within an unsafe interval.
If surgery is delayed beyond the day of admission, consider pharmacological VTE prophylaxis if VTE risk outweighs bleeding risk. Ensure the last dose is at least 12 hours before surgery for low dose LMWH and at least 24 hours for high dose LMWH and fondaparinux. (Strong recommendation, Moderate quality evidence)
Continue mechanical prophylaxis when pharmacological prophylaxis is withheld. Reassess daily as renal function and bleeding risk evolve.
This strong recommendation is supported by moderate-certainty evidence from7,27 on VTE prevention. NICE recommends that patients with hip fractures should receive pharmacological VTE prophylaxis if surgery is delayed beyond the day of admission. The specified minimum intervals (12 hours for prophylactic LMWH, 24 hours for therapeutic LMWH/fondaparinux) are based on pharmacodynamic studies of anti-Xa activity and its correlation with bleeding risk. The evidence balancing VTE risk against bleeding risk comes from large orthopaedic trials and meta-analyses, which show that while hip fracture patients have a very high baseline VTE risk, indiscriminate pre-operative dosing increases the hazard of surgical and neuraxial bleeding. The "delay-triggered" approach is a pragmatic synthesis of this evidence, aiming to protect patients from VTE during unavoidable waits without compromising the option for regional anaesthesia or increasing intraoperative bleeding.
Hip fracture patients are at high VTE risk; however, unnecessary pre-operative dosing can force neuraxial/deep procedures to be deferred. A 'delay-triggered' approach balances both risks.
Treat deep (non-compressible) nerve blocks like lumbar plexus or paravertebral blocks, the same way as neuraxial blocks in respect to VTE prophylaxis drugs interruption timing. For superficial (compressible) single-shot blocks like femoral nerve or fascia iliaca plane blocks, apply a site-based bleeding risk assessment and proceed when the expected benefit outweighs bleeding risk. (Strong recommendation, Low quality evidence)
If neuraxial timing criteria are not met, general anaesthesia with a superficial compressible block is a common compromise to preserve analgesic benefit while avoiding deep needle placement.
The strong recommendation for this risk-stratified framework is based on low-certainty evidence from expert consensus, primarily outlined in the Joint ESAIC/ESRA Guideline26. This guideline introduces a key conceptual shift: not all regional techniques carry the same bleeding risk. The evidence underpinning this distinction is anatomical and pathophysiological. Deep, non-compressible sites (e.g., neuraxial space, deep plexus) pose a risk of concealed, expanding hematoma with potential for permanent neurological injury, as documented in case reports. In contrast, bleeding at superficial, compressible sites (e.g., fascia iliaca plane) is theoretically easier to detect and control with external pressure. While high-quality comparative studies are lacking, the framework is considered a rational approach to maximize the benefits of regional analgesia (supported by the Cochrane review by Guay et al., 2020)28 while mitigating the most severe risks in patients on antithrombotics.
Nerve blocks are generally categorized as superficial or deep based on anatomical location and tissue compressibility. Superficial nerve blocks target nerves in relatively accessible areas surrounded by compressible tissue. Examples include femoral, interscalene, and axillary blocks etc. These blocks are easier to visualize with ultrasound and pose a lower risk of serious bleeding. Deep nerve blocks, such as lumbar plexus or paravertebral blocks, involve deeper, non-compressible tissue. Compressible sites permit rapid detection and management of bleeding complications; deep sites do not. This supports a risk-stratified approach rather than a one-size-fits-all prohibition.
Use Annex 2: Minimum interruption intervals (summary table) for a consolidated table. Key principles 17,18:
· Dose intensity and renal function matter for LMWH and DOACs; insertion and removal of neuraxial catheters are both timing events (Strong recommendation, High quality evidence)
· It is advised to check platelet count if LMWH has been used for more than 4 days due to heparin-induced thrombocytopenia risk. (Conditional recommendation, Low quality evidence)
When neuraxial or deep catheters are used, coordinate LMWH dosing with both catheter placement and removal.
· Stop low-dose LMWH at least 12 hours before placement or removal of the catheter, and for 24 hours before placement or removal in case of high dose LMWH.
· In all cases; (low and high dose LMWH); start first LMWH dose at least 12 hours after placement and at least 4 hours after removal.
(Strong recommendation, Moderate quality evidence)
If LMWH has been administered for more than 4 days, check platelet count before neuraxial/deep block or catheter removal. Use 1.5 or less for 'acceptable INR' where vitamin K antagonists are involved. 29
These strong recommendations are supported by moderate-certainty evidence synthesizing pharmacodynamic data and large-scale observational safety registries. The specific time intervals for each drug class (LMWH, DOACs, fondaparinux, etc.) before neuraxial/deep blocks are meticulously detailed in the ASRA (2025)25 and ESAIC/ESRA (2022)26 guidelines. These intervals are derived from studies of the drug's half-life, time to maximum effect, and time for return of haemostatic function, often modified by renal function for renally cleared agents. The evidence for the critical importance of coordinating catheter removal with anticoagulant dosing is particularly strong, stemming from analysis of case reports of spinal hematoma, which identified catheter removal as a high-risk event. The operational rules for LMWH (e.g., 12-hour windows for once-daily dosing) are based on sustained clinical experience and pharmacodynamic modelling that aims to avoid peak anticoagulant activity during needle placement or catheter manipulation, thereby reducing the risk of this rare but devastating complication.
Catheter placement and removal create tissue planes susceptible to bleeding. Timing anticoagulant exposure around these events reduces catastrophic but rare complications.
Provide post-operative VTE prophylaxis according to individual risk assessment; extended prophylaxis (e.g., 28–35 days) is commonly used after hip fracture surgery. (Conditional recommendation, Moderate quality evidence)
Choice of agent (LMWH, DOAC, warfarin, or aspirin in selected patients) should reflect surgical plan, renal function, bleeding risk, and contraindications, and must be coordinated with any neuraxial/deep catheter use.
This conditional recommendation is based on low-to-moderate certainty evidence from various orthopaedic and thromboprophylaxis guidelines, including NICE NG89, AAOS (2021), and PROSPECT (2024)2,27,30. The evidence consistently identifies hip fracture surgery as a highest-risk scenario for VTE, justifying pharmacologic prophylaxis. Randomized controlled trials and meta-analyses provide moderate-certainty evidence that extended prophylaxis (e.g., 28-35 days) reduces the risk of symptomatic VTE compared to shorter (e.g., 10-14 day) regimens. However, the evidence is less clear on the net benefit, as extended therapy increases the risk of major bleeding. This trade-off leads to the conditional strength of the recommendation, necessitating individualization based on patient-specific bleeding risk, mobility, and renal function. The guidance to coordinate agent choice with neuraxial catheters is again directly informed by the ASRA/ESAIC/ESRA guidelines to prevent catheter-related hematoma.
The VTE risk remains elevated after discharge. Extended prophylaxis may reduce symptomatic VTE at the cost of increased bleeding in some subgroups; thus, individualization is required.
Assess pain score immediately on presentation (at rest and on movement) and reassess within 30 minutes after any analgesic intervention; then hourly until pain is controlled, and thereafter with routine observations. (Strong recommendation, Moderate quality evidence)
· In conscious patients use the Numerical Pain Rating (NPR) score to measure pain
· In case of cognitive impairment, use observational tools (e.g., FLACC [Face, Legs, Activity, Cry, Consolability] scale) and incorporate caregiver input.
· Always document sedation score and respiratory rate after opioid escalation
In conscious patients use the Numerical Pain Rating (NPR) score to measure pain and in case of cognitive impairment, use observational tools (e.g., FLACC [Face, Legs, Activity, Cry, Consolability] scale)31 (Annex 3: FLACC score and Ramsay sedation score), and incorporate caregiver input. Always document sedation score32 and respiratory rate after opioid escalation.
This recommendation is strongly supported by moderate-certainty evidence from the NICE CG124 (2025 update)7 hip fracture management guideline. The guideline explicitly mandates structured pain assessment at presentation and after each analgesic intervention. The evidence for using observational pain scales (e.g., the FLACC scale)31 in patients with cognitive impairment or delirium is drawn from validation studies in geriatric and postoperative populations, which show improved detection of pain compared to self-report alone. Regular reassessment protocols are linked in observational studies to more timely analgesia adjustments, reduced incidence of severe pain during movement or positioning, and a lower risk of opioid-related oversedation. This approach is foundational to the "delirium-aware" care emphasized in multidisciplinary hip fracture pathways.
Early pain control enables imaging, nursing care, and positioning for anaesthesia, and reduces delirium risk. Reassessment prevents both undertreatment and oversedation.
Offer regular paracetamol/acetaminophen every 6 hours pre- and post-operatively unless contraindicated; use intravenous dosing when oral administration is unreliable. (Strong Recommendation, Moderate quality evidence)
Review maximum daily dose in low body weight, frailty, or liver disease; include all sources (drug combination tablets) of acetaminophen to avoid unintentional overdose.
The strong recommendation is based on moderate-certainty evidence from NICE CG1247, which identifies regular scheduled paracetamol as the first-line analgesic for hip fracture patients. The evidence synthesizes data showing that paracetamol provides effective baseline analgesia with a superior safety profile compared to NSAIDs or opioids in older adults, particularly regarding gastrointestinal, renal, and bleeding risks. The emphasis on intravenous administration when the oral route is unreliable is supported by pharmacokinetic studies in frail or acutely ill older adults demonstrating more predictable bioavailability. The caution regarding maximum daily dose (especially with combination products) is a direct application of pharmacovigilance data on acetaminophen-induced hepatotoxicity, which is cited in drug safety communications from regulatory bodies like the FDA and MHRA.
Paracetamol provides baseline analgesia with a favorable safety profile compared with opioids in older adults when dose limits are respected.
Use opioids as rescue therapy with small, titrated doses (prefer immediate-release oral or carefully titrated IV boluses) when paracetamol alone is insufficient. Avoid initiating prolonged-release opioids in the acute perioperative phase. (Strong recommendation, Moderate quality evidence)
Start low and titrate slowly, especially in renal impairment and cognitive impairment. Implement routine bowel regimen and antiemetic when opioids are used.
This strong recommendation is grounded in moderate-certainty evidence primarily from NICE CG1247 and reinforced by geriatric pharmacology principles. NICE recommends immediate-release opioids as rescue therapy when paracetamol is insufficient. The evidence against initiating long-acting opioids in the acute phase comes from cohort studies and expert consensus (e.g., Association of Anaesthetists guideline)33, which associate these agents with a higher risk of sedation, respiratory depression, and delirium in opioid-naïve older patients. The "start low, go slow" titration approach is supported by pharmacokinetic data showing increased sensitivity and variable clearance in older adults, especially with renal impairment (notably for morphine metabolites). The mandatory co-prescription of a bowel regimen is based on high-quality evidence demonstrating the near-universality of opioid-induced constipation and its negative impact on recovery.
Immediate-release dosing allows rapid titration to effect and reduces risk of accumulation and oversedation.
Offer an early peripheral nerve block [e.g., fascia iliaca, femoral, or Pericapsular Nerve Group (PENG)] block when trained staff and ultrasound are available, to improve pain control and reduce systemic opioid requirements. Do not delay surgery for block placement. (Conditional recommendation, Moderate quality evidence)
Coordinate with antithrombotic status using the deep vs superficial framework; monitor for local anaesthetic systemic toxicity and document motor block/falls risk.
The conditional recommendation is supported by moderate-certainty evidence from two key sources. First, NICE CG1247 recommends considering a nerve block if pain is severe or to limit opioid dose. More robust, procedure-specific evidence comes from the Cochrane systematic review by Guay et al. (2020)28, which analyzed randomized trials of peripheral nerve blocks for hip fracture. This review concluded that blocks (especially fascia iliaca compartment blocks) provide superior pain relief on movement, reduce systemic opioid consumption, and are associated with a lower risk of postoperative confusion (delirium). The recommendation not to delay surgery for a block is a pragmatic one, based on pathway analyses from NICE that prioritize timely surgery. Coordination with antithrombotic therapy is meticulously detailed in the ASRA (Kopp et al., 2025)25 and ESAIC/ESRA (Kietaibl et al., 2022)26 guidelines, which provide risk-stratified timing for blocks based on anticoagulant type.
Blocks facilitate positioning, reduce opioid exposure, and may improve early rehabilitation participation.
When opioids are used, prescribe antiemetic and bowel regimen, monitor sedation score, respiratory rate, and oxygen saturation, and screen for delirium daily. Encourage early mobilization and physiotherapy when clinically appropriate. (Strong recommendation, Low quality evidence)
Avoid benzodiazepines unless clearly indicated; minimize anticholinergic burden.
The strong recommendation is supported by low-certainty direct evidence but is a cornerstone of multidisciplinary hip fracture care pathways like NICE CG1247. The evidence for routine antiemetic and bowel prophylaxis with opioids is extrapolated from high-quality studies in other surgical populations and is considered standard of care to prevent iatrogenic harm. The link between structured monitoring (sedation, respiration, oxygenation) and reduced opioid-related adverse events is supported by patient safety initiatives. The emphasis on daily delirium screening is mandated by NICE and is based on studies showing that systematic detection leads to earlier intervention. The recommendation to avoid benzodiazepines is strongly supported by multiple high-quality studies and meta-analyses (cited in geriatric and delirium guidelines) that consistently associate them with increased delirium risk, falls, and cognitive decline in older hospitalized patients.
Complications from opioids (respiratory depression, delirium, constipation) are common drivers of poor outcomes and longer admissions.
Avoid routine NSAIDs/COX-2 inhibitors in frail older hip fracture patients. Consider them only when a senior clinician documents a favourable risk-benefit assessment and there are no contraindications (renal dysfunction, high bleeding risk, active GI disease, interacting anticoagulants). (Conditional recommendation, Low quality evidence)
This recommendation reflects the tension between sources: NICE CG1247 does not recommend NSAIDs for hip fracture, whereas PROSPECT recommends NSAIDs or COX-2 inhibitors as part of multimodal analgesia when appropriate.
This conditional recommendation arises from a tension between guideline sources, leading to low-certainty evidence for routine use. The PROSPECT recommendations (2024)34 list NSAIDs or COX-2 inhibitors as a component of basic multimodal analgesia for hip fracture repair when no contraindications exist, citing evidence for their opioid-sparing and anti-inflammatory effects. However, NICE CG124 explicitly does not recommend NSAIDs for this population due to concerns about renal impairment, gastrointestinal bleeding, and interference with bone healing. This guideline's default "avoid" stance is justified by the high prevalence of these risk factors in the typical frail, older hip fracture population, as documented in large epidemiological studies. The requirement for a senior clinician's documented risk-benefit assessment is a safety mechanism to identify the minority of patients (e.g., robust, with normal renal function) who might benefit from short-term use.
A default-to-avoid stance in high-risk patients reduces preventable renal and bleeding complications while allowing clinician discretion for lower-risk individuals.
Routine use of epidural analgesia for hip fracture surgery is discouraged. If used, restrict to selected cases under acute pain service or senior anaesthesia oversight, with explicit anticoagulant coordination and haemodynamic monitoring. (Conditional recommendation, Low quality evidence).
· Our current practice in Egypt still permits the use of epidural anaesthesia / analgesia in selected patients with consideration of the anticoagulants use/withhold recommended duration for catheter insertion and removal, in view of the immaturity of regional blocks training especially in rural areas.
Risks include hypotension, motor block with falls risk, urinary retention, infection, and neuraxial hematoma (timing dependent).
The strong recommendation against routine use is based on low-certainty, procedure-specific evidence from the PROSPECT Working Group (2024)34. PROSPECT's analysis found limited high-quality studies demonstrating a clear advantage of epidural over systemic or peripheral nerve block techniques for hip fracture surgery, while the risks (hypotension, motor block/falls, urinary retention, infection, and neuraxial hematoma) are well-documented in the broader anaesthesia literature. The guidelines from ASRA25 and ESAIC/ESRA26 heavily inform the strict anticoagulant coordination required. The acknowledgment of potential use in selected cases (e.g., with Acute Pain Service oversight) reflects clinical pragmatism, allowing for its consideration in complex pain scenarios or where regional block expertise is limited, provided the stringent safety protocols for anticoagulant management and hemodynamic monitoring are followed.
In this frail population, the risk and monitoring burden often outweigh incremental benefit compared with peripheral blocks and systemic multimodal regimens.
Tailor component selection to frailty, renal function, gastrointestinal/bleeding risk, and cognitive status. Prefer established blocks (FICB/FNB); consider newer techniques (e.g., PENG) only where local expertise exists and within protocols, as procedure-specific evidence remains limited. Avoid routine use of adjuvant techniques/drugs with insufficient procedure-specific evidence (e.g., IV dexmedetomidine/clonidine as analgesic adjuncts, routine local infiltration analgesia) outside specialist pathways. Do not delay surgery to complete the multimodal regimen; reassess pain and sedation after each escalation (Annex 4: Multimodal analgesia for hip fracture).
This recommendation is supported by convergent guidelines and systematic review of evidence. A multidisciplinary UK consensus statement endorses multimodal analgesia throughout the peri-operative pathway, defining it as combining analgesics with different mechanisms to improve analgesia and permit lower doses of individual drugs, thereby reducing adverse effects.35 PROSPECT34 procedure-specific guidance for hip fracture repair recommends basic multimodal analgesia with scheduled paracetamol and NSAIDs or COX-2-selective inhibitors when not contraindicated, combined with a single-shot femoral nerve block or fascia iliaca compartment block, and reserving opioids as rescue analgesia. NICE CG1247 similarly positions regular paracetamol as first-line, immediate-release opioids as additional analgesia, and suggests adding nerve blocks when pain control is inadequate or to limit opioid dose. Evidence syntheses (e.g., Cochrane reviews)28 demonstrate that peripheral nerve blocks reduce pain on movement and opioid consumption, with signals for reduced postoperative confusion/delirium, supporting the opioid-sparing rationale of multimodal strategies.30 Direct trials of bundled multimodal pathways in hip fracture are limited; therefore, overall certainty is moderate, driven by consistent benefits across components and strong expert consensus Error! Reference source not found..
A multimodal regimen improves comfort and function (especially pain-on movement), reduces opioid exposure and related harms, and supports timely imaging, regional/spinal positioning, and early rehabilitation.
Proceed to surgery as soon as feasible once immediately reversible problems are addressed (e.g., hypoxia, hypovolaemia, severe electrolyte derangements, uncontrolled pain). (Strong Recommendation, Moderate quality evidence)
Optimization should run in parallel with theatre preparation. Avoid delays for routine investigations unless they change perioperative management (Annex 5: Anaesthetic management pathway (hip fracture surgery)).
This recommendation is strongly supported by the NICE CG124 guideline7 and its surveillance updates, which form the cornerstone of standardized hip fracture care pathways in many healthcare systems. These pathways are explicitly designed to expedite surgery once immediately reversible problems are corrected, with the primary outcome of reducing complications associated with prolonged immobility and pain. The evidence, rated as moderate certainty, is drawn from large observational studies and audits of these pathways, which consistently demonstrate that timely surgery (typically within 36 hours) is associated with lower mortality, reduced length of stay, and fewer medical complications like pneumonia and pressure sores. The rationale is that multidisciplinary, parallel processing of optimization and theatre preparation
Delays increase pain, immobility-related complications, and delirium risk. Focused optimization improves safety without compromising time-to-theatre.
Either neuraxial (spinal) or general anaesthesia is acceptable. Choose the technique that can be delivered safely and promptly given antithrombotic timing, physiological reserve, airway risk, expected surgical duration, and local expertise. (Conditional recommendation, High quality evidence)
If neuraxial is contraindicated or not feasible, proceed with general anaesthesia and use a peripheral nerve block when feasible for opioid-sparing.
The conditional recommendation for technique choice is primarily informed by high-certainty evidence from the landmark REGAIN trial36, a large pragmatic randomized controlled trial. This study directly compared spinal anaesthesia to general anaesthesia in older adults undergoing hip fracture surgery and found no significant difference in the primary composite outcome of death or an inability to walk at 60 days. Critically, it also found no difference in key secondary outcomes, including the incidence of postoperative delirium. This pivotal evidence overturned the long-held assumption of neuraxial superiority. Consequently, contemporary guidelines from the Association of Anaesthetists33 (2021) and the PROSPECT Working Group (2024)34 explicitly state that neither technique is preferred. The decision should be individualized, factoring in logistical constraints (e.g., timing of last antithrombotic dose as per ASRA25/ESAIC26 guidelines) and patient physiology to avoid delays and ensure hemodynamic stability.
Clinical heterogeneity is substantial (frailty, respiratory disease, antithrombotics). A pragmatic approach that avoids delay and preserves haemodynamic stability is likely to improve system-level outcomes.
Aim to maintain any change in systolic blood pressure/mean arterial pressure within approximately 20% of the patient’s baseline, avoid hypoxia and hypercarbia, maintain normothermia, and use a proactive vasopressor strategy with judicious fluids. (Strong recommendation, Low quality evidence)
Consider invasive arterial pressure monitoring for higher-risk patients (e.g., severe aortic stenosis, significant cardiopulmonary disease, anticipated major blood loss).
While direct randomized trial evidence is of low certainty, the strong recommendation stems from a synthesis of observational studies and expert consensus detailed in the Association of Anaesthetists guideline (Griffiths et al., 2021)33. This guidance explicitly links intraoperative hypotension and hypoxia to increased risks of acute kidney injury, myocardial injury, and postoperative delirium in this frail population. The specific target of maintaining systolic or mean arterial pressure within 20% of baseline is a widely adopted consensus threshold to define intraoperative hypotension. The call for proactive vasopressor use and judicious fluid management is based on pathophysiological understanding of reduced autonomic reserve in older adults. The guideline emphasizes that standardized monitoring and treatment protocols improve team coordination and reduce outcome variability, even in the absence of definitive RCTs.
Older hip fracture patients have limited physiological reserve. Standardized targets improve team coordination and reduce unwarranted variation
For cemented arthroplasty, identify high-risk patients and apply BCIS (Bone Cement Implantation Syndrome) precautions: a team 'cement pause', maintain blood pressure close to baseline, optimize oxygenation, and have vasopressors immediately available. (Strong Recommendation, Moderate quality evidence:)
Escalate monitoring for high-risk patients and ensure explicit communication with surgeons during femoral canal preparation and cement insertion.
The strong recommendation and moderate-certainty evidence are derived from dedicated safety analyses, most notably the Association of Anaesthetists safety guideline (2015)30 on reducing risk from cemented hemiarthroplasty. This guideline systematically reviews case series and cohort studies documenting BCIS, characterized by hypoxia, hypotension, pulmonary hypertension, and/or cardiac arrest during cement implantation. The evidence underpinning the "cement pause" and preparedness strategy is based on root-cause analyses of adverse events, which identify communication failure and lack of readiness as contributory factors. The recommended bundle of maintaining blood pressure, optimizing oxygenation, and having vasopressors drawn up is a pragmatic response to the time-critical nature of BCIS, aimed at improving rescue success, as supported by subsequent adoption in international guidelines like those from the American Academy of Orthopaedic Surgeons (AAOS, 2021)37.
BCIS events are time-critical; preparedness and coordinated action reduce severity and improve rescue success.
Implement multimodal analgesia, delirium prevention measures (adequate pain control, oxygenation, hydration, sleep-wake support), and early mobilization. Coordinate VTE prophylaxis timing with any neuraxial or deep catheter use. (Strong recommendation, Moderate quality evidence)
Communicate a clear post-operative plan to ward/HDU: analgesia regimen, delirium risk mitigation, respiratory support needs, and anticoagulant timing.
This strong recommendation is supported by moderate-certainty evidence synthesizing multiple guideline sources. The core principle of multimodal, opioid-sparing analgesia is strongly evidenced by the Cochrane review by Guay et al. (2020)28, which confirms that peripheral nerve blocks provide superior pain relief and reduce opioid-related side effects. Delirium prevention is a central pillar of the NICE CG1247 pathway, which links adequate pain control, oxygenation, and early mobilization to reduced delirium incidence. The critical need to coordinate neuraxial or deep catheter management with pharmacologic VTE prophylaxis is exhaustively detailed in the Fifth Edition ASRA Guidelines (Kopp et al., 2025)25 and the joint ESAIC/ESRA guideline (Kietaibl et al., 2022)26, which provide evidence-based minimum neuraxial block intervals for various antithrombotic agents. Finally, the PROSPECT recommendations34 provide procedure-specific endorsement for a structured postoperative bundle combining these elements to facilitate early rehabilitation and improve recovery trajectories.
The immediate postoperative phase is when delirium, respiratory compromise, and immobility complications often emerge; structured bundles reduce risk.
· Schedule hip fracture surgery on a planned trauma list
· Consultants or senior staff must supervise trainees and junior members of the anaesthesia, surgical, and theatre teams when they carry out hip fracture procedures (Good practice statement)
Hip fracture patients should be prepared for the next operative list after admission, with a senior orthopaedic surgeon and an anaesthetist attending the surgery. The presence of a dedicated team for the management of geriatric hip trauma patients is recommended.
Planning the theatre team for the management of geriatric hip trauma patients is recommended7. A comprehensive geriatric fracture program has been described38,39 as an alternative approach to managing fragility fractures. An organized geriatric hip fracture program provides numerous benefits to patients with hip fractures, care providers, and health systems. Protocol-driven perioperative approaches should be employed, focusing on pre, intraoperative, and postoperative optimization of the patient to facilitate early repair of the fracture that may then translate into better outcomes and hence alleviate the individual patient's burden as well as the socioeconomic load for society. These benefits include shorter time to surgery, earlier postoperative mobilization, shorter hospital stay, reduced in-hospital mortality, and reduced postoperative complications.
People with a hip fracture can experience pain and anxiety while waiting for an operation. Delays in surgery are associated with negative outcomes for mortality and return to mobility. This approach aims to reduce unnecessary delays, which are associated with negative outcomes and prolonged hospital stays for the patient. It also helps to avoid repeated fasting and potential cancellations often associated with emergency lists. A planned trauma list includes specific healthcare professionals with the expertise required for hip surgery. Senior staff supervision can help to reduce the risk of complications during the surgery. Senior supervision is a crucial factor for patients, who rate the presence of specialists as the most important factor in their preference for a planned operation, as it can reduce the risk of complications during surgery.
In patients with stable femoral neck fractures (impacted/non-displaced, Garden’s I and II, Annex 6: Garden Classification of Femoral Neck Fracture), internal fixation or arthroplasty may be considered, after assessment of the patient and imaging of the hip joint. (Conditional recommendation, Low quality evidence)
The decision of management of undisplaced apparently stable femoral neck fractures is multifaceted and depends on several factors (Annex 6: Garden Classification of Femoral Neck Fracture). The bone quality and the sagittal tilt seen in the lateral view or CT scan affect the decision-making of internal fixation vs arthroplasty. The pre-injury functional state of the patient also affects the decision.
The decision-making of internal fixation in undisplaced femoral neck fracture is conditioned on the true stability of the fracture, Garden classifications I and II without posterior or anterior tilt 40, 41 and the relatively good bone quality for the anchor of the internal fixation tools. There is no reported superior long-term outcome of arthroplasty compared to internal fixation 42, 2, 7.
Internal fixation may be the preferred treatment for physiologically fit elderly patients with Garden I and II, with posterior tilt <20°, good bone quality, independent ambulation, and reasonable life expectancy. Primary arthroplasty should be considered when the probability of fixation failure is high. It is indicated when posterior tilt >20° (Okike K et al. 2019, Papadelis E et al. 2023), associated severe osteoporosis, frailty, and poor compliance of the patient, and pre-existing hip osteoarthritis. Age >80 years with multiple risk factors is also an indication. Arthroplasty did not show superior long-term outcomes compared to internal fixation of non-displaced femoral neck fractures.
For displaced (Garden III/IV) fractures neck femur in ambulatory or functionally independent elderly patient, HA or THA is strongly recommended over internal fixation. (Strong Recommendation, High quality evidence:).
Fixation is associated with high failure rates (25–40%), frequent reoperations, and inferior functional outcomes. Compared with the internal fixation group, patients that underwent hemiarthroplasty had a lower reoperation rate and an equivalent overall mortality rate 7,37,43-45
1. Patient was non ambulatory pre fracture (bedbound or wheelchair- dependent)
2. Life expectancy is less than 12 months (metastatic cancer, end stage organ failure)
3. High surgical risk (ASA IV, not optimized despite best efforts)
In ambulatory patient with unstable fractures femoral neck, Arthroplasty is recommended over fixation
Arthroplasty is preferred when:
1. Patient is active and can benefit from better functional outcomes
2. Minimizing reoperation risk is a priority
3. Patient needs faster return to walking with less pain
Internal Fixation may be considered when:
1. Patient has low activity levels or advanced dementia
2. Patient has limited life expectancy
3. High surgical risk Favors shorter procedure time
Important Notes:
1. Mortality rate is similar in both groups (~25% at 1 year)
2. Decision should focus on expected quality of life rather than survival alone
3. Shared decision-making with patient/family is essential after explaining risks and benefits
1. Reoperation Rate 46
· Internal Fixation: Very high (26–32%)
· Arthroplasty: Low (6–9%)
· Relative Risk: 0.29 (Favors arthroplasty)
o This means the risk of reoperation is 3.4 times higher with internal fixation
2. Non-union/Avascular Necrosis (AVN)
· Internal Fixation: Common problem (20–40%)
· Arthroplasty: Very rare (<2%)
· Not applicable for relative risk calculation (too rare with arthroplasty)
3. 1-Year Mortality Rate
· Identical in both groups (~25%)
· No statistically significant difference
4. 1-Year Functional Outcomes
· Internal Fixation: Worse mobility, more pain
· Arthroplasty: Better walking ability, less pain
· Standardized mean difference: +0.4 (Favors arthroplasty)
Use a femoral stem design other than Austin Moore or Thompson stems for arthroplasties. Unipolar (Austin Moore or Thompson) prosthesis should be used in strictly limited conditions, e. g. Unavailable bipolar prosthesis. (Good practice statement, Moderate quality evidence:)
Where the unipolar head has a single articulation between the prosthesis and the acetabulum, the bipolar head offers a second articulation between an inner smaller head and the polyethylene liner of the larger outer head. In theory this reduces stress on the acetabular surface and thereby acetabular erosion. Acetabular erosion is believed to cause pain and impaired hip function.
RCTs comparing unipolar and bipolar, showed better Health-related quality of life and hip function for bipolar. The average four years follow-up showed less acetabular erosion by using bipolar47-53.
In spite that both replace the femoral head for hip fractures, but bipolar's dual articulation aims for better preservation of the natural socket (acetabulum), and for a better range of motion
Recommendation 1: For fit, active elderly patients (≥60 years) with displaced femoral neck fractures, Total Hip Arthroplasty (THA) is suggested rather than Hemiarthroplasty (HA) to improve function and reduce revision risk. (Conditional recommendation, Moderate quality evidence)
Recommendation 2: For frail, medically complex, or cognitively impaired patients with limited mobility, Hemiarthroplasty (HA) may be preferred due to shorter operative time and reduced perioperative risk. (Conditional recommendation, Moderate quality evidence)
Recommendation 3: Decisions should incorporate individual patient comorbidities, cognition, pre-fracture mobility, surgical risk, and patient preference. (Strong recommendation, Moderate quality evidence)
The pathways below integrate evidence
quality with clinical risk stratification to provide
decision support.![]()
Pathway A: Fit, Active Elderly (>60, Independent, Low Comorbidity)
Goal: Maximize postoperative function and quality of life.
Recommendation:
· Total Hip Arthroplasty (THA) preferred.
Rationale:
Considerations:
Pathway B: Medically Complex, High Surgical Risk (≥60, Multiple Comorbidities, Frailty)
Goal: Minimize perioperative risk and complications.
Recommendation:
· Hemiarthroplasty (HA) preferred.
Rationale:
Pathway C: Intermediate Risk (Moderate Comorbidity, Ambulatory but Dependent)
Goal: Balance function and surgical risk.
Recommendation:
· Consider HA if frailty is significant; THA if moderate comorbidity but preserved cognition and activity.
Rationale:
The evidence suggests that THA provides slightly better functional outcomes and quality of life than HA, with comparable revision rates and mortality. HA, however, may be preferable in patients with higher surgical risk due to shorter operative time and lower dislocation risk.
A. Functional Outcomes and Quality of Life
|
Outcome |
Evidence Source |
Effect |
Certainty (GRADE) |
Comments |
|
Hip function (Harris Hip Score) |
RCTs + Meta-analyses |
THA modestly higher HHS at 1–5 years |
Moderate |
Meta-analyses show small functional benefit with THA44. |
|
Patient-reported quality of life |
Systematic reviews |
Slightly better with THA |
Moderate |
Data from multiple systematic reviews show improved EQ-5D metrics for THA56. |
|
Early mobility / pain |
RCTs (e.g., NEJM trial) |
Trend favouring THA |
Low-Moderate |
Individual RCTs suggest better early function and pain control with THA58. |
B. Revision and Reoperation
|
Outcome |
Evidence Source |
Effect |
Certainty (GRADE) |
Comments |
|
Revision / Reoperation rates |
Meta-analyses (25 RCTs) |
THA lower or similar |
Moderate |
Some analyses find lower revision with THA; others find no significant difference54. |
|
Mid-term implant survivorship |
RCT/registry analyses |
Comparable |
Moderate |
Registry and trial data suggest similar survivorship up to ~5 years59. |
C. Complications and Risks
|
Outcome |
Evidence Source |
Effect |
Certainty (GRADE) |
Comments |
|
Dislocation |
Observational analyses |
Slightly higher with THA |
Moderate |
Large cohort data show increased dislocation risk with THA (absolute difference small)55. |
|
Operative time |
Meta-analyses |
Longer with THA |
Moderate |
Consistent finding: THA takes longer than HA56. |
|
Mortality |
Meta-analyses |
No clear difference |
Low |
Mortality differences not consistently significant60. |
|
Periprosthetic fracture / infection |
Meta-analyses |
Similar |
Low-Moderate |
Complication trends similar across groups56. |
4. Summary of Evidence
|
Outcome |
Direction of Effect (THA vs HA) |
Magnitude |
Certainty (GRADE) |
Source |
|
Functional outcome (Harris Hip Score) |
THA > HA |
Small–moderate improvement |
Moderate |
RCT meta-analyses (n > 3000) |
|
Health-related quality of life (EQ-5D) |
THA > HA |
Small benefit |
Moderate |
RCT & systematic reviews |
|
Reoperation / Revision |
Similar or lower with THA |
Minimal difference |
Moderate |
RCT + registry |
|
Dislocation |
Higher with THA |
1–2 % absolute increase |
Low–Moderate |
Observational + registry |
|
Operative time |
Longer with THA |
+20–30 min on average |
Moderate |
RCT pooled |
|
Mortality (30–90 days) |
No difference |
Neutral |
Low |
Pooled analyses |
|
Long-term implant survival |
Comparable |
Neutral |
Moderate |
Registry data |

Figure 1: Forest plot summarizing comparative outcomes for THA versus HA across revision rate, functional outcome, dislocation, and mortality
|
Outcome |
No. of Studies (RCTs) |
Participants (n) |
Relative Effect (95% CI) |
Absolute Effect (per 1000) |
Certainty (GRADE) |
|
Revision/Reoperation44,56 |
25 RCTs |
~3,100 |
RR 0.67 (0.48–0.93) |
70 → 47 fewer events |
Moderate |
|
Functional Outcome58,61 |
18 RCTs |
~2,800 |
SMD 0.59 (0.04–1.08) |
+4 HHS points |
Moderate |
|
Dislocation56,58 |
16 RCTs + registries |
>10,000 |
RR 1.25 (0.81–1.91) |
+4 events per 1000 |
Low |
|
Mortality44,56 |
22 RCTs + observational |
>12,000 |
RR 0.94 (0.81–1.09) |
No difference |
Low–Moderate |
Fit, Active Elderly Patients Population:
Patients ≥60 years, cognitively intact, ambulatory, independent, with low
surgical risk (ASA I–II).
Recommendation: Perform total hip arthroplasty (THA) rather than hemiarthroplasty to optimize function and quality of life.
Rationale:
Implementation notes:
Frail or Medically Complex Patients Population:
Patients ≥75 years, frail, with multiple comorbidities (ASA III–IV), limited ambulation, or cognitive impairment.
Recommendation: Perform hemiarthroplasty (HA) rather than total hip arthroplasty to minimize operative risk.
Rationale:
Implementation notes:
Intermediate Risk / Mixed Profile Population:
Patients with moderate comorbidities (ASA II–III), ambulatory with aids, or
mildly dependent.
Recommendation: Individualize the choice based on cognitive status, pre-fracture activity, and surgical expertise.
Rationale:
Implementation Considerations
Cemented stem implants are preferred in patients undergoing surgery with arthroplasty. (Conditional recommendation, High quality evidence)
The use of cement in arthroplasty has the potential to secure the implant in an osteoporotic patient and reduce the need for revision secondary to loosening of the prosthesis.
Evidence based studies and RCTs showed that cemented fixation in THA after hip fractures is associated with lower revision rates, but similar mortality compared to cementless fixation62-68
Some concerns exist around the use of cement and the possibility of bone cement implantation syndrome. Bone cement implantation syndrome is a poorly understood phenomenon which is characterised by one or more of the following: hypoxia, hypotension, cardiac arrhythmias, increased pulmonary vascular resistance and cardiac arrest. It can occur at a number of stages during an arthroplasty including during femoral reaming, insertion of cement or the prosthesis and at the time of reduction of the joint. Its exact aetiology and pathophysiology remain poorly understood as does an accurate figure of the true incidence of the syndrome.
In patients undergoing treatment of femoral neck fractures with hip arthroplasty, evidence does not show a favoured surgical approach. Select approach based on surgeon’s experience and preference (Good practice statement)
The data in newer studies show no difference in the dislocation rates between the different surgical approaches, including the posterior approach. This contrasts with the earlier data in older publications which showed higher dislocation rate with the posterior approach in comparison to the lateral approach.
One high quality study69, seven moderate quality studies70-76 and two low quality studies77,78 were included in the evidence for this recommendation.
The high-quality study75 compared hemiarthroplasty with the anterolateral approach to hemiarthroplasty with the direct lateral approach and reported that while there were elevated levels of serum creatine kinase (CK) observed in the anterolateral approach group, no correlation between CK levels and the Timed Up and Go test or the Trendelenburg sign at 3 months were found.
There were also 8 citations about surgical approach in the surgical treatment of femoral neck fractures with moderate evidence strength. Jianbo (2019)70 reported on a prospective, randomized study of 100 patients. They specifically compared the clinical outcomes and complications of using either the conventional posterior approach, or with using a minimally invasive surgery (MIS) and muscle preserving approach (the Suprapath approach). There was less blood loss, and low transfusion rate in the MIS group. There was less pain, and better function within the first week in the minimally invasive group, but no differences between the groups at the 3-month interval. Repantis (2015)73 reported on the comparative results of a prospective, randomized study in 80 patients using either a MIS approach or in using the posterior approach. It was a single-surgeon series. There was less pain in the MIS group in the short term. There was no difference in any of the other outcomes or complications up to 4 years of follow up. In another comparative study, Saxer (2018)74 reported on the results of 190 patients using either a MIS or using the lateral approach. There was less pain, and faster ambulation in the first 3 weeks in the MIS group. There was no difference in any of the other outcomes, or in the complications between the groups. Verzellotti (2019)76 reported on the comparative results of using the direct anterior (DA) which is muscle preserving, or in using the posterior approach in 100 patients. There was less pain in the DA group in the first month after surgery. There was no difference in the other outcomes or complications between the groups. The operative time was longer in the DA group. Parker (2015)72 reported the comparative results of a multi-centre, prospective, randomized study in 216 patients using either the posterior or the lateral approach. There was no difference in any of the outcome measures analyzed between the groups. In a prospective, randomized study in 150 patients, Ugland (2018)69 reported higher risk of post-surgery Trendelenburg gait when the arthroplasty was done using the lateral approach in contrast to using the anterolateral approach (more abductor muscle preserving). Two low strength articles77,78 (Biber 2012, Skoldenberg 2010) compared the posterior approach to the direct lateral approach for performing arthroplasty in the patients with femoral neck fractures. While neither of the included studies specifically addressed any functional outcomes, they both demonstrated statistically significant differences in dislocation rates, favouring the direct lateral approach.
The existing evidence does not support superiority of one surgical approach. Future well designed RCTs should include a comparison of the anterior approach with the posterior and the lateral approach. Any future studies related to surgical approach should also include pain and functional data associated with the approaches. This may have important implications for patient selection and recovery needs such as assistive devices or therapy needs.
In patients with stable intertrochanteric fractures, use of either a sliding hip screw or a cephalomedullary device is recommended. Use a dynamic hip screw (DHS) in preference to an intramedullary nail in patients with stable intertrochanteric fractures (Strong recommendation, High quality evidence)
Stable trochanteric fractures are simple two-part intertrochanteric fractures with posteromedial cortical continuity and lateral wall integrity. This fracture pattern is considered stable as it will resist medial compressive loads once reduced.
Sliding hip screw versus intramedullary nail for trochanteric fracture
Parker et al. (2012)79 compared the sliding hip screw with the Targon PF intramedullary nail in the treatment of 600 cases of trochanteric hip fracture among 598 patients (mean age=82 years, 80% women). Patients were randomised to treatment with a sliding hip screw or intramedullary nail, and all operations were either performed or supervised by a single orthopaedic surgeon. Patients were reviewed 6 weeks after discharge, and followed up at 3, 6, and 12 months after injury by a research nurse blinded to treatment.
There were no significant differences between groups for total hospital stay (p=0.3), wound healing complications (p=1), other fracture-related complications (p values ranging from 0.12 to 1), loss of hip flexion (p=0.31), or shortening (p=1) at 6 weeks. There were also no significant differences between groups at 1 year for mortality (indicated by Kaplan-Meier curve) or pain (p=0.26). There was, however, a significantly greater recovery of mobility at 1 year with intramedullary nail versus sliding hip screw (difference in mobility score of approximately 0.5 on a scale from 0 to 9, p=0.01).
Cai et al. (2016) 80 in a prospective, randomised blinded study included patients aged over 65 years with stable intertrochanteric fractures (Evans grades I and II). The patients were allocated to one of two groups treated via extramedullary or intramedullary fixation. Extramedullary (compared with intramedullary) fixation of stable intertrochanteric fractures significantly reduces perioperative blood loss but affords similar functional outcomes and times to union. In view of the morbidity and complications associated with acute anaemia and transfusions, extramedullary fixation may be the optimal choice for treatment of stable fractures, being associated with reduced blood loss.
Lewis et al. (2022)81 included randomised controlled trials (RCTs) and quasi-RCTs comparing cephalomedullary nails with extramedullary implants for treating fragility extracapsular hip fractures in older adults. They concluded that Extramedullary devices, most commonly the sliding hip screw, yield very similar functional outcomes to cephalomedullary devices in
the management of extracapsular fragility hip fractures. There is a reduced risk of infection and non-union with cephalomedullary nails; however, there is an increased risk of implant-related fracture that is not attenuated with newer designs.
Sliding hip screw versus proximal femoral locking compression plate for stable intertrochanteric fracture
Zhong B et al. (2014) 82 compared proximal femoral locking compression plate (PFLCP) and DHS fixation in intertrochanteric fractures. They concluded that PFLCP can offer better functional outcomes and fewer complications for subtrochanteric femoral fractures. DHS fixation is preferable for stable intertrochanteric fractures. For unstable intertrochanteric fractures, the value of PFLCP fixation needs to be confirmed by further clinical studies.
Stable trochanteric fractures have posteromedial continuity and have lateral wall integrity that enables these fractures to resist compressive medial loads, and if they are well reduced and varus reduction is avoided, both intramedullary and extramedullary implants will maintain the fracture reduction and resist failure. This will allow early weight bearing of patients, whether they are operated upon by intramedullary or extramedullary implant. The cost of cephalomedullary devices is generally more than sliding hip screw fixation in most institutions. Cephalomedullary nail fixation reduces the length of hospital stay and fewer complications (Xu 2018), which can decrease the overall costs with cephalomedullary devices.
In patients with unstable intertrochanteric fractures, the use of cephalomedullary device is recommended. (Strong recommendation, High quality evidence)
Unstable trochanteric fractures are fractures with comminution, posteromedial fragment, deficient lateral wall, reversed oblique, and subtrochanteric extension. This fracture pattern is considered unstable as it will drift into varus and/or medialization with exposure to compressive loads.
In a systematic review and meta-analysis conducted by Zeelenberg ML et al. (2024)83, current literature shows that several functional outcomes, complications, and surgical outcomes were statistically in favor of intramedullary fixation when compared with extramedullary fixation of AO/OTA 31-A2 fractures. However, as several of the differences found appear not to be clinically relevant and for many outcomes data remains sparse or heterogeneous, complete superiority of IM fixation for AO type 31-A2 fractures remains to be confirmed.
Kassem et al. (2022)84, in another systematic review and meta-analysis to compare DHS with trochanter stabilizing plate (TSP) and short proximal femoral nails (PFNs) in unstable trochanteric fractures in terms of the functional and radiological outcomes. They concluded that the use of PFN in unstable trochanteric fractures was associated with a shorter time until union and a faster return to the pre-fracture level of activity than the DHS+TSP. However, postoperative hip function, walking independence, as well as complication and one-year mortality rates were comparable. Based on these findings, they suggested that PFN is the first-choice implant for the unstable (AO/OTA 31-A2) intertrochanteric fractures.
Lewis et al. (2022), in a systematic review, included older adults with both stable and unstable extracapsular fractures. Their findings indicate that there may be no difference between cephalomedullary nails versus dynamic fixed-angle plates
Proximal femoral locking compression plate versus intramedullary nailing for unstable intertrochanteric fracture
Zhong B et al. (2014)82 concluded that in unstable intertrochanteric fractures, the value of PFLCP fixation needs to be confirmed by further clinical studies. Fixation with an intramedullary nail is still the best option for patients with unstable intertrochanteric fractures; however, controlled studies are needed.
Zhang S et al. (2025)85 conducted a systematic review and meta-analysis of randomized controlled trials with the aim of summarizing the latest evidence for the effectiveness and safety of a variety of implants for fixation of intertrochanteric fractures. They concluded that InterTAN nail (ITN) clearly reduces the incidence of non-mechanical major post-surgery complications and non-specific mechanical complications; however, it is associated with an increased risk of intraoperative complications. No differences were observed between SHS and other implants regarding Harris hip score, reoperation rate, and overall mechanical complications. Most comparisons evaluating the efficacy of these implants are supported by moderate confidence of evidence. Further large-scale, longitudinal, randomized controlled trials are necessary to provide more robust and consistent evidence.
Unstable intertrochanteric fractures are fractures that may have comminution, posteromedial fragment, deficient lateral wall, reversed oblique, or subtrochanteric extension. This fracture pattern is considered unstable as it will drift into varus and/or medialization with exposure to compressive loads. Fixation with an intramedullary nail is still the best option for patients with unstable intertrochanteric fractures, as it is biomechanically superior to an extramedullary implant.
In patients with subtrochanteric or reverse obliquity fractures a cephalomedullary device is recommended. (Strong recommendation, High quality evidence)
Reverse obliquity fractures are a subset of intertrochanteric/peritrochanteric fractures that are an unstable pattern. Though subtrochanteric fractures are more of a proximal femur fracture, they can be a component of an intertrochanteric fracture as well.
Xie et al. (2019) 86 in a meta-analysis suggested that intramedullary fixation for subtrochanteric fracture might be superior to extramedullary fixation in terms of shorter operation time, less intraoperative blood loss, shorter length of incision, length of stay, and better functional outcomes. Meanwhile, intramedullary fixation had a lower rate of fixation failure and reoperation. Therefore, intramedullary fixation is recommended as the treatment of subtrochanteric fractures. Larger multi-centre and high-quality RCTs are required for further research.
The results of a meta-analysis conducted by Wang J et al. (2020)87 revealed that intramedullary fixation can confer shorter union time, lower non-union, and reoperation rates compared with extramedullary fixation. They considered intramedullary nailing as the first selection for the treatment of patients with subtrochanteric fractures.
Plating may be considered in select cases, such as periprosthetic fractures, proximal deformities, or salvage situations.88
Intramedullary nailing is the implant of choice in subtrochanteric fractures and reverse obliquity fractures. It is biomechanically superior to a surface implant.
A blood transfusion threshold of no higher than 8g/dl is suggested in asymptomatic postoperative hip fracture patients. (Conditional recommendation, Moderate quality evidence)
Moderate-strength evidence suggests that restrictive transfusion practices reduce utilization of transfusions and may decrease infections without increasing adverse outcomes in major orthopaedic surgery. 89-93
1. Hemodynamic status (stable/unstable)
2. Haemoglobin (Hb) level
3. Symptoms of anaemia (tachycardia, hypotension, dyspnoea, chest pain, dizziness)
4. Cardiovascular comorbidities
· Hb < 8 g/dL → transfuse
· Hb 8–10 g/dL → transfuse if symptomatic or high cardiac risk
· Hb >10 g/dL → no transfusion, monitor
· Restrictive strategy preferred
· Number of units per transfusion (usually 1 unit at a time, reassess Hb)
· Monitor for transfusion reactions
· Post-transfusion Hb
· Re-evaluate symptoms
· Repeat transfusion only if Hb < 8 g/dL or persistent symptoms
· Ensure hemodynamic stability
· Correct coagulopathy if present
· Proceed to surgery once stable
· Non-operative/palliative care for patients with limited life expectancy or refusal of transfusion
· Consider erythropoietin or iron supplementation if appropriate
When an elderly hip-fracture patient needs transfusion but refuses 93-96
· Assess and document decision-making capacity.
· Clearly explain:
· Why blood may be needed
· Risks of refusing transfusion (anaemia, cardiac events, death)
· Available alternatives
· Obtain written informed refusal (ideally with a witness).
· If the patient lacks capacity → follow advance directives or legally authorized surrogate.
If the patient has capacity, their refusal must be respected, even if life-threatening.
Many patients who refuse “blood” may accept:
· Cell salvage (closed circuit)
· Acute normovolaemic haemodilution
· Albumin
· Coagulation factors (e.g., fibrinogen, PCC)
· Erythropoietin
· Iron therapy
Do not assume refusal of all blood products — ask and document precisely.
If surgery can be delayed safely (24–48 h max in hip fractures):
· IV iron (e.g., ferric carboxymaltose)
· Erythropoietin (EPO)
· Folic acid + vitamin B12
· Minimize blood sampling
Surgical
· Prefer hemiarthroplasty over THA when appropriate
· Cemented stems (shorter operative time)
· Meticulous haemostasis
· Minimize operative time
Anaesthetic
· Regional anaesthesia (spinal) if feasible
· Controlled hypotension (careful in elderly)
· Tranexamic acid (TXA) — IV ± topical
· TXA significantly reduces blood loss in hip fracture surgery
· Cell salvage if acceptable
· Maintain normothermia
· Restrictive transfusion thresholds (already transfusion-free)
· Tolerate lower Hb if patient is asymptomatic
· Oxygen therapy
· Treat anaemia aggressively with iron/EPO
· Early mobilization to reduce complications
· Autonomy overrides beneficence in a competent adult
· Forced transfusion = assault
· Thorough documentation protects both patient and physician
· Involve:
· Ethics committee (if available)
· Hospital legal team (high-risk cases)
A restrictive red blood cell transfusion strategy is supported by high-quality evidence in elderly patients with hip fractures. Randomized controlled trials, including the FOCUS trial92, demonstrated that transfusing asymptomatic patients only when hemoglobin falls below 8g/dL does not increase mortality, cardiovascular complications, functional recovery impairment, length of hospital stay, or loss of independent ambulation compared with a liberal transfusion strategy.
International guidelines, including those from the AABB93, NICE91, and AAOS2, therefore recommend a restrictive transfusion threshold for most elderly hip fracture patients, while emphasizing that symptomatic anemia, ongoing bleeding, hemodynamic instability, or evidence of tissue hypoxia may justify transfusion at higher hemoglobin levels.
For patients who decline blood transfusion, patient blood management measures such as intravenous iron, erythropoietin, tranexamic acid, meticulous surgical hemostasis, minimization of phlebotomy, optimization of oxygen delivery, and early mobilization are recommended to reduce transfusion requirements.
The evidence supporting a restrictive transfusion threshold in elderly hip fracture patients2,7,91-93,97,98 is considered high quality, with strong consistency across randomized trials and major international guidelines.
A restrictive transfusion strategy is recommended for most elderly patients with hip fractures. Current high-quality evidence demonstrates that using a haemoglobin threshold of 8 g/dL (unless the patient is symptomatic or has ongoing bleeding) is safe and effective. Compared with a liberal transfusion strategy, it does not increase:
· 30- or 60-day mortality
· Cardiovascular complications
· Functional recovery
· Independent walking ability
· Length of hospital stay
· Discharge destination
Restrictive transfusion also reduces unnecessary exposure to blood products and transfusion-related complications while conserving healthcare resources (Annex 7: Blood transfusion in elderly hip fracture patients (flowchart)).
Tranexamic acid should be administered to reduce blood loss and blood transfusion in patients with hip fractures. (Strong recommendation, High quality evidence)
Tranexamic acid was not associated with higher incidence of mortality or symptomatic thromboembolic events.
· Confirm hip fracture requiring surgery (intracapsular or extracapsular)
· Age > 65 years
· Check for contraindications:
o Active thromboembolic disease (DVT, PE)
o History of stroke or myocardial infarction within 6 months
o Active intravascular clotting disorder
o Known hypersensitivity to TXA
o Severe renal impairment
· IV TXA is preferred
· Typical regimen:
o Bolus: 1 g IV preoperatively (within 30 min before incision)
o Optional second dose: 1 g IV postoperatively or infusion over 8 hours in high-risk bleeding patients
· Adjust dose for renal impairment
· Preoperative: ideally at induction of anaesthesia
· Some protocols allow additional intraoperative/topical dose if significant bleeding risk
· Watch for thromboembolic complications
· Monitor haemoglobin postoperatively
· Assess need for transfusion
· Early mobilization
· Thromboprophylaxis as per institutional protocol (e.g., LMWH or DOAC)
· Reassess bleeding risk and renal function
· Avoid TXA if active clotting risk or severe renal impairment
· Consider alternative blood conservation strategies
High-quality evidence demonstrates that tranexamic acid (TXA) significantly reduces perioperative blood loss and the need for allogeneic blood transfusion in elderly patients undergoing hip fracture surgery without increasing the risk of venous thromboembolism (VTE), myocardial infarction, stroke, or all-cause mortality99-101.
Multiple randomized controlled trials102 and meta-analyses99-101 have consistently shown reductions in total blood loss (approximately 200–400 mL) and transfusion rates (relative reduction of approximately 30–50%) compared with placebo or standard care. These benefits are observed across different surgical procedures, including hemiarthroplasty, total hip arthroplasty for fracture, and internal fixation.
Current evidence indicates that both intravenous and topical TXA are effective. Intravenous administration is supported by the largest body of evidence, while topical TXA provides a reasonable alternative when systemic administration is contraindicated. No clear superiority of one route over the other has been demonstrated.
Large observational studies and systematic reviews have found no significant increase in symptomatic deep vein thrombosis, pulmonary embolism, myocardial infarction, stroke, or mortality when TXA is used in appropriately selected patients receiving standard thromboprophylaxis.
Based on the consistency of evidence, major international organizations, including the American Academy of Orthopedic Surgeons (AAOS)2 and the National Institute for Health and Care Excellence (NICE)7, recommend considering routine TXA administration in hip fracture surgery unless contraindications exist.
Strength of Evidence
|
Outcome |
Quality of Evidence |
Overall Conclusion |
|
Reduction in perioperative blood loss |
High |
Significant reduction |
|
Reduction in blood transfusion |
High |
Significant reduction |
|
Reduction in postoperative hemoglobin drop |
High |
Significant benefit |
|
Risk of DVT/PE |
High |
No significant increase |
|
Risk of myocardial infarction or stroke |
Moderate–High |
No significant increase |
|
Mortality |
Moderate |
No increase in mortality |
|
Length of hospital stay |
Moderate |
Little or no consistent benefit |
Guideline Statement
High-certainty evidence supports the use of tranexamic acid in elderly patients undergoing hip fracture surgery. TXA consistently reduces perioperative blood loss and transfusion requirements without increasing thromboembolic or cardiovascular complications when used with standard venous thromboembolism prophylaxis. Therefore, routine perioperative administration of TXA should be considered in the absence of contraindications (Annex 8: Tranexamic acid (TXA) in elderly hip fracture patients).
Patients with hip fractures may benefit from TXA to reduce blood loss and subsequent transfusion. Use of tranexamic acid in hip fracture patients may result in lower blood loss and transfusion rates compared to placebo in several high-quality studies. Studies were unable to detect any difference in adverse events with use of tranexamic acid such as infection, wound complication, DVT, CVA, PE or MI7,37,102-107
On admission, offer patients a formal, acute orthogeriatric or orthopaedic ward-based fracture program that includes the following steps:
· Comprehensive orthogeriatric assessment to evaluate both current and baseline level of functioning
· Rapid optimization to make patient fit for surgery
· Identify individual goals for multidisciplinary rehabilitation to recover mobility and independence, and to achieve return to pre-fracture residence when possible
· Offer longitudinal, coordinated, orthogeriatric and multidisciplinary review
· Provide liaison or integration with related services, particularly mental health (delirium prevention), falls prevention, bone health, primary care and social services
· Clinical and service governance responsibility for all stages of the pathway of care and rehabilitation, including those provided in the community.
(Conditional recommendation, High quality evidence)
It is a comprehensive interdisciplinary evidence-based model of immediate and longitudinal interdisciplinary assessment, management and discharge planning7. Instead of the traditional model of orthopaedic care followed by routine transfer for rehabilitation elsewhere (e.g. orthopaedic or general rehabilitation units), interdisciplinary model provides many benefits including expediting and organizing both assessment and care in the acute hospital, promoting prompt discharge (wherever possible) to the patient’s normal home setting. It is more cost-effective compared to traditional model as established following the latest NICE CG124 (Clinical Guideline 124) evidence review7,108.
Prompt, effective analgesia, anaesthesia and surgery, coordinated with structured, medical and multidisciplinary management from presentation to hospital discharge, are therefore needed and have been shown to deliver improved outcomes cost-effectively7.
The medical and multidisciplinary ‘ortho-geriatrician’ role was developed by physicians in clinical gerontology but is applicable to the care of hip fractures in adults of all ages109.
A RCT (Randomized Clinical Trial)110 of 199 patients analysed admittance to a geriatric rehabilitation ward (comprising a geriatric team applying comprehensive geriatric assessment) versus regular orthopaedic care immediately postoperative to hip fracture surgery. Patients randomized to geriatric ward had less postoperative delirium (being shorter in those who developed it), fewer pressure ulcers, less malnutrition, fewer urinary tract infections, fewer falls, fewer new fractures during hospitalization, shorter hospital length of stay, and a 3-fold odds ratio of walking independently 1 year after. They also found that the best effect was seen in patients with dementia.
Another RCT111 of 459 patients with hip fracture compared orthogeriatric co-management versus care by a geriatric consultant team versus standard orthopaedic care. Compared with standard care and geriatric consultant team care, orthogeriatric care showed significantly better outcomes in terms of time-to-surgery and in-hospital medical complications. Versus standard care, orthogeriatric care was also associated with significant reductions in hospital length of stay and in-hospital mortality.
Ortho-geriatric team involvement in care provision for hip fracture patients from admission to discharge reduces complications, improves both in-hospital and long-term outcomes and reduces cost of care.
In patients undergoing surgical stabilization of hip fractures, early mobilization, including functional movement within 24–48 hours postoperatively is recommended, provided the patient is medically and mobilization is consistent with the surgeon’s postoperative instructions (Strong recommendation, High quality evidence)
Mobilization should begin with bed mobility and progress to sitting, standing, and assisted ambulation as tolerated. Progression should be individualized according to pain levels, hemodynamic stability, cardiopulmonary status, and overall medical condition. Delays in mobilization may be necessary in cases of medical instability but should be minimized whenever possible.
Multiple randomized controlled trials112 and systematic reviews113,114 have consistently demonstrated that early mobilization following hip fracture surgery is associated with reduced postoperative complications, including pneumonia, thromboembolic events, delirium, and pressure injuries. Early mobilization has also been shown to improve functional recovery, reduce length of hospital stay, and enhance the likelihood of returning to pre-fracture mobility levels. Across studies, mobilization initiated within the first 24–48 hours is superior to delayed mobilization strategies.
Early mobilization mitigates the adverse physiological effects of prolonged bed rest, supports cardiovascular and pulmonary function, and promotes neuromuscular activation necessary for recovery of mobility, independence, and overall functional outcomes.
Following hip fracture surgery, weight-bearing should be initiated as early as clinically feasible, with full weight-bearing as tolerated recommended after stable fixation, unless contraindicated by surgical or patient-specific factors (Conditional recommendation, Low quality evidence)
In cases of uncertain fixation stability, complex fracture patterns, or compromised bone quality, temporary partial or restricted weight-bearing may be considered. Decisions should be guided by operative findings, implant stability, surgeon recommendations, patient cognitive status, and safety within the rehabilitation environment.
Available evidence, primarily from observational studies115 and cohort analyses2,116-118, suggests that early weight-bearing after stable fixation does not increase the risk of implant failure, non-union, or reoperation. Several studies report improved functional outcomes and earlier return to ambulation with early weight-bearing strategies119. However, high-quality randomized controlled trials specifically comparing weight-bearing protocols after hip fracture surgery remain limited.
Early weight-bearing facilitates functional recovery, improves patient confidence during ambulation, and reduces complications related to immobility, while allowing clinicians to individualize care based on surgical stability and patient safety considerations.
Rehabilitation after hip fracture surgery should follow a structured, phased pathway, spanning the acute inpatient phase, home or inpatient rehabilitation services, and outpatient rehabilitation, aligned with the patient’s recovery stage and care setting (Conditional recommendation, Low Quality evidence)
The rehabilitation pathway should prioritize early mobility and functional independence during hospitalization, followed by progressive strengthening, balance training, and gait restoration after discharge. Coordination among healthcare providers across settings is essential to ensure continuity of care.
Studies evaluating multidisciplinary and continuity-based rehabilitation models120,121 demonstrate improvements in mobility, functional outcomes, and discharge disposition. However, variability in rehabilitation protocols, intensity, and care settings limits the ability to identify a single optimal pathway. Evidence supports the concept of structured progression rather than any specific standardized protocol.
A structured rehabilitation pathway ensures continuity of care, promotes timely progression of functional goals, optimizes resource utilization, and addresses the evolving physical and functional needs of patients recovering from hip fractures.
Fall prevention strategies should begin with identification and management of underlying fall risk factors, including muscle weakness, balance deficits, cognitive impairment, medication-related side effects, orthostatic hypotension, visual impairment, and environmental hazards. These strategies should be systematically integrated into all phases of postoperative rehabilitation following hip fracture surgery (Conditional recommendation, High quality evidence)
Fall prevention interventions should include fall risk assessment, balance and strength training, home based exercise program, medication review, environmental hazard modification, vision assessment, and appropriate prescription and training in assistive device use.
Strong evidence from randomized controlled trials and meta-analyses122-124 demonstrates that multifactorial fall prevention programs significantly reduce fall risk in older adults. Although many studies include broader geriatric populations, evidence supports similar benefits in individuals recovering from hip fracture, who are at particularly high risk for recurrent falls and secondary fractures.
Patients recovering from hip fractures are vulnerable to recurrent falls due to residual weakness, balance impairment, and fear of falling. Addressing modifiable risk factors is essential to ensure long-term safety, preserve functional gains, and prevent secondary injuries.
Standardized functional and mobility outcome measures, such as the Timed Up and Go Test (TUG test), should be used regularly to guide rehabilitation progression and monitor recovery after hip fracture surgery. (Conditional recommendation, Low quality evidence)
Outcome measures should be feasible, clinically meaningful, and sensitive to change in older adults. Assessments may include measures of mobility, balance, gait performance, activities of daily living, and pain.
Although outcome measures such as gait speed, Timed Up and Go, and functional mobility scales are widely used in clinical practice and research, evidence supporting the superiority of any single tool in guiding rehabilitation outcomes remains limited. Current evidence125,126 supports consistent and repeated use of standardized measures rather than reliance on subjective assessment alone.
Regular outcome assessment facilitates individualized goal setting, enhances communication among care providers, and allows early identification of delayed recovery, complications, or need for modification of the rehabilitation plan.
Discharge planning should begin early during hospitalization and be individualized based on medical stability, functional recovery, cognitive status, family support, and access to rehabilitation services. In the Egyptian healthcare setting, most patients require a short inpatient stay followed by home-based or facility-based rehabilitation. Early discharge within 24–48 hours may be considered for selected, medically stable patients with adequate family support and rehabilitation access. Same-day or next-day discharge should be limited to exceptional cases. (Conditional recommendation, Low quality evidence)
Discharge planning should address discharge destination, functional readiness (safe transfers and assisted ambulation), caregiver education, provision of walking aids, and coordination of outpatient or home-based rehabilitation. Family caregivers play a central role in post-discharge care in Egypt and should be included early in planning and education.
Hip fracture specific randomized evidence for same-day discharge is limited. Observational studies indicate that structured, early discharge planning improves care transitions and functional outcomes without increasing readmissions when rehabilitation continuity is ensured. Evidence from elective arthroplasty populations shows that same-day or 1-day discharge can be safe in selected patients, supporting a readiness-based rather than time-based discharge approach, though direct extrapolation to hip fracture patients should be cautious127,128.
Early and coordinated discharge planning reduces risks associated with prolonged hospitalization, including delirium and deconditioning, and supports safe transition to rehabilitation. Discharge timing should prioritize patient safety, caregiver preparedness, and continuity of rehabilitation rather than length of stay alone.
Following hip fracture surgery, appropriate assistive devices should be prescribed and regularly reassessed to support safe ambulation. A walker is recommended in the early postoperative phase, with progression to a cane held in the contralateral hand to the operated limb as balance, strength, and weight-bearing tolerance improve. (Good practice statement, Low quality evidence)
Assistive device selection should be individualized based on balance capacity, lower-limb strength, pain, cognitive status, and environmental demands. Proper fitting, patient education, and supervised training are essential. Transition from a walker to a cane should be guided by functional performance rather than time since surgery alone.
Systematic reviews and biomechanical studies demonstrate that walkers provide greater stability during early postoperative ambulation, while cane use improves gait efficiency during later recovery. Biomechanical evidence consistently shows that using a cane in the contralateral hand reduces hip joint reaction forces and hip abductor demand on the operated side. Clinical practice guidelines support this progression strategy, although randomized controlled trials specific to hip fracture populations remain limited126,129.
Assistive devices enhance safety and confidence during ambulation after hip fracture surgery. Using a cane in the contralateral hand optimizes biomechanical unloading of the operated hip, improves gait symmetry, and reduces fall risk while promoting progressive independenc
It is crucial to offer the patients (or when appropriate, their carers) information about their medical diagnosis and its implications and treatment options and management plan either verbally or in printed form (Good practice statement).
Family, friends and carers can provide support to patients to prepare for the first few weeks after discharge. From simple tasks like measuring the heights of patient’s bed, toilet and chair to providing physical and emotional support, the role of carers is important for the patients.
Decision making process must be based on information, involving family and carers can be crucial in cases where the patient is incapacitated due to delirium and can help as proxy in making informed medical decisions.
The care burden following hip fracture may decrease over time; however, it often lasts for over 12 months. Caregivers tend to experience the greatest stress for the first 2 months post-fracture, with the stress being associated with increased care demands and care cost130-133. Educating them beforehand sets realistic expectation to carers.
Providing clear information to patients and carers supports shared decision-making, treatment adherence, realistic expectations, and active participation in rehabilitation, ultimately contributing to safer and more patient-centred care. Details should include their exact diagnosis, choices available for analgesia and other medications, surgical procedures, choices of anaesthesia, possible complications, postoperative care and rehabilitation plans, short and long term expected outcomes and which healthcare professionals are involved7.