EHC has developed the present evidence-informed recommendations with a view to promoting the best possible clinical practices for the Prevention and Treatment of Hypertension in Pregnancy.
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Strength |
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Definitions And Classification |
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HDPs should be classified according to the criteria and definitions presented in “Glossary” |
GPS |
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Diagnose Hypertension in pregnancy when systolic blood pressure is ≥140mmHg and/or diastolic blood pressure is ≥90mmHg, based on the average of at least 2 measurements, taken at least 15minutes apart, using the same arm. |
Strong |
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Severe hypertension (sBP ≥ 160 and/or dBP ≥ 110 mmHg), can be confirmed within a short interval (minutes) to facilitate timely antihypertensive therapy |
Conditional |
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Gestational hypertension is hypertension that develops for the first time at > 20 weeks, without evidence of preeclampsia |
Conditional |
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Women with gestational hypertension should undergo testing for preeclampsia to rule it out. |
Strong |
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Diagnose preeclampsia in women with new onset hypertension after 20 weeks and new-onset proteinuria or one/more adverse conditions (defined as a maternal end organ complication or evidence of uteroplacental dysfunction) |
Strong |
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Strong |
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Do not use an elevation in BP to make a diagnosis of preeclampsia superimposed on chronic hypertension. |
Conditional |
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Risk factors |
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Risk factors for developing preeclampsia should be included in the antenatal assessment of all pregnant women. |
GPS |
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Screening |
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All pregnant women should be screened for their risk of developing preeclampsia early in the pregnancy. |
Strong |
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The screening tool utilized should be determined based on the locally available resources |
Conditional |
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Blood Pressure measurement |
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During every antenatal visit, screening for preeclampsia in pregnant women with blood pressure measurements throughout pregnancy is strongly recommended |
Strong |
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Testing For Proteinuria |
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Screen for proteinuria with urinary dipstick at first visit and at each subsequent visit |
Conditional |
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More definitive testing for proteinuria (by urinary protein:creatinine ratio or 24-hour urine collection) is encouraged when there is a suspicion of preeclampsia, including: ≥1+ dipstick proteinuria in women with hypertension and rising blood pressure and in women with normal blood pressure, but symptoms or signs suggestive of preeclampsia |
Conditional |
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When quantitative methods are not available or rapid decisions are required, a urine protein dipstick reading can be substituted using 2+ as the discriminant value |
Conditional |
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Proteinuria testing does not need to be repeated once significant proteinuria in the setting of confirmed pre-eclampsia has been detected |
Conditional |
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Biomarkers and ultrasonography screening |
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The use of a combined first trimester screen (combined maternal features, biomarkers and sonography) to identify women at risk of developing preeclampsia is conditionally recommended based on local availability and access to the required resources |
Conditional |
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Risk Reduction |
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Low dose Aspirin |
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To reduce the risk of developing preeclampsia, pregnant women with one high risk factor or two or more moderate risk factors for developing preeclampsia should receive low dose aspirin (100 mg -150 mg daily) beginning at 12 weeks gestation and till delivery. |
Strong |
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The use of aspirin at bedtime is conditionally recommended |
Conditional |
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Cessation of aspirin between 34 weeks gestation and birth is conditionally recommended. Exact timing of cessation should be based on individualized clinical judgment and informed, shared decision taking with the women |
Conditional |
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Oral calcium Supplementation |
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The use of supplemental calcium is strongly recommended in pregnant women with low dietary calcium intake (<1g/day) for the prevention of preeclampsia, preterm birth, and gestational hypertension |
Strong |
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Calcium supplementation at doses of 1.5–2.0 g elemental calcium/day is recommended from the first antenatal visit till delivery, to reduce the risk of developing preeclampsia |
Strong |
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Education |
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Pregnant women with hypertension or with risk factors for developing preeclampsia should be educated about the symptoms and signs that require immediate attention and referral to health care facilities. |
Strong |
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A clear referral plan should be discussed with each woman |
Conditional |
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Educate pregnant women to seek a healthcare professional immediately if they experience any of the symptoms of pre-eclampsia |
Strong |
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Exercise and diet |
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Moderate intensity exercise, in the form of aerobic, stretching and/or muscle resistance exercises, for a total of 2.5-5 hours a week, as recommended exercise regimen for general pregnancy wellbeing is encouraged. |
Conditional |
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What is Not recommended for risk reduction |
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Dietary salt restriction, for prevention of preeclampsia, is not recommended given the lack of evidence of benefit |
Conditional |
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The use of oral omega-3 long-chain polyunsaturated fatty acids LCPUFA supplementation for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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The use of oral garlic supplementation, specifically for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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The use of oral vitamin C and E supplementation, specifically for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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There is inadequate data to recommend for the use or against the use of oral magnesium supplementation specifically for the prevention of preeclampsia. More data on the safety profile is required |
Conditional |
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The use of progesterone replacement, specifically for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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The use of statins, specifically for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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The use of low molecular weight heparin (LMWH) alone (without aspirin) in women without a history of thrombophilia or APLS can be considered if a contraindication to aspirin is present. The decision to use LMWH (at a prophylactic dose) should be individualized based on women’s clinical and obstetric history and through a shared, informed decision-making process |
Conditional |
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LMWH should not replace the use of aspirin in women without contraindications to aspirin |
Conditional |
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The use of low molecular weight heparin (LMWH) in addition to aspirin for prevention of preeclampsia in women without a history of thrombophilia or APLS is not recommended |
Conditional |
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The use of nitric oxide (either in donor or precursor forms) for the prevention of preeclampsia is not recommended until more data are available |
Conditional |
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The use of metformin, specifically for the prevention of preeclampsia is not recommended until more data are available |
Conditional |
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The use of oral vitamin D supplementation for the prevention of preeclampsia, is not recommended until more data are available |
Conditional |
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The use of proton pump inhibitors for prevention of preeclampsia is not recommended until more data are available |
Conditional |
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The use of clopidogrel for prevention of preeclampsia is not recommended until human data are available |
GPS |
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TREATMENT OF PRE-ECLAMPSIA SYNDROME AND GESTATIONAL HYPERTENSION |
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Hospital Admission Versus Ambulatory Outpatient Management |
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Ambulatory outpatient management at home is an option only for women with mild to moderate gestational hypertension and requires frequent fetal and maternal evaluation |
Strong |
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Hospitalization is appropriate for Women with gestational hypertension in whom adherence to frequent monitoring is a concern and for patients diagnosed with preeclampsia |
Strong |
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Ambulatory outpatient management |
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At each antenatal care visit, following the detection of hypertension in pregnancy, a systematic clinical evaluation of symptoms, signs, laboratory investigations and fetal wellbeing must be performed |
Strong |
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Frequency of appointments is based on the individual clinical needs; suggested review is initially weekly to fortnightly (every 2 weeks) at a minimum |
Conditional |
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Women with non-severe hypertension during pregnancy should not be offered antihypertensive drug treatment when adequate resources for good quality antenatal care follow-up may be lacking |
Conditional |
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Inpatient Care |
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Women with preeclampsia should have additional tests to detect multisystem involvement, and should have fetal surveillance to assure fetal wellbeing |
Strong |
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A clear referral plan for patients with severe preeclampsia must be developed and implemented in every health care unit |
GPS |
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Complete bed rest is not advised for fear of thromboembolism, however minimal activities with 2 hours afternoon nap and 8 hours night sleep is recommended. |
GPS |
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Non-severe hypertension should be treated with the first-line agents oral methyldopa, labetalol, or nifedipine |
Conditional |
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Severe hypertension in pregnancy (i.e., sBP ≥ 160 mmHg or dbp ≥ 110 mmHg) requires urgent antihypertensive therapy, in a monitored setting |
Strong |
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Severe hypertension should be treated with the first-line agents oral nifedipine, oral labetalol, IV labetalol, or IV hydralazine |
Conditional |
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The target BP for antihypertensive therapy should be a dBP of 85 mmHg, regardless of sBP |
Conditional |
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Use of corticosteroid (either betamethasone or dexamethasone) is recommended in women with preeclampsia who are at risk of birth at < 34 weeks’ gestation |
Conditional |
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There are insufficient data to recommend routine use of corticosteroid in women with preeclampsia who are at risk of birth between 34- and 36-weeks’ gestation. Delivery should not be delayed for the administration of steroids in the late preterm period |
Conditional |
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The use of magnesium sulphate for fetal neuroprotection in women with preeclampsia at risk of preterm birth at < 30 weeks’ gestation is strongly recommended |
Strong |
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As part of expectant management, in-utero transfer to a tertiary-level centre with neonatal intensive care capacity should be considered |
GPS |
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Inpatient Expectant care versus Delivery |
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Inpatient Expectant care |
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Women with mild to moderate gestational hypertension or preeclampsia without severe features, expectant management up to 37 0/7 weeks of gestation is recommended |
Conditional |
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In low-resource setting where maternal and neonatal care and adequate resources for close monitoring by healthcare personnel may be lacking or is not available, the GDG recommend against expectant management for preeclampsia with severe hypertension or other severe features |
Conditional |
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Capabilities for the evaluation of fetal wellbeing and detection of fetal compromise should be available in healthcare facilities providing care for pregnant women with hypertensive disorders |
Conditional |
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Transfer of women with hypertension of pregnancy should be considered in situations where the health care provider believes that the health care facility is unequipped to manage the complications of hypertension of pregnancy |
GPS |
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Birth and Delivery |
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Time of Birth |
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Initiate birth at ≥ 37 weeks gestation, in women with preeclampsia |
Conditional |
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At < 37 weeks gestation, the decision on expectant management with continued surveillance is appropriate for women with non-severe preeclampsia. |
Conditional |
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At 34+0 till 36+6 weeks gestation for women with preeclampsia in presence of any feature of severity initiation of delivery should is considered. Delivery should not be delayed for the administration of steroids in the late preterm period |
Conditional |
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From fetal viability until <34+0 weeks gestation, Expectant management should be considered, but only in hospitals where very preterm infants and sick mothers can be cared for. Initiation of birth is considered in the absence of available resources for maternal and neonatal care |
Conditional |
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Maternal stabilization and labor management of pre-eclampsia and eclampsia |
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Prevention and treatment of convulsions |
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The prevention of eclampsia is empirically based on the timely delivery once preeclampsia has been diagnosed |
GPS |
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Prophylactic magnesium sulphate with an intravenous loading dose of 4g followed by maintenance at 1g/hr for 24 hours in total or time of last seizure is strongly recommended in women at risk of eclampsia or recurrent eclampsia |
Conditional |
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There is inadequate evidence to support an alternative magnesium regimen or the use of anticonvulsants for the prevention of eclampsia |
Conditional |
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It is recommended that magnesium sulfate should be used for the prevention and treatment of seizures in women with severe hypertension or severe preeclampsia, or eclampsia and birth is planned within 24 hours |
Conditional |
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The prophylactic use of magnesium sulfate for the prevention of seizures in women with gestational hypertension or preeclampsia without severe features is Conditionally recommended |
GPS |
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Women with eclampsia should receive magnesium sulphate to prevent recurrent seizures |
Conditional |
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Control of acute severe hypertension |
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Severe hypertension in pregnancy (i.e., sBP ≥ 160 mmHg or dBP ≥ 110 mmHg) requires urgent antihypertensive therapy, in a monitored setting |
Conditional |
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Severe hypertension should be treated with the first-line agents oral nifedipine, oral labetalol, intravenous (IV) labetalol, or IV hydralazine |
Strong |
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The target BP for antihypertensive therapy should be a dBP of 85 mmHg, regardless of sBP |
Conditional |
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Non-severe hypertension should be treated with the first-line agents oral methyldopa, labetalol, or nifedipine |
Conditional |
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Control of other complications: HELLP syndrome |
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For women with severe preeclampsia with features of HELLP expectant management is harmful. Plan birth as soon as feasible |
Strong |
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Platelet transfusion should be considered if a woman’s platelet count is <20 _ 109/L before vaginal delivery or <50 _ 109/L before cesarean delivery, or at any time if there is excessive active bleeding, known platelet dysfunction, rapidly falling platelet count, or coagulopathy |
Conditional |
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Vaginal delivery is the preferred modality, unless urgent delivery is necessary for maternal stabilization or for fetal indications. The delivery options should be discussed by a multidisciplinary team and consider the safest mode of delivery to the mother, how fast she is expected to deliver, what are the resources of blood products and other supportive mechanisms available, and can she sustain a surgery |
Conditional |
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In rapidly progressing preeclampsia with severe features or HELLP syndrome, vaginal delivery may be attempted if cervical conditions are favorable and delivery is anticipated within a short timeframe (e.g., ≤2 hours). If labor progress is slow (>6 hours) or maternal/fetal status worsens, immediate cesarean delivery is indicated |
Conditional |
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In small to medium size health care facilities, it is important to estimate whether their blood bank can support a massive blood trans fusion and, if necessary, contact regional or larger hospitals for assistance or for transferring the patient |
GPS |
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Mode of Birth |
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For women with any HDP, vaginal delivery should be considered unless a cesarean delivery is required for obstetrical indications. |
Strong |
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Vaginal delivery may require early cervical ripening and induction |
Conditional |
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If urgent or emergent delivery is required for maternal and/or fetal indications, an emergency cesarean delivery may be indicated |
Strong |
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Urgency ot Birth |
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Health facilities in Egypt should provide local protocols of management for their health care providers in accordance with WHO recommendations. |
Strong |
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GDG recommends to nationally adopt a color-triage system for acute obstetric emergencies (Modified Early obstetric warning score -MEOWS) |
GPS |
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TREATMENT OF CHRONIC HYPERTENSION |
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Expectant Management |
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Offer expectant management for women with Chronic hypertension who are <37 weeks and, whose blood pressure is lower than 160/110 mmHg with or without antihypertensive treatment, unless there are other medical indications62 |
Strong |
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Offer antihypertensive treatment to pregnant women who have chronic hypertension and who are not already on treatment if they have sustained systolic blood pressure of 140 mmHg or higher or sustained diastolic blood pressure of 90 mmHg or higher |
Strong |
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The target BP for antihypertensive therapy should be a dBP of 85 mmHg, regardless of sBP |
Strong |
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Consider labetalol to treat chronic hypertension in pregnant women. Consider nifedipine for women in whom labetalol is not suitable or methyldopa if both labetalol and nifedipine are not suitable. Base the choice on any pre-existing treatment, side-effect profiles, risks (including fetal effects) and the woman's preference |
Conditional |
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Continue with existing antihypertensive treatment if safe in pregnancy, or switch to an alternative treatment, unless sustained systolic blood pressure is less than 110 mmHg or sustained diastolic blood pressure is less than 70 mmHg or the woman has symptomatic hypotension |
Conditional |
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Offer pregnant women with chronic hypertension aspirin 150 mg once daily from 12 weeks |
Strong |
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Give the same advice on rest, exercise and work to women with chronic hypertension or at risk of hypertensive disorders during pregnancy as healthy pregnant women |
Conditional |
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Offer PLGF testing between 20–36+6 weeks to rule out pre-eclampsia in women with chronic hypertension if clinical suspicion arises |
Conditional |
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In chronic hypertension with suspected pre-eclampsia, monitor proteinuria 1–2x weekly alongside BP checks |
Strong |
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A complete blood count and levels of serum transaminases, lactate dehydrogenase, and uric acid should be checked on diagnosis then weekly |
Conditional |
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Timing of birth |
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Do not offer planned early birth (before 37 weeks) to women with chronic hypertension whose blood pressure is lower than 160/110 mmHg, with or without antihypertensive treatment, unless there are other medical indications |
Strong |
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Offer planned birth to women with chronic hypertension whose blood pressure is lower than 160/110 mmHg with or without antihypertensive treatment after 37 weeks |
Strong |
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Determination of timing should be agreed between the woman and the obstetrician. Initiation of delivery can be offered at 38+0 to 39+6 weeks |
Conditional |
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Offer planned early birth before 37 weeks to women with chronic hypertension or gestational hypertension if inability to control maternal blood pressure despite using 3 or more classes of antihypertensives in appropriate doses or if any of the known features of severe superimposed preeclampsia develop |
Strong |
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Care for women with hypertension during labor and postpartum |
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Intrapartum Care |
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During labour, measure blood pressure hourly. In women with severe hypertension measure blood pressure every 15 to 30 minutes until blood pressure is less than 160/110 mmHg. |
Conditional |
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Continue use of antenatal antihypertensive treatment during labour |
Conditional |
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Do not preload women who have severe pre-eclampsia with intravenous fluids before establishing low-dose epidural analgesia or combined spinal epidural analgesia |
Conditional |
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Do not routinely limit the duration of the second stage of labour in women with controlled hypertension |
Conditional |
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Consider operative or assisted birth in the second stage of labour for women with severe hypertension whose hypertension has not responded to initial treatment |
Conditional |
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As women with preeclampsia are at increased risk of postpartum hemorrhage, the third stage of labour should be actively managed |
Conditional |
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Ergometrine should not be administered to women with any hypertensive disorder of pregnancy, particularly preeclampsia or gestational hypertension; alternative oxytocic drugs should be considered |
Strong |
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Postpartum care for women with HDP |
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There remains inadequate data to suggest the superiority of a single agent or group of agents in selecting antihypertensives for the management of hypertension in the postpartum period. The choice of antihypertensive (beta-blockers, methyldopa, hydralazine, nifedipine, enalapril, clonidine) should be made through a shared decision-making process, particularly in breastfeeding/lactating women |
Conditional |
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Women should be informed of the long-term risks associated with preeclampsia, gestational hypertension and chronic hypertension and the importance of postpartum follow up prior to discharge from hospital |
Conditional |
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Antihypertensive therapy administered antepartum should be continued after birth. Also, consideration should be given to administering antihypertensive therapy for any hypertension diagnosed before six days postpartum |
Conditional |
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The target dBP for postpartum antihypertensive treatment should be 85 mmHg, as antenatally |
Conditional |
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Non-steroidal anti-inflammatory drugs (NSAIDs) for postpartum analgesia may be used in women with pre-eclampsia if other analgesics are ineffective, and there is no acute kidney injury (AKI) or other risk factors for it |
Conditional |
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Breastfeeding is recommended |
Strong |
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Counselling should be provided about the risks of gestational hypertension (at least 4%) or pre-eclampsia (at least 15%) in future pregnancy |
Conditional |
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At 3 months postpartum, all women should be reviewed to ensure that BP, urinalysis, and any laboratory abnormalities have normalised. If proteinuria or hypertension persist, then appropriate referral for further investigations should be initiated |
Conditional |
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At 6 months postpartum, where possible, all women should be reviewed again, at which point we suggest that BP ≥ 120/80 mmHg lead to discussion of lifestyle change |
Conditional |
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Following hypertensive pregnancy, particularly pre-eclampsia, counselling should be provided about the heightened health risks for the mother (particularly cardiovascular) and the offspring |
Strong |