| Site: | EHC | Egyptian Health Council |
| Course: | Infection Prevention and Control Guidelines |
| Book: | Management of Environmental Safety and Cleaning in Hospitals |
| Printed by: | Guest user |
| Date: | Sunday, 26 July 2026, 9:50 AM |
Transmission of infectious microorganisms from the environment to patients may occur through direct contact with contaminated equipment or indirectly. Environmental surfaces can be safely decontaminated using less rigorous methods than those used on medical instruments and devices.
|
Recommendations |
|
Clean housekeeping surfaces (e.g., floors, tabletops) on a regular basis, when spills occur, and when these surfaces are visibly soiled (Good practice statement) |
|
Clean and disinfect environmental surfaces on a regular basis (e.g., daily, three times per week) and when surfaces are visibly soiled (Good practice statement) |
|
Follow manufacturers’ instructions for proper use of disinfecting (or detergent) products -such as recommended use-dilution, material compatibility, storage, shelf-life, and safe use and disposal (Good practice statement) |
|
Clean walls, blinds, and window curtains in patient-care areas when these surfaces are visibly contaminated or soiled. (Good practice statement) |
|
Prepare disinfecting (or detergent) solutions as needed and replace it with fresh solution frequently (e.g., replace floor mopping solution every three patient rooms or hourly), according to the facility’s policy (Strong recommendation) |
|
Decontaminate mop heads and cleaning cloths regularly to prevent contamination (e.g., launder and dry at least daily). (Good practice statement) |
|
Detergent and water are adequate for cleaning surfaces in nonpatient-care areas (e.g., administrative offices). (Good practice statement) |
|
Do not use high-level disinfectants/liquid chemical sterilant for disinfection of non-critical surfaces. (Strong recommendation) |
|
Disinfect noncritical surfaces with an EDA and/or MoHP -registered hospital disinfectant according to the label’s safety precautions and use directions(Conditional recommendation) |
|
Do not use disinfectants to clean infant bassinets and incubators while these items are occupied. If disinfectants are used for the terminal cleaning of infant bassinets and incubators, thoroughly rinse the surfaces of these items with water and dry them before these items are reused. (Strong recommendation) |
|
Promptly clean and decontaminate spills of blood and other potentially infectious materials. (Strong recommendation) |
|
For site decontamination of spills of blood or other potentially infectious materials (OPIM), implement the following procedures. Use protective gloves and other PPE (e.g., when sharps are involved use forceps to pick up sharps and discard these items in a puncture-resistant container) appropriate for this task. Disinfect areas contaminated with blood spills using an EDA and/or MoHP -registered tuberculocidal agent, (Conditional recommendation) |
|
If sodium hypochlorite solutions are selected use 1000 ppm to decontaminate nonporous surfaces after a small spill (e.g., <10 mL) of either blood or OPIM. If a spill involves large amounts (e.g., >10 mL) of blood or OPIM, or involves a culture spill in the laboratory, use 5000 ppm chlorine for the first application of hypochlorite solution before cleaning in order to reduce the risk of infection during the cleaning process in the event of a sharp injury. Follow this decontamination process with a terminal disinfection, using 1000 ppm of sodium hypochlorite. (Strong recommendation) |
|
If the spill contains large amounts of blood or body fluids, clean the visible matter with disposable absorbent material, and discard the contaminated materials in appropriate, labeled containment. (Conditional recommendation) |
|
Use protective gloves and other PPE appropriate for this task (site decontamination of spill). (Conditional recommendation) |
|
An EDA and/or MoHP-registered sodium hypochlorite product is preferred, but if such products are not available, generic versions of sodium hypochlorite solutions (e.g., household chlorine bleach) can be used. (Good practice statement) |
|
Do not perform disinfectant fogging for routine purposes in patient-care areas. These refer to spraying or fogging of chemicals (e.g., formaldehyde, phenol-based agents, or quaternary ammonium compounds) as a way to decontaminate environmental surfaces or disinfect the air in patient rooms. (Strong recommendation) |
|
Other Disinfection Methods |
|
Hydrogen peroxide vapour disinfection is not recommended as a routine adjunct in healthcare facilities as the evidence of added value compared with conventional cleaning and disinfection is not well established (Strong recommendation) |
|
Ultraviolet light disinfection, ultraviolet light in combination with sodium hypochlorite and other novel approaches to healthcare environment disinfection are not recommended as routine adjuncts in healthcare facilities as the evidence of added value compared with conventional cleaning and disinfection is not well established. (Strong recommendation) |
|
The use of surfaces, fittings or furnishings containing materials with antimicrobial properties in healthcare facilities is not recommended as the evidence of added value compared with conventional cleaning and disinfection is not well established. (Strong recommendation) |
|
Recommendations |
|
Clean housekeeping surfaces (e.g., floors, tabletops) on a regular basis, when spills occur, and when these surfaces are visibly soiled (Good practice statement) |
|
Clean and disinfect environmental surfaces on a regular basis (e.g., daily, three times per week) and when surfaces are visibly soiled (Good practice statement) |
|
Follow manufacturers’ instructions for proper use of disinfecting (or detergent) products -such as recommended use-dilution, material compatibility, storage, shelf-life, and safe use and disposal (Good practice statement) |
|
Clean walls, blinds, and window curtains in patient-care areas when these surfaces are visibly contaminated or soiled. (Good practice statement) |
|
Prepare disinfecting (or detergent) solutions as needed and replace these with fresh solution frequently (e.g., replace floor mopping solution every three patient rooms or hourly), according to the facility’s policy (Strong recommendation, Moderate grade evidence) |
|
Decontaminate mop heads and cleaning cloths regularly to prevent contamination (e.g., launder and dry at least daily). (Good practice statement) |
|
Detergent and water are adequate for cleaning surfaces in nonpatient-care areas (e.g., administrative offices). (Good practice statement) |
|
Do not use high-level disinfectants/liquid chemical sterilant for disinfection of non-critical surfaces. (Strong recommendation, Moderate grade evidence) |
|
Disinfect noncritical surfaces with an EDA and/or MoHP -registered hospital disinfectant according to the label’s safety precautions and use directions (Conditional recommendation, Moderate grade evidence) |
|
Do not use disinfectants to clean infant bassinets and incubators while these items are occupied. If disinfectants are used for the terminal cleaning of infant bassinets and incubators, thoroughly rinse the surfaces of these items with water and dry them before these items are reused. (Strong recommendation, Moderate grade evidence) |
|
Promptly clean and decontaminate spills of blood and other potentially infectious materials. (Strong recommendation, Moderate grade evidence) |
|
For site decontamination of spills of blood or other potentially infectious materials (OPIM), implement the following procedures. Use protective gloves and other PPE (e.g., when sharps are involved use forceps to pick up sharps and discard these items in a puncture-resistant container) appropriate for this task. Disinfect areas contaminated with blood spills using an EDA and/or MoHP -registered tuberculocidal agent, (Conditional recommendation, Moderate grade evidence) |
|
If sodium hypochlorite solutions are selected use 1000 ppm to decontaminate nonporous surfaces after a small spill (e.g., <10 mL) of either blood or OPIM. If a spill involves large amounts (e.g., >10 mL) of blood or OPIM, or involves a culture spill in the laboratory, use 5000 ppm for the first application of hypochlorite solution before cleaning in order to reduce the risk of infection during the cleaning process in the event of a sharp injury. Follow this decontamination process with a terminal disinfection, using 1000 ppm of sodium hypochlorite. (Strong recommendation, Moderate grade evidence) |
|
If the spill contains large amounts of blood or body fluids, clean the visible matter with disposable absorbent material, and discard the contaminated materials in appropriate, labeled containment. (Conditional recommendation, Moderate grade evidence) |
|
Use protective gloves and other PPE appropriate for this task (site decontamination of spill). (Conditional recommendation, Moderate grade evidence) |
|
An EDA and/or MoHP-registered sodium hypochlorite product is preferred, but if such products are not available, generic versions of sodium hypochlorite solutions (e.g., household chlorine bleach) can be used. (Good practice statement) |
|
Do not perform disinfectant fogging for routine purposes in patient-care areas. These refer to spraying or fogging of chemicals (e.g., formaldehyde, phenol-based agents, or quaternary ammonium compounds) as a way to decontaminate environmental surfaces or disinfect the air in patient rooms. (Strong recommendation, Moderate grade evidence) |
|
Other Disinfection Methods |
|
Hydrogen peroxide vapour disinfection is not recommended as a routine adjunct in healthcare facilities as the evidence of added value compared with conventional cleaning and disinfection is not well established (Strong recommendation, , weak grade evidence) |
|
Ultraviolet light disinfection, ultraviolet light in combination with sodium hypochlorite and other approaches to healthcare environment disinfection are not recommended as routine adjuncts in healthcare facilities as the evidence of added value compared with conventional cleaning and disinfection is not well established. (Strong recommendation, weak grade evidence) |
|
The use of surfaces, fittings or furnishings containing materials with antimicrobial properties in healthcare facilities is not recommended as the evidence of added value compared with conventional cleaning and disinfection is not well established. (Strong recommendation, weak grade evidence) |
The determination of environmental cleaning procedures for patient care areas, including the cleaning frequency, method, and process, should be based on the risk of pathogen transmission.
This risk is a function of the:
● Probability of contamination: Heavily contaminated surfaces and items require more frequent and thorough environmental cleaning than moderately contaminated surfaces, which in turn require more frequent and rigorous environmental cleaning than lightly or non-contaminated surfaces and items.
● Vulnerability of the patients to infection: Surfaces and items in care areas containing vulnerable patients (e.g., immunosuppressed) require more frequent and rigorous environmental cleaning than surfaces and items in areas with less vulnerable patients.
● Potential for exposure (i.e., high-touch vs low-touch surfaces): High-touch surfaces (e.g., bed rails) require more frequent and rigorous environmental cleaning than low-touch surfaces (e.g., walls).
➡️Every facility should develop cleaning schedules, including:
▪️ Identifying the person responsible.
▪️ The frequency.
▪️ The method (product, process).
▪️ Detailed standard operating procedures for environmental cleaning of surfaces in every type of patient care area.
➡️General environmental cleaning techniques
▪️ For all environmental cleaning procedures, always use the following general strategies:
We would like to acknowledge the Infection Control Guidelines Committee for developing these guidelines.
Head of IPC Guidelines Committee
Professor Ghada Ismail (Professor of Clinical Pathology (Clinical Microbiology), Faculty of Medicine, Ain Shams University, Secretary of Supreme IPC Committee, SCUH, Member of WHO Global Guidelines Groups (GDG) for Infection Prevention)
Secretary of IPC Guidelines Committee
Professor Walaa Abd El-Latif (Professor of Medical Microbiology and Immunology, Faculty of Medicine Ain Shams University, IPC Consultant)
Members of the Committee
▪ Professor Amal Sayed (Deputy Manager of Environmental Affair, Infection Control Director, Cairo University Hospitals)
▪ Professor Amani El-Kholy (Clinical Pathology Department (Microbiology), Faculty of Medicine, Cairo University, Infection Control Consultant)
▪ Dr Asmaa Mohamed Abdelfatah Mohamed (Lecturer, Faculty of Nursing MTI University)
▪ Dr Gehan Mohamed Fahmy (Professor clinical microbiology ASUSH consultant infection control, Board member of IFIC EMERO region)
▪ Professor Hebatallah Gamal Rashed (Clinical Pathology Department (Microbiology), Faculty of Medicine, Assuit University, Infection Control Consultant)
▪ Dr Iman Afifi (Consultant Clinical Pathology (Microbiology) and IPC, Ain Shams University, Director IPC units of Ain Shams internal medicine and Geriatric hospitals
▪ Professor Maha El Touny (Department of internal medicine. Faculty of Medicine, Ain Shams University. Infection Control Consultant)
▪ Professor Nagwa Khamis (Emeritus Consultant Clinical Pathology (Microbiology) and IPC, ASU Director IPC Department and CEO Consultant IPC, CCHE-57357)
▪ Professor Nesrine Fathi Hanafi (Professor in Medical Microbiology and Immunology Faculty of Medicine Alexandria University, Head of Infection Prevention and Control, Alexandria University Hospitals)
▪ Dr. Reham Lotfy Abdel Aziz (Environmental Health Director, EEAA, Hazardous Waste Consultant, WMRA, Ministry of Environment)
▪ Professor Sherin ElMasry (Professor of Clinical Pathology, Ain Shams University, Chief Director of IPC ASU, Health Care Quality & Patient Safety Consultant)
▪ Dr Shimaa El-Garf (Coordinator): Clinical Pathology Specialist, Coordinator of HAI Surveillance and Audit Electronic System for University Hospitals, RLEUH- SCUH
● Cleaning products (also known as cleaning agents): Liquids, powders, sprays, or granules that remove organic material (e.g., dirt, body fluids) from surfaces and suspend grease or oil. Can include liquid soap, enzymatic cleaners, and detergents.
● Cleaning solution: A combination of water and cleaning product (e.g., detergent) in a ratio specified by the manufacturer.
● Contact time: The time that a disinfectant must be in contact with a surface or device to ensure that appropriate disinfection has occurred. For most disinfectants, the surface should remain wet for the required contact time.
● Detergent: A synthetic cleansing agent that can emulsify and suspend oil. Contains surfactant or a mixture of surfactants with cleaning properties in dilute solutions to lower surface tension and aid in the removal of organic soil and oils, fats, and greases.
● Disinfectant fogging: Misting or fogging a liquid chemical disinfectant to disinfect environmental surfaces in an enclosed space.
● High-touch surfaces: Surfaces, often in patient care areas, that are frequently touched by healthcare workers and patients (e.g. overbed table, IV pole, doorknobs, medication carts).
● Noncritical patient care equipment: Equipment, such as stethoscopes, blood pressure cuffs, and bedpans, that comes into contact with intact skin.
● Safety data sheet (SDS): A document by the supplier or manufacturer of a chemical product that contains information on the product's potential hazards (health, fire, reactivity, and environmental) and how to work safely with it. It also contains information on the use, storage, handling, and emergency procedures.
● Patient Rooms: Regular cleaning and disinfection of high-touch surfaces such as bed rails, bedside tables, light switches, and doorknobs.
● Common Areas: Cleaning and disinfection of shared spaces like waiting rooms, corridors, and restrooms.
● Clinical Areas: Thorough cleaning and disinfection of operating rooms, procedure rooms, and other clinical areas.
● Equipment Handling: Cleaning and disinfection of medical equipment to prevent cross-contamination.
● Air Quality: Maintaining adequate cleaning of ventilation and air filtration systems to reduce airborne pathogens.
Purpose of Environmental Safety and Cleaning in Hospitals
● Prevent the Spread of Infection: By reducing the number of microorganisms on surfaces, cleaning helps to prevent the transmission of HAIs.
● Protect Patient Health: A clean environment contributes to patient safety and well-being.
● Comply with Regulatory Standards: Hospitals must adhere to specific cleaning and disinfection protocols to meet regulatory requirements.
● Enhance Patient Experience: A clean and well-maintained hospital environment can positively impact patient satisfaction.
➡️Management Considerations
● Cleaning and Disinfection Protocols: Developing and implementing standardized protocols for cleaning and disinfection, including specific cleaning agents and procedures.
● Staff Training: Providing regular training to cleaning staff on proper cleaning techniques, the importance of hand hygiene, and the use of personal protective equipment (PPE).
● Monitoring and Evaluation: Implementing a system to monitor cleaning practices and identify areas for improvement.
● Quality Assurance: Conducting regular audits to ensure compliance with cleaning protocols and standards.
● Resource Allocation: Allocating sufficient resources, including cleaning staff, cleaning agents, and equipment, to maintain a clean environment.
By effectively managing environmental cleaning, hospitals can significantly reduce the risk of HAIs and improve overall patient safety.
A comprehensive search for guidelines was undertaken to identify the most relevant guidelines to consider for adaptation.
Inclusion/ exclusion criteria followed in the search and retrieval of guidelines to be adapted:
● Selecting only evidence-based guidelines (guideline must include a report on systematic literature searches and explicit links between individual recommendations and their supporting evidence)
● Selecting only national and/or international guidelines
● Specific range of dates for publication (using Guidelines published or updated in 2013 and later)
● Selecting peer reviewed publications only
● Selecting guidelines written in English language
● Excluding guidelines written by a single author, not on behalf of an organization to be valid and comprehensive, a guideline ideally requires multidisciplinary input.
● Excluding guidelines published without references as the panel needs to know whether a thorough literature review was conducted and whether current evidence was used in the preparation of the recommendations.
The following characteristics of the retrieved guidelines were summarized in:
● Developing organization/authors
● Date of publication, posting, and release
● Country/language of publication
● Date of posting and/or release
● Dates of the search used by the source guideline developers.
All retrieved Guidelines were screened and appraised using AGREE II instrument (www.agreetrust.org) by at least three members. The panel decided on a cut-off point or ranked the guidelines (any guideline scoring above 50% on the rigor dimension was retained). The committee decided to adapt from:
1. CDC Recommendations for Disinfection and Sterilization in Healthcare Facilities Guideline for Disinfection and Sterilization in Healthcare Facilities (2008) updated December 7, 2023
2. CDC Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings (2007) updated November 27, 2023
3. CDC AND HICPAC Recommendations guidelines for environmental infection control in health-care facilities (2023) updated December 14, 2023
4. Irish Infection Prevention and Control (IPC): National clinical guideline no. 30 May 2023 vol 1
➡️Evidence assessment
According to WHO Handbook for Guidelines, we used the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach to assess the quality of a body of evidence, develop and report recommendations. GRADE methods are used by WHO because these represent internationally agreed standards for making transparent recommendations. Detailed GRADE information is available on the following sites:
● GRADE working group: https://www.gradeworkinggroup.org/
● GRADE online training modules: http://cebgrade.mcmaster.ca/
Table (1) Quality and Significance of the four levels of evidence in GRADE
|
Quality |
Definition |
Implications |
|
High |
The guideline development group is very confident that the true effect lies close to that of the estimate of the effect |
Further research is very unlikely to change confidence in the estimate effect |
|
Moderate |
The guideline development group is moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibly that it is substantially different |
Further research is likely to have an important impact on confidence in the estimate of the effect and may change the estimate |
|
Low |
Confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the true effect |
Further research is very likely to have an important on confidence in the estimate of effect and is unlikely to change the estimate |
|
Very low |
The group has very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of the effect |
Any estimate of the effect is very uncertain |
Table (2) Factors that determine How to upgrade or downgrade the quality of evidence.
|
Downgrade in presence of |
Upgrade in presence of |
|
Study limitations. 1- Serious limitations 2- Very serious limitations |
Dose- response gradient. +1 Evidence of a dose-response gradient |
|
Consistency 1- Important inconsistency |
Direction of plausible bias + All plausible confounders would have reduced the effect |
|
Directness 1- Some uncertainty 2- Major uncertainty |
Magnitude of the effect +1 Strong, no plausible Confounder, consistent and direct evidence |
|
Precision 1- Imprecise data |
+2 very strong, no major threats to validity and direct evidence |
|
Reporting bias 1- High probability of reporting bias |
|
➡️The strength of the recommendations
The strength of a recommendation communicates the importance of adherence to the recommendation.
● Strong recommendations
With strong recommendations, the guideline communicates the message that the desirable effects of adherence to the recommendation outweigh the undesirable effects. This means that in most situations the recommendation can be adopted as policy.
● Conditional recommendations
These are made when there is greater uncertainty about the four factors above or if local adaptation has to account for a greater variety in values and preferences, or when resource use makes the intervention suitable for some, but not for other locations. This means that there is a need for substantial debate and involvement of stakeholders before this recommendation can be adopted as policy.
When not to make recommendations?
When there is lack of evidence on the effectiveness of an intervention, it may be appropriate not to make a recommendation.


Annex 3. Table (3): PPE for Cleaning by Task and Type.
|
Type of cleaning task |
Required personal protective equipment for cleaning staff |
|
Routine cleaning (standard precautions) |
None (unless spills or contamination risk—see below) |
|
Terminal cleaning (standard precautions) |
Reusable rubber gloves |
|
Blood and body fluid spills and high contamination risk areas (e.g., cleaning bed of an incontinent patient, labor and delivery wards) |
● Gown and/or plastic apron ● Reusable rubber gloves ● Face mask with either goggles or face shield (if splash risk or large spill) |
|
Droplet precautions (routine and terminal cleaning) |
● Gown and/or plastic apron ● Reusable rubber gloves ● Face mask with either goggles or face shield (if splash risk or large spill) |
|
Contact precautions (routine and terminal cleaning) |
● Gown and/or plastic apron ● Reusable rubber gloves |
|
Airborne precautions (routine and terminal cleaning) |
● Respirator (N95 or FPP2), fit tested ● Reusable rubber gloves |
|
Preparation of disinfectant products and solutions |
● According to specifications in SDS (manufacturer instructions) ● If SDS not available, then: o Chemical-resistant gloves (e.g., nitrile) o Gown and/or apron o Face mask with either goggles or face shield |
● Association for Professionals in Infection Control and Epidemiology (APIC): APIC Text of Infection Control and Epidemiology, 4th Edition, 2014.
● Best Practices for Environmental Cleaning for Infection Prevention and Control: In All Health Care Settings, 3rd Edition, Public Health Ontario, 2018. Available at: https://www.publichealthontario.ca
● CDC AND HICPAC Recommendations guidelines for environmental infection control in health-care facilities (2023) updated December 14, 2023
● CDC Best Practices for Environmental Cleaning in Global Healthcare Facilities with Limited Resources (2024): Environmental Cleaning Procedures
● CDC Recommendations for Disinfection and Sterilization in Healthcare Facilities Guideline for Disinfection and Sterilization in Healthcare Facilities (2008) updated December 7, 2023
● Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings (2007) updated November 27, 2023
● IRISH Infection Prevention and Control (IPC): National clinical guideline no. 30 May 2023 vol 1
● Rutala, W. A., Weber, D. J., & the Healthcare Infection Control Practices Advisory Committee (HICPAC). “Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008.” Infection Control and Hospital Epidemiology, 29(S1), S61-S62.
● The Joint Commission Standard EC.02.06.01: The Hospital Maintains a Safe, Functional Environment Available at: https://www.jointcommission.org/
● WHO Guidelines on Core Components of Infection Prevention and Control Programmes at the National and Acute Health Care Facility Level, 2016. Available at: https://apps.who.int/iris/handle/10665/251730