This document contains a monthly checklist for assessing performance measures related to patient safety, infection control, and environmental safety standards. It includes items to observe directly, such as proper hand hygiene and patient identification procedures. It also contains items to assess through record reviews, like medication reconciliation documentation. Staff are expected to conduct assessments using this checklist on a monthly basis and record any issues to address on page 10. The goal is continual monitoring and education to maintain compliance with regulatory standards.
The document discusses hospital waste management. It classifies hospital waste into hazardous and non-hazardous categories. Hazardous waste includes infectious waste from medical procedures and laboratories as well as chemical and radioactive waste. Proper segregation, treatment, and disposal of hospital waste is important to prevent health hazards. Key steps include waste minimization, segregation, storage, treatment, transportation, and final disposal.
This document defines key concepts related to pharmaceutical storage and provides guidelines for best practices. It discusses definitions of storage, materials, and quality control. It also outlines procedures for warehouse site selection, receipt of incoming materials, storage, stock rotation, and dispatch. Temperature requirements are provided for vaccine storage. Guidance is given for sanitation, housekeeping, fire prevention, security, and stability follow-up to ensure safe and effective storage of pharmaceutical products.
The document discusses the importance of biosafety and monitoring in the central sterile supply department (CSSD) of hospitals. It outlines the key role of the CSSD in providing sterile supplies and supporting infection control. Proper training of CSSD staff and consistently following processes are emphasized. Various methods of monitoring sterilization are discussed, including mechanical, chemical, and biological indicators. The document focuses on the importance of biological indicators for directly measuring the effectiveness of sterilization, as chemical indicators can sometimes provide inaccurate results. It also defines the different classes of chemical indicators.
Practice Guidelines Endocopic disinfection & ReprocessingHossam Ghoneim
This document provides guidelines for endoscope disinfection and reprocessing. It defines key terms like cleaning, disinfection, sterilization and single-use accessories. The basic steps for endoscope reprocessing are outlined as cleaning, rinsing, disinfection, drying, rinsing and storage. Optimal, normal and minimal standards are discussed. Principles that apply to all standards include pre-cleaning, cleaning, rinsing, disinfection, final rinsing, drying and storage. Common disinfectants like glutaraldehyde and alternatives are described. The document emphasizes that effective disinfection requires the use of appropriate chemicals, temperatures, exposure times and equipment to eliminate pathogens from hardest to easiest.
The document provides guidelines for equipping Primary Health Centres (PHCs) in India. It recommends standard lists of equipment tailored for PHCs to aid in budgeting, procurement, and prioritization. Equipment is categorized as vital, essential, or non-essential. Appropriate equipment must consider local conditions, compatibility, acceptability, and safety/performance standards. Lists include consumables, medical devices, surgical kits, laboratory reagents, furniture, and other supplies needed for basic maternal and child health services, family planning, treatment of common illnesses, and running a functional health centre. Maintenance and infection control are also addressed.
This document outlines the 9 key steps for reprocessing flexible gastrointestinal endoscopes: 1) precleaning, 2) leak testing, 3) manual cleaning, 4) rinsing after cleaning, 5) visual inspection, 6) high level disinfection, 7) rinsing after disinfection, 8) drying, and 9) storage. It emphasizes that manual cleaning is the most important step for removing debris and that all 9 steps must be followed diligently to ensure endoscope decontamination and prevent patient infection. Proper reprocessing according to manufacturer guidelines is critical for patient and staff safety.
The document discusses proper care and maintenance of medical equipment used for patient care. It emphasizes that all equipment must be thoroughly cleaned and disinfected or sterilized between each use to prevent transmission of infections. General principles include cleaning equipment to remove organic matter, keeping items clean and in working order, following manufacturer's instructions for appropriate disinfectants, and storing equipment in a clean, dry location. Proper maintenance such as periodic calibration and repairs is important to ensure safe and effective use of medical devices.
The document provides information about medical laboratories and laboratory procedures. It discusses the different departments in a clinical laboratory including clinical chemistry, hematology, microbiology, and blood bank. It also covers topics like laboratory personnel, regulations, quality control, safety, specimen collection, use of microscopes, and standard precautions. Laboratory equipment like centrifuges and autoclaves are described along with their proper use and safety.
The document discusses hospital waste management. It classifies hospital waste into hazardous and non-hazardous categories. Hazardous waste includes infectious waste from medical procedures and laboratories as well as chemical and radioactive waste. Proper segregation, treatment, and disposal of hospital waste is important to prevent health hazards. Key steps include waste minimization, segregation, storage, treatment, transportation, and final disposal.
This document defines key concepts related to pharmaceutical storage and provides guidelines for best practices. It discusses definitions of storage, materials, and quality control. It also outlines procedures for warehouse site selection, receipt of incoming materials, storage, stock rotation, and dispatch. Temperature requirements are provided for vaccine storage. Guidance is given for sanitation, housekeeping, fire prevention, security, and stability follow-up to ensure safe and effective storage of pharmaceutical products.
The document discusses the importance of biosafety and monitoring in the central sterile supply department (CSSD) of hospitals. It outlines the key role of the CSSD in providing sterile supplies and supporting infection control. Proper training of CSSD staff and consistently following processes are emphasized. Various methods of monitoring sterilization are discussed, including mechanical, chemical, and biological indicators. The document focuses on the importance of biological indicators for directly measuring the effectiveness of sterilization, as chemical indicators can sometimes provide inaccurate results. It also defines the different classes of chemical indicators.
Practice Guidelines Endocopic disinfection & ReprocessingHossam Ghoneim
This document provides guidelines for endoscope disinfection and reprocessing. It defines key terms like cleaning, disinfection, sterilization and single-use accessories. The basic steps for endoscope reprocessing are outlined as cleaning, rinsing, disinfection, drying, rinsing and storage. Optimal, normal and minimal standards are discussed. Principles that apply to all standards include pre-cleaning, cleaning, rinsing, disinfection, final rinsing, drying and storage. Common disinfectants like glutaraldehyde and alternatives are described. The document emphasizes that effective disinfection requires the use of appropriate chemicals, temperatures, exposure times and equipment to eliminate pathogens from hardest to easiest.
The document provides guidelines for equipping Primary Health Centres (PHCs) in India. It recommends standard lists of equipment tailored for PHCs to aid in budgeting, procurement, and prioritization. Equipment is categorized as vital, essential, or non-essential. Appropriate equipment must consider local conditions, compatibility, acceptability, and safety/performance standards. Lists include consumables, medical devices, surgical kits, laboratory reagents, furniture, and other supplies needed for basic maternal and child health services, family planning, treatment of common illnesses, and running a functional health centre. Maintenance and infection control are also addressed.
This document outlines the 9 key steps for reprocessing flexible gastrointestinal endoscopes: 1) precleaning, 2) leak testing, 3) manual cleaning, 4) rinsing after cleaning, 5) visual inspection, 6) high level disinfection, 7) rinsing after disinfection, 8) drying, and 9) storage. It emphasizes that manual cleaning is the most important step for removing debris and that all 9 steps must be followed diligently to ensure endoscope decontamination and prevent patient infection. Proper reprocessing according to manufacturer guidelines is critical for patient and staff safety.
The document discusses proper care and maintenance of medical equipment used for patient care. It emphasizes that all equipment must be thoroughly cleaned and disinfected or sterilized between each use to prevent transmission of infections. General principles include cleaning equipment to remove organic matter, keeping items clean and in working order, following manufacturer's instructions for appropriate disinfectants, and storing equipment in a clean, dry location. Proper maintenance such as periodic calibration and repairs is important to ensure safe and effective use of medical devices.
The document provides information about medical laboratories and laboratory procedures. It discusses the different departments in a clinical laboratory including clinical chemistry, hematology, microbiology, and blood bank. It also covers topics like laboratory personnel, regulations, quality control, safety, specimen collection, use of microscopes, and standard precautions. Laboratory equipment like centrifuges and autoclaves are described along with their proper use and safety.
This document provides information on infection prevention and control strategies during construction and renovation projects in healthcare facilities. It discusses the objectives of preventing microbial spread from construction sites. It outlines various infection control measures that should be implemented, including erecting barriers, controlling dust and debris, maintaining proper ventilation, educating workers, and monitoring the project. The document emphasizes doing a risk assessment, relocating high-risk patients if needed, establishing traffic control, and ensuring ventilation and filtration. It also discusses strategies for internal projects, such as barrier containment, dust control, and cleaning and commissioning spaces after completion. The overall goal is to minimize infection risks during construction through planning and coordination.
The document outlines the essential factors for an ideal medical laboratory setup. It discusses the necessary infrastructure requirements including adequate laboratory premises, heating/ventilation/lighting systems, drainage, electricity, fire safety facilities, storage areas, IT systems, and qualified medical and non-medical personnel. It emphasizes the importance of proper biomedical waste management and maintaining a safe, clean, and hygienic environment for sample collection, analysis, and reporting. The document also highlights the roles of various laboratory staff in ensuring quality testing and delivery of diagnostic services.
This document defines biomedical waste and provides guidelines for its proper handling and disposal at the University of Ottawa. It outlines roles and responsibilities, defines key terms, and provides detailed procedures for waste segregation, containment, labelling, treatment, handling, transportation, storage, collection, and disposal. Biomedical waste must be properly contained and labelled according to type before undergoing required treatment such as autoclaving or chemical disinfection, and ultimately collection by the Office of Risk Management for off-site disposal. Adhering to these guidelines ensures biomedical waste is safely managed in compliance with regulations.
The document provides an overview of the Central Sterile Supply Department (CSSD) in a hospital. It describes the CSSD's functions like receiving, cleaning, sterilizing and distributing medical supplies and equipment. It outlines the layout, staffing, equipment and processes used in different areas of the CSSD like receiving, cleaning, packing and sterilization. Quality assurance procedures like the use of indicators and records maintained are also summarized.
This document discusses the management of hospital waste. It defines medical waste, regulated medical waste, and infectious waste. Regulated medical waste includes seven categories such as human pathological wastes and sharps. Infectious waste is categorized into seven groups like isolation wastes and contaminated sharps. An infectious waste management plan should include designation of infectious waste, segregation, packaging, storage, treatment, disposal, contingency measures, and staff training. Common treatment methods mentioned are autoclaving, incineration, thermal inactivation, gas/vapor sterilization, chemical disinfection, and sterilization by irradiation. The document emphasizes the importance of a clean environment for public health.
The document discusses biomedical waste management in hospitals. It defines different types of medical waste and their sources. It notes that most waste is non-infectious (80%) while pathological and infectious waste makes up 15%. It outlines 10 categories of biomedical waste and procedures for waste segregation, collection, storage, transportation, and treatment. Key steps include effective waste segregation at source using color coding, safe primary collection and storage, authorized transportation, and final treatment through incineration or other methods. Occupational safety and training of healthcare workers is also emphasized.
The document provides guidelines for endoscope disinfection and reprocessing. It defines key terms and outlines the optimal 6 step process: cleaning, rinsing, high-level disinfection, drying, rinsing, and storage. The steps involve manually cleaning with detergent followed by automatic disinfection, rinsing and drying in a reprocessor. The document also discusses control measures, disinfectants like glutaraldehyde, efficacy against different pathogens, advantages of automatic reprocessing, and different standards for areas with limited resources.
The document discusses medical and laboratory waste management. It defines infectious waste and outlines various types of waste generated from medical facilities. Key elements of infectious waste management are identified, including identification, segregation, packaging, storage, transport, treatment, and disposal. Common treatment methods like incineration are described. The importance of microbial inactivation testing to ensure treatment effectiveness is emphasized. Guidelines for acceptable levels of pathogen reduction are provided. The document concludes with recommendations around improving waste treatment guidelines and prioritizing occupational health and safety in medical waste management.
The Program file is created from various peer reviewed, and world standard protocols in implantation of Safe Operation theater standards for wider use in the world, In India still we do not have any set standards and practices, As good beginning is half done, I wish all my professional friends go through the article, your opinions and comments are highly appreciated for future developments,
Dr.T.V.Rao MD
This document provides a summary of the content areas and competencies tested on the Medical Laboratory Technician (MLT) certification examination. It is organized into six main sections: Blood Bank, Chemistry, Hematology, Microbiology, Urinalysis/Other Body Fluids, and Laboratory Operations. Each section lists the specific topics covered, such as blood typing and crossmatching in Blood Bank or electrolyte and protein testing in Chemistry. Competencies involve technical skills like performing laboratory tests, problem solving abnormal results, verifying quality control, and communicating with clinicians. The examination evaluates knowledge, interpretation, and problem-solving skills through multiple choice questions.
The document provides guidelines for hospital waste management in India based on the Bio-Medical Waste (Management & Handling) Rules, 1998. It outlines 10 categories of hospital waste and appropriate treatment and disposal methods for each category, including incineration, deep burial, autoclaving, microwaving, shredding, and secured landfilling. The guidelines emphasize segregation of waste, use of colored containers, and proper treatment to minimize health and safety risks from hazardous hospital waste.
Analytical instruments in clinical chemistry, uses and maintenanceJennifer Giovanna
The document provides guidelines for the proper use and maintenance of various analytical instruments used in clinical chemistry laboratories. It discusses spectrophotometers, flame photometers, pipettes, balances, centrifuges, autoclaves, refrigerators, freezers, ovens, water baths, and pH meters. Proper calibration and preventative maintenance are emphasized for ensuring accurate test results and extending the life of the equipment.
The document provides information about the Central Sterile Service Department (CSSD) and Biomedical Engineering Department at YMCH. It describes the functions, workflow, and processes of CSSD, including receiving, cleaning, packaging, sterilizing, storing and distributing instruments. It also outlines the roles and responsibilities of the Biomedical Engineering Department, such as maintaining medical equipment inventory, conducting planned and breakdown maintenance, and calibration.
The Leading Manufacturer and supplier of disinfection control system and infection control equipment. Owing to our quality proven range we have been able to carve a niche foothold in the industry such as Steam Sterilizers, Flash Sterilizers, Bulk Sterilizers, ETO Sterilizers, Pass Box, Wash Station With 2 Sinks, Linen Fold Table, Free Standing Basket Rack, Motorized Lift Table, Hydraulic Lift Tables, Fully Electric Bi-Position Painless Delivery Table, Motorised Lifting Multi-Position C-Arm Compatible Table, O.T. Lights - IS-24T, O.T. Lights - IS-7Rz, O.T. Lights - IS-5Rz, O.T. Lights - IS-4 Rz...
The document discusses the importance of maintaining proper standards in operation theatres to prevent surgical site infections. It emphasizes the need for surveillance of operation theatres which includes monitoring the quality of air. Air sampling methods like settle plate method and slit sampler are recommended to measure bacterial counts and ensure the air quality meets acceptable limits. Adhering to guidelines regarding zoning, ventilation, temperature, humidity and regular environmental monitoring can help minimize risks of infections.
This document provides guidelines for disinfecting ultrasound probes based on their level of use and contact. It outlines three levels of probe use - non-critical (intact skin), semi-critical (mucous membranes or non-intact skin), and critical/sterile procedures. For each level, it details the appropriate disinfection method, including cleaning, low-level disinfection, or high-level disinfection/sterilization. Proper cleaning is emphasized as the most important first step before disinfection. Storage and documentation requirements are also covered to ensure probes are properly processed between patients.
This document discusses various aspects of laboratory management including organizing the laboratory space, storing equipment and chemicals, purchasing supplies, and record keeping. It emphasizes the importance of proper storage, labeling, and stock control to ensure safety, availability of materials, and cost effectiveness. Key recommendations include storing chemicals by type in labeled cabinets and containers, maintaining minimum and maximum stock levels, and having processes for requisition, receipt, and auditing of all laboratory items.
1. A study examined the effectiveness of different cleaning methods for laryngoscope handles in reducing bacterial contamination.
2. Laboratory experiments showed that wipes containing chlorhexidine and alcohol were highly effective at eliminating bacteria immediately after cleaning and provided residual sterilization for up to 24 hours.
3. An audit of laryngoscope handles in a hospital found high levels of bacterial contamination before changing cleaning protocols, but contamination was significantly reduced after implementing the use of chlorhexidine wipes between patients.
Project Information
Accommodation Name:
Location: Company Name:
Date: Time :
Sl No. ITEMS TO BE CHECKED Yes No N/A Comments
Audit Check List for Laundry
1 The premises are cleaned & situated in an environment which has minimum risk for contamination.
2 Sufficient area for storage of unwashed clothes & washed clothes.
3 Washing & drying premises was found cleaned & in good condition.
4 There are arrangements to control the entry of rodents, insects and birds.
5 Clothes are collected washed & dried separately.
Infection Control Checklist Laundry Personnel
1 Clean, neat, untorn and appropriate clothing is worn
2 Closed toe shoes with safety soles and in good repair are worn
3 Good personal hygiene (including hair and body cleanliness) is practiced
4 Fingernails are clean and trimmed
5 Hair is neat and protected by covering
6 Strict clothing and linen handling procedures are followed to avoid contamination
7 Direct resident contact is avoided except in emergency situations
8 Rubber gloves and protective covering are worn when handling and loading soiled linen
9 Disposable gloves are worn when handling isolation supplies
10 Injuries and suspected infections are reported immediately
11 Personnel are oriented to infection control policies on hiring; this is documented
12 Personnel attend department/facility-wide infection control in services monthly
13 Personnel are screened for infectious diseases on hiring and at further facility discretion
14 Personnel are informed of potential dangers/toxicities of cleaning compounds
15 Personnel, when informed of these potential dangers, follow safety procedures/precautions
16 Personnel are aware of methods to handle supplies and disposal of globes/equipment
Washing/Folding/Cleaning/Storage
1 Wash/rinse temperatures are maintained at a minimum of _____of for regular linen
2 Dryer temperatures are set at _____of for linen and regular clothes
3 Clean linens are transported in covered containers and stored in covered areas
4 Dirty linens are separated from clean ones at all times
5 Soiled linens are kept in a covered barrel at all times
6 Linen barrels are lined with plastic bags which cover the inside surface at all time
7 Isolation linen is transported as outlined in the Infection Control Manual
8 Linen folding surfaces are cleaned with a detergent germicide solution
9 All laundry appliances (washers/dryers, carts) are cleaned daily with detergent germicide solution
10 Supplies for clothing/equipment cleaning approved by Infection Control Committee
11 Equipment and supply problems are immediately reported to the administrator
………………………………………………….………………………………………………………………………………………………………………………………………..
Laundry Condition & Specific Location if needed: Initial
This document provides information on infection prevention and control strategies during construction and renovation projects in healthcare facilities. It discusses the objectives of preventing microbial spread from construction sites. It outlines various infection control measures that should be implemented, including erecting barriers, controlling dust and debris, maintaining proper ventilation, educating workers, and monitoring the project. The document emphasizes doing a risk assessment, relocating high-risk patients if needed, establishing traffic control, and ensuring ventilation and filtration. It also discusses strategies for internal projects, such as barrier containment, dust control, and cleaning and commissioning spaces after completion. The overall goal is to minimize infection risks during construction through planning and coordination.
The document outlines the essential factors for an ideal medical laboratory setup. It discusses the necessary infrastructure requirements including adequate laboratory premises, heating/ventilation/lighting systems, drainage, electricity, fire safety facilities, storage areas, IT systems, and qualified medical and non-medical personnel. It emphasizes the importance of proper biomedical waste management and maintaining a safe, clean, and hygienic environment for sample collection, analysis, and reporting. The document also highlights the roles of various laboratory staff in ensuring quality testing and delivery of diagnostic services.
This document defines biomedical waste and provides guidelines for its proper handling and disposal at the University of Ottawa. It outlines roles and responsibilities, defines key terms, and provides detailed procedures for waste segregation, containment, labelling, treatment, handling, transportation, storage, collection, and disposal. Biomedical waste must be properly contained and labelled according to type before undergoing required treatment such as autoclaving or chemical disinfection, and ultimately collection by the Office of Risk Management for off-site disposal. Adhering to these guidelines ensures biomedical waste is safely managed in compliance with regulations.
The document provides an overview of the Central Sterile Supply Department (CSSD) in a hospital. It describes the CSSD's functions like receiving, cleaning, sterilizing and distributing medical supplies and equipment. It outlines the layout, staffing, equipment and processes used in different areas of the CSSD like receiving, cleaning, packing and sterilization. Quality assurance procedures like the use of indicators and records maintained are also summarized.
This document discusses the management of hospital waste. It defines medical waste, regulated medical waste, and infectious waste. Regulated medical waste includes seven categories such as human pathological wastes and sharps. Infectious waste is categorized into seven groups like isolation wastes and contaminated sharps. An infectious waste management plan should include designation of infectious waste, segregation, packaging, storage, treatment, disposal, contingency measures, and staff training. Common treatment methods mentioned are autoclaving, incineration, thermal inactivation, gas/vapor sterilization, chemical disinfection, and sterilization by irradiation. The document emphasizes the importance of a clean environment for public health.
The document discusses biomedical waste management in hospitals. It defines different types of medical waste and their sources. It notes that most waste is non-infectious (80%) while pathological and infectious waste makes up 15%. It outlines 10 categories of biomedical waste and procedures for waste segregation, collection, storage, transportation, and treatment. Key steps include effective waste segregation at source using color coding, safe primary collection and storage, authorized transportation, and final treatment through incineration or other methods. Occupational safety and training of healthcare workers is also emphasized.
The document provides guidelines for endoscope disinfection and reprocessing. It defines key terms and outlines the optimal 6 step process: cleaning, rinsing, high-level disinfection, drying, rinsing, and storage. The steps involve manually cleaning with detergent followed by automatic disinfection, rinsing and drying in a reprocessor. The document also discusses control measures, disinfectants like glutaraldehyde, efficacy against different pathogens, advantages of automatic reprocessing, and different standards for areas with limited resources.
The document discusses medical and laboratory waste management. It defines infectious waste and outlines various types of waste generated from medical facilities. Key elements of infectious waste management are identified, including identification, segregation, packaging, storage, transport, treatment, and disposal. Common treatment methods like incineration are described. The importance of microbial inactivation testing to ensure treatment effectiveness is emphasized. Guidelines for acceptable levels of pathogen reduction are provided. The document concludes with recommendations around improving waste treatment guidelines and prioritizing occupational health and safety in medical waste management.
The Program file is created from various peer reviewed, and world standard protocols in implantation of Safe Operation theater standards for wider use in the world, In India still we do not have any set standards and practices, As good beginning is half done, I wish all my professional friends go through the article, your opinions and comments are highly appreciated for future developments,
Dr.T.V.Rao MD
This document provides a summary of the content areas and competencies tested on the Medical Laboratory Technician (MLT) certification examination. It is organized into six main sections: Blood Bank, Chemistry, Hematology, Microbiology, Urinalysis/Other Body Fluids, and Laboratory Operations. Each section lists the specific topics covered, such as blood typing and crossmatching in Blood Bank or electrolyte and protein testing in Chemistry. Competencies involve technical skills like performing laboratory tests, problem solving abnormal results, verifying quality control, and communicating with clinicians. The examination evaluates knowledge, interpretation, and problem-solving skills through multiple choice questions.
The document provides guidelines for hospital waste management in India based on the Bio-Medical Waste (Management & Handling) Rules, 1998. It outlines 10 categories of hospital waste and appropriate treatment and disposal methods for each category, including incineration, deep burial, autoclaving, microwaving, shredding, and secured landfilling. The guidelines emphasize segregation of waste, use of colored containers, and proper treatment to minimize health and safety risks from hazardous hospital waste.
Analytical instruments in clinical chemistry, uses and maintenanceJennifer Giovanna
The document provides guidelines for the proper use and maintenance of various analytical instruments used in clinical chemistry laboratories. It discusses spectrophotometers, flame photometers, pipettes, balances, centrifuges, autoclaves, refrigerators, freezers, ovens, water baths, and pH meters. Proper calibration and preventative maintenance are emphasized for ensuring accurate test results and extending the life of the equipment.
The document provides information about the Central Sterile Service Department (CSSD) and Biomedical Engineering Department at YMCH. It describes the functions, workflow, and processes of CSSD, including receiving, cleaning, packaging, sterilizing, storing and distributing instruments. It also outlines the roles and responsibilities of the Biomedical Engineering Department, such as maintaining medical equipment inventory, conducting planned and breakdown maintenance, and calibration.
The Leading Manufacturer and supplier of disinfection control system and infection control equipment. Owing to our quality proven range we have been able to carve a niche foothold in the industry such as Steam Sterilizers, Flash Sterilizers, Bulk Sterilizers, ETO Sterilizers, Pass Box, Wash Station With 2 Sinks, Linen Fold Table, Free Standing Basket Rack, Motorized Lift Table, Hydraulic Lift Tables, Fully Electric Bi-Position Painless Delivery Table, Motorised Lifting Multi-Position C-Arm Compatible Table, O.T. Lights - IS-24T, O.T. Lights - IS-7Rz, O.T. Lights - IS-5Rz, O.T. Lights - IS-4 Rz...
The document discusses the importance of maintaining proper standards in operation theatres to prevent surgical site infections. It emphasizes the need for surveillance of operation theatres which includes monitoring the quality of air. Air sampling methods like settle plate method and slit sampler are recommended to measure bacterial counts and ensure the air quality meets acceptable limits. Adhering to guidelines regarding zoning, ventilation, temperature, humidity and regular environmental monitoring can help minimize risks of infections.
This document provides guidelines for disinfecting ultrasound probes based on their level of use and contact. It outlines three levels of probe use - non-critical (intact skin), semi-critical (mucous membranes or non-intact skin), and critical/sterile procedures. For each level, it details the appropriate disinfection method, including cleaning, low-level disinfection, or high-level disinfection/sterilization. Proper cleaning is emphasized as the most important first step before disinfection. Storage and documentation requirements are also covered to ensure probes are properly processed between patients.
This document discusses various aspects of laboratory management including organizing the laboratory space, storing equipment and chemicals, purchasing supplies, and record keeping. It emphasizes the importance of proper storage, labeling, and stock control to ensure safety, availability of materials, and cost effectiveness. Key recommendations include storing chemicals by type in labeled cabinets and containers, maintaining minimum and maximum stock levels, and having processes for requisition, receipt, and auditing of all laboratory items.
1. A study examined the effectiveness of different cleaning methods for laryngoscope handles in reducing bacterial contamination.
2. Laboratory experiments showed that wipes containing chlorhexidine and alcohol were highly effective at eliminating bacteria immediately after cleaning and provided residual sterilization for up to 24 hours.
3. An audit of laryngoscope handles in a hospital found high levels of bacterial contamination before changing cleaning protocols, but contamination was significantly reduced after implementing the use of chlorhexidine wipes between patients.
Project Information
Accommodation Name:
Location: Company Name:
Date: Time :
Sl No. ITEMS TO BE CHECKED Yes No N/A Comments
Audit Check List for Laundry
1 The premises are cleaned & situated in an environment which has minimum risk for contamination.
2 Sufficient area for storage of unwashed clothes & washed clothes.
3 Washing & drying premises was found cleaned & in good condition.
4 There are arrangements to control the entry of rodents, insects and birds.
5 Clothes are collected washed & dried separately.
Infection Control Checklist Laundry Personnel
1 Clean, neat, untorn and appropriate clothing is worn
2 Closed toe shoes with safety soles and in good repair are worn
3 Good personal hygiene (including hair and body cleanliness) is practiced
4 Fingernails are clean and trimmed
5 Hair is neat and protected by covering
6 Strict clothing and linen handling procedures are followed to avoid contamination
7 Direct resident contact is avoided except in emergency situations
8 Rubber gloves and protective covering are worn when handling and loading soiled linen
9 Disposable gloves are worn when handling isolation supplies
10 Injuries and suspected infections are reported immediately
11 Personnel are oriented to infection control policies on hiring; this is documented
12 Personnel attend department/facility-wide infection control in services monthly
13 Personnel are screened for infectious diseases on hiring and at further facility discretion
14 Personnel are informed of potential dangers/toxicities of cleaning compounds
15 Personnel, when informed of these potential dangers, follow safety procedures/precautions
16 Personnel are aware of methods to handle supplies and disposal of globes/equipment
Washing/Folding/Cleaning/Storage
1 Wash/rinse temperatures are maintained at a minimum of _____of for regular linen
2 Dryer temperatures are set at _____of for linen and regular clothes
3 Clean linens are transported in covered containers and stored in covered areas
4 Dirty linens are separated from clean ones at all times
5 Soiled linens are kept in a covered barrel at all times
6 Linen barrels are lined with plastic bags which cover the inside surface at all time
7 Isolation linen is transported as outlined in the Infection Control Manual
8 Linen folding surfaces are cleaned with a detergent germicide solution
9 All laundry appliances (washers/dryers, carts) are cleaned daily with detergent germicide solution
10 Supplies for clothing/equipment cleaning approved by Infection Control Committee
11 Equipment and supply problems are immediately reported to the administrator
………………………………………………….………………………………………………………………………………………………………………………………………..
Laundry Condition & Specific Location if needed: Initial
The document outlines the key components of an effective hospital infection control program, including establishing an infection control team, committee, and manual. It emphasizes the importance of surveillance to monitor infection rates, preventive activities like standard precautions, and staff training. Standard precautions include proper hand hygiene, use of barriers like gloves and gowns, safe handling of sharps and contaminated materials, and maintaining a clean patient environment. The goal of the program is to reduce infection risk and increase safety.
The document provides guidelines for infection prevention and occupational health programs at the Faculty of Dentistry, October 6 University. It outlines policies for developing and maintaining infection prevention programs, including having training for staff on standard precautions, exposure risks, and proper use of personal protective equipment. It also details procedures for sterilizing dental instruments, cleaning the clinical environment, and managing exposures to infectious materials to minimize risk of disease transmission.
This document provides guidelines and best practices for high-level disinfection (HLD) of flexible endoscopes. It discusses the importance of cleaning prior to HLD to remove debris, and identifies the Spaulding Classification system for classifying medical devices based on infection risk. Critical and semi-critical devices that contact sterile tissues or mucous membranes must be sterilized or undergo HLD. The document outlines the HLD process, including pre-cleaning, leak testing, manual cleaning with brushes, rinsing, HLD with chemical agents, rinsing again, drying and storing. It emphasizes that cleaning is the most important step to remove debris before disinfection.
mantoux TEST GUIDELINE11111111111111 .pdfdmfrmicro
This document provides guidance for administering the Mantoux tuberculin skin test to test for latent tuberculosis infection. It outlines the necessary supplies, including tuberculin solution and syringes. It describes the two-part procedure of administering the injection and later reading the results. Key steps include patient education, selecting the injection site, cleaning the skin with alcohol, and ensuring the patient returns within 48-72 hours to read the results. Proper technique and following guidelines are important for accurately identifying those with latent TB infection.
This document provides guidelines for infection control measures related to Hepatitis B in a dental setting. It outlines procedures for immunizing dental personnel against Hepatitis B, managing exposures, testing involved individuals, and administering post-exposure prophylaxis if needed. It also details protocols for cleaning and sterilizing dental instruments and equipment, disinfecting surfaces, and properly disposing of contaminated waste to prevent the spread of infection. The document emphasizes the importance of thorough cleaning, use of protective equipment, and established decontamination procedures to control transmission of Hepatitis B and other pathogens in dental facilities.
Project Management- Hospital and Healthcare Management NaheedaFatimaKhan
Planning 25 bed hospital in an emergency to be used as an isolation facility for patients of covid-19 in a rural area.
Elaboration for staffing and other requirements
The document discusses guidelines for developing and implementing an effective infection control program in hospitals, including establishing an infection control team, conducting surveillance to monitor infection rates, implementing standard precautions like hand hygiene and proper waste disposal, and using antimicrobials appropriately through an understanding of their mechanisms of action and developing resistance.
The document outlines standards for hospital infection control (HIC) at the pre-accreditation entry level. It discusses three main HIC standards: HIC 1 specifies that the hospital must have an updated infection control manual and conduct surveillance activities to monitor cleanliness, disinfection practices, and laundry management. HIC 2 requires the hospital to take measures to prevent hospital-acquired infections through proper hand hygiene, use of personal protective equipment, and provision of post-exposure prophylaxis. HIC 3 mandates that the hospital follow bio-medical waste management practices, including proper segregation, collection, and disposal of waste in accordance with regulatory provisions.
1) The document discusses safely conducting urine drug and alcohol tests (UDAT) during the COVID-19 pandemic.
2) Proper personal protective equipment, social distancing, sanitization measures, and specific guidelines for cleaning breathalyzers between each use are outlined to minimize risks.
3) Legal and operational safety considerations for UDAT are also reviewed, including ensuring facilities and processes meet basic infection control standards and legal regulations.
Laboratory waste management in medical/health universityShira Shahid
Laboratory waste management in medical and health universities must follow regulations and guidelines to properly handle and dispose of waste. Regulations in Malaysia are set by the Department of Environment and classify waste as clinical, radioactive, chemical, or general. Waste must be segregated by color-coded containers and properly labeled. Proper procedures include contracting licensed services for disposal. Students should be trained on guidelines to mitigate health and environmental risks. While Malaysia has regulations, its management system could be improved compared to international standards by more strictly enforcing rules.
The document outlines Good Laboratory Practices (GLP) which were introduced in response to cases of fraudulent activities and poor lab practices discovered by the FDA in the 1970s. GLP helps ensure data submitted is a true reflection of study results and can be relied upon for risk assessments. It establishes standards for laboratory facilities, equipment, personnel qualifications, organization, standard operating procedures, test and control articles, protocol for conducting studies, and maintenance of raw data. Adhering to GLP helps assure regulatory authorities that submitted safety data is of high quality and integrity.
Cleaning and disinfection waste management disposalGerinorth
This document summarizes best practices for infection control related to waste management, cleaning and disinfection, sharps management, and linen management in a nursing home setting. The key points covered include:
- Proper segregation of waste types and use of color-coded bags and bins for hazardous, infectious, and general waste.
- Cleaning and disinfection techniques including types of cleaning, frequency of routine cleaning for high-touch and low-touch areas, and steps for terminal cleaning.
- Safe practices for sharps disposal and management of needlestick injuries.
- Segregation of clean, used, soiled and infectious linen and proper handling, transportation, and storage.
IC in ICU.pdf infections in icu and how to deal with it perfectlyswiftkeys339
This document discusses infection control in the ICU. It outlines several factors that increase patients' risk of infection, including therapeutic interventions, host factors like compromised immune systems, and environmental issues. To reduce risk, it recommends measures related to host factors like proper isolation and antibiotic use. It also suggests improving therapeutic practices through antibiotic stewardship, medical/surgical asepsis, and medication preparation. Additionally, it advises environmental strategies like ensuring proper ICU design with adequate space, traffic flow, and ventilation; regularly cleaning patient equipment and the environment; and maintaining appropriate liquid container hygiene. The goal is to break the chain of infection through multidisciplinary preventative measures.
Clinic A clinic Was investigated in Chief Albert Luthuli Local municip.pdfemilemathez
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WASH evaluation To evaluate access to WASH, a Water and Sanitation for Health Facility
Improvement Tool (WASH FIT) dealing with WASH conditions, availability, supply, sanitation,
hygiene, and waste management was used to obtain WASH aspects of the health care clinics
(WHO, 2017). The WASHFIT used is divided into essential and advanced indicators for the four
domains which include water, sanitation and healthcare waste, and hygiene. Three domains of
the WASHFIT including water, sanitation and hygiene were investigated in this study. The
indicators for each domain were ranked from meets target, partially meets target, and does not
meet target; this ranking was explained by the tool for each indicator. For instance, a water
indicator on improved water supply piped into the premises of the facility (clinic). According to
the tool this indicator is met when there is improved supply within the facility and available,
partially met when water supply is outside of facility building and available, and the target is not
met when there is no improved water source within facility grounds (WHO, 2017). Sample
collection Samples were collected in 290 mL Sodium Thiosulphate sampling bottles and
transported on ice. Four tap water samples were collected from each site which included
kitchen, bathroom, consultation room and an outside tap. Physicochemical parameters such as
pH, temperature, electrical conductivity, and total dissolved solids were measured onsite using
the pH/EC meter (HANNA Instruments, USA). Total and Free chlorine was measured using the
YSI 900 chlorine meter .Turbidity was measured using the TN-100 EUTECH. The
microbiological analysis of the samples was carried out within 6 hours of collection. For this
analysis,100 mL of the sample was used in the detection of E. coli and coliforms using the
IDEXX Colilert Quanti-Tray/2000 assay according to manufacturers instructions. The following
tables answered interview question show the results which were found in the clinic Questions
AND answers for semi-structured Interviews To find out the challenges faced by the clinics in
terms of WASH 1. What is the main source of water in the facility? Municipal 2. Any backup or
alternative source of water? -JoJo Tanks 3. Does it happen that the facility stays without water
supply from the main source? Yes 3.1. How long does it usually take? -1 TO 2 WEEKS 4. Who
do you report to when experiencing water shortages? - Municipality 4.1. What is being done
when you report water shortages? -Tanks get filled with water by municipal trucks 5. How often
do hygienic products (Sanitizers, soaps, cleaning material) get supplied in a year?- irregular 6.
Do you have to apply for hygienic products to be supplied? -ordered 6.1. Who do you apply to?
-Caroline hospital 6.2. How long does delivery take after application?- 2 weeks 7. Are there any
challenges you face in terms of the supply .
This document defines an investigational product and outlines requirements for its use in clinical trials. An investigational product refers to a drug, biologic, device, or other therapy being studied for safety and efficacy. Key points covered include that investigational products must be manufactured and handled according to Good Manufacturing Practice standards and used per the approved trial protocol. Labeling, storage, and distribution of investigational products are also discussed.
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The document provides data on staff data quality in various departments at WRNMMC. It shows the percentage of staff in each department that have complete data profiles in the DRMSi system, ranging from 5% in DRO to 100% in DRM. It identifies five key elements for data quality: comparing to DRMSi, new account registration, email, date of birth, and supervisor. It provides contact information for the WRNMMC Safety Representative Coordinator to address data quality issues.
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This document outlines metrics and programs to promote excellence, quality, safety, and a culture of respect at a Regional Health Command facility. It discusses visions of taking care of patients, employees, and self through compassionate care. Various references are provided relating to continuous process improvement, lean management, safety culture, and reducing risk through teamwork. The goal is to innovate teamship, simplify processes, and deliver initiatives from 2016-2017 to align safety reporting, risk management, and achieve a high reliability organization through employee pledges, training, and communication.
This document outlines metrics and programs to promote excellence, quality, safety, and a culture of respect at a Regional Health Command facility. It discusses visions of taking care of patients and employees while taking care of oneself. Programs are described to optimize patients and employees through a learning experience and campaign centered on Army values. Specific metrics and references are listed to guide readiness, education, teamwork, process improvement, and access to care. Goals and assessments are outlined for patient safety, organizational safety, reporting, investigation, and counseling. The document provides references for continuous improvement and transforming safety culture.
1. PATIENTCARE VERSION
Schedule: Completed by: Initials
JAN / /
FEB / /
MAR / /
APR / /
MAY / /
JUN / /
JUL / /
AUG / /
SEP / /
OCT / /
NOV / /
DEC / /
Ref: (a) The Joint Commission Accreditation Standards for Ambulatory Care, Environment of Care, 2016
/
CoZAR system owner: Naval Health Clinic Patuxent River, Environment of Care Committee
CONSOLIDATED ZONE ASSESSMENT REPORT (CoZAR) ANNUAL TRACKER FOR DEPT:
Directions: The CoZAR may be completed anytime during each month. One purpose is to cross assign and involve several staff in a continual
department education and inspection system as they look around their departmental spaces, and talk with staff.
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Environment of CareInfection Control
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DirectorDept HeadTraining
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p.2 p.3 p.4 p.5
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2016
Page 1 tracks use, pages 2-9 are the CoZAR (Tool), and page 10 tracks deficiencies. The CoZAR (Help) is 6 pages.
p.6 p.7 p.8 p.9
/
CY
/
/
Due qtrly Due qtrlyDue
Submit CeZAR for BHCs and Directorates before the 5th monthly at
https://nhcpr-intra.nmed.ds.med.navy.mil/safe/CeZAR/Forms/AllItems.aspx
Reviewed by: Initial / Date
Patient Safety/Risk Mgmt
Due 5th monthly
NHCPR 5100 ( ) Page 1 of 10
2. # opportunities observed
/
# times 2 identifiers used
# Observed / # times
specimens are labeled in
front of patient
Fall Prevention Program
JUL AUG SEP OCT NOV DEC
Number
Reviewed: 0Goal 1: Improve the accuracy of patient identification
1. Verifies name & DOB with patient or family member when staff administers
meds and verifies 2 identifiers with records.
Direct
Observation
(Minimum: 5)
Month
JAN FEB MAR APR MAY JUN
JUL AUG SEP OCT NOV DEC
2. Verifies name & DOB with patient or family member when taking blood or
other specimens for clinical tests.
3. Verifies name & DOB with patient or family member when providing
treatments/testing (i.e. Radiology)
4. Containers used for blood and other specimens are labeled in the presence of
the patient (i.e. pap smears, bx containers)
Goal 7: Reduce the risk of health care-associated infections
Number
Compliant: 0
Month
JAN FEB MAR APR MAY JUN
Patient Safety (PS)
Goal 3: Improve the safety of using medications
5. Critical test results are reported to the ordering physician/provider or
designee within 60 minutes. (Lab)
# reviewed /
# of reports per policy
2. Medication list is reconciled via Ahlta and documented that reconciliation was
documented.
3. Medications are reconciled at each outpatient, including OTCs, herbal, and
other supplements via AHLTA.
1. Comply with current hand hygiene guidelines.
2. Measure procedure site infection rates for the first 30 days following
procedures.
Review 10
records
# records reviewed
/ # of records with proper
reconciliation
1. UP 1 Operative ite Marking completed by person performing the case and
consist of that person's initials.
2. UP 1 "Time-out" completed and documented.
# records reviewed
/
# of records with proper
reconciliation
4. Provide the patient (or family as needed) with written information on the medications
the patient should be taking. Explain the importance of managing medication information
to the patient at the end of the episode of care.
Review 10
records
6. Critical test results are reported to the ordering physician/provider or
designee within 60 minutes. (Radiology)
# critical tests reviewed
/ # instances where
report was given per
policy
1. Can staff identify how to report a fall/unsafe condition?
# records reviewed
/ # of records that
document current list of
meds.
Yes or No
# of procedures requiring site marking /
# of site markings done
# of procedures reviewed /
# time-outs documented
Review 5
records
1. Medications, containers, and solutions are labeled. This includes medications on sterile and
unsterile fields. (i.e. syringes, medicine cups, basins, or other containers)
Review 10
records
# opportunities observed /# times correct
PERFORMANCE MEASURES (POC Mr. Akbari at 301-342-3097)
UNIVERSAL PROTOCOL (UP) "Time-Out and Verification Process
NHCPR 5100 ( ) Page 2 of 10
3. 28. Receptacles designated for shredding PHI/PAI/PPI are properly monitored and regularly
emptied? Check trash/waste receptacles for improper disposal of documents?
27. Documents/etc. with Protected Health Information (PHI), Privacy Act information (PAI) or Personal
Private Information (PPI) are properly stored, protected, and/or disposed?
0
OCT NOV DEC JUL AUG
# No Total: 0
25. Monthly AED Operator's Checklist is completed?
26. Staff know the policy and process of proper handling and disposal of documents/media with
PHI/PAI/PPI information and how to report violations? (contact Privacy Officer)
HIPAA (POC: Ms. Foster)
# COTS Total:
24. The phone number to call for all medical emergencies is known? Answer: 911 for all codes.
22. High alert medications are readily identified by staff?
23. The code for cardiac emergency is known? Answer: Code Blue.
Resuscitation (POC: Dr Culp)
#COTS Total: # No Total:0 0
0 # No Total:
17. If temperature out of range, was action documented on the form (does staff know process to
follow when refer temperatures are out of range)?
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
N/A
Risk Management (RM)
18. Are medications within their expiration date?
Medications (POC: LT Martin)
# COTS Total: 0
19. Multiple-dose vials are dated with date entered and 28 day expiration date (or expiration per
manufacturer's recommendations)?
20. Single dose vials are destroyed after single use, after one hour of opening or one hour after seal
puncture?
21. Sound Alike Look Alike Medications are readily identified by staff?
Month Month
JAN FEB MAR APR MAY JUN JAN FEB MAR APR MAY JUN
JUL AUG SEP
16. Immunization refrigerators temperatures are logged TWICE every day?
SEP OCT DECNOV
# Assess-
ed
PERFORMANCE MEASURES
NHCPR 5100 ( ) Page 3 of 10
4. 38. Expiration dates are checked monthly on all containers of hand soap and waterless hand
hygiene products. Expired items are removed and replaced with items ready for use.
32. Infection control training is conducted annual on SWANK Health
33. Staff know that the Infection Control Manual is accessible on the NHCPR Intranet and can
demonstrate how to use it. F:0000 ALLINFECTION CONTROL MANUAL
46. Observation of clinical workspaces shows them to be free of all food and drink items.
47. Space below sinks free of patient care items. (Examples of exceptions: Properly labeled cleaning
supplies, unused sharp’s containers, plastic bags)
40. Separate refrigerators used to store biological specimens, medications, and food.
41. Biohazardous waste or infectious waste is segregated correctly. In Red bag trash, and sharp
containers.
42. Soiled utility room maintained in clean, organized manner.
43. Dirty linen is handled appropriately and closed containers used.
44. Patient care equipment cleaned and decontaminated correctly.
45. Cardboard shipping boxes removed from sterile/clean storage and patient care spaces.
39. Medication, specimens, and food are appropriately handled to avoid cross contamination.
34. Personal protective equipment is readily available and staff can explain when to use it.
35. Staff employ correct hand hygiene measures. Hands washed before and after patient contact.
Dispensers are not above or adjacent to electrical items, 48 inches high and separate.
36. Clean/sterile patient care supplies are stored appropriately (floor clearance: 8-10" sterile, >3"
clean. 18" from ceiling, liquids below solids, separated from dirty, prefer sterile above clean, expirable
items together, FIFO).
37. Expiration dates are checked monthly on sterile/non-sterile patient care supplies. Expired items
are removed and replaced with items ready for use.
# COTS Total: 0 # No Total: 0
30. The unit/area presents a clean appearance (without dust or debris) paying particular attention to
equipment, patient furniture, exam tables, chairs, etc.
31. In areas where toys are made available in the department, these items are cleaned DAILY and
whenever necessary using an approved hospital grade cleaner/disinfectant.
MAY JUN
JUL
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
N/A
Month Month
JAN FEB MAR APR JAN FEB MAR APR MAY JUN
AUG SEP
General-Direct Observation (see)
OCT NOV DEC JUL AUG SEP OCT NOV DEC
Infection Control (IC) / Department IC Representative
# Assess-
ed
PERFORMANCE MEASURES
NHCPR 5100 ( ) Page 4 of 10
5. Respiratory Etiquette / Other # COTS Total: 0 # No Total: 0
51. Dirty linen carts are covered and bags not left in corridors unattended.
56. Waste receptacle and alcohol based hand sanitizer are present and maintained in waiting area by use
of patients/visitors. Patients are provided a mask when they present signs or symptoms of a cold or flu.
N/A
AUG SEP OCT
53. Recapping is by scoop or one hand method. (passive technique)
54. Sharps containers are changed when ¾ full or have foul odor, then disposed of properly.
55. Sharps containers in patient care areas are wall mounted or if on floor, secured and out of reach of
children. Optimal distance for standing is 52 to 56 inches high and 11 to 19 inches reach.
Sharps # COTS Total: 0 # No Total: 0
52. SAFETY DEVICE is immediately activated with one hand after use.
Rolling Stock # COTS Total: 0 # No Total: 0
48. Bottles of irrigating solution such as sterile water or saline are one time use only.
49. Low level disinfectant (CaviWipes XL Wipe, 2 minute wait time) is used to clean patient transport
devices, countertops and surfaces - when?
50. Clean linen carts are covered, have solid bottom shelves and protected from dirt/dust.
Month Month
JAN FEB MAR APR MAY JUN JAN FEB MAR APR MAY JUN
JUL NOV DEC JUL AUG SEP OCT NOV DEC
Infection Control (IC) / Department IC Representative
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
# Assess-
ed
PERFORMANCE MEASURES
Infection Control Comments:
NHCPR 5100 ( ) Page 5 of 10
6. Environment of Care (EC) Zone Assessment Report: Patient Care Departments
74. Lead Apron and Collar devices are hung on should hangers and not laid over items. Examined
before each use for holes, rips and tears - include shoulder straps. If defective, turn into DRMO.
73. Operator's Manual available in department or on Sharepoint?
71. Patient injury because of medical equipment malfunctions are reported using a PSR?
72. PM sticker and ECN# are on equipment / DATE NOT Overdue?
69. Full acceptance procedures known before using medical equipment?
70. Broken or malfunction medical equipment / Defective Equipment Tag and procedure known?
DEC
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
N/A JAN FEB MAR APR MAY JUN JAN JUNMAR APR MAY
Month Month
JUL AUG SEP OCT NOV DEC JUL AUG
FEB
SEP OCT NOV
68. Unlock toilet or room where a patient can lock themselves in? (Try coin to unlock. Know where to
find keys to all rooms)
67. ESAMS: Is staff email and supervisor (safety rep.) accurate? Is date of birth entered?
66. ESAMS: Are staff transferred to deactivated so ESAMS roster is accurate?
65. Emergency call system at patient toilet is tested & functions? Total # ____
64. ESAMS: Have all staff been added and completed initial log-in at this command?
62. Pediatric toys and treats are non-chokable; will not hurt eye or puncture skin?
63. Chairs with wheels prohibited for patient use?
61. Patient waiting area - chairs, connectors, and furniture in good, safe condition?
59. Alarm sounds differ and recognized by staff? Test an alarm and reset per local procedures.
58. Emergency Electrical Power. Outlets are labled "emergency power" or identified in red? Staff
know equipment, outlets and areas on emergency power when the generator is activated?
60. Patient lift devices and methods known by staff?
57. Safety needle device is used immediately after withdrawal using one hand method? Needles,
syringes and sharps are controlled to prevent unauthorized access?
Additional items not addressed on pages 6 (to customize for your people, spaces and processes) # COTS Total: 0 # No Total: 0
Medical Equipment # COTS Total: 0 # No Total: 0
Safety # COTS Total: 0 # No Total: 0
# Assess-
ed
PERFORMANCE MEASURES
NHCPR 5100 ( ) Page 6 of 10
7. 87. Safety Data Sheet and, symptoms of exposure and first aid readily found by staff?
96. Code Red Drill during inspection. Staff able to locate Fire Station Bill, call Code Red, and verbalize
emergency exits and muster location? RACE (Rescue, Alarm, Contain, Evacuate)
94. Fire Extinguisher inspected Monthly - unobstructed, seal not broken and tag initialed?
95. Sprinkler heads have an 18-inch clearance in entire room? (exception in helps)
92. Corridors are unobstructed. Temporary items not left over 30 minutes?
93. Doors fully open and close, without sticking? When pulled closed - it must latch.
90. Medical Gas Shutoff - Location and procedures known?
91. PASS procedures known for fire extinguisher use? (Pull pin, Aim nozzle, Squeeze handle, Sweep
nozzle). Locate department fire extinguishers and tell what type they are?
88. Emergency eyewash/showers are tested weekly and a log maintained with signature and date
tested? Staff are trained on location and use eyewash/showers? Not blocked?
89. Medical Gas Cylinders are secured, empty and full are labeled and seperated? Caps on?
85. Hazardous Material Authorized Use List (HMAUL) was last updated no more than 12 months
ago and is used as the table of content for the Safety Data Sheet (SDS) Binder?
86. Hazardous Material containers are labeled clearly with manufacturer's label? Flammables and
corrosives are properly stored. Hazardous waste properly stored and disposed of?
83. Asbestos and lead materials in the building is in good condition - not damaged?
84. Code Orange procedures for hazardous material spill cleanup is known?
# No Total:
81. Storage/Supplies are maintained to prevent creating a safety hazard? (not stacked too high or
unstable, not stored in front of fire doors, fire extinguishers, fire exits or electrical panels)
82. Personal Protective Equipment is available, in good condition & staff explain when to use?
79. Monthly Safety Talk is read by 100% of staff?
80. Slip, trip and fall hazards are promptly repaired or removed? (floors maintained in a dry condition
and clear of trip hazards? (e.g. electrical cords, telephone wires, computer cables)
78. Ergonomic - Back Injury Prevention methods known? No related discomfort or pain?
77. Indoor Air Quality is comfortable; with no toxic, unhealthy or unpleasant exposures?
OCT NOV DEC
JUN
JUL AUG SEP
Environment of Care (EC) Zone Assessment Report: Patient Care & ALL Departments
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
N/A JAN FEB MAR APR MAY JUN JAN FEB MAR APR MAY
75. Annual safety goal for 2016? Increase Enterprise Safety Analysis Management System (ESAMS)
training compliance from 50% to 90%.
Month Month
OCT NOV DEC JUL AUG SEP
76. Safety Bulletin Board location and identify at least one item? (Unsafe Condition Report - OPNAV
5100/11, Civil Service and MLC employee mishap information, DD Form 2272, etc.)
# COTS Total: 0 # No Total: 0Fire Safety
Hazardous Material and Waste
Safety and Security # COTS Total: # No Total:0 0
0 0# COTS Total:
# Assess-
ed
PERFORMANCE MEASURES
NHCPR 5100 ( ) Page 7 of 10
8. FEB MAR APR MAY JUN
Month Month
NOV DECDEC JUL AUG SEP OCTJUL AUG SEP OCT NOV
N/A JAN FEB MAR APR MAY JUN JAN
Environment of Care Zone (EC) Assessment Report: Patient Care & ALL Departments
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
113. Are all exits signs fully iluminated? Are exit lights tested monthly for 30 seconds? 90 minutes
annually?
Environment of Care Comments.
112. Plumbing handles/fixtures operate appropriately? Not loose or leaking? Showers/ faucets
operate properly? Water temperature and pressure? Commodes flush properly?
110. Recycling options are used within their workspaces? (Blue bins for white paper, brown bins for dry
cell recycle batteries, and bins by soda machines for bottles and cans)
111. Heat maximum 20 ℃ in winter. Cool minimum 25 ℃ iin summer.
108. Environmental Goal for 2016? .
109. Energy Conservation - are lights and air / heat secured when nobody is present?
106. Smoking policy is enforced? No smoking allowed at grounds? No cigarrette butts found?
107. Environmental Policy - Are personnel aware of the CO's Environmental Policy Statement?
# COTS Total: 0 # No Total: 0
104. Electric Safety: extension cords/multiple outlets are not used for refrigerators, coffee pots,
mircowaves, space-food-water heaters? No damage, wear or tear? Dept. Self-Inspections.
105. Space heaters have written authorization from Facilities Managemente. Only oil cooled space
heaters are used in admin rooms?
102. Signage is accurate and facilitates patient traffic flow? Signage is on approved bulletin boards and
laminated in patient care spaces (not taped or thumb tacked to walls or doors)?
103. Staff food refrigerator clean? Refrigerator labeled with magnetic sign from Safety Office?
100. Inspect floor - is it intact, free from damage and no soiled carpet?
101. Good Housekeeping - orderliness, cleanliness, and no gear adrift? No clutter in storage areas?
Items marked for DRMO and processed promptly?
98. Inspect furniture - for safe and good condition? (no broke armrests, legs or components, no soiled
or torn fabric. If need replaced, order through Materials Management)
99. Inspect ceiling - lights are working and ceiling tiles are not broken, stained, or need replaced?
97. Inspect walls - decorations, cabinetry for finish quality, holes, permanent stains, damage. All in
good condition? Cables & wires are secure, covered & neatly organized-removed if unused?
# COTS Total: 0 # No Total: 0
Additional items not addressed on pages 7 & 8 (to customize for your people, spaces and processes) # COTS Total: 0 # No Total: 0
Environmental and Energy Conservation
Facilities: Submit DMLSS Work Request
# Assess-
ed
PERFORMANCE MEASURES
NHCPR 5100 ( ) Page 8 of 10
9. SEAT Comments:
Training
Yes is default answer. # Assessed. "N/A" 1st time. Corrected On The Spot (COTS). If not able to COTS, No - Note action on page 10.
N/A
Month Month
JAN FEB MAR APR MAY JUN JAN FEB MAY JUN
JUL AUG SEP OCT NOV DEC JUL AUG SEP OCT NOV DEC
# COTS Total: 0 # No Total: 0
1. Do all staff members have a work-space specific competency completed, including annual updates
within their training jacket?
2. Do all staff members have a completed EOC orientation within 48 hours of check in to the work center
in their training jacket?
3. Do all staff members have a current, signed position description in their training jacket?
4. Do all staff members have a signed Privacy Act statement that does not contain their full SSN in their
training jacket?
29. Dept SOPs "say what they do and do what they say"
5. Are all clinical staff currently certified in BLS skills?
# Assess-
ed
PERFORMANCE MEASURES MAR APR
NHCPR 5100 ( ) Page 9 of 10
10. Note: Please add another page now.
31 Jun 2013Y
HM2 Sharp submitted DMLSS Work Request to repair on
16 Jun 2013.
99
EXAMPLE: Ceiling tile broken in corridor - 1/2 hole on
left corner. Outside of room 2C35. 15 Jun 2013
Completed Y/N - dateAction (DMLSS Work Request, Purchase Req., Trng.)
Deficiency (No) Tracker - Not able to Correct On The Spot (COTS)
Item Description, location, and date
NHCPR 5100 ( ) Page 10 of 10