Hazardous drugs used in healthcare can harm workers through occupational exposure. Exposure risks depend on a drug's toxicity, route of exposure, physical/chemical properties, formulation, and workplace activities. Closed system drug transfer devices (CSTDs) can help minimize exposure by mechanically preventing drug transfer outside the system. National Institute for Occupational Safety and Health (NIOSH) recommends using CSTDs during handling and administering hazardous drugs as part of a safety program including training, exposure assessment, and emergency procedures. NIOSH is developing a test protocol to evaluate CSTD performance in containing hazardous drugs.
This document outlines patient safety goals and standards. It defines key terms like risk and safety. It lists international patient safety goals such as identifying patients correctly and reducing healthcare associated infections. National patient safety goals are discussed in more detail and include accurately identifying patients, improving caregiver communication, safely using medications, reducing anticoagulant therapy harm, maintaining accurate medication information, reducing clinical alarm hazards, and preventing healthcare associated infections. The document provides specific requirements for implementing several of the national goals.
Under the former NJ Governor Christie administration, a 2017 law was passed to begin the process of identifying stakeholders who may be able to construct legislation to protect healthcare workers who are exposed to hazardous drugs in oncology. Some work practices place pharmacists, animal handlers, veterinarians, oncologists and nurses at risk of contact with these toxic drugs. Many of these drugs cause terratogenic and mutagenic effects in both men, women, and offspring. The National Institute for Occupational Safety and Health (NIOSH) identified 204 hazardous drugs, which may be toxic to exposed workers. In addition, both the State of Washington and California have enacted legislation to protect all workers from exposure, which includes training, biological monitoring and medical surveillance. This is a very important issue that needs further review and consideration.
This document provides guidelines for improving the labelling and packaging of injectable medicines to enhance patient safety. It summarizes research conducted with healthcare professionals and experts in design. The guidelines illustrate design practices that clearly identify contents and minimize the risk of selection errors. Specific recommendations are provided for ampoules, vials, pre-filled syringes, and infusion bags. Adopting standard practices for prominence of generic names, font size and type, contrast, and critical information can help reduce medication incidents.
Patient safety is a fundamental principle of healthcare. Adverse events can result from problems in various areas of care and improving safety requires a complex, system-wide effort. Ensuring safety involves assessing risks, preventing harm, reporting and analyzing incidents, learning from mistakes, and implementing solutions. Guidelines include proper identification of patients, hand hygiene, medication reconciliation, and fall prevention.
Pharmacovigilance involves monitoring the safety of drugs at all stages, from development through post-marketing. It aims to detect, understand, and prevent adverse drug reactions through activities like adverse event reporting, drug monitoring, and studying medication errors and drug-related deaths. Pharmacovigilance is important for protecting public health as patterns of drug use change over time with globalization and advances in technology and medicine.
Glossary of terms used in pharmacovigilance. FINAL.pdfAlfiaAnsari2
1. The document defines key terms related to pharmacovigilance including adverse drug reactions, adverse drug events, side effects, serious adverse events, and differences between them.
2. An adverse drug reaction is an unwanted reaction that is related to the pharmacological properties of the drug. A side effect is also an unwanted effect but is mild and expected based on the drug's properties.
3. An adverse drug event may or may not be related to the drug and includes any medical occurrence during treatment, while a serious adverse event poses a serious threat to health.
Health care workers (HCWs) involved with hazardous drugs (HDs) may be exposed to them in the air, on work surfaces, clothing, patient excreta, etc. At-risk workers include pharmacists, pharmacy technicians, nurses, physicians, operating room staff, environmental services workers, research laboratory workers, home HCWs, and others. Studies have linked workplace HD exposures with health effects such as skin rashes, adverse reproductive outcomes, leukemia, and other cancers. Because risk is influenced by the extent of HD exposure as well as the potency and toxicity of HDs, USP standards have been developed to minimize exposure and promote HCW safety. Although there is an increased awareness of the risks of HD exposure, these safety standards are not universally implemented and compliance is often inadequate. Occupational health/safety professionals are responsible for executing a comprehensive HD program that includes hazard communication, administrative, and engineering controls.
This document outlines patient safety goals and standards. It defines key terms like risk and safety. It lists international patient safety goals such as identifying patients correctly and reducing healthcare associated infections. National patient safety goals are discussed in more detail and include accurately identifying patients, improving caregiver communication, safely using medications, reducing anticoagulant therapy harm, maintaining accurate medication information, reducing clinical alarm hazards, and preventing healthcare associated infections. The document provides specific requirements for implementing several of the national goals.
Under the former NJ Governor Christie administration, a 2017 law was passed to begin the process of identifying stakeholders who may be able to construct legislation to protect healthcare workers who are exposed to hazardous drugs in oncology. Some work practices place pharmacists, animal handlers, veterinarians, oncologists and nurses at risk of contact with these toxic drugs. Many of these drugs cause terratogenic and mutagenic effects in both men, women, and offspring. The National Institute for Occupational Safety and Health (NIOSH) identified 204 hazardous drugs, which may be toxic to exposed workers. In addition, both the State of Washington and California have enacted legislation to protect all workers from exposure, which includes training, biological monitoring and medical surveillance. This is a very important issue that needs further review and consideration.
This document provides guidelines for improving the labelling and packaging of injectable medicines to enhance patient safety. It summarizes research conducted with healthcare professionals and experts in design. The guidelines illustrate design practices that clearly identify contents and minimize the risk of selection errors. Specific recommendations are provided for ampoules, vials, pre-filled syringes, and infusion bags. Adopting standard practices for prominence of generic names, font size and type, contrast, and critical information can help reduce medication incidents.
Patient safety is a fundamental principle of healthcare. Adverse events can result from problems in various areas of care and improving safety requires a complex, system-wide effort. Ensuring safety involves assessing risks, preventing harm, reporting and analyzing incidents, learning from mistakes, and implementing solutions. Guidelines include proper identification of patients, hand hygiene, medication reconciliation, and fall prevention.
Pharmacovigilance involves monitoring the safety of drugs at all stages, from development through post-marketing. It aims to detect, understand, and prevent adverse drug reactions through activities like adverse event reporting, drug monitoring, and studying medication errors and drug-related deaths. Pharmacovigilance is important for protecting public health as patterns of drug use change over time with globalization and advances in technology and medicine.
Glossary of terms used in pharmacovigilance. FINAL.pdfAlfiaAnsari2
1. The document defines key terms related to pharmacovigilance including adverse drug reactions, adverse drug events, side effects, serious adverse events, and differences between them.
2. An adverse drug reaction is an unwanted reaction that is related to the pharmacological properties of the drug. A side effect is also an unwanted effect but is mild and expected based on the drug's properties.
3. An adverse drug event may or may not be related to the drug and includes any medical occurrence during treatment, while a serious adverse event poses a serious threat to health.
Health care workers (HCWs) involved with hazardous drugs (HDs) may be exposed to them in the air, on work surfaces, clothing, patient excreta, etc. At-risk workers include pharmacists, pharmacy technicians, nurses, physicians, operating room staff, environmental services workers, research laboratory workers, home HCWs, and others. Studies have linked workplace HD exposures with health effects such as skin rashes, adverse reproductive outcomes, leukemia, and other cancers. Because risk is influenced by the extent of HD exposure as well as the potency and toxicity of HDs, USP standards have been developed to minimize exposure and promote HCW safety. Although there is an increased awareness of the risks of HD exposure, these safety standards are not universally implemented and compliance is often inadequate. Occupational health/safety professionals are responsible for executing a comprehensive HD program that includes hazard communication, administrative, and engineering controls.
This document outlines patient safety in healthcare facilities. It defines key terms like patient safety, psychological safety, and safety culture. It discusses the roles of the patient safety committee and the components of a patient safety plan. Specific patient safety issues in the intensive care unit are examined, like collaboration among ICU staff and common errors. International patient safety goals are provided, such as accurately identifying patients and reducing healthcare-associated infections. Root cause analysis is introduced as a way to investigate incidents and prevent future errors.
Medication Safety- Administration and monitoring.pptxLatha Venkatesan
The document discusses medication safety and reducing medication errors. It covers several key points:
1) Medication errors are common, especially during transitions of care between settings. The WHO aims to reduce medication-related harm by 50% through their "Medication Without Harm" challenge.
2) Medication errors can occur at various stages like prescribing, transcribing, dispensing, and administering. High-risk medications and situations like polypharmacy also increase error risk.
3) Strategies to improve safety include training, protocols, technology like CPOE, reconciliation, and empowering patients. A multidisciplinary team approach is important to strengthen systems and practices.
The document discusses the International Patient Safety Goals (IPSG) which were developed by the Joint Commission International to help improve patient safety. It provides background on how the IPSG were adapted from the National Patient Safety Goals established by the Joint Commission. The document then outlines several of the IPSG, including proper patient identification, improving staff communication, reducing risks associated with medications, and preventing wrong site/procedure surgery. The goals are aimed at reducing common safety issues and medical errors in healthcare facilities.
Pharmacovigilance is the science of monitoring the safety of medicines. It aims to detect adverse effects from drugs, understand their causes, and prevent patient harm. Pharmacovigilance programs collect reports of adverse drug reactions and analyze the data to identify safety issues, quantify risks, and communicate safety information to patients and healthcare professionals. The ultimate goals are to protect patients and promote the safe use of medicines.
Patient safety goals effective january 1, 2016Hisham Aldabagh
Includes the patient safety goals which must be achieved during the year 2016, focusing on patient identification, proper patient medication, protection patient against infection, and strict per operative patient safety procedures
The document discusses the importance of pharmacovigilance in health care. It defines pharmacovigilance as the science related to detecting, assessing, understanding, and preventing adverse effects of drugs. The main goals of pharmacovigilance are to improve patient safety, assess the risk-benefit profiles of medicines, and encourage their safe and effective use. Pharmacists can play important roles in pharmacovigilance by monitoring for and reporting adverse drug reactions. Pharmacovigilance programs in health systems should include ongoing surveillance, reporting, analysis, and education to prevent adverse drug events.
The document discusses international patient safety goals in hospital settings. It outlines 6 main goals: [1] Identify patients correctly; [2] Improve communication among caregivers; [3] Improve safety of high-alert medications; [4] Ensure correct procedures and patients; [5] Reduce health care-associated infections; [6] Reduce risk of falls. The goals aim to prevent medical errors and harm to patients by establishing safety protocols for identification, communication, medication use, surgery, infection control, and fall prevention.
safe injection practice as per NABH.pptxanjalatchi
Safe injection practices are intended to prevent the transmission of infectious diseases between patients or between patients and healthcare personnel. The key steps of safe injection practices include cleaning the work space, proper hand hygiene, using sterile syringes and needles for each patient, properly disinfecting medication vials, safely collecting sharps, and properly disposing of waste. Healthcare facilities should provide regular training to all personnel on safe injection practices and periodically observe practices to ensure they are being followed correctly.
This document discusses occupational health hazards faced by nurses from exposure to chemicals, including chemotherapeutic drugs. It notes that nurses are at risk of various health issues from regular exposure to sterilizing agents, disinfectants, anesthetic gases, and antineoplastic drugs used in chemotherapy. Precautions like proper use of personal protective equipment, ventilation, limiting exposure times, and hygiene practices can help reduce risks. However, studies show nurses still experience high rates of injury from improper protective measures or lack of awareness regarding chemical hazards of their work environment.
Hospital Pharmacy Isolator Solutions for USP <797> Compliance from EscoEsco Group
The document discusses guidelines and regulations for handling hazardous drugs in hospitals, including USP <797>. It outlines the risks of exposure to hazardous drugs, such as cancer risks. Engineering controls are important for compounding sterile preparations to reduce contamination, including biological safety cabinets and compounding isolators. Personal protective equipment and proper work practices are also needed to safely handle hazardous drugs.
Occupational health hazards among health care workers can include:
- Biological hazards like infectious diseases from needle sticks or exposure to pathogens.
- Chemical hazards such as exposure to disinfectants, anesthetic gases, or hazardous drugs.
- Physical hazards including noise, radiation, temperature extremes, and electric shock. Ergonomic and psychosocial hazards are also common in health care settings. Protective measures and training can help reduce risks for staff.
Goal 1 improve the accuracy of patient identification.npsssuser47f0be
The document discusses patient identification and reducing errors related to misidentification. It focuses on using two patient identifiers, which can help reliably identify individuals and match them to the correct service or treatment. Newborns are at higher risk given their inability to communicate and lack of distinguishing features. The document provides examples of methods to prevent misidentification of newborns such as distinct naming systems and standardized identification banding practices.
Pharmacovigilance (PV) is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. WHO established its Programme for International Drug Monitoring in response to the thalidomide disaster detected in 1961. Together with the WHO Collaborating Centre for International Drug Monitoring, Uppsala, WHO promotes PV at the country level. At the end of 2010, 134 countries were part of the WHO PV Programme. The aims of PV are to enhance patient care and patient safety in relation to the use of medicines; and to support public health programmes by providing reliable, balanced information for the effective assessment of the risk-benefit profile of medicines.
This document discusses industrial hygiene and toxicology. It begins by defining toxicology as the study of how toxicants enter and affect the body and how they are eliminated. Industrial hygiene aims to prevent or reduce exposure to toxicants. The key aspects of an industrial hygiene study are: hazard identification through tools like safety data sheets; hazard evaluation including monitoring exposures and comparing to standards; and hazard control through methods like engineering and administrative controls. Laws and regulations in Malaysia and the US govern industrial hygiene through agencies like OSHA, NIOSH, EPA and process for developing and enforcing regulations.
Patient safety is a fundamental principle of healthcare. Adverse events may result from problems in practice, products, procedures or systems. Improving patient safety demands a complex, system-wide effort involving performance improvement, risk management, infection control, safe clinical practices, and a safe environment of care. Unsafe injections expose millions of people to infections worldwide each year. Ensuring single-use injection devices and safety boxes are available in every healthcare facility can prevent reuse and unsafe waste disposal.
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Role of Human Resource Department in the Management of Drug Safety in Pharmaceutical Industry..
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This document discusses dangerous substances and risk assessment. It defines dangerous substances as liquids, gases or solids that pose risks to worker health or safety. The document outlines a 5-step process for risk assessment of dangerous substances: 1) identify hazards and those at risk, 2) evaluate and prioritize risks, 3) decide on preventive actions like elimination or substitution, 4) take action, and 5) monitor and review the assessment. The goal of risk assessment is to protect workers from harm by implementing controls for dangerous substances in the workplace.
The Role of Pharmacovigilance in Ensuring Drug Safety and EfficacyClinosolIndia
Pharmacovigilance plays a vital role in ensuring drug safety and efficacy throughout the entire lifecycle of a pharmaceutical product. Here are the key aspects of pharmacovigilance in safeguarding public health:
Early Detection of Adverse Drug Reactions (ADRs): Pharmacovigilance systems collect and analyze data on ADRs reported by healthcare professionals and patients. This enables the early detection of potential safety concerns associated with drugs, including known and previously unrecognized adverse effects.
Signal Detection and Evaluation: Pharmacovigilance activities involve the systematic identification and evaluation of safety signals, which are indications of potential risks associated with a drug. Signals are assessed by analyzing data from various sources, such as spontaneous reports, clinical trials, literature, and real-world evidence, to determine their clinical significance and inform regulatory action if necessary.
Risk Assessment and Benefit-Risk Evaluation: Pharmacovigilance assesses the balance between the benefits and risks of drugs. The collected data are evaluated to determine whether the benefits of a drug outweigh its risks or if any additional safety measures are required. This information guides regulatory decisions, such as labeling changes, restrictions, or even withdrawal of the drug from the market.
Post-Marketing Surveillance: Pharmacovigilance is crucial in monitoring the safety of drugs after they have been approved and marketed. It involves ongoing surveillance and analysis of real-world data, including ADR reports, electronic health records, and other sources, to identify new or rare adverse effects that may emerge in larger patient populations or specific subgroups.
patient safety and staff Management system ppt.pptxanjalatchi
Patient Safety is a health care discipline that emerged with the evolving complexity in health care systems and the resulting rise of patient harm in health care facilities. It aims to prevent and reduce risks, errors and harm that occur to patients during provision of health care.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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This document outlines patient safety in healthcare facilities. It defines key terms like patient safety, psychological safety, and safety culture. It discusses the roles of the patient safety committee and the components of a patient safety plan. Specific patient safety issues in the intensive care unit are examined, like collaboration among ICU staff and common errors. International patient safety goals are provided, such as accurately identifying patients and reducing healthcare-associated infections. Root cause analysis is introduced as a way to investigate incidents and prevent future errors.
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The document discusses the International Patient Safety Goals (IPSG) which were developed by the Joint Commission International to help improve patient safety. It provides background on how the IPSG were adapted from the National Patient Safety Goals established by the Joint Commission. The document then outlines several of the IPSG, including proper patient identification, improving staff communication, reducing risks associated with medications, and preventing wrong site/procedure surgery. The goals are aimed at reducing common safety issues and medical errors in healthcare facilities.
Pharmacovigilance is the science of monitoring the safety of medicines. It aims to detect adverse effects from drugs, understand their causes, and prevent patient harm. Pharmacovigilance programs collect reports of adverse drug reactions and analyze the data to identify safety issues, quantify risks, and communicate safety information to patients and healthcare professionals. The ultimate goals are to protect patients and promote the safe use of medicines.
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The document discusses the importance of pharmacovigilance in health care. It defines pharmacovigilance as the science related to detecting, assessing, understanding, and preventing adverse effects of drugs. The main goals of pharmacovigilance are to improve patient safety, assess the risk-benefit profiles of medicines, and encourage their safe and effective use. Pharmacists can play important roles in pharmacovigilance by monitoring for and reporting adverse drug reactions. Pharmacovigilance programs in health systems should include ongoing surveillance, reporting, analysis, and education to prevent adverse drug events.
The document discusses international patient safety goals in hospital settings. It outlines 6 main goals: [1] Identify patients correctly; [2] Improve communication among caregivers; [3] Improve safety of high-alert medications; [4] Ensure correct procedures and patients; [5] Reduce health care-associated infections; [6] Reduce risk of falls. The goals aim to prevent medical errors and harm to patients by establishing safety protocols for identification, communication, medication use, surgery, infection control, and fall prevention.
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This document discusses occupational health hazards faced by nurses from exposure to chemicals, including chemotherapeutic drugs. It notes that nurses are at risk of various health issues from regular exposure to sterilizing agents, disinfectants, anesthetic gases, and antineoplastic drugs used in chemotherapy. Precautions like proper use of personal protective equipment, ventilation, limiting exposure times, and hygiene practices can help reduce risks. However, studies show nurses still experience high rates of injury from improper protective measures or lack of awareness regarding chemical hazards of their work environment.
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The document discusses patient identification and reducing errors related to misidentification. It focuses on using two patient identifiers, which can help reliably identify individuals and match them to the correct service or treatment. Newborns are at higher risk given their inability to communicate and lack of distinguishing features. The document provides examples of methods to prevent misidentification of newborns such as distinct naming systems and standardized identification banding practices.
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This document discusses industrial hygiene and toxicology. It begins by defining toxicology as the study of how toxicants enter and affect the body and how they are eliminated. Industrial hygiene aims to prevent or reduce exposure to toxicants. The key aspects of an industrial hygiene study are: hazard identification through tools like safety data sheets; hazard evaluation including monitoring exposures and comparing to standards; and hazard control through methods like engineering and administrative controls. Laws and regulations in Malaysia and the US govern industrial hygiene through agencies like OSHA, NIOSH, EPA and process for developing and enforcing regulations.
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Early Detection of Adverse Drug Reactions (ADRs): Pharmacovigilance systems collect and analyze data on ADRs reported by healthcare professionals and patients. This enables the early detection of potential safety concerns associated with drugs, including known and previously unrecognized adverse effects.
Signal Detection and Evaluation: Pharmacovigilance activities involve the systematic identification and evaluation of safety signals, which are indications of potential risks associated with a drug. Signals are assessed by analyzing data from various sources, such as spontaneous reports, clinical trials, literature, and real-world evidence, to determine their clinical significance and inform regulatory action if necessary.
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Post-Marketing Surveillance: Pharmacovigilance is crucial in monitoring the safety of drugs after they have been approved and marketed. It involves ongoing surveillance and analysis of real-world data, including ADR reports, electronic health records, and other sources, to identify new or rare adverse effects that may emerge in larger patient populations or specific subgroups.
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Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
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Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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Occupational exposure to hazardous drugs has been linked to a
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pose some serious risks to healthcare and
pharmaceutical staff. These drugs can effectively
kill cancer cells. The trade-off is that they also kill
healthy cells in the process, which is why patients
undergoing chemotherapy experience undesirable
side effects such as hair loss. For people who are
battling cancer, often, the benefits outweigh the
risks and side effects.
2 The Risks of Occupational Exposure to Hazardous Drugs
4. •For people who don't have
cancer, though, exposure offers no
benefit. There are a number of
measures healthcare leaders can
put in place, including the use of
CSTDs, that can help minimize
dangerous exposure to these
drugs. This makes pharmaceutical
care safer for everyone
involved, including patients and
caregivers.
5. Hazardous drugs used to treat
patient illnesses can harm
unprotected healthcare
workers in their workplaces
How Exposures Can Occur
3
6. •so in order to protect them it is
recommended that workplaces assess the
hazards specific to their workplace and
develop hazard control strategies to mitigate
those hazards. These may include use of
engineering controls, such as ventilated
hoods and enclosures , such as establishing
safe handling policies, and routine training
reviews for potentially exposed individuals;
and supplying personal protective
equipment (PPE), such as chemotherapy
gloves and gowns.
7. Steps you can take to protect workers. No
single approach can protect all workers in
healthcare workplaces against all hazardous
drugs. These steps, however, can lessen the
chance that hazardous drugs will do harm:
Minimizing Occupational Exposure to Hazardous
Drugs - Safety Protocols and Equipment
4
8. STEPS
Clearly label all hazardous drugs so workers will know to carefully handle
them.
Do not use automated counting machines for hazardous drugs. The
machines can produce powder and contaminate the work area.
Use liquid formulations when possible to avoid crushing tablets or
opening capsules.
avoid cutting, crushing, or otherwise manipulating pills or capsules. This
might produce powder that can contaminate a workplace .
10. conclusion
•Consider relevant factors when
determining appropriate hazard
control strategies. For example,
administering unopened, intact
tablets and capsules may have
lower risk of exposure than
preparing syringes or IV bags of
injectable drugs
11.
12. The potential exposure of workers from handling a hazardous drug depends on
several factors unique to each work setting. Such factors include:
1-A drug’s toxicity .
2-Route of exposure .
3-A drug’s physical and chemical properties .
4-Drug formulation .
5-Workplace activity .
NIOSH (National Institute of Occupational Safety and Health )
Publications
5
13. Drug’s toxicity
•This refers to the type of harm a drug
can cause to a person’s health. For
example, cytotoxic drugs are used to
kill cancer cells, but they can also cause
cancer or other harm to healthcare
workers who work with or handle them
without adequate protection. Some
drugs may harm a person’s ability to
have healthy children.
14. Route of exposure
•How workers may be exposed to a drug is
an important factor to consider in
developing strategies for controlling
exposure. Workers can be exposed to
hazardous drugs through breathing vapors,
dusts, or aerosols, absorbing it through
skin contact swallowing it, or accidental
injection.
15. Drug’s physical and chemical properties
•The physical and chemical properties of drugs that
influence their hazard include vapor pressure, physical
state (solid, liquid, or gas) and molecular weight of the
drug . For example, when a drug has a high molecular
weight, like a monoclonal antibody, and its typical
dosing regimen is via injection, the drug would
generally be absorbed through intact skin very poorly
Of course, there may still be a risk of exposure to such
drugs from accidental needle sticks or inhalation of
dusts or droplets.
16. Drug formulation
•This refers to the form the drug takes for
administration such as a powder, liquid,
capsule, or prefilled syringe. Like a drug’s
physical and chemical properties, the
formulation of the drug is an important
indicator of the types of precautions needed to
avoid exposure. Different risk management
strategies are needed for powders than pre-filled
syringes.
17. Workplace activity
•This involves how workers use and
handle the drug in the workplace such as
administering the drug, compounding it,
shipping it, or receiving it. Different
activities have very different potential for
healthcare worker exposure.
18. Possible Solutions
•Institutions should have formal written
programs to manage hazards. Such programs
should include training, exposure assessment,
emergency procedures for spills, policies for
managing staff with reproductive concerns, and
most importantly, ways to ensure that the
institution is adhering to critical national
standards.
19. CSTD bag or infusion adapter attached to an IV bag.
NIOSH defines a Closed System Drug-Transfer Device (CSTD) as
“a drug transfer device that mechanically prohibits the transfer of
environmental contaminants into the system and the escape of the
hazardous drug or vapor concentrations outside the system”
[NIOSH 2004]. Currently, CSTDs generally follow one of two
design concepts, using either a physical barrier or an air-cleaning
technology to prevent the escape of hazardous drugs into the work
environment. When appropriately designed and used, CSTDs offer
enhanced protection against potentially hazardous exposures to
healthcare workers during the compounding and administration of
hazardous drugs.
Introduction
How CSTDs(Closed system drug-transfer devices)
Help Keep You Safe
6
20. •NIOSH recommends healthcare workers use a CSTD throughout the
hazardous drug- handling chain, from pharmaceutical compounding to
patient dose administration [NIOSH 2004]. While all CSTDs may not be
equally protective, research shows that CSTD use can reduce hazardous
drug contamination [Vyas 2013]. CSTDs should not be the only means
of worker protection. They should be used as part of a hazardous drug
safety program and used in conjunction with other engineering controls
[NIOSH 2004].
21. CSTD Performance Standards
•As CSTD designs and available models changed,
NIOSH and its industry partners realized the need for an
independent testing method for CSTD performance.
•While CSTD performance standards are available that
apply to sterile practice and patient protection, no CSTD
performance standards are available for drug
containment [Douglass et al. 2012]. To address this gap,
NIOSH researchers are developing a test protocol that
evaluates a CSTD’s containment of hazardous drugs.
22. NIOSH Research on CSTD Test protocol
•The following is information on NIOSH CSTD
research activities and includes links to early draft
protocols, other associated documents, and public
comments. Also provided is an update on the
research status of the most -recent NIOSH draft
CSTD test protocol. This is a unified test protocol
for both air-cleaning and barrier type CSTDs. Check
back for more on this continuing NIOSH research
project and other relevant CSTD information.
23. The Importance of CSTDs in Protecting Health
Care Professionals
•CSTDs help protect health care professionals from
hazardous drugs, including pharmacists preparing
medications and nurses administering medication. It
has been estimated that 8 million health care
professionals are exposed to hazardous drugs each
year, increasing the risk of chromosomal abnormalities,
teratogenicity, and cancer. More than 100 studies
substantiate the increased risk, and more than 50
studies have documented harm to health care
25. Conclusions
•CSTDs have an important role in
protecting health care professionals from
the risks of long -term low-level exposure
to hazardous drugs both during preparation
in the pharmacy and during administration
at the bedside by nurse.
26. Prepared By
- Abobaker Nasser Sheikh .
- Ahmad Radwan Ahmad .
- Ahmed Ashraf Mostafa .
- Ahmad Sami Al Hammady .
- Ahmed Sameh Eladl .
- Ahmed Amir Elkasir .
- Ahmed ashraf abdullah.
- Ahmed Ibrahim Abdalla