“KILL KINETICS “Emerging Trends in Sterile Supply by Dr.Mahboob Khan Phd
CSSD's role lies in receiving, cleaning, packing, disinfecting, sterilising, storing and distributing instruments as per well-delineated protocols and standardised procedures
Dr.Mahboob ali khan Phd
The Central Sterile Supply Department (CSSD) in recent times has expanded from a mere support entity which consisted of steam sterilisation units to process instrument and linen packs. Today, CSSD is the heart of hospital infection control and the most important unit of clinical support services.
The anti-bacterial powers of nano silver and nano copper combine into a power...NanoSpaTech, Inc.
HAI infections kill tens of thousands of patients every year and present a major problem for all hospitals, who lack product, skills and budgets to effectively kill all harmful organisms around patients room and hospital equipment. NanoSpa presents a solution in the wave of new technology.
The anti-bacterial powers of nano silver and nano copper combine into a power...NanoSpaTech, Inc.
HAI infections kill tens of thousands of patients every year and present a major problem for all hospitals, who lack product, skills and budgets to effectively kill all harmful organisms around patients room and hospital equipment. NanoSpa presents a solution in the wave of new technology.
The Central Sterile Supply Department (CSSD) is the service responsible for receiving, storing, processing, distributing and controlling the professional supplies and equipment (both sterile and non-sterile) for all user unit of hospital for the care and safety of patient under strict quality control
You will be able to have a brief idea about CSSD from this ppt
Thanks
At Aseptic Technologies we developed and manufacture innovative solutions for aseptic filling operations. Our equipment and devices are designed to provide safer & easier sterility assurance for aseptic fill and finish of biologicals, potent drugs and products requiring cryopreservation.
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...
This write up shows that Therapure offers fill/finish services for their client's bulk drug substance either produced off-site or as an add-on to Therapure's own cGMP manufacturing services. Therapure is an ideal partner for biotech companies as they can provide this integrated service from manufacturing to fill/finish to storage and distribution of finished product.
“ NK & PP Túi ép tiệt trùng y tế – Găng tay y tế VN, Malaysia : Găng tay có bột, không bột (powder Free), Nitrile, Vinyl không bột, găng tay phẩu thuật tiệt trùng không bột- Vật tư khoa chống nhiễm khuẩn – Dung dịch tiệt khuẩn – Giấy gói y tế Crepe paper – Trang phục phòng mổ – Vật tư tiêu hao dành cho bệnh viện, phòng khám đa khoa, nha khoa, cty sx dược phẩm”
CÔNG TY TNHH THƯƠNG MẠI DỊCH VỤ ĐỈNH VIỆT
TSC: 132 Đường Số 18,Ấp 2, Xã Bình Hưng, Huyện Bình Chánh,TPHCM
MST: 0309797133
Tel : (848)22443084 – Mobile: 0909 39 68 38 – 0938 06 98 38 (Mr. Kiệt)
Web: www.tuihaptiettrung.com;www.tuihaptiettrung.vn ; www.dinhvietmedical.com
E-mail: dinhvietmedical@yahoo.com
Sterilization Validation for Medical DevicesDocKetchum
Every medical device produced must be sterilized before being shipped to hospitals, doctors’ offices, and other medical locations.
Random samples of these devices must then be tested to be sure the sterilization kills disease causing microbes including bacteria, fungus, and spores in every device.
These are some of the most common ways that sterilization validation is performed.
The Central Sterile Supply Department (CSSD) is the service responsible for receiving, storing, processing, distributing and controlling the professional supplies and equipment (both sterile and non-sterile) for all user unit of hospital for the care and safety of patient under strict quality control
You will be able to have a brief idea about CSSD from this ppt
Thanks
At Aseptic Technologies we developed and manufacture innovative solutions for aseptic filling operations. Our equipment and devices are designed to provide safer & easier sterility assurance for aseptic fill and finish of biologicals, potent drugs and products requiring cryopreservation.
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...
This write up shows that Therapure offers fill/finish services for their client's bulk drug substance either produced off-site or as an add-on to Therapure's own cGMP manufacturing services. Therapure is an ideal partner for biotech companies as they can provide this integrated service from manufacturing to fill/finish to storage and distribution of finished product.
“ NK & PP Túi ép tiệt trùng y tế – Găng tay y tế VN, Malaysia : Găng tay có bột, không bột (powder Free), Nitrile, Vinyl không bột, găng tay phẩu thuật tiệt trùng không bột- Vật tư khoa chống nhiễm khuẩn – Dung dịch tiệt khuẩn – Giấy gói y tế Crepe paper – Trang phục phòng mổ – Vật tư tiêu hao dành cho bệnh viện, phòng khám đa khoa, nha khoa, cty sx dược phẩm”
CÔNG TY TNHH THƯƠNG MẠI DỊCH VỤ ĐỈNH VIỆT
TSC: 132 Đường Số 18,Ấp 2, Xã Bình Hưng, Huyện Bình Chánh,TPHCM
MST: 0309797133
Tel : (848)22443084 – Mobile: 0909 39 68 38 – 0938 06 98 38 (Mr. Kiệt)
Web: www.tuihaptiettrung.com;www.tuihaptiettrung.vn ; www.dinhvietmedical.com
E-mail: dinhvietmedical@yahoo.com
Sterilization Validation for Medical DevicesDocKetchum
Every medical device produced must be sterilized before being shipped to hospitals, doctors’ offices, and other medical locations.
Random samples of these devices must then be tested to be sure the sterilization kills disease causing microbes including bacteria, fungus, and spores in every device.
These are some of the most common ways that sterilization validation is performed.
Introduction to CSSD, Decontamination is an entry-level program for new entra...Talal Albudayri
Decontamination is an entry-level program for new
entrants to the field of decontamination and sterilization in
a hospital, dental or ambulatory clinic setting.
In this module, we will discuss about reusable medical
device reprocessing, the facilities required to carry out
this function, and how the life cycle of a reusable medical
device fits in.
Infection Control Guidelines the responsibility of allA-dec Australia
The ADA infection control guidelines applying to dental surgeries (incorporating Australian Standards AS/NZS 4815:2006 and AS/NZS 4187:2014) have been updated in the latest ADA Guidelines for Infection Control - Third edition published in October 2015.
Batch Control Identification (BCI) in the dental setting allows dental practitioners to demonstrate that any critical dental instruments used on a patient have been through a particular steriliser cycle with verifiable performance data.
White paper - Key factors for developing a pharmaceutical cleaning strategyFedegari Group
Pharmaceutical Cleaning Strategies: What are the key factors to consider when developing a quality procedure?
Cleaning is an essential practice for any pharmaceutical activity: it is impossible to manufacture drugs in dirty conditions, even if dirt is not evident. Many aspects need to be considered in setting up a cleaning procedure. This is certainly a multidisciplinary issue that involves various company areas: from “Regulations” to Engineering, from Quality Control lab to Production department. Contributions of all these areas together can lead to a robust and reproducible cleaning process.
In these conditions, even regulatory bodies struggle. Essentially, they allow manufacturers considerable flexibility in establishing their own cleaning specifications. The FDA, for example, does not define methods describing how a cleaning process should be validated.
Therefore, there are many aspects to be considered when approaching the issue of pharmaceutical cleaning. First of all, one has to consider where to perform cleaning activity: in-place (CIP) or out-of-place (COP).
TIPS issue on the 2004 Joint Commission National Patient Safety Goals (NPSGs) - Starting with this issue, I authored or co-authored every annual issue on the NPSGs through 2010.
CSSD EQUIPMENT .. AS AN INCORPORATED UNIT INSIDE CLINICS AND MEDICAL CARE OFF...Talal Albudayri
WHAT IS CSSD EQUIPMENT?
AS AN INCORPORATED UNIT INSIDE
CLINICS AND MEDICAL CARE OFFICES,
THE CSSD PERFORMS CLEANSING AND
OTHER RELATED ACTIVITIES ON
CLINICAL CONSUMABLES, EQUIPMENT,
AND DEVICES.
THESE THINGS WILL AT THAT POINT BE
UTILIZED WHERE ASEPTIC TECHNIQUES
ARE PERFORMED —
, FOR EXAMPLE, IN
THE WORKING THEATER, IN INJURY
STITCHING, AND IN THE CAREFUL,
PEDIATRIC, AND MATERNITY WARDS.
Process flow, CSSD IS A SERVICE UNIT IN A HOSPITALTalal Albudayri
CSSD IS A SERVICE UNIT IN A HOSPITAL THAT
PROCESSES, ISSUE & CONTROLS THE STERILE
STORES SUPPLY TO ALL DEPARTMENTS OF THE
HOSPITAL.
CSSD IS THE DEPARTMENT WHICH DEALS WITH
RECEIVING, CLEANING, PACKING,
DISINFECTING, STERILIZING, STORING AND
DISTRIBUTING ALL SURGICAL INSTRUMENTS
AND EQUIPMENTS AS PER WELL-DELINEATED
PROTOCOLS AND STANDARDIZED PROCEDURES.
White paper - Decontamination by hydrogen peroxide: use and technical develop...Fedegari Group
This article compares the concepts of sterilization, disinfection and decontamination with reference to the different scopes thereof. Decontamination by hydrogen peroxide vapor and its use for conditioning the Sterility Test Isolators are discussed. A technologically new method for the vaporization of the hydrogen peroxide and its dosage control is presented. Author: V. Mascherpa - Senior consultant R&D Fedegari Group
White Paper : Need for Standardization of Tests for Plant Viruseskrishgen
Plant virus testing in India requires standardization. There is a need for Department of Biotechnology, under the Ministry of Agriculture to work towards encouraging Indian manufacturers to develop and offer test kits at low costs suited to Indian farmers.
January 2024. Healthcare Waste (HCW), also called Medical Waste, refers to the hazardous and non-hazardous waste generated from healthcare facilities, including used needles, blood, body parts, chemicals, diagnostic samples, medical devices, and pharmaceuticals.
HCW sources include hospitals, laboratories, blood banks, dental clinics, ambulance centers, nursing homes, autopsy centers, veterinary clinics, and medical colleges.
Hazardous HCW types include infectious, pathological, pharmaceutical, genotoxic, and radioactive.
Non-hazardous HCW types include paper, plastic packaging, food (organic), aerosols, electronics, and glass.
Improper handling and disposal of HCW has negative impacts on the environment, human health, and on the economy: Incineration of waste produces carbon and GHG emissions, releases harmful pollutants, and can contaminate groundwater. Health risks include transmission of infectious diseases, radiation burns, immune and endocrine system impairment. Economically, lack of recycling leads to increased waste volume and higher landfill costs, while lost productivity is due to health problems associated with exposure to contaminants. Healthcare facilities failing to comply face large fines.
Healthcare Waste Management (HCWM) is defined as the sustainable disposal of HCW using environmentally safe and cost-effective technologies while minimizing health risks associated with waste handling.
A sustainable HCW management strategy aims to avoid creating HCW from the beginning, or minimizing it to a large degree by (1) Using recyclable materials and biodegradable plastics (2) Reusing items such as glass, ceramic cups, and thermometers (3) Reducing packaging and medication waste and (4) Using food waste for compost and biofuel production.
Sustainable HCW management stages are (1) Collection by healthcare facility staff (2) Segregation of waste into regular non-hazardous waste, which will be sent to conventional municipal treatment facilities, and HCW. (3) Transportation of HCW from the healthcare facility to HCW treatment facility (4) Treatment using appropriate methods to achieve desired disinfection and (5) Disposal of treated waste in a HCW designated landfill.
Policy wise, in 2015, the World Health Organization (WHO) and the United Nations Children's Fund (UNICEF) launched a global initiative to ensure adequate water, sanitation and hygiene services in healthcare facilities, including addressing proper HCW treatment. Successful and sustainable global HCW management system can significantly contribute to achieving Sustainable Development Goals (SDGs) 3, 6, 8 ,12, and 13.
In this slideshow, you will learn about the definition, sources, types, effects, sustainable HCW management, UN policy, and global statistics of healthcare waste. For more slideshows on environmental sustainability, please visit s2adesign.com
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KILL KINETICS “Emerging Trends in Sterile Supply by Dr.Mahboob ali Khan Phd.
1. 1
“KILL KINETICS “Emerging Trends in Sterile Supply by
Dr.Mahboob Khan Phd
CSSD's role lies in receiving, cleaning, packing, disinfecting, sterilising,
storing and distributing instruments as per well-delineated protocols and
standardised procedures
The Central Sterile Supply Department (CSSD) in
recent times has expanded from a mere support
entity which consisted of steam sterilisation units to
process instrument and linen packs. Today, CSSD is
the heart of hospital infection control and the most
important unit of clinical support services.
CSSD's role lies in receiving, cleaning, packing,
disinfecting, sterilising, storing and distributing
instruments (both multi-use and single-use devices),
as per well-delineated protocols and standardised
procedures. However, with newer techniques of
surgery and subsequent sophisticated instruments,
these functions have become critical and
specialised. Modern medical technology has thus given a host of
transformations, which have helped to ensure that the sterile supply remains—
sterile. Broadly, the reflections could be felt in the following points:
New-age Sterilisers & Modalities
Manual sterilisers are now a passe and now fully
automated pre-vacuum-assisted sterilisers are
replacing them. These sterilisers are generally more
efficient and leave very little space for error.
Computer-operated sterilisers with automated
recording system are also available now-a-days
which record vital details like temperature, pressure,
etc. Also, they record the load weight, cycle time and other details vital to
business analysis.
On the other hand, ETO is now not the preferred choice for sterilising the
thermo labile items due to their toxicity and environmental hazards. Hydrogen
Peroxide sterilisers and Gamma irradiation have shown a new way to safe and
speedy sterilisation.
Dr.Mahboob ali khan
Phd
2. 2
Process Challenge Devices
With the change and sophistication of surgical sciences, sophisticated minimally
invasive instruments (MIS) have also come into picture, which generally have
very narrow lumen. Improperly maintained old sterilisers generally cannot put
air out of the lumen, which is an essential element for kill kinetics. This could
not be detected by normal chemical indicators, rather a process challenge device
and PCD Bowie Dick indicator is required to get this checked and corrected.
PCD tests the steriliser by simulating worst situations which can happen while
sterilisation.
Biological & Chemical Indicators
Biological and chemical indicators remain a preferred choice for testing the
sterility. However, with recently launched chemical integrators, it is easy to
check for multiple parameters at the same go in every cycle/pack.
Quality & Documentation
A modern CSSD must follow well-established Quality Management System
like EN ISO 14937, EN 550, 552. ISO 900:2001 (with reference to ISO 13487),
which states the requirements for a quality management system for sterile
supply services department.
Batch Processing Label System
Another useful device is the batch monitoring system. In case of sterilisation
breakdown, when the entire lot needs to be retrieved from various parts of the
hospital, this system comes handy.
The entire lot could be just called back by simply identifying the packets with
the label bearing the same lot number. Also, the label gives you the sterilisation
and the expiry date, ruling out chances of error while calculating 48 hours or
seven days time frame. The presence of autoclave number and the operator code
also helps to identify the malfunctioning machine and fix the accountability.
3. 3
Lubricants & Enzymatic Detergents
Instruments, generally, have a tendency to develop crust or sometimes even rust
near the grooves and hinges, which may be a potential source of infection. Also,
they decrease the life of the instruments drastically, which could be prevented
by using instrument lubricants.
Lubricant generally develops a protective film on the instruments. In addition,
some of these lubricants have anti-bacterial property, which prevents pathogenic
growth on the instruments. It is true that whatever is not clean cannot be
sterilised. This is where the enzymatic detergents come into picture. These
enzymatic detergents clean the human enzymes from the tiny instruments and
thus decrease the bio burden to ensure proper sterilisation.
Management & Training
CSSD is no longer run by nurses and general technicians, but by hospital
management graduates and senior technological officers, who are specially
trained in varied techniques of quality management. You will also come across
CSSD departments having a MoU with the sterilisation product companies who
take steps for complete training and quality assurance of the department.
Re-useMost Indian hospitals use devices like catheters, balloons, octopauss and
tissue stabilisers multiple times in order to minimise cost to the patient.
However, if not done properly, this could be a health hazard. Therefore, the
sterile supply department must ensure adoption of a standard protocol with non-
toxic marking of the items with non-toxic markers. These single use items
generally get defected on using for few times and thus it is very important to
know their number of use for patient safety.
Mahboob804@yahoo.co.in Dr.Mahboob ali khan is chief healthcare consultant
and a NABH/JCI assessor responsible for maintaining the hospital as per ISO &
NABH /JCI standards