Research

S. No.	Category of staff	Trained
1	Doctors	79
2	Nurses	211
3	Paramedical staff	414
4	Sanitation staff (SA/HA)	56
TOTAL		760

2) VACCINATION

S.No.	Category of staff	For Hepatitis B Vaccinated( first and second dose)
1	Biotec(CMBWTF)	21
2	Sanitary / Hospital attendants	324
TOTAL		345

NEEDLE STICK INJURY

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PROTOCOL

Immediate
1. For Injury: Wash with soap and running water.
2. For Non intact Skin Exposure: Wash with soap and water.
3. For Mucosal Exposure: Wash thoroughly.
Reporting
1. All sharps injury and mucosal exposure MUST be reported to the immediate supervisor, and to the Casualty Medical Officer to evaluate the injury. Details of the needle-stick injury should be filled by the supervisor and handed over to the HIC nurse for further follow-up.
Management
1. Management is on a case to case basis.
Follow-Up
1. Follow-up and statistics of needle-stick injury are done by the HIC nurse on a weekly basis. This information is presented at the HICC meeting and preventive actions to avoid needle-stick injuries, if any, are recorded.

POST-HIV EXPOSURE MANAGEMENT / PROPHYLAXIS (PEP)

Occupational exposure:

Occupational exposure refers to exposure to potential blood-borne infections (HIV, HBV and HCV) that occurs during performance of job duties.

“Exposure” which may place an HCP at risk of blood-borne infection is defined as:

a percutaneous injury (e.g. needle-stick or cut with a sharp instrument),
contact with the mucous membranes of the eye or mouth,
contact with non-intact skin (particularly when the exposed skin is chapped, abraded, or afflicted with dermatitis), or
contact with intact skin when the duration of contact is prolonged (e.g. several minutes or more) with blood or other potentially infectious body fluids.

What is infectious and what is not?

TABLE 12.3.4 POTENTIALLY INFECTIOUS BODY FLUIDS
Exposure to body fluids considered ‘at risk’	Exposure to body fluids considered ‘not at risk’
Blood	Tears	Unless these secretions contain visible blood
Semen	Sweat
Vaginal secretions	Urine and Faeces
Cerebrospinal fluid	Saliva
Synovial, pleural, peritoneal, pericardial fluid
Amniotic fluid
Other body fluids contaminated with visible blood

Protocol:

It is necessary to determine the status of the exposure and the HIV status of the exposure source

before starting post exposure prophylaxis (PEP).

Step 1: Immediate measures

For skin — if the skin is broken after a needle-stick or sharp instrument:

· Immediately wash the wound and surrounding skin with water and soap, and rinse. Do not scrub.

· Do not use antiseptics or skin washes (bleach, chlorine, alcohol, betadine).

After a splash of blood or body fluids on unbroken skin:

· Wash the area immediately

· Do not use antiseptics

For the eye:

· Irrigate exposed eye immediately with water or normal saline. Sit in a chair, tilt head back and ask a colleague to gently pour water or normal saline over the eye.

· If wearing contact lens, leave them in place while irrigating, as they form a barrier over the eye and will help protect it. Once the eye is cleaned, remove the contact lens and clean them in the normal manner. This will make them safe to wear again

· Do not use soap or disinfectant on the eye.

For mouth:

· Spit fluid out immediately

· Rinse the mouth thoroughly, using water or saline and spit again. Repeat this process several times

· Do not use soap or disinfectant in the mouth

· Consult the designated physician of the institution for management of the exposure immediately.

Don’ts

· Do not panic

· Do not put pricked finger in mouth

· Do not squeeze wound to bleed it

· Do not use bleach, chlorine, alcohol, betadine, iodine or any antiseptic or detergent

Step II: Prompt reporting:

a) All needle-stick/sharp injuries should be reported to the immediate supervisor, and then to the Casualty Medical Officer.

b) An entry is made in the Needle-Stick Injury Register in the Casualty.

Step III: Post exposure treatment:

The decision to start PEP is made on the basis of degree of exposure to HIV and the HIV statusof the source from where the exposure/infection has occurred. More so, it should begin as soon as possible preferably within two hours, and is notrecommended after 72 hours.

PEP is not needed for all types of exposures:The HIV seroconversion rate of 0.3% after an AEB (accidental exposure to blood) (for percutaneous exposure) is an average rate. The risk of infection transmission is proportional to the amount of HIV transmitted, which depends on the nature of exposure and the status of the source patient. A baseline rapid HIV testing of exposed and source person must be done for PEP. However, initiation of PEP should not be delayed while waiting for the results of HIV testing of the source of exposure. Informed consent should be obtained before testing of the source as per national HIV testing guidelines.

First PEP dose within 72 hours

A designated person/trained doctor must assess the risk of HIV and HBV transmission following an AEB. This evaluation must be quick so as to start treatment without any delay, ideally within two hours but certainly within 72 hours; PEP is not effective when given more than 72 hours after exposure. The first dose of PEP should be administered within the first 72 hours of exposure. If the risk is insignificant, PEP could be discontinued, if already commenced.

Step IV: Counselling for PEP

Exposed persons (clients) should receive appropriate information about what PEP is about and the risk and benefits of PEP in order to provide informed consent for taking PEP. It should be clear that PEP is not mandatory.

Step V: Psychological support

Many people feel anxious after exposure. Every exposed person needs to be informed about the risks, and the measures that can be taken. This will help to relieve part of the anxiety. Some clients may require further specialised psychological support.

Step VI: Documentation of exposure
Documentation of exposureis essential. Special leave from workshould be considered initially for a period of two weeks. Subsequently, it can be extended based on the assessment of the exposed person’s mental state, side effects and requirements.

IMPORTANT: Seek expert opinion in case of

· Delay in reporting exposure (> 72 hours).

· Unknown source

· Known or suspected pregnancy, but initiate PEP

· Breastfeeding mothers, but initiate PEP

· Source patient is on ART

· Major toxicity of PEP regimen.

Step VII: Follow-up of an exposed person

Whether or not post-exposure prophylaxis is started, a follow up is needed to monitor for possible infections and to provide psychological support.

Clinical follow-up

In the weeks following an AEB, the exposed person must be monitored for the eventual appearance of signs indicating an HIV seroconversion: acute fever, generalized lymphadenopathy, cutaneous eruption, pharyngitis, non-specific flu symptoms and ulcers of the mouth or genital area. These symptoms appear in 50%-70% of individuals with an HIV primary (acute) infection and almost always within 3 to 6 weeks after exposure. When a primary (acute) infection is suspected, referral to an ART centre or for expert opinion should be arranged rapidly.

An exposed person should be advised to use precautions (e.g., avoid blood or tissue donations, breastfeeding, unprotected sexual relations or pregnancy) to prevent secondary transmission, especially during the first 6–12 weeks following exposure. Condom use is essential.Drug adherence and side effect counselling should be provided and reinforced at every follow-up visit. Psychological support and mental health counselling is often required.

Laboratory follow-up

Exposed persons should have post-PEP HIV tests. HIV-test at 3 months and again at 6 months is recommended. If the test at 6 months is negative, no further testing is recommended.

Photo Gallery

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AIIMS First Prize winner of kaya kalp	Bio Medical Waste Trolleys
Card board boxes for glassware	Clean & Green AIIMS poster
Colour coded foot operated bins
Kaya Kalp Inspection	Resource Material
Sewage Treament Plant	STP Sludge
Temporary Storage Facility	Training Session for Bio Medical Waste mgmt workers
Training session
Bio Medical Waste poster

BIO-MEDICAL WASTE MANAGEMENT

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Biomedical waste Android App link

INTRODUCTION

As per the act passed by the Ministry of Environment and Forests in 1986 & notified the Bio Medical Waste (Management and Handling) Rules in July 1998, it is the duty of every “occupier”, (in the case of AIIMS, the Director, AIIMS) i.e. a person who has the control over the institution or its premises, to take all steps to ensure that waste generated is handled without any adverse effect to human health and environment.

The biomedical waste management policy followed at AIIMS is as per the Biomedical Waste Management Rules 2016, notified by the Ministry of Environment, Forest and Climate Change, Government of India as per the gazette notification dated 28^th March 2016. Prior to this notification, AIIMS had been following the Bio-medical Waste (Management & Handling) Rules 1998 notified by the same ministry. At present, the biomedical waste management at AIIMS has been outsourced to a common biomedical waste management facility, M/S Biotic Waste Solutions Pvt. Ltd..

DEFINITIONS

• Hospital waste: refers to all waste, biological or non‐ biological that is discarded and not intended for further use.

• Bio-medical waste means any waste, which is generated during the diagnosis, treatment or immunization of human beings or animals or in research activities pertaining thereto or in the production or testing of biologicals, and including categories mentioned in Schedule I, of the BMW rules, 2016.

SALIENT FEATURES:

The major salient features of BMW Management Rules, 2016 include the following:-

(a) The ambit of the rules has been expanded to include vaccination camps, blood donation camps, surgical camps or any other healthcare activity;

(b) Phase-out the use of chlorinated plastic bags, gloves and blood bags within two years;

(c) Pre-treatment of the laboratory waste, microbiological waste, blood samples and blood bags through disinfection orsterilization on-site in the manner as prescribed by WHOor NACO;

(d) Provide training to all its health care workers and immunize all health workers regularly;

(e) Establish a Bar-Code System for bags or containers containing bio-medical waste for disposal;

(f) Report major accidents;

(g) The new rules prescribe more stringent standards for incinerator to reduce the emission of pollutants in environment;

(h) Existing incinerators to achieve the standards for retention time in secondary chamber and Dioxin and Furans within two years;

(i) Bio-medical waste has been classified in to 4 categories instead of 10 to improve the segregation of waste at source;

(j) Procedure to get authorization simplified. Automatic authorization for bedded hospitals. The validity of authorization synchronized with validity of consent orders for Bedded HCFs. One time Authorization for Non-bedded HCFs;

(k) No occupier shall establish on-site treatment and disposal facility, if a service of `common bio-medical waste treatment facility is available at distance of seventy-five kilometers.

(l) Operator of a common bio-medical waste treatment and disposal facility to ensure the timely collection of bio-medical waste from the HCFs and assist the HCFs in conduct of training.

ORGANOGRAM

BIO MEDICAL WASTE RULE 2016

AUTHORIZATION OF AIIMS UNDER BIO MEDICAL WASTE MANAGEMENT RULES (ARCHIVE)

a) RENEWAL OF AUTHORIZATION OF AIIMS UNDER BIO MEDICAL WASTE MANAGEMENT RULES-2016.

b) CONSENT TO OPERATE

a) PRESENTATIONS ON BMW Rules

BIOMEDICAL WASTE MANAGEMENT: STATUS REVIEW & THE LABORATORY WASTE PERSPECTIVE

BIOMEDICAL WASTE MANAGEMENT RULES 2016: OVERVIEW, SALIENT FEATURES & IMPLICATION

BIO MEDICAL WASTE MANAGEMENT LECTURE FOR HEALTHCARE WORKERS:ENGLISH

CAPACITY BUILDING IN BMW MANAGEMENT

BIO MEDICAL WASTE MANAGEMENT LECTURE FOR HEALTHCARE WORKER :HINDI

b) DELHI POLLUTION CONTROL COMMITTEE GUIDE ON BIO MEDICAL WASTE MANAGEMENT

CURRENT AGREEMENT: under finalization

6. REPORTS

a) ANNUAL

b) MONTHLY REPORT

7. STAFF HEALTH ACTIVITIES:

8. NEEDLE STICK INJURY

9. PHOTO GALLERY

10. Biomedical waste management manual

11. Guidelines for Handling, Treatment and Disposal of Waste generated during Treatment/Diagnosis/Quarantine of COVID-19 patients at AIIMS, New Delhi

11. Mode of disposal of Biomedical waste: Through CBWTF

12. Name and Address of the CBWTF:
      Biotic Waste Solutions Pvt. Ltd.
      46-47, SSI Industrial Area,
      G.T. Karnal Road, Delhi-110033
      Ph:+91-11-47528106/07

13. CONTACT DETAILS

Nodal Officer:

Dr. Vijaydeep Siddharth: Asstt. Professor, Dept. of Hospital Administration, AIIMS

Contact no.: Landline: 011-26593323

Sanitation Officer: Mr. R.D. Munda:

Contact no.:

Mobile no. 9868023974

Landline: 011-26593369, 011-26594367 (available 24 X 7)