Policies and Procedures On Continuous Quality Improvement
Policies and Procedures On Continuous Quality Improvement
Policies and Procedures On Continuous Quality Improvement
No. of Pages :
Date of Implementation :
Approved By : Designation :
Name :
Signature :
AMENDMENT SHEET
The holder of the copy of this Manual shall maintain it in current status by inserting latest amendments as and
when the amended versions are received.
Quality Manager is responsible for issuing the amended copies to the copyholders, the copyholder should
acknowledge the same and he /she should return the obsolete copies to the Quality Manager.
The amendment sheet, to be updated (as and when amendments received) and referred for details of
amendments issued.
The manual is reviewed once a year and is updated as relevant to the hospital policies and procedures. Review
and amendment can happen also as corrective actions to the non-conformities raised during the self-assessment
or assessment audits by NABH.
The procedure manual with original signatures of the above on the title page is considered as ‘Master Copy’,
and the photocopies of the master copy for the distribution are considered as ‘Controlled Copy’.
S.No. Designation
1 ……………………….
2 ……………………….
3 ……………………….
CONTENTS
2.0 Scope 5
3.0 Responsibility 5
4.0 Abbreviations 5
5.0 Definitions 5
6.0 Reference 6
7.0 Policy 6
8.0 Procedures 6
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1.0 PURPOSE:
1.1 To guide and ensure the continuous improvement of quality services provided by ………
(Hospital name)
1.2 To fix key indicators for the processes, to organize measurement process to assess the
performance index on such key indicators.
1.3 Scheduling of periodical measurement of performance index of key indicators explained above.
1.4 To identify appropriate tools for continual improvement.
2.0 SCOPE:
2.1 Hospital Wide – All Inpatient care areas
2.2 Applicable to all employees of the hospital
3.0 RESPONSIBILTY:
3.1 Consultants / Doctors
3.2 All hospital staff
3.3 Core/Quality Assurance Committee
4.0 ABBREVIATION:
4.1 NABH : National Accreditation Board For Hospitals and Healthcare
providers
4.2 CQI : Continuous Quality Improvement
5.0 DEFINITION:
5.1 Quality Indicators: Quality indicators are the means to judge the real performance of certain
clinical as well as managerial parameters selected for monitoring and evaluation.
5.2 Sentinel Events: An unexpected occurrence involving death or serious physical or
psychological injury, or the risk thereof to a patient, visitor, or an employee.
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5.3 Quality improvements: It is an ongoing response to quality assessment data about a service
in ways that improve the process by which services are provided to the patients.
5.4 Risk management: Clinical and administrative activities to identify evaluate and reduce the
risk of injury.
6.0 REFERENCE:
6.1 NABH: Pre Accreditation Entry Level Standards for Hospitals, Fifth Edition
7.0 POLICY:
7.1 Organization has designated a person as NABH coordinator to meet the quality standards.
7.2 Quality improvement and patient safety programme shall be implemented by Quality & Safety
Team.
7.3 The Hospital management makes available adequate resources required for quality improvement
and patient safety program.
7.4 The hospital management has identified key performance indicators to monitor the clinical and
managerial areas.
8.0 PROCEDURE:
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8.1 Approach To Designing, Measuring, Assessing And Improving Quality:
8.1.1 Planning: Planning for the improvement of patient care and health outcomes includes a
hospital-wide approach.
8.1.2 Designing: Processes, functions or services are designed effectively based on: Mission
and vision of Karkinos Healthcares’ needs and expectations of patients, staff, and others.
8.1.3 Measurement: Data is collected for a comprehensive set of Quality measures. Data is
collected as a part of continuing measurement, in addition to data collected for priority
issues. Data collection considers measures of processes and outcomes. Data collection
includes at least the following processes or outcomes:
8.1.3.1 Patient assessment
8.1.3.2 Laboratory safety & quality
8.1.3.3 Diagnostic Radiology safety & quality
8.1.3.4 Processes related to medication use
8.1.3.5 Processes related to anesthesia
8.1.3.6 Processes related to the use of blood and blood components
8.1.3.7 Processes related to medical records content, availability and use
8.1.3.8 Risk management activities
8.1.4 Assessment:
8.1.4.1 The assessment process involves the relevant departments to draw conclusions
about the need for more intensive measurement.
8.1.4.2 A systematic process is used to assess collected data in order to determine
whether it is possible to make improvement of existing processes, actions taken
to improve the Quality Improvement processes, and whether changes in the
processes resulted in improvement.
8.1.4.3 Collected data is assessed at least annually and findings are documented and are
forwarded through the proper channels.
8.1.4.4 When assessment of data indicates, a variation in Quality, more intensive
measurement and analysis will be conducted and in addition, the
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department/service or team will reassess its Quality measurement activities and
re-prioritize them as deemed necessary.
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8.3.1 Documents such as regulations, standards, policies, SOPs, manuals and other normative
documents as well as drawings, software form part of the Hospital Quality Management
System.
8.3.2 A copy of each of these controlled documents shall be archived for future reference and
the documents shall be retained in their respective department the documents are
maintained in paper or electronic media as appropriately required.
8.3.3 Documents are identified and established as two levels namely:
8.3.3.1 Quality Manual;
8.3.3.2 Hospital Policies & Procedures;
8.3.4 The Heads of the Departments of the respective departments shall review all documents
issued to personnel as a part of management system annually and they shall approve it
for the use. The Head of Quality issues the finalized document.
8.3.5 The Head of Quality ensures that:
8.3.5.1 Authorized editions of appropriate documents are available at all locations where
operations essential to the effective functioning of the Hospital are performed.
8.3.5.2 Documents are periodically reviewed and revised where necessary to ensure
suitability and compliance with applicable requirements.
8.3.5.3 Invalid or obsolete documents are promptly removed from all prints of issue or
use, or otherwise assured against unintended use.
8.3.5.4 Obsolete documents are retained for either legal and / or knowledge preservation
purposes are suitably marked or destroyed or the record and the record of this
maintained in a separate register.
8.3.6 Document Changes:
8.3.6.1 Revision of management systems documents is carried out when necessary by the
original author and updated at least once in two years.
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8.3.6.2 When alternate persons are designated for review, they shall first familiarize
themselves with pertinent background information upon which to base their
review and approval.
8.3.6.3 Document control system does not follow for the amendments by hand unless
there is an extreme circumstance.
8.3.6.4 These amendments shall be marked, initialed and dated only by the Head of the
Department.
8.3.6.5 The amendment shall be brought to the notice of the Quality coordinator and the
same shall be reissued
8.4 Preventive Actions:
8.4.1 The NABH Coordinator shall be perpetually vigilant and identify potential sources of
non-compliance and areas that need improvement.
8.4.2 These may include trend analysis of specific markers such as turnaround time, risk
analysis, etc.
8.4.3 Where preventive action is required, a plan is prepared and implemented.
8.4.4 All preventive actions must have control mechanisms and monitor for efficacy in
reducing any occurrence of non-compliance or producing opportunities for improvement.
8.5 Corrective Action:
8.5.1 The Quality Coordinator takes all necessary corrective action when any
deviation is detected in Quality Management System.
8.6 Root Cause Analysis: Deviations are detected by:
8.6.1 Patient complaints/feedbacks.
8.6.2 Non-compliance receipt of items/sample.
8.6.3 Non-compliance at Internal/external Quality Audit. Management Reviews.
8.6.4 The Quality coordinator conducts and coordinates the detailed analysis of the nature and
root cause of non-compliance along with the responsible persons from the respective
sections.
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8.7 Selection and Implementation of Corrective Actions: Potential corrective actions are
identified and the one that is most likely to eliminate the problem is chosen for implementation.
Corrective action is taken into consideration the magnitude and degree of impact of the problem.
All changes from corrective action is documented and implemented.
8.8 Monitoring of Corrective Actions: The NABH/Quality Coordinator shall monitor the outcome
parameters to ensure that corrective actions taken have been effective in eliminating the
problem.
8.9 Procedures for Internal Quality Audit:
8.9.1 Internal audit shall be conducted by the internal audit team members once in six
months.
8.9.2 Internal audit team members shall be trained on Pre Accreditation Entry Level
NABH standards either internally (a trained person who in turn trains the other
members of the team) or externally (training conducted by Quality Council of India).
8.9.3 Audit starts with the opening meeting. All departmental heads shall be informed
about the purpose of audit, audit timings and duration of audit etc.
8.9.4 All minor correction shall be suggested then and there by the auditor to the
departmental staff.
8.9.5 Audit gets over with the closing meeting, over all observations shall be summarized
by the chief auditor. Audit observations shall be handed over to the chairman of the
quality assurance committee in a standardized format.
8.9.6 All the audit reports shall be discussed with the core committee members and the
observations noticed will be presented to the Chairman for improvements.
8.9.7 The Audit reports shall be forwarded to the concerned Departmental Heads.
Corrective and preventive actions will be done by the department staff based on the
audit observations. Reports of the corrective and preventive actions will be submitted
to the Quality department by the concerned Head of the department.
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8.10 Procedure for collection of data, interpretation and analysis of Quality Indicators:
8.10.1 Collection of Data: Reports of all key indicators as decided by the management will be
submitted to the quality coordinator at the end of every month by the Head of each
department. All the data will be collected in the standardized format.
8.10.2 Analysis of Data: All the data will be assessed in the form of Structure, process and the
outcome.
8.10.3 Structure: Structure includes the facilities provided to the staff. Formula used for
calculation. Training or awareness of the set formulas / quality improvement programme.
8.10.4 Process: Strict adherence of developed procedures in the daily work routine. In case of
deviations same will be documented in the quality indicator reporting form with proper
reasoning.
8.10.5 Out Come: Based on the reports received trend analysis will be done and the same will be
reported to the chairman/ Management.
STANDAR
SL
INDICATOR NUMERATOR DENOMENATOR DIZATION Definition
NO
FACTOR
Time for The time shall begin
Initial Sum of time Total number of from the time that the
1 patient has arrived at the
Assessment of taken patients 100 bed of the ward till the
Indoor patients
time that the initial
assessment has been
conducted by a doctor.
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14 of
of 16
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assessment completed by
Page
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the doctor
Re-scheduling of patients
Percentage of
Number of cases Total number of includes cancellation and
3 re-scheduling 100
re-scheduled surgeries performed postponement (beyond 4
of surgery
hours) of the surgery.
A medication error is any
preventable event that
may cause or lead to
inappropriate medication
usage or harm to a
Percentage of Number of patient. Eg: errors in
Number of patients
4 medication medication 100 prescribing, transcribing,
under medication
errors errors reported dispensing, administering
and monitoring of
medications; wrong drug,
wrong dose, or wrong
strength errors; wrong
patient errors
Percentage of
Number of Medication chart with
medication number of
medication chart illegible handwriting and
5 chart with error medication chart 100
with error prone unaccepted error prone
prone reviewed
abbreviations abbreviations
abbreviations
Anesthesia plan is the
outcome of preanesthesia
Percentage of Number of cases Total number of assessment. Any changes
6 modification of where anesthesia patients given 100 done after this shall be
anesthesia plan plan is modified anaesthesia considered as
modification of
anesthesia plan.
Adverse drug event is any
untoward medical
Number of occurance that may
Percentage of
patients who Number of patients present during treatment
Adverse
7 developed who underwent 100 with anesthetic product
Anesthesia but which does not
adverse anesthesia
Events necessarily have causal
anesthesia events
relationship with this
treatment
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Page 15 aofsystemic
16 response of
Page
Percentage of the body to the
Number of
blood and Number of blood administration of blood
transfusion
8 blood products and blood products 100 in compatible with that
reactions
transfusion transfusions done of the recipient. The
occurred
reactions causes include red cell
incompatibility.
A medical record is
Total number of considered as missing,
Percentage of
Number of medical records when it could not be
9 missing 100
records generated per found out from the MRD
records
month after 72nd hour of record
request
Urinary Number of patients
Number of
Tract who were inserted
Urinary
Infection with Urinary As per latest CDC
10 Catheter 1000
Rate due to Catheter guidelines
associated
urinary
UTIs
catheter
Ventilator Number of
associated ventilator Number of patients As per latest CDC
11 1000
pneumonia associated on a ventilator guidelines
Rate pneumonias
Number of
Surgical Site surgical site Number of surgeries As per latest CDC
12 100
Infection Rate infections performed guidelines
loss of upright position
that results in landing
on the floor, ground or
an object or furniture or
a sudden uncontrolled
Incidence of Number of unintentional,
13 Number of falls 100
falls Admissions nonpurposeful
downward displacement
of the body towards
floor/ floor or hitting
another object like a
stair or chair.
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Pre exposure prophylaxis
is any medical or public
Percentage of Number of
health procedure used
employees employees Total No of
before exposure to the
14 provided provided with Employees in the 100
disease causing agent, its
preexposure Pre-exposure hospital
purpose is to prevent,
prophylaxis prophylaxis
rather than treat or cure a
disease.
NSI is a penetrating stab
wound from a needle that
Number of Number of may result in exposure to
15 needle stick needle stick Number of IP days 100 blood or other body
injuries injuries reported fluids. NSI are wounds
caused by needles that
accidently puncture.
Percentage of
admissions Number of patients
16 Number of ADR 100
with adverse under medication
drug reactions
Every anesthesia plan
shall invariably mention
Number of if there is a possibility of
Percentage of patients the patient requiring
unplanned requiring Number of patients Ventillation followed by
17 Ventillation unplanned who underwent 100 anesthesia. Every case
followed by Ventillation anesthesia wherein patient requires
anesthesia followed by Ventillation but this was
anesthesia not captured in the
anesthesia plan shall be
part of numerator
Number of
Incidence of patients who
Number of
18 bedsore after requiring new/ 100
Admissions
admission worsening of
pressure ulcer
19 Waiting time Sum of TAT Number of patients 100
for diagnostic (patient in reported for
procedures , time for Multiple x rays
X RAY: procedure - taken
reporting
time)
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Waiting time Sum of TAT
for diagnostic (patient in
Number of patients
19 a procedures ,lab time for 100
reported
investigations procedure -
reporting time)
Percentage of
Number of
medical
medical records
records not Number of
20 not having 100
having discharges and death
discharge
discharge
summary
summary