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Establishing a Drug Information

Centre

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Definition
World Health Organization (WHO) defines drug
information centre as an independent centre that is
accessible to any healthcare professional to ask all
questions about drug therapy

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Introduction
There are three physical criteria, which define an
information centre:

1. Specific room set aside as location for drug


information centre
2. At least one dedicated and trained pharmacist
must be available to answer queries
3. Sufficient information resources should be
available to answer a broad scope of queries
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Introduction
A strategic plan should be developed when establishing a
drug information centre

The plan should include:


mission statement
goals and objectives
action plan with performance indicators
details of budget
methods for evaluating the services provided
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Introduction
Establishment of a drug information centre needs the
consideration of:

Justification of the need for a centre


Services to be offered by the centre
Resources, facilities and ongoing maintenance for the
centre.
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Establishment and minimum requirements


To be successful, DI centre requires a
-- stable location and environment
-- idealistic commitment to provide needed drug
information
-- physical space to house the service
-- basic information references
-- staff
-- equipment to support information access and
dissemination, and communication equipment
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Establishment and minimum requirements


Essential components
-- Philosophical commitment
-- Location of the centre
-- Space allocation
-- Facilities and equipments
-- Financial issues
-- Staff

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Establishment and minimum requirements


Essential components
-- Organization
-- Resources
-- Operational Procedures
-- Documentation
-- Quality assurance

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Philosophical commitment
Drug information centers should work both in
reactive and proactive ways
The reactive or passive responsibilities of the centers include
providing the information to the individuals who approach
the centre
Proactive responsibilities include reaching out with drug
information for the people who need it, in a format that is
convenient and effective
The centers should work according to the needs and
expectations of its users and should create demand and
expectations
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Location of the centre


Should be centrally located & the location selected should
have good access to requestors and not too much of
distraction

Few ideal locations


-- In or adjacent to a hospital
-- Medical teaching institution
-- Within the hospital
-- University/academic institution
-- Within/adjacent to a medical / pharmacy association
-- Relevant governmental agency (such as ministry of health,
drug control authority, drug approval unit, or quality control lab)
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Space allocation
An independent area must be set aside for the drug
information services
It may depend upon the size of the centre and the number of
queries received by the centre

A secure space of 25 square meters in one or two rooms


allows for office workspace, storage of references, placement
of communication equipment, research and educational
activities, and space for visitors to use the drug information
resources
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Facilities and equipments


DIC should have sufficient lighting, ventilation and aeration
It should also have essential access to a medical library
The basic equipments needed for effective functioning of a
drug information centre include, basic office equipment,
photocopier
(preferably),
microfiche
reader/printer,
computer equipment and Internet, printer, telephones,
calculator (or computer programs), visual aids and fax
machine.

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The minimum equipments required for effective operation of a major


teaching hospital based drug information centre
Equipment

Number(s)

Chair

10

Desk

Working table with chair

Filing systems/cabinet

Microfiche filing system cabinet

Book and journal shelf

Journal display rack

Notice board

Teaching board

Computer desk with chair

Table for microfiche reader/printer

Photocopier* (with facility to produce multiple collated copies, capable of copying bound volumes,
capable of photocopying overhead transparencies, facility to reduce and enlarge)

Microfiche reader/printer (compatible with database requirements)

Computer (compatible with the database requirements, with printing facility, appropriate
software programs, internet access with separate telephone lines)

Telephone (preferably with STD access)

Calculator or computer program (with facility for pharmacokinetic calculations and basic
statistical functions)
Overhead projector

Fax machine

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1
1

Financial issues
The source of finance depends on the objectives and
operational modalities
Ideally funding may be sought from governmental
authorities [as DI is public service]
Other sources
--donors supporting essential drugs projects
-- professional associations,
-- universities/pharmacy and medical institutions
-- non-governmental organizations
Collation of several of these groups can also fund the drug
information centers
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Financial issues
No matter how the drug information centre is financed, the
integrity of the unit is paramount
No special interests should be able to influence what
information is or is not given out
Drug information centre should devote suitable amount for both
human resources and non human resources

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Sample budget for establishing & maintaining a DI centre


* Approximate annual cost

Set up costs*
(Rs)
(First year)

Running costs*
(Rs)
(Subsequent years)

Salaries (1 pharmacist, 1 assistant / clerical staff)

180,000=00

180,000=00

Journals

50,000=00

50,000=00

Books

200,000=00

50,000=00

Databases

300,000=00

300,000=00

Equipment & office furniture

200,000=00

Nil

Bulletins/Newsletters (4 per year)

30,000=00

30,000=00

Telephone and Internet

20,000=00

15,000=00

Stationary

15,000=00

15,000=00

Conferences/Continue education programs


(2 per year)

10,000=00

10,000=00

Photocopying costs

5,000=00

5,000=00

Item

Total

10,10, 000=00
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6, 55, 000=00

Staff
The DI centre should have a multidisciplinary team
Ideally the number of personnel should be related to call
volume
In case of hospital based drug information centre, the number
depends on beds strength

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Staff

Number of full time equivalent pharmacists and other staff required for
operating a drug information centre (minimum required)

No. of beds in
the hospital

Less than 200

200 - 500

More than 500

No. of full time


equivalent
pharmacists
required
1

Assistant / clerical
staff

3-4

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Staff
Basic requirements for drug information pharmacists

-- Master of Pharmacy degree


(Preferably Clinical Pharmacy / Pharmacy Practice)

-- Registered pharmacist
-- Training in computer based information systems
-- Two years of experience in DI services
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Staff
Basic requirements for drug information pharmacists

-- Knowledge about literature identification, selection,


utilization and critical
evaluation
--Training in verbal,
communication skills

written

and

telephone

-- Involvement with in-service educational activities


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Organization
The drug information services should have an organization
that should involve in the preparation of

guidelines & policies


procedures
manuals
establishment of staff
allocation of staff
deciding the hours of the operation
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Organization
The policy and procedure prepared by the organization
should answer the following questions:

What must be done?


What is the purpose?
When it should be done?
Who should do it?
How it should be done?
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Organization
The guidelines and policies prepared by the centre should
serve as:

Guide for training new employees


Control tool in ensuring a defined procedure for
performing a task
Means for evaluating job performance
Important element for action arising from an
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error

Resources
The drug information centre must well equipped with
current information resources based on services
provided
The source of information may include primary,
secondary and tertiary resources
The collection of resources must represent variety of
pharmaceutical and therapeutic literature available and
must be adequate to ensure timely response to the
enquiries
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Resources
The drug information centre should have:

Access to the medical journals (local and international),


which may be through a library attached to the hospital
Adequate number of appropriate reference texts
In house information system (with relevant articles)
Access to on-line data retrieval systems and drug
information databases for obtaining the published
articles
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Tertiary sources
(minimum requirements)
Title
Standard references and textbooks
AHFS Drug Information. Mc Evoy GK, ed.
Australian Medicine Handbook
Averys Drug Treatment. Speigth TM, ed.
Basic skills in interpreting the laboratory data illustrated with
case studies. Traub SL, ed
Current Medical Diagnosis and Treatment. Tierney LM, ed.
Davidsons principles and practice of medicine. Haslett C, ed.
Drug Information Handbook. Lacy C.
Drugs in Pregnancy and Lactation. Briggs GG.
Drug Interactions. Stockley IH.
Drug Interaction and updates. Hansten PD.
Drug Interaction facts. Tatro DS, ed.
Drug Prescribing in Renal Failure: Dosing Guidelines for
Adults. Aronoff GR.
Ellenhorns Medical Toxicology.www.revolutionpharmd.com
Ellenhorn MJ.

Requirement
E
D
E
D
D
D
E
E
E
E
E
E
E

Tertiary sources
(minimum requirements)
Formulary manuals
British National Formulary

Indian Pharmacopoeia

British Pharmacopoeia

United States Pharmacopoeia

USP National Formulary

Australian Pharmaceutical Formulary and Handbook

Pediatric Pharmacopoeia. Kemp CA, ed.

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Tertiary sources
(minimum requirements)
Standard treatment manuals
Essential Drug List

Hospital Level Standard Treatment Guidelines

Periodicals
Current Index for Medical Specialties

Drug Index

Drug Today

Indian Drug Review

E
Medical Dictionaries

Stedmans Medical Dictionary

Oxford Concise Medical Dictionary

Dorlands Medical Dictionary

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Tertiary sources
(minimum requirements)
Drug bulletins and newsletters
Australian Adverse Drug Reactions Bulletin

Uppsala Reports

Clinical Pharmacy Newsletter JSS College of Pharmacy,


Mysore

Clinical Pharmacy Newsletter JSS College of Pharmacy, Ooty

Clinical Pharmacy Newsletter College of pharmaceutical


Sciences, Manipal.

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Secondary sources
(minimum requirements)
Title

Requirements

Medline

International Pharmaceutical Abstracts

Chemical Abstracts

Iowa Drug Information Service

Drugdex

Poisindex

E
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Primary sources
(minimum requirements)
Title
Annals of Pharmacotherapy
Journal of American Medical Association
British Medical journal
Drugs
Drugs and Therapeutics Bulletin
Lancet
Medical Letter on Drugs and Therapeutics
New England Journal of Medicine
Australian Prescriber
Pharmaceutical Journal
Hospital Pharmacist
Journal of Clinical Pharmacy and Therapeutics
Indian Journal of Clinical Practice
Journal of Association of Physicians of India
National Medical Journal of India
Indian Journal of Medical Sciences
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Drugs safety

Requirement
EA
EA
EA
D
EA
EA
EA
EA
EA
E
E
D
D
D
E
E
EA

Operational Procedures
A. Services to be offered

The drug information centre should clearly indicate


the scope of service provided

For example:
Oncology services
Pregnancy lactation services

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Operational Procedures
A. Services to be offered
A. Services to be offered

Drug information centre should involve in following activities:

Providing medication information to patients, healthcare professionals and other personnel/public


Establishing and maintaining formulary based on
scientific evidence of efficacy and safety, cost, and
patient factors
Developing and participating in efforts to prevent
medication misadventure, including adverse drug
event and medication error reporting and analysis
programs
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Operational Procedures
A. Services to be offered

Developing methods of changing patient and healthcare provider behaviors to support optimal
medication use
Educating health-care providers about medication
related policies and procedures
Publishing newsletters to educate patients, families,
and health-care professionals on medication use
Coordinating program to support population-based
medication practices
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Operational Procedures
A. Services to be offered

Coordinating investigational drug services


Providing continuing-education service to healthcare professional staff
Educating pharmacy students and residents
Applying health economic and outcome analysis
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Operational Procedures
A. Services to be offered

Developing and maintaining the active research


program
Drug utilization evaluation program
Toxicology service
Therapeutic drug monitoring
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Operational Procedures
B. Enquiry response

The drug information can be initiated by


pharmacists or requested by other health care
professionals, patients and their caretakers or the
general public
The pharmacist must not only accumulate and
organize the literature but also objectively evaluate
and apply the information from the literature to a
particular patient or situation
Modified systematic approach should be followed
for answering the drug information enquiries
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Operational Procedures
C. Hours of Service

The drug information centre must make known


when it will be available to receive the enquiries
As a minimum the centre should operate during the
normal working hours of the hospital
In case of after hours of service appropriate
arrangements should be in place for after hour
enquiries [e.g., use of answering machine/ automatic call diversion system]
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Operational Procedures
D. Fee for Service

Services must be free of charges to the enquirers,


particularly in the emergency cases
If the charges are to be fixed only minimum charges
may be collected and the charge per call should be
fixed on the basis of no loss and no profit

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Documentation
Documentation is one of the essential elements in the
practice of drug information service in terms of both
legal and future reference purpose
should maintain the documentation of drug
information queries received and the responses
provided
All the documented enquiries should be stored for a
minimum of 5 years and may be for the longer
period (25 years) for the queries related to pregnancy
and lactation
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Documentation
The documentation of the drug information requests and
responses should include the following:

Date and time of receipt of the enquiry.


Requesters
name,
address,
professional
status/occupation/discipline, method of contact (e.g.,
telephonically, direct access)
Previous references consulted by the enquirer
Information about the pharmacist receiving the
enquiry
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Documentation
The documentation of the drug information requests and
responses should include the following:

Category of the enquiry


Question asked
Patient data [specific information related to the enquiry]
Answer provided
Date and time of answering
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Documentation
The documentation of the drug information requests and
responses should include the following:

References used for answering the enquiry


Mode of reply [e.g., verbal, written, printed literature]
Method of delivery [e.g., telephone, personal visit, mail]
Time spent in answering the enquiry
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Documentation
The documentation of the drug information requests and
responses should include the following:

Information about the pharmacist answering


the enquiry
Follow-up information

[e.g., impact on patient outcome,


improvement in medication use, requestor satisfaction]

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Quality assurance
The aims of the drug information centre need to be
met and this can be assessed by the application of
quality assurance program
The drug information centre should measure how
well the services were provided, and if the services
were not found to be acceptable or optimal, centre
should undertake some correctional measures to
ensure that future services will be acceptable

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Quality assurance
General assessment techniques that can be used for the
quality assurance of DI services

Workload statistics
Auditing
Peer review
Enquirers assessment/Users survey
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Quality
assurance
Key areas of drug information where in the quality should be monitored
Inputs level

Staff
Resources
Organization

Processes level

Receiving enquiries
Search strategy
Data collection
Literature evaluation
Formulation and communication of response
Documentation and storage

Outputs level

User satisfaction
Patient outcome
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publications

Quality assurance
A quality assurance program for a drug information centre
should involve the following steps:

Assigning responsibility for monitoring quality


assurance activities
Describing the scope of services provided by the
centre
Identification of the most important aspects of the
services provided
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Quality assurance
A quality assurance program for a drug information centre
should involve the following steps:

Identification of the indicators for monitoring the


important aspects of services provided
Establishment of the threshold/minimum expected
level of performance
Monitoring by collecting and organizing the data on
indicators
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Quality assurance
A quality assurance program for a drug information centre
should involve the following steps:

Identification of the problems and opportunities to


improve the services offered by evaluation of the
data collected
Taking actions to improve the services or correct the
identified problems

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Quality assurance
A quality assurance program for a drug information centre
should involve the following steps:

Assessment of the effectiveness of correction and


documentation of the improvement in services
provided
Communication of the results of quality assurance
program
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Conclusion
Adequate infrastructures with well-qualified and
trained staff are must for the effective functioning of
any drug information centres
Pharmacists as "medication managers" can not only
play a vital role in the patient management but may
also find suitable place in the healthcare system by
developing and maintaining image and credibility
through effective provision of drug information
services
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