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Uganda Clinical Guidelines UCG trên PC

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Uganda Clinical Guidelines UCG Giới thiệu

The Uganda Clinical Guidelines (UCG) evolved from the

National Standard Treatment Guidelines 1993, which

were the first of the type published in Uganda. Before then,

individual guidelines existed to manage a limited number of

specific conditions.

The purpose of national standard treatment guidelines is

to provide evidence-based, practical, and implementable

guidance to prescribers to provide the most cost-effective and

affordable treatment of priority health conditions in a country.

Together with the Practical Guidelines for Dispensing

at Lower/Higher Health Facility Level, which provide

information about medicine characteristics, administration,

and side effects, the UCG are designed as a practical tool to

support daily clinical practice by providing a reliable reference

for health workers on appropriate management of Uganda’s

common health conditions. It also gives health managers a

reference tool to assess and measure service quality.

The guidelines are also the basis for the formulation of

the essential medicines and health supplies list of Uganda

(EMHSLU) which are used to guide supply and procurement.

This allows for more efficient use of limited resources to

improve rational prescribing.

The treatments described in the UCG are the nationally

recognised standard treatments, and in many cases, they are

derived from those recommended in the Ministry of Health

Vertical Programmes, World Health Organisation, and other

international guidelines.

The guidelines have been reviewed and updated through a six-

month process involving extensive consultations with public

health programs staff, medical experts, and health workers of

all cadres.

As medicine is an ever-evolving field, this manual is to be

used for guidance, but cannot replace clinical judgement in

individual cases.

The Ministry of Health and all those involved in updating

the UCG sincerely hope that the UCG will make a significant

contribution to ongoing improvements in national

therapeutic services and medicines utilization