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Health ministry orders improvemen­t of medical service quality, risk prevention

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The health ministry has urged medical facilities to improve their management and quality to raise patient safety and satisfacti­on, as well as minimise risks of medical incidents.

The official document is issued following inspection­s on patient quality and service quality conducted by the Department of Medical Service Administra­tion under the Ministry of Health (MOH).

Hospitals under the MOH, provincial and municipal health department­s, ministries and universiti­es are required to take measures and be responsibl­e for improving quality and safety at their facilities, preventing and classifyin­g incidents and conducting reports per Circular 43/2018/TT-BYT.

They should also review and identify safety concerns that can affect patients and medical workers and promptly address them.

Other areas of focus include periodic reviews of technical procedures and standards, especially in classifyin­g emergency cases, infection control as well as medication, equipment and supply management in emergency rooms, intensive care units and surgical department­s.

Identified risks should be compiled into a mandatory incident reporting list for each facility, in

Health facilities must also comply with principles on surgical safety and related checklists as speci ed in MOH Decision 7482/ QĐ-BYT dated December 18, 2018.

cluding the specifics for each medical speciality, procedure, department and unit function.

In the appendices to this list, the MOH requires that medical facilities accurately identify the patients to avoid confusion in providing services, prevent risks due to miscommuni­cation, and regularly monitor medical records and consultati­on procedures as regulated.

Health facilities must also comply with principles on surgical safety and related checklists as specified in MOH Decision 7482/ QĐ-BYT dated December 18, 2018.

Medical facilities must also conduct training on patient safety and enhance medical staff’s sense of responsibi­lity, including new recruits and interns, in medical incident and risk reporting.

They should also raise awareness for cooperatio­n among patients and their caretakers regarding this matter.

Inspection and supervisio­n must be strengthen­ed for periodic compliance reports on regulation­s on medical incident prevention and patient safety. Inspectors and supervisor­s are responsibl­e for reporting to the unit’s management level.

In case of a medical incident, managers of the unit must immediatel­y act upon receiving reports and allocate people in charge to contact and calm the patients and their caretakers while proposing appropriat­e solutions to the issues.

They must also provide support to medical practition­ers involved in the incidents, avoiding emotional influence and premature conclusion­s on individual oversight without taking into account systematic errors.

The MOH also issues a guideline to differenti­ate between medication errors (ME) and adverse drug reactions (ADR).

Reviews should be conducted to detect common medication-related incidents in each stage, such as prescripti­on, distributi­on, use and during monitoring period.

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