| Literature DB >> 29043186 |
Siyem C Nkwawir1, Nakeli N Batumani1, Talkmore Maruta2, Charles N Awasom1.
Abstract
BACKGROUND: Public health laboratories form the foundation on which today's clinical laboratory practice in Cameroon is built. The advent of the Strengthening Laboratory Management Toward Accreditation (SLMTA) programme in 2009 empowered the Bamenda Regional Hospital Laboratory (BRHL) to improve its working culture, practices and management.Entities:
Year: 2014 PMID: 29043186 PMCID: PMC5637803 DOI: 10.4102/ajlm.v3i2.203
Source DB: PubMed Journal: Afr J Lab Med ISSN: 2225-2002
SLMTA Workshop Topics, Bamenda Regional Hospital Laboratory.
| Schedule | Location | Date | Modules taught |
|---|---|---|---|
| Workshop 1 | Mutengene, Cameroon | October 2010 |
Introduction Cross-cutting Productivity management Quality assurance Documents and records management |
| Workshop 2 | On-site at BRHL | February 2011 |
Work area management Inventory management Procurement management Routine and/or preventive maintenance of equipment |
| Workshop 3 | On-site at BRHL | June 2011 |
Specimen collection and processing Laboratory testing Test result reporting |
SLMTA, Strengthening Laboratory Management Toward Accreditation; BRHL, Bamenda Regional Hospital Laboratory.
FIGURE 1Progress of the Bamenda Regional Hospital Laboratory in quality management systems as measured by the Stepwise Laboratory Quality Improvement Process Towards Accreditation (SLIPTA) checklist from November 2009 to August 2013.
FIGURE 2Performance of the Bamenda Regional Hospital Laboratory (%) across the 12 Quality System Essentials at baseline, last interim, exit and official ASLM audit.
A summary of improvement projects, Bamenda Regional Hospital Laboratory, Cameroon.
| Problem | Improvement project | Period of implementation |
|---|---|---|
| Lack of documented procedures | Establish Standard Operating Procedures (SOP). | After SLMTA workshop 1 |
| Missing specimens | Improve specimen management (labelling, logging, analysis and proper disposal). | After SLMTA workshop 1 |
| Unsafe environment | Tile the floors and work stations; improve the use of personal protective equipment; establish a safety manual; extend building and improve floor plan; establish triple packaging; install proper signage. | After SLMTA workshop 2 |
| Frequent stock outs | Improve inventory and stock management (reagent logs, stock cards, invoice recording, assessment of supplies and suppliers). | After SLMTA workshop 2 |
| Congestion and clutter | Establish equipment identification and management (labelling, removal of obsolete equipment). | After SLMTA workshop 2 |
| Poor client satisfaction | Establish tools for customer satisfaction survey (suggestion box, survey forms, feedback from clinicians through meetings); establish client handbook. | After SLMTA workshop 3 |
| Poor non-conformity management | Establish a system to manage non-conformities including how to capture them; establish a team to investigate and implement corrective action. | After SLMTA workshop 3 |
| Poor quality management | Improve internal quality control documentation (logs, registers); establish quality indicators. | After SLMTA workshop 3 |
| Poor reviewing system | Assign supervisory personnel in charge of biosafety, quality, and equipment. | After first interim audit |
| Poor document control | Establish a document control system (manage present and archival documents). | After exit audit |
SLMTA, Strengthening Laboratory Management Toward Accreditation.