African Journal of Laboratory Medicine最新文献

{"title":"GeneXpert rollout in three high-burden tuberculosis countries in Africa: A review of pulmonary tuberculosis diagnosis and outcomes from 2001 to 2019.","authors":"Victor Williams, Marianne Calnan, Bassey Edem, Chukwuemeka Onwuchekwa, Chika Okoro, Christine Candari, Rhodora Cruz, Kennedy Otwombe","doi":"10.4102/ajlm.v11i1.1811","DOIUrl":"10.4102/ajlm.v11i1.1811","url":null,"abstract":"<p><strong>Background: </strong>The rollout of GeneXpert aimed at increasing early diagnosis of tuberculosis to improve treatment outcomes and global tuberculosis targets.</p><p><strong>Objective: </strong>This study evaluated trends in tuberculosis diagnosis and outcomes pre- and post-introduction of GeneXpert in three African countries - the Democratic Republic of the Congo (DRC), Nigeria and South Africa.</p><p><strong>Methods: </strong>Data from 2001 to 2019 were extracted from the World Health Organization's data repository. Descriptive analysis, paired <i>t</i>-tests and interrupted time series models were used.</p><p><strong>Results: </strong>Estimated tuberculosis incidence decreased from 327/100 000 to 324/100 000 in the DRC, and from 1220/100 000 to 988/100 000 in South Africa. Incidence remained at 219/100 000 in Nigeria. The tuberculosis case notification rate did not change significantly. Increases in the new case treatment success rates were statistically significant (DRC: <i>p</i> = 0.0201; Nigeria: <i>p</i> = 0.0001; South Africa: <i>p</i> = 0.0017); decreases in mortality were also statistically significant (DRC: <i>p</i> = 0.0264; Nigeria: <i>p</i> = 0.0001; South Africa: <i>p</i> < 0.0001). Time series models showed insignificant increases in new tuberculosis cases in DRC (<i>n</i> = 1856, <i>p</i> = 0.085) and Nigeria (<i>n</i> = 785, <i>p</i> = 0.555) from 2011 to 2019; and a statistically significant decrease in South Africa (<i>n</i> = 15 269, <i>p</i> = 0.006).</p><p><strong>Conclusion: </strong>Improvements in tuberculosis treatment outcomes were achieved, but little progress has been made in new case notification due to varied implementation and scale-up of GeneXpert across the three countries. Implementation barriers need to be addressed to achieve the required tuberculosis targets.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2022-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453189/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33459936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Tuberculosis-loop-mediated isothermal amplification implementation in Cameroon: Challenges, lessons learned and recommendations.","authors":"Valerie F Donkeng-Donfack,&nbsp;Suzanne M Ongoulal,&nbsp;Yvonne J Djieugoue,&nbsp;Yannick Kamdem Simo,&nbsp;Henri Manga,&nbsp;Danielle A D Tollo,&nbsp;Edwige M A Belinga,&nbsp;Vincent Mbassa,&nbsp;Jean L Abena,&nbsp;Sara Eyangoh","doi":"10.4102/ajlm.v11i1.1792","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1792","url":null,"abstract":"<p><strong>Background: </strong>Until 2016, microscopy was the main tool for the early detection of pulmonary tuberculosis in Cameroon, especially in remote settings. Due to the poor sensitivity of microscopy, there was a need to implement a molecular assay in order to improve tuberculosis case detection.</p><p><strong>Intervention: </strong>In 2017, tuberculosis loop-mediated isothermal amplification (TB-LAMP), a molecular rapid diagnostic test recommended by the World Health Organization, was implemented in Cameroon as a replacement test of microscopy for initial diagnosis of pulmonary tuberculosis and also as a follow-on test to microscopy for smear-negative sputum specimens. A roll out plan for TB-LAMP implementation in Cameroon had been developed from January 2017 to April 2017, followed by initial implementation at four sites in May 2017. Additional sites were added progressively.</p><p><strong>Lessons learnt: </strong>The use of TB-LAMP as a follow-on test to microscopy for smear-negative sputum specimens helped in the detection of tuberculosis in 14.77% of those who were sputum-smear negative in 2019. Tuberculosis-loop-mediated isothermal amplification usage as an initial test, followed by testing with Xpert MTB/RIF for rapid tuberculosis and rifampicin resistance detection during tuberculosis mass screening campaigns, reduced the turn-around time by 73.23% as compared to when the Gene Xpert instrument was used alone.</p><p><strong>Recommendations: </strong>The implementation and scaling up of TB-LAMP in Cameroon contributed to increase access to tuberculosis molecular diagnosis in remote settings and as such improved tuberculosis case notification. However, to better enhance this notification and optimise the use of a TB-LAMP instrument, a suitable sample transport system is recommended.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453169/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33459932","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Bacteriological profile and antibiogram of blood culture isolates from bloodstream infections in a rural tertiary hospital in Nigeria.","authors":"Oluwalana T Oyekale,&nbsp;Bola O Ojo,&nbsp;Adewale T Olajide,&nbsp;Oluwatoyin I Oyekale","doi":"10.4102/ajlm.v11i1.1807","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1807","url":null,"abstract":"<p><strong>Background: </strong>Bloodstream infections (BSIs) are a cause of significant morbidity and mortality requiring urgent antibiotic treatment. However, there is widespread antibiotic-resistance from the bacterial causes, necessitating regular surveillance for drug-resistant bacteria and their antibiograms.</p><p><strong>Objective: </strong>This study isolated and identified various bacterial causes of BSIs, determined their antibiotic susceptibility patterns, and determined the best empirical treatment for cases of BSI in the setting.</p><p><strong>Methods: </strong>A cross-sectional study was carried out at the Federal Teaching Hospital, Ido-Ekiti, Nigeria between June 2020 and February 2021 on 177 blood culture samples from cases of BSI. Identification of isolated bacteria and antibiotic susceptibility testing of the isolates were carried out following the standard protocol.</p><p><strong>Results: </strong>Culture positivity in this study was 19.2%. No significant difference was seen in culture positivity between male and female participants (<i>p</i> = 0.97). Gram-negative enteric bacteria were predominantly isolated (67.6%), including <i>Escherichia coli</i> (29.4%) and <i>Klebsiella aerogenes</i> (20.6%). <i>Staphylococcus aureus</i> was the most common Gram-positive bacterium isolated (23.5%). Three (37.5%) <i>S. aureus</i> isolates were methicillin-resistant. All isolates were sensitive to meropenem, and 97.1% were sensitive to imipenem; other sensitivity patterns were: ceftazidime (85.3%), ciprofloxacin (79.4%), ofloxacin (79.4%), and gentamicin (76.5%). There was low sensitivity to ampicillin (32.4%) and cotrimoxazole (38.2%). All Gram-positive isolates, including methicillin-resistant <i>S. aureus</i>, were sensitive to vancomycin.</p><p><strong>Conclusion: </strong>Regular surveillance of isolate sensitivity patterns, formulation of hospital antibiotic policies based on existing data and compliance with treatment guidelines will promote rational antibiotic use and reduce resistance among bacteria.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453184/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33459935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Establishment of haemoglobin A₂ reference intervals in Pretoria, South Africa: A retrospective secondary data analysis.","authors":"Cailin Nieuwenhuizen,&nbsp;Tshiphiri Netshidzivhani,&nbsp;Johan Potgieter","doi":"10.4102/ajlm.v11i1.1841","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1841","url":null,"abstract":"<p><strong>Background: </strong>Haemoglobinopathies are one of the most common inherited diseases worldwide. Quantification of haemoglobin A₂ is necessary for the diagnosis of the beta thalassaemia trait. In this context, it is important to have a reliable reference interval for haemoglobin A₂ and a local reference range for South Africa has not been established.</p><p><strong>Objective: </strong>This study aimed to establish reference intervals for haemoglobin A₂ using stored patient laboratory data.</p><p><strong>Methods: </strong>This descriptive study used retrospective data to evaluate haemoglobin A₂ levels determined using high-performance liquid chromatography at the National Health Laboratory Service haematology laboratory in Pretoria, South Africa. All tests performed from 01 October 2012 to 31 December 2020 were screened for inclusion; of these, 144 patients' data met the selection criteria. The reference interval was calculated using descriptive statistics (mean and standard deviation) with a 95% confidence interval.</p><p><strong>Results: </strong>Analysed data from enrolled patients showed a normal distribution. The mean age of the patients was 40 years (range: 3-84 years). The reference interval for haemoglobin A₂ calculated from this data was 2.3% - 3.6%. The minimum haemoglobin A₂ was 2.3% and the maximum was 3.9% with a mean of 2.95% and a standard deviation of 0.357%.</p><p><strong>Conclusion: </strong>A normal reference interval has been established for the population served by the laboratory that will assist with accurate diagnosis of the beta thalassaemia trait. This reference interval may also be useful to other laboratories that employ the same technology, especially smaller laboratories where obtaining a sufficiently large number of normal controls may be challenging.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453124/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33459934","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Efficacy of diversely isolated lytic phages against multi-drug resistant <i>Enterobacter cloacae</i> isolates in Kenya.","authors":"Ivy J Mutai,&nbsp;Angela A Juma,&nbsp;Martin I Inyimili,&nbsp;Atunga Nyachieo,&nbsp;Anthony K Nyamache","doi":"10.4102/ajlm.v11i1.1673","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1673","url":null,"abstract":"<p><strong>Background: </strong><i>Enterobacter cloacae</i> causes nosocomial infections in 15% of patients in low- and middle-income countries with emergence of carbapenem resistance. The utilisation of bacteriophages for therapeutic purposes is crucial for eradicating these resistant bacterial strains.</p><p><strong>Objective: </strong>This study evaluated the efficacy of lytic phages on bacterial isolates of <i>E. cloacae</i> and determined their stability in various physicochemical conditions.</p><p><strong>Methods: </strong>Twenty-nine lytic phages were isolated from the waste water of six informal settlements in Nairobi County, Kenya, from July 2019 to December 2020 and cross-reacted with 30 anonymised clinical isolates of <i>E. cloacae.</i> Six phages were then selected for physicochemical property studies. Phages were described as potent upon lysing any bacterial strain in the panel.</p><p><strong>Results: </strong>Selected phages were stable at 4 °C - 50 °C with a 5.1% decrease in titre in four of six phages and a 1.8% increase in titre in two of six phages at 50 °C. The phages were efficient following two weeks incubation at 4 °C with optimal activity at human body temperature (37 °C) and an optimal pH of 7.5. Phages were active at 0.002 M and 0.015 M concentrations of Ca²⁺ ions. The efficiency of all phages decreased with increased exposure to ultraviolet light. All phages (<i>n</i> = 29) showed cross-reactivity against anonymised clinical isolates of <i>E. cloacae</i> strains (<i>n</i> = 30). The most potent phage lysed 67.0% of bacterial strains; the least potent phage lysed 27.0%.</p><p><strong>Conclusion: </strong>This study reveals the existence of therapeutic phages in Kenya that are potent enough for treatment of multi-drug resistant <i>E. cloacae.</i></p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453119/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33459938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Prevalence of hepatitis B virus core antibodies among blood donors in Nigeria: Implications for blood safety.","authors":"Foluke A Fasola,&nbsp;Adeola A Fowotade,&nbsp;Adedayo O Faneye,&nbsp;Adeyeni Adeleke","doi":"10.4102/ajlm.v11i1.1434","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1434","url":null,"abstract":"<p><strong>Background: </strong>Anti-hepatitis B core antibody (anti-HBc) testing improves transfusion safety by detecting past and current hepatitis B virus (HBV) infection while detecting hepatitis B surface antigen (HBsAg) in serology-negative HBV infection. However, occult HBV infection (OBI) (serum or liver HBV DNA-positive but HBsAg-negative) remains unaddressed among replacement blood donors - family members or friends who donate to replace blood transfused to a relative.</p><p><strong>Objective: </strong>This study assessed risk factors for a positive anti-HBc test among donors with OBI and determined the anti-HBc-positive status of replacement donors.</p><p><strong>Methods: </strong>The study was conducted at the University College Hospital Blood Bank, Ibadan, Nigeria, using blood samples collected from blood donors between April 2019 and May 2019. Donors were screened for HBsAg by rapid diagnostic test (RDT) and enzyme-linked immunosorbent assay (ELISA) and anti-HBc by ELISA, while HBV DNA was detected using a semi-nested polymerase chain reaction.</p><p><strong>Results: </strong>Of the 274 participants, 15 (5.5%) were HBsAg-positive by RDT and 36 (13.1%) by ELISA, while 133 (48.5%) were anti-HBc positive. Out of 232 HBsAg-negative donors, 107 (46.1%) were anti-HBc positive. Of the 107 HBsAg-negative but anti-HBc-positive samples, only one (0.93%) was HBV DNA-positive. The HBV DNA-positive donor was HBsAg-negative by both RDT and ELISA tests.</p><p><strong>Conclusion: </strong>This study establishes a potential risk for HBV transmission from isolated anti-HBc-positive donors to blood recipients. HBc immunoglobulin (antibody) M testing to identify blood units requiring further screening with polymerase chain reaction to detect OBI can prevent HBV transmission through blood transfusion.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350478/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40701405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"COVID-19 mass testing and sequencing: Experiences from a laboratory in Western Kenya.","authors":"John N Waitumbi,&nbsp;Esther Omuseni,&nbsp;Josphat Nyataya,&nbsp;Clement Masakhwe,&nbsp;Faith Sigei,&nbsp;Allan Lemtudo,&nbsp;George Awinda,&nbsp;Eric Muthanje,&nbsp;Brian Andika,&nbsp;Rachel Githii,&nbsp;Rehema Liyai,&nbsp;Gathii Kimita,&nbsp;Beth Mutai","doi":"10.4102/ajlm.v11i1.1737","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1737","url":null,"abstract":"<p><strong>Background: </strong>The Basic Science Laboratory (BSL) of the Kenya Medical Research Institute/Walter Reed Project in Kisumu, Kenya addressed mass testing challenges posed by the emergent coronavirus disease 2019 (COVID-19) in an environment of global supply shortages. Before COVID-19, the BSL had adequate resources for disease surveillance and was therefore designated as one of the testing centres for COVID-19.</p><p><strong>Intervention: </strong>By April 2020, the BSL had developed stringent safety procedures for receiving and mass testing potentially infectious nasal specimens. To accommodate increased demand, BSL personnel worked in units: nucleic acid extraction, polymerase chain reaction, and data and quality assurance checks. The BSL adopted procedures for tracking sample integrity and minimising cross-contamination.</p><p><strong>Lessons learnt: </strong>Between May 2020 and January 2022, the BSL tested 63 542 samples, of which 5375 (8.59%) were positive for COVID-19; 1034 genomes were generated by whole genome sequencing and deposited in the Global Initiative on Sharing All Influenza Data database to aid global tracking of viral lineages. At the height of the pandemic (August and November 2020, April and August 2021 and January 2022), the BSL was testing more than 500 samples daily, compared to 150 per month prior to COVID-19. An important lesson from the COVID-19 pandemic was the discovery of untapped resilience within BSL personnel that allowed adaptability when the situation demanded. Strict safety procedures and quality management that are often difficult to maintain became routine.</p><p><strong>Recommendations: </strong>A fundamental lesson to embrace is that there is no 'one-size-fits-all' approach and adaptability is the key to success.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350206/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40678160","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Therapeutic drug monitoring of phenytoin and valproic acid in critically ill patients at Windhoek Central Hospital, Namibia.","authors":"Bonifasius S Singu,&nbsp;Helen Morrison,&nbsp;Lydia Irengeya,&nbsp;Roger K Verbeeck","doi":"10.4102/ajlm.v11i1.1628","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1628","url":null,"abstract":"<p><strong>Background: </strong>Phenytoin and valproic acid, anticonvulsants, have a low therapeutic index and are highly plasma protein bound, mainly to albumin. Hypoalbuminaemia is common in critically ill patients and increases the unbound drug concentration. Thus, monitoring unbound rather than total plasma drug concentrations is recommended to optimise the dosing of these drugs.</p><p><strong>Objective: </strong>This retrospective study determined unbound plasma concentrations of phenytoin and valproic as a more accurate value of drug levels than total plasma drug concentrations.</p><p><strong>Methods: </strong>Total plasma concentrations were retrieved for 56 Intensive Care Unit patients for phenytoin and 93 for valproic acid. Total drug concentrations were converted to unbound concentrations using a serum albumin-based normalising equation.</p><p><strong>Results: </strong>Total phenytoin plasma concentration was below (41.1% of patients), within (46.4%) or above (12.5%) the therapeutic range (10 μg/mL - 20 μg/mL). However, the predicted unbound plasma concentration of phenytoin was above the therapeutic range (1 μg/mL - 2 μg/mL) in the majority of patients (57.1%). For valproic acid, the total plasma concentration of most patients (87.1%) was below the therapeutic range (50 μg/mL - 100 μg/mL); among remaining patients (12.9%), it was within the therapeutic range. In the majority of patients (91.4%), the predicted unbound plasma concentration of valproic acid was between 2.5 μg/mL and 20 μg/mL.</p><p><strong>Conclusion: </strong>The usefulness of monitoring the total phenytoin or valproic acid levels for dose optimisation is limited as it is an inaccurate indicator of a patient's drug therapeutic state. Thus, the unbound plasma drug concentrations should be quantified experimentally or predicted in resource-limited settings.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350491/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40678156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Occurrence and antimicrobial susceptibility patterns of <i>Salmonella</i> species from poultry farms in Ibadan, Nigeria.","authors":"Terese G Orum,&nbsp;Olayinka O Ishola,&nbsp;Oluwawemimo O Adebowale","doi":"10.4102/ajlm.v11i1.1606","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1606","url":null,"abstract":"<p><strong>Background: </strong><i>Salmonella</i> species are among the major foodborne pathogens causing diseases of economic and public health implications in poultry and humans globally.</p><p><strong>Objective: </strong>This study aimed to determine the occurrence and antimicrobial susceptibility patterns of <i>Salmonella</i> isolates from chickens in poultry farms in Ibadan, Southwest Nigeria.</p><p><strong>Methods: </strong>Cloacal swab samples (<i>n</i> = 360) were obtained from chickens randomly selected from 10 poultry farms in five local government areas of Ibadan, Oyo State, from 04 April 2018 to 20 November 2018. Bacterial identification and antimicrobial susceptibility testing were performed using established protocols. Data were analysed using descriptive statistics and Pearson's chi-squared test at <i>P</i> ≤ 0.05 significance level.</p><p><strong>Results: </strong>The overall prevalence of <i>Salmonella</i> was 21.4%. There were statistically significant associations between <i>Salmonella</i> prevalence and the farm location (<i>p</i> = 0.003), age of chickens (<i>p</i> < 0.001), and health status of chickens (<i>p</i> < 0.001). All <i>Salmonella</i> isolates (<i>n</i> = 77; 100.0%) were resistant to cefuroxime. The isolates were also highly resistant to cotrimoxazole (<i>n</i> = 74; 96.1%), chloramphenicol (<i>n</i> = 73; 94.8%), meropenem (<i>n</i> = 72; 93.5%), gentamicin (<i>n</i> = 69; 89.6%), and tetracycline (<i>n</i> = 64; 83.1%).</p><p><strong>Conclusion: </strong>The presence of drug-resistant <i>Salmonella</i> in commercial layer chickens in Ibadan is a potential threat to consumer health as it increases the risk of carcass contamination and pathogen propagation, and limits the options to control and treat infections in humans and animals. Well-integrated national surveillance systems for monitoring <i>Salmonella</i> and antimicrobial resistance in poultry are critical.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350445/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40701412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Challenges with the pursuit of ISO 15189 accreditation in a public health laboratory in Ghana.","authors":"Seth Attoh,&nbsp;Francis K M Tetteh,&nbsp;Mary McAddy,&nbsp;Kingsley Ackah,&nbsp;Richmond Kyei,&nbsp;Marcus Moroti,&nbsp;Cynthia Boateng,&nbsp;Laurinda Adusu-Donkor,&nbsp;Joseph Boafo,&nbsp;Alhassan Yakubu,&nbsp;Sarah Kwao,&nbsp;Emmanuel Sarkodie,&nbsp;Nana-Banyin Koranteng,&nbsp;Monica A Addo,&nbsp;Frederick Hobenu,&nbsp;Kwasi Agyeman-Bediako,&nbsp;Raymond D Fatchu","doi":"10.4102/ajlm.v11i1.1448","DOIUrl":"https://doi.org/10.4102/ajlm.v11i1.1448","url":null,"abstract":"<p><strong>Background: </strong>Accreditation is important for all medical laboratories, particularly public health laboratories in developing countries. Several laboratories in Ghana implemented the requirements of the International Organization for Standardization (ISO) 15189 but were unable to proceed to accreditation. This article describes the challenges faced by the Pathology Division Laboratory of the 37 Military Hospital, Accra, Ghana, during the acquisition of ISO 15189 accreditation and suggests solutions for a better approach.</p><p><strong>Intervention: </strong>Following ISO 15189 accreditation in 2017, an online survey was conducted between 01 and 30 March 2020 among the laboratory staff. Respondents were required to grade, on a scale of 0 (least) to 5 (most), the extent to which 16 key challenges influenced the process of obtaining accreditation. Key informant interviews were also held with laboratory personnel who were directly involved in the establishment of the quality management system in the laboratory and the accreditation acquisition process.</p><p><strong>Lessons learnt: </strong>Documentation, laboratory safety measures, laboratory management support, and reagent unavailability were estimated as the challenges that most affected the acquisition of laboratory accreditation. Challenges such as poor communication, staff apathy and workload had the least effect on the accreditation process. There was no difference in challenges identified between persons who worked in the laboratory before or after accreditation (<i>p</i> = 0.11).</p><p><strong>Recommendations: </strong>To surmount the anticipated challenges, there is the need for national strategic direction for laboratory accreditation, hospital and laboratory management support for the accreditation acquisition and maintenance processes, and sufficient technical assistance in the form of training and mentorship.</p>","PeriodicalId":45412,"journal":{"name":"African Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350552/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40701407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}