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1.
World J Surg ; 48(7): 1616-1625, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38757867

ABSTRACT

BACKGROUND: In Tanzania, inadequate infrastructures and shortages of trauma-response training exacerbate trauma-related fatalities. McGill University's Centre for Global Surgery introduced the Trauma and Disaster Team Response course (TDTR) to address these challenges. This study assesses the impact of simulation-based TDTR training on care providers' knowledge/skills and healthcare processes to enhance patient outcomes. METHODS: The study used a pre-post-interventional design. TDTR, led by Tanzanian instructors at Muhimbili Orthopedic Institute from August 16-18, 2023, involved 22 participants in blended online and in-person approaches with simulated skills sessions. Validated tools assessed participants' knowledge/skills and teamwork pre/post-interventions, alongside feedback surveys. Outcome measures included evaluating 24-h emergency department patient arrival-to-care time pre-/post-TDTR interventions, analyzed using parametric and non-parametric tests based on data distributions. RESULTS: Participants' self-assessment skills significantly improved (median increase from 34 to 58, p < 0.001), along with teamwork (median increase from 44.5 to 87.5, p < 0.003). While 99% of participants expressed satisfaction with TDTR meeting their expectations, 97% were interested in teaching future sessions. The six-month post-intervention arrival-to-care time significantly decreased from 29 to 13 min, indicating a 55.17% improvement (p < 0.004). The intervention led to fewer ward admissions (35.26% from 51.67%) and more directed to operating theaters (29.83% from 16.85%), suggesting improved patient management (p < 0.018). CONCLUSION: The study confirmed surgical skills training effectiveness in Tanzanian settings, highlighting TDTR's role in improving teamwork and healthcare processes that enhanced patient outcomes. To sustain progress and empower independent trauma educators, ongoing refresher sessions and expanding TDTR across low- and middle-income countries are recommended to align with global surgery goals.


Subject(s)
Clinical Competence , Patient Care Team , Tanzania , Humans , Patient Care Team/organization & administration , Male , Female , Simulation Training/methods , Traumatology/education , Adult , Wounds and Injuries/therapy
2.
Afr Health Sci ; 15(3): 810-8, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26957969

ABSTRACT

BACKGROUND: Prevention and treatment of malaria during pregnancy is crucial for reduction of malaria in pregnancy and its adverse outcomes. The spread of parasite resistance to Sulphadoxine-Pyrimethamine (SP) used for Intermittent Preventive Treatment for malaria in pregnancy (IPTp), particularly in East Africa has raised concerns about the usefulness and the reliability of the IPTp regimen. We aimed to assess the effectiveness of two doses of SP in treating and preventing occurrence of adverse pregnancy outcomes. METHODOLOGY: The study was an analytical cross sectional study which enrolled 350 pregnant women from Kibiti Health Centre, South Eastern Tanzania. Structured questionnaires were used to obtain previous obstetrics and medical history of participants and verified by reviewing antenatal clinic cards. Maternal placental blood samples for microscopic examination of malaria parasites were collected after delivery. Data was analyzed for associations between SP dosage, risk for PM and pregnancy outcome. Sample size was estimated based on precision. RESULTS: Prevalence of placental maternal (PM) was 8% among pregnant women (95%CI, 4.4-13.1%). Factors associated with increased risk of PM were primigravidity (P<0.001) and history of fever during pregnancy (P= 0.02). Use of at least 2 doses of SP for IPTp during pregnancy was insignificantly associated with reducing the risk PM (P=0.08), low birth weight (P=0.73) and maternal anemia (P=0.71) but associated significantly with reducing the risk of preterm birth (P<0.001). CONCLUSION: Two doses of SP for IPTp regime are ineffective in preventing and treating PM and adverse pregnancy outcome. Hence a review to the current IPTp regimen should be considered with possibility of integrating it with other malaria control strategies.


Subject(s)
Antimalarials/therapeutic use , Malaria/drug therapy , Placenta/parasitology , Pregnancy Complications, Parasitic/prevention & control , Adult , Cross-Sectional Studies , Dose-Response Relationship, Drug , Drug Combinations , Female , Humans , Infant, Low Birth Weight , Infant, Newborn , Malaria/prevention & control , Pregnancy , Pregnancy Outcome/epidemiology , Pregnant Women , Prevalence , Pyrimethamine/administration & dosage , Pyrimethamine/therapeutic use , Risk Factors , Severity of Illness Index , Sulfadoxine/administration & dosage , Sulfadoxine/therapeutic use , Tanzania/epidemiology , Treatment Outcome , Young Adult
3.
Trop Med Int Health ; 19(9): 1048-56, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24965022

ABSTRACT

OBJECTIVE: To assess the effectiveness of IPTp in two areas with different malaria transmission intensities. METHODS: Prospective observational study recruiting pregnant women in two health facilities in areas with high and low malaria transmission intensities. A structured questionnaire was used for interview. Maternal clinic cards and medical logs were assessed to determine drug intake. Placental parasitaemia was screened using both light microscopy and real-time quantitative PCR. RESULTS: Of 350 pregnant women were recruited and screened for placental parasitaemia, 175 from each area. Prevalence of placental parasitaemia was 16.6% (CI 11.4-22.9) in the high transmission area and 2.3% (CI 0.6-5.7) in the low transmission area. Being primigravida and residing in a high transmission area were significant risk factors for placental malaria (OR 2.4; CI 1.1-5.0; P = 0.025) and (OR 9.4; CI 3.2-27.7; P < 0.001), respectively. IPTp was associated with a lower risk of placental malaria (OR 0.3; CI 0.1-1.0; P = 0.044); the effect was more pronounced in the high transmission area (OR 0.2; CI 0.06-0.7; P = 0.015) than in the low transmission area (OR 0.4; CI 0.04-4.5; P = 0.478). IPTp use was not associated with reduced risk of maternal anaemia or low birthweight, regardless of transmission intensity. The number needed to treat (NNT) was four (CI 2-6) women in the high transmission area and 33 (20-50) in the low transmission area to prevent one case of placental malaria. CONCLUSION: IPTp may have an effect on lowering the risk of placental malaria in areas of high transmission, but this effect did not translate into a benefit on risks of maternal anaemia or low birthweight. The NNT needs to be considered, and weighted against that of other protective measures, eventually targeting areas which are above a certain threshold of malaria transmission to maximise the benefit.


Subject(s)
Anemia/prevention & control , Infant, Low Birth Weight , Malaria/prevention & control , Parasitemia/complications , Placenta/parasitology , Pregnancy Complications/prevention & control , Pyrimethamine/therapeutic use , Sulfadoxine/therapeutic use , Adult , Anemia/etiology , Anemia/parasitology , Antimalarials/administration & dosage , Antimalarials/therapeutic use , Birth Weight , Drug Combinations , Female , Humans , Infant, Newborn , Malaria/parasitology , Malaria/transmission , Malaria, Falciparum , Numbers Needed To Treat , Parasitemia/epidemiology , Parasitemia/parasitology , Placenta Diseases/parasitology , Placenta Diseases/prevention & control , Pregnancy , Pregnancy Complications/epidemiology , Pregnancy Complications/parasitology , Pregnancy Complications, Parasitic/epidemiology , Pregnancy Complications, Parasitic/parasitology , Pregnancy Complications, Parasitic/prevention & control , Prevalence , Prospective Studies , Pyrimethamine/administration & dosage , Risk , Sulfadoxine/administration & dosage , Tanzania/epidemiology , Treatment Outcome , Young Adult
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