The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania.

Journal: BMC hematology

Volume: 18

Issue: 

Year of Publication: 

Affiliated Institutions:  Emergency Medicine Department, Muhimbili University of Health and Allied Sciences, P.O. Box , Dar es salaam, Tanzania. Division of Emergency Medicine, University of Cape Town, Cape Town City, South Africa. Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Abstract summary 

Sickle cell anaemia (SCA) is prevalent in sub-Saharan Africa, with high risk of complications requiring emergency care. There is limited information about presentation of patients with SCA to hospitals for emergency care. We describe the clinical presentation, resource utilization, and outcomes of SCA patients presenting to the emergency department (ED) at Muhimbili National Hospital (MNH) in Dar es Salaam, Tanzania.This was a prospective cohort study of consecutive patients with SCA presenting to ED between December 2014 and July 2015. Informed consent was obtained from all patients or patients' proxies prior to being enrolled in the study. A standardized case report form was used to record study information, including demographics, relevant clinical characteristics and overall patients outcomes. Categorical variables were compared with chi-square test or Fisher's exact test; continuous variables were compared with two-sample t-test or Mann-Whitney U-test.We enrolled 752 (2.7%) people with SCA from 28,322 patients who presented to the MNH-ED. The median age was 14 years (Interquartile range [IQR]: 6-23 years), and 395 (52.8%) were female. Pain 614 (81.6%), fever 289 (38.4%) were the most frequent presenting complaint. Patients with fever, hypoxia, altered mental status and bradycardia had statistically significant relative risk of mortality of 10.4, 153, 50 and 12.1 ( < 0.0001) respectively, compared to patients with normal vitals. Overall, 656 (87.2%) patients received Complete Blood Cell counts test, of these 342 (52.1%) had severe anaemia (haemoglobin < 7 g/dl), and a 30.3 ( = 0.02) relative risk of relative risk of mortality compare to patients with higher haemoglobin. Patients who had malaria, elevated renal function test and hypoglycemia, had relative risk of mortality of 22.9, 10.4 and 45.2 ( < 0.0001) respectively, compared to patient with normal values. Most 534 (71.0%) patients were hospitalized for in patients care, and the overall morality rate was 16 (2.1%).We described the clinical presentation, management, and outcomes of patients with SCA presenting to the largest public ED in Tanzania, as well as information on resource utilization. This information can inform development of treatment guidelines, clinical staff education, and clinical research aimed at optimizing care for SCA patients.

Authors & Co-authors:  Sawe Hendry R HR Reynolds Teri A TA Mfinanga Juma A JA Runyon Michael S MS Murray Brittany L BL Wallis Lee A LA Makani Julie J

Study Outcome 

Source Link: Visit source

Statistics
Citations :  CDC - Sickle Cell Disease, Data and Statistics - NCBDDD [Internet]. [cited 2013 Mar 13]. Available from: http://www.cdc.gov/ncbddd/sicklecell/data.html.
Authors :  7
Identifiers
Doi : 25
SSN : 2052-1839
Study Population
Male,Female
Mesh Terms
Other Terms
Anaemia;Emergency department;Sickle cell anaemia;Sub-Saharan Africa
Study Design
Cohort Study,Case Study,Cross Sectional Study
Study Approach
Country of Study
Tanzania
Publication Country
England