Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/42999
Title: Unraveling the Complexity of Vaso-Occlusive Crises in Sickle Cell Disease: Insights from a Resource-Limited Setting
Authors: Kaponda, Ali
Muya, Kalunga
Panda, Jules
Koto, Kodondi Kule
BONNECHERE, Bruno 
Issue Date: 2024
Publisher: MDPI
Source: JOURNAL OF CLINICAL MEDICINE, 13 (9) (Art N° 2528)
Abstract: Background/Objectives: This study investigated vaso-occlusive crises (VOCs) in sickle cell disease in Lubumbashi, Democratic Republic of Congo, aiming to understand the disease complexities amidst limited resources. With sickle cell hemoglobinopathies on the rise in sub-Saharan Africa, this nine-year study explored factors associated with VOCs and hematological components. Methods: This study comprised 838 patients, analyzing VOCs and hematological changes over time. Demographic characteristics and blood composition changes were carefully categorized. A total of 2910 crises were observed and managed, with analyses conducted on severity, localization, and age groups using statistical methods. Results: The majority of crises were mild or moderate, primarily affecting osteoarticular regions. Statistical analysis revealed significant disparities in crisis intensity based on location and age. The association between blood samples and the number of comorbidities was investigated. Significant positive associations were found for all parameters, except monocytes, indicating a potential link between blood variables and complication burden. Survival analysis using Cox regression was performed to predict the probability of experiencing a second crisis. No significant effects of medication or localization were observed. However, intensity (p < 0.001), age (p < 0.001), and gender (p < 0.001) showed significant effects. Adjusted Hazard Ratios indicated increased risk with age and male gender and reduced risk with mild or severe crisis intensity compared to light. Conclusions: This research sheds light on the complexities of VOCs in resource-limited settings where sickle cell disease is prevalent. The intricate interplay between clinical, laboratory, and treatment factors is highlighted, offering insights for improved patient care. It aims to raise awareness of patient challenges and provide valuable information for targeted interventions to alleviate their burden.
Notes: Bonnechere, B (corresponding author), Univ Hasselt, Fac Rehabil Sci, Rehabil Res Ctr, REVAL, B-3590 Hasselt, Belgium.; Bonnechere, B (corresponding author), Univ Hasselt, Data Sci Inst, Technol Supported & Data Driven Rehabil, B-3590 Hasselt, Belgium.; Bonnechere, B (corresponding author), PXL Univ Appl Sci & Arts, Dept PXL Healthcare, Hasselt, Belgium.
alik@unilu.ac.cd; kalunga.muya@unilu.ac.cd; jupand@hotmail.com;
k_kodondi@yahoo.fr; bruno.bonnechere@uhasselt.be
Keywords: sickle cell disease;vaso-occlusive crises;resource-limited setting;hematological parameters;patient care
Document URI: http://hdl.handle.net/1942/42999
ISSN: 2077-0383
e-ISSN: 2077-0383
DOI: 10.3390/jcm13092528
ISI #: 001220566300001
Rights: 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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