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Updated: May 21, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Physical activity, vaso-occlusive crises and pain in patients with sickle cell anaemia in Senegal
Mor Diaw1,2, Mame Saloum Coly3, Keyne Charlot4,5
1Laboratoire de Physiologie Humaine, Faculté de Médecine, de Pharmacie et d'Odontologie, Université Cheikh Anta Diop, Dakar, Senegal.
Abstract:
Acute physical exercise may trigger vaso-occlusive crises (VOC) in patients with sickle cell anaemia (SCA), creating uncertainty around physical activity (PA) recommendations. This cross-sectional study examined the relationships between PA, VOC and steady-state pain in 104 Senegalese male patients with SCA. PA was objectively measured over 5 weeks, recording daily steps and time spent in different PA intensities (expressed in metabolic equivalent of task, MET). VOC occurrence was tracked, and steady-state days excluded VOC days plus 2 days before and after. Pain frequency and intensity on steady-state days were recorded via diaries, and blood viscosity was measured. Ninety-eight patients (29 ± 8 years old) completed the study, averaging 9611 ± 4040 steps/day, with 293 ± 108, 64 ± 69 and 28 ± 32 min in ≥1.5, ≥3.0, and ≥6.0 MET PA respectively. Median daily step count and PA duration were not associated with VOC occurrence. However, higher step counts and more time in ≥1.5 and ≥6.0 MET PA correlated with lower pain frequency and intensity (on steady-state days) and lower blood viscosity. These findings suggest that PA may benefit patients with SCA, but further research is needed to establish guidelines.
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