Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain |
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| Authors: | Maha Khaleel Mammen Puliyel Payal Shah John Sunwoo Roberta M. Kato Patjanaporn Chalacheva Wanwara Thuptimdang Jon Detterich John C. Wood Jennie Tsao Lonnie Zeltzer Richard Sposto Michael C. K. Khoo Thomas D. Coates |
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| Affiliation: | 1. Section of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, Los Angeles, California;2. Biomedical engineering, Viterbi School of Engineering, Los Angeles, California;3. Division of Pulmonology, Children's Hospital Los Angeles, Keck School of Medicine, Los Angeles, California;4. Division of Cardiology, Children's Hospital Los Angeles, Keck School of Medicine, Los Angeles, California;5. Pediatric Pain Program, University of California Los Angeles, Los Angeles, California;6. Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California |
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| Abstract: | The painful vaso‐occlusive crises (VOC) that characterize sickle cell disease (SCD) progress over hours from the asymptomatic steady‐state. SCD patients report that VOC can be triggered by stress, cold exposure, and, pain itself. We anticipated that pain could cause neural‐mediated vasoconstriction, decreasing regional blood flow and promoting entrapment of sickle cells in the microvasculature. Therefore, we measured microvascular blood flow in the fingers of both hands using plethysmography and laser‐Doppler flowmetry while applying a series of painful thermal stimuli on the right forearm in 23 SCD patients and 25 controls. Heat pain applied to one arm caused bilateral decrease in microvascular perfusion. The vasoconstriction response started before administration of the thermal pain stimulus in all subjects, suggesting that pain anticipation also causes significant vasoconstriction. The time delay between thermal pain application and global vasoconstriction ranged from 5 to 15.5 seconds and increased with age (P < .01). Although subjective measures, pain threshold and pain tolerance were not different between SCD subjects and controls, but the vaso‐reactivity index characterizing the microvascular blood flow response to painful stimuli was significantly higher in SCD patients (P = .0028). This global vasoconstriction increases microvascular transit time, and may promote entrapment of sickle cells in the microvasculature, making vaso‐occlusion more likely. The rapidity of the global vasoconstriction response indicates a neural origin that may play a part in the transition from steady‐state to VOC, and may also contribute to the variability in VOC frequency observed in SCD patients. |
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