- ►annals.org [PDF] WR Smith, LT Penberthy, VE Bovbjerg, DK … - Annals of Internal Medicine, 2008 - Am Coll Physicians Background: Researchers of sickle cell disease have traditionally used health
care utilization as a proxy for pain and underlying vaso-occlusion. However,
utilization may not completely reflect the amount of self-reported pain or ... Cited by 17 - Related articles - BL Direct - All 5 versions
[CITATION] Daily Assessment of Pain in Adults with Sickle Cell Disease.
VG Nolan, Y Zhang, T Lash, P Sebastiani, MH … - British Journal of Haematology, 2008 - ccmjournal.org The role of the weather as a trigger of sickle cell acute painful episodes has
long been debated. To more accurately describe the role of the weather as a
trigger of painful events, we conducted a case-crossover study of the ... Cited by 4 - Related articles - All 4 versions
C Dampier, BN Setty, B Eggleston, D Brodecki, … - Journal of Pediatric Hematology/Oncology, 2004 - journals.lww.com Summary: Vaso-occlusive pain is a frequent manifestation of sickle cell disease,
but most clinical studies have documented only those pain episodes for which
patients seek acute care or require hos- pitalization. Based on limited ... Cited by 20 - Related articles - All 3 versions
S Jones, ER Duncan, N Thomas, J Walters, … - British journal of haematology, 2005 - critcaremed.org Sickle cell disease (SCD) is characterised by intermittent episodes of acute
severe pain, related to vaso-occlusion. Environmental factors are thought to
play an important role, and studies in tropical countries have suggested ... Cited by 10 - Related articles - Cached - BL Direct - All 7 versions
DK McClish, LT Penberthy, VE Bovbjerg, JD … - Health and Quality of Life Outcomes, 2005 - biomedcentral.com We administered the Medical Outcomes Study 36-item Short-Form to 308 patients in
the Pain in Sickle Cell Epidemiology Study (PiSCES) to assess HRQOL. Scales
included physical function, physical and emotional role function, bodily ... Cited by 34 - Related articles - Cached - All 11 versions
KA Anie, A Steptoe - The Hematology Journal, 2003 - online.haematologica.org Patients with sickle cell disease show wide variations in their experience of
pain, and in the impact of pain on everyday functioning. This study examined
relations between pain, mood, physical activity, and medication use in a ... Cited by 12 - Related articles - BL Direct - All 5 versions
- ►nih.gov [PDF] WR Smith, VE Bovbjerg, LT Penberthy, DK … - Journal of the National Medical Association, 2005 - pubmedcentral.nih.gov Until recent decades, sickle cell disease (SCD) was associated with recurrent.,
disabling pain, organ failure and death in child- hood or early adulthood. SCD
treatment advances have now decreased pain and prolonged survival, but ... Cited by 22 - Related articles - All 4 versions
V Cumming, L King, R Fraser, G Serjeant, M … - British Journal of Haematology, 2008 - ccmjournal.org Clinical features and potential risk factors for chronic leg ulceration
(duration >6 months) in homozygous sickle cell (SS) disease were examined in 225
subjects in the Jamaican Cohort Study. Potential risk factors included the ... Cited by 3 - Related articles - All 6 versions
