A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease

CL Edwards, MT Scales, C Loughlin… - International journal of …, 2005 - Springer
abstract Sickle cell disease (SCD) is the most common genetic disorder of the blood. The
disease produces significantly abnormal hemoglobin (Hgb) molecules in red blood cells …

Psychosocial and affective comorbidities in sickle cell disease

LH Pecker, DS Darbari - Neuroscience letters, 2019 - Elsevier
Psychosocial and affective comorbidities are common in sickle cell disease (SCD) and can
strongly influence disease outcomes, especially those related to pain such as frequency and …

Psychosocial treatments in pain management of sickle cell disease

LKY Edwards, CL Edwards - Journal of the National Medical Association, 2010 - Elsevier
The principal symptom of sickle cell disease (SCD) is pain. Many studies have been
conducted on pain management strategies for this illness. There is recognition that …

Pathological basis of symptoms and crises in sickle cell disorder: implications for counseling and psychotherapy

OO Ilesanmi - Hematology reports, 2010 - mdpi.com
Abstract Sickle Cell Disorder (SCD) is a congenital hemoglobinopathy. There is little in
literature regarding the psychological variables affecting individuals living with SCD and all …

Depression and functioning in relation to health care use in sickle cell disease

MM Grant, KM Gil, MY Floyd, M Abrams - Annals of Behavioral Medicine, 2000 - Springer
The purpose of the current study was to investigate depression and health care use in
patients with sickle cell disease (SCD). Forty-four adults with SCD were interviewed and …

The psychosocial problems of sickle cell disease sufferers and their methods of coping

JU Ohaeri, WA Shokunbi, KS Akinlade… - Social Science & Medicine, 1995 - Elsevier
We interviewed 170 sickle cell disease (SCD) patients (mean age 25 years) with a modified
version of the Frankfurter Befindlichkeitskala (FBS, 33-item) and the 12-item General Health …

Sickle cell disease: Pain, coping and quality of life in a study of adults in the UK

KA Anie, A Steptoe, DH Bevan - British journal of health …, 2002 - Wiley Online Library
Objective: To examine the relationship between pain, coping, and quality of life in adult
patients with sickle cell disease (SCD) in the UK, and to assess the influence of these factors …

Psychosocial adaptation of children and adolescents with sickle cell disease

LP Barakat, LA Lash, MJ Lutz… - … handbook of childhood …, 2006 - books.google.com
Sickle Cell has brought me both pain and joy My school friends make fun of my yellow eyes
And along with the sickle cell pain, my friends make it worst I have to learn to cope with my …

The social and cultural context of coping with sickle cell disease: I. A review of biomedical and psychosocial issues

OA Barbarin, M Christian - Journal of Black Psychology, 1999 - journals.sagepub.com
Sickle cell disease (SCD) is widely conceived in the United States as a group of blood
disorders that principally affect African Americans. Although pain is its principal feature …

Psychosocial considerations in sickle cell disease (SCD): The transition from adolescence to young adulthood

ML Baskin, MH Collins, F Brown, JR Griffith… - Journal of Clinical …, 1998 - Springer
Sickle cell disease (SCD) occurs in 1 of every 400 to 500 African American births. Despite its
prevalence, there has been a relative dearth of attention paid to SCD in the psychological …