Journal ArticleInt J Psychiatry Med · 2014
Differentiating somatic from emotional influences on the experience of chronic pain has been of interest to clinicians and researchers for many years. Although prior research has not well specified these pathways at the anatomical level, some evidence, bot ...
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Journal ArticleJournal of African American Studies · March 1, 2011
Sickle cell disease (SCD) affects developmental maturation causing a delay in secondary sex characteristics associated with puberty. There is little data on the impact of SCD on body image, a well-established risk factor for eating disorders among young wo ...
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Journal ArticleHemoglobin · 2011
While pain is one of the most debilitating symptoms of sickle cell disease, narcotics remain an effective although controversial widely practiced intervention. Vaso-occlusive crises are the most common cause for seeking pharmacological treatment. The influ ...
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Journal ArticleHemoglobin · 2011
The impact of cerebrovascular events (CVE) on cognitive functioning in adults with sickle cell disease is not well understood. Sequelae of CVEs can adversely impact their quality of life. We reviewed neurocognitive presentation and testing in adults with s ...
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Journal ArticleJ Natl Med Assoc · November 2010
The unpredictable nature of sickle cell disease (SCD) and its social and environmental consequences can produce an unhealthy and almost exclusive focus on physical functioning. At the upper range of this focus on health concerns is somatization. In the cur ...
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Journal ArticleClin J Pain · 2010
OBJECTIVE: The present paper examines the literature that addresses psychologic aspects involved in complex regional pain syndrome from a historic perspective to provide a rationale for the emergence of psychologic theories to explain its pathogenesis. The ...
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Journal ArticleJ Natl Med Assoc · November 2009
There is a strong relationship between suicidal ideation, suicide attempts, and depression. Rates of successful suicides are relatively high among the chronically ill compared to other populations but are reduced with treatment. Depression and suicide rate ...
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Journal ArticleJ Pain · October 2009
UNLABELLED: Although there has been a rapid increase in Latino populations in the United States over the last 10 years, health research with Latino cultural groups is sorely lacking. In the area of pain-coping research, one consequence of the limited resea ...
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Journal ArticleJournal of African American Studies · March 1, 2009
The current study tested a non-linear model of religious coping among Black patients with Sickle Cell Disease (SCD). We predicted that moderate prayer and church attendance would be associated with less severe affective and sensory ratings of pain, lower l ...
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Journal ArticleJournal of African American Studies · March 1, 2009
Coping is recognized as an increasingly important consideration in the management of chronic disease. Prayer, hostility and John Henryism appeared to be the most frequently discussed but least understood coping strategies associated with health outcomes in ...
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Journal ArticleNeuropsychiatr Dis Treat · June 2008
The current study examined the effects of electroconvulsive therapy (ECT) on neuropsychological test performance. Forty-six patients completed brief neuropsychological and psychological testing before and after receiving ECT for the treatment of recalcitra ...
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Journal ArticleJ Natl Med Assoc · March 2008
Blacks experience disproportionately elevated rates of tobacco-related morbidity and mortality. Blacks experience delayed smoking initiation relative to other racial/ethnic groups, highlighting the importance of examining smoking correlates occurring in la ...
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Journal ArticleNeuropsychiatr Dis Treat · December 2007
Traditionally, neuropsychological deficits due to Sickle Cell Disease (SCD) have been understudied in adults. We have begun to suspect, however, that symptomatic and asymptomatic Cerebrovascular Events (CVE) may account for an alarming number of deficits i ...
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Journal ArticleClin J Pain · October 2007
OBJECTIVES: Fear of movement (ie, kinesiophobia) has emerged as a significant predictor of pain-related outcomes including disability and psychologic distress across various types of pain (eg, back pain, headache, fibromyalgia, complex regional pain syndro ...
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Journal ArticleJ Natl Med Assoc · September 2006
For many years, we have known of deficits in our system of training mental health professionals, particularly in recognizing and integrating diversity. Recently, we have begun to understand that our literature must more authentically reflect the experience ...
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Journal ArticleJ Natl Med Assoc · March 2006
There is increasing interest from a social learning perspective in understanding the role of parental factors on adult health behaviors and health outcomes. Our review revealed no studies, to date, that have evaluated the effects of parental substance abus ...
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Journal ArticleJ Natl Med Assoc · December 2005
In this exploratory study, we evaluated weight status and dietary intake patterns during painful episodes in adult patients with SCD. Specifically, we explored the relation between pain severity and body mass index (BMI), and we tested the hypothesis that ...
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Journal ArticleInt J Behav Med · 2005
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 (RBCs). The sickling of RBCs occurs when partially or totally deoxygenated Hgb molecules d ...
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