Sickle cell disease pain: Relation of coping strategies to adjustment.

Gil, Karen M.; Abrams, Mary Ann; Phillips, George; Keefe, Francis J.

doi:10.1037/0022-006x.57.6.725

Cited by 196 publications

(236 citation statements)

References 21 publications

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“…37 Available evidence shows that affective disturbance and psychosocial factors are involved in negative medical outcomes, including increased frequency, duration, and intensity of painful episodes and adverse psychosocial consequences in patients with SCD. 7,11,[38][39][40] Further, negative or maladaptive cognitions, a particular feature of depression, are associated with poorer medical outcomes, passive adherence to medical directives, increased levels of psychological distress, and decreased capacity to cope with pain. 38,[41][42][43] Our data show that one-third of SCD patients had clinical depression.…”

Section: Discussionmentioning

confidence: 99%

“…7,11,[38][39][40] Further, negative or maladaptive cognitions, a particular feature of depression, are associated with poorer medical outcomes, passive adherence to medical directives, increased levels of psychological distress, and decreased capacity to cope with pain. 38,[41][42][43] Our data show that one-third of SCD patients had clinical depression. Of these, 72% were women, which is similar to 65% found in the general population.…”

Section: Discussionmentioning

confidence: 99%

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Depression, quality of life, and medical resource utilization in sickle cell disease

et al. 2017

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Key Points• Depression was found in 35.2% of adult SCD patients and was strongly associated with worse physical and mental quality-of-life outcomes.• Total health care costs for adult SCD patients with depression were more than double those of SCD patients without depression.Sickle cell disease (SCD) is a chronic, debilitating disorder. Chronically ill patients are at risk for depression, which can affect health-related quality of life (HRQoL), health care utilization, and cost. We performed an analytic epidemiologic prospective study to determine the prevalence of depression in adult patients with SCD and its association with HRQoL and medical resource utilization. Depression was measured by the Beck Depression Inventory and clinical history in adult SCD outpatients at a comprehensive SCD center. HRQoL was assessed using the SF36 form, and data were collected on medical resource utilization and corresponding cost. Neurocognitive functions were assessed using the CNS Vital Signs tool.Pain diaries were used to record daily pain. Out of 142 enrolled patients, 42 (35.2%) had depression. Depression was associated with worse physical and mental HRQoL scores (P , .0001 and P , .0001, respectively). Mean total inpatient costs ($25 000 vs $7487, P 5 .02) and total health care costs ($30 665 vs $13 016, P 5 .01) were significantly higher in patients with depression during the 12 months preceding diagnosis. Similarly, during the 6 months following diagnosis, mean total health care costs were significantly higher in depressed patients than in nondepressed patients ($13 766 vs $8670, P 5 .04). Depression is prevalent in adult patients with SCD and is associated with worse HRQoL and higher total health care costs. Efforts should focus on prevention, early diagnosis, and therapy for depression in SCD.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Depression, quality of life, and medical resource utilization in sickle cell disease

et al. 2017

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“…7 As suas complicações comprometem a QV do paciente com DF e pode levar à invalidez. 8,9 Nesse contexto, estudo de Platt e colaboradores 10 mostrou expectativa de vida de 42 anos para homens e 48 anos para mulheres com hemoglobina SS. Para pacientes com a Hemoglobina SC, a expectativa de vida foi de 60 e 68 anos, para homem e mulher, respectivamente.…”

Section: Introductionunclassified

Doença falciforme e qualidade de vida: um estudo da percepção subjetiva dos pacientes da Fundação Hemominas, Minas Gerais, Brasil

Pereira¹,

Cardoso²,

Brener³

et al. 2008

Rev. Bras. Hematol. Hemoter.

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H E M O T E R A P I A IntroduçãoA doença falciforme (DF) originou-se na Ásia Menor e na África, foi trazida às Américas pela imigração forçada dos nativos africanos para trabalho escravo e é hoje encontrada em toda a Europa e Ásia. 1No Brasil distribuiu-se heterogeneamente, sendo mais prevalente onde a proporção de negros é maior. Ocorre também entre brancos, decorrente da miscigenação da população brasileira. No sudeste do Brasil, a prevalência média de portadores (heterozigotos) é de 2%, e entre os negros essa prevalência eleva-se para 10%. Pela sua alta prevalência, a DF configura-se como um importante problema de saúde pública no país.

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“…The subscale score is the mean of all 6 items, and higher scores indicate more frequent pain catastrophizing. The Catastrophizing scale of the CSQ has demonstrated excellent internal consistency reliability and validity in numerous studies.e.g., 13,15,33 Its validity has been demonstrated by associations with measures of psychosocial dysfunction and depression. 11,18,25,39…”

Section: 37mentioning

confidence: 99%

Pain Catastrophizing and Beliefs Predict Changes in Pain Interference and Psychological Functioning in Persons With Spinal Cord Injury

Hanley

Raichle

Jensen

et al. 2008

The Journal of Pain

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The current study sought to examine how changes in pain-related beliefs and coping responses are related to changes in pain interference and psychological functioning in individuals with spinal cord injuries (SCI) and pain. To measure longitudinal changes in these variables, respondents completed a survey which included measures of pain intensity, pain interference, and psychological functioning, as well as specific psychosocial variables (pain-related beliefs, coping, and social support), and then completed the same survey 6 months later; analyses included only the individuals who reported pain at both times (N = 40). Demographic and injury-related variables were also assessed, but none were found to be significantly associated with changes in functioning. Changes in catastrophizing and belief in one's ability to control pain were each significantly associated with changes in the outcome variables: greater pain interference and poorer psychological functioning. Changes in specific coping strategies and social support were not predictors of changes in pain, interference, or psychological functioning . These findings support a biopsychosocial model of pain in persons with SCI. Intervention studies targeting maladaptive pain-related beliefs and catastrophizing may help to identify the causal nature of these relationships and may improve multidisciplinary treatment of pain in SCI.Perspective-Intervention studies targeting catastrophizing and maladaptive pain-related beliefs may be the next step in determining which variables play a causal role in the pain interference and psychological functioning of individuals with pain and SCI. Keywords coping; cognitions; spinal cord injury; pain; mental health; catastrophizing Pain is a common 8,16 and often difficult to treat 4,50,51 problem in persons with spinal cord injuries (SCI) which can be associated with increased physical and psychological dysfunction, independent of the effects of the injury. 16,27,32,41,43 Given the refractory nature of pain in

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Sickle cell disease pain: Relation of coping strategies to adjustment.

Cited by 196 publications

References 21 publications

Depression, quality of life, and medical resource utilization in sickle cell disease

Depression, quality of life, and medical resource utilization in sickle cell disease

Doença falciforme e qualidade de vida: um estudo da percepção subjetiva dos pacientes da Fundação Hemominas, Minas Gerais, Brasil

Pain Catastrophizing and Beliefs Predict Changes in Pain Interference and Psychological Functioning in Persons With Spinal Cord Injury

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