Literature DB >> 23407129

Psychological aspects and hospitalization for pain crises in youth with sickle-cell disease.

Jennie C I Tsao1, Eufemia Jacob, Laura C Seidman, Mary A Lewis, Lonnie K Zeltzer.   

Abstract

Sickle-cell disease is a genetic disorder characterized by severe pain episodes or "vaso-occlusive crises" that may require hospitalization. This study examined the associations among emotion regulation, somatization, positive and negative affect, and hospitalizations for pain crises in youth with sickle-cell disease. Multivariate analyses indicated that emotional suppression and somatization were significantly associated with more frequent hospitalizations for pain crises in the previous year after controlling for sickle-cell disease type and pain. These results suggest that efforts to reduce emotional suppression and somatization may assist in decreasing the frequency of hospitalizations for pain crises among youth with sickle-cell disease.

Entities:  

Keywords:  adolescence; children; emotion regulation; health-care utilization; somatization

Mesh:

Year:  2013        PMID: 23407129      PMCID: PMC3744610          DOI: 10.1177/1359105312471570

Source DB:  PubMed          Journal:  J Health Psychol        ISSN: 1359-1053


  31 in total

1.  Individual differences in two emotion regulation processes: implications for affect, relationships, and well-being.

Authors:  James J Gross; Oliver P John
Journal:  J Pers Soc Psychol       Date:  2003-08

2.  Spontaneous emotion regulation during evaluated speaking tasks: associations with negative affect, anxiety expression, memory, and physiological responding.

Authors:  Boris Egloff; Stefan C Schmukle; Lawrence R Burns; Andreas Schwerdtfeger
Journal:  Emotion       Date:  2006-08

3.  Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation.

Authors:  Danitza Nebor; Andre Bowers; Marie-Dominique Hardy-Dessources; Jennifer Knight-Madden; Marc Romana; Harvey Reid; Jean-Claude Barthélémy; Vanessa Cumming; Olivier Hue; Jacques Elion; Marvin Reid; Philippe Connes
Journal:  Haematologica       Date:  2011-07-12       Impact factor: 9.941

4.  Changes in intensity, location, and quality of vaso-occlusive pain in children with sickle cell disease.

Authors:  Eufemia Jacob; Christine Miaskowski; Marilyn Savedra; Judith E Beyer; Marsha Treadwell; Lori Styles
Journal:  Pain       Date:  2003-03       Impact factor: 6.961

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Authors:  G A Walco; C D Dampier
Journal:  J Pediatr Psychol       Date:  1987-06

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Authors:  D Cioffi; J Holloway
Journal:  J Pers Soc Psychol       Date:  1993-02

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

Authors:  M M Grant; K M Gil; M Y Floyd; M Abrams
Journal:  Ann Behav Med       Date:  2000

8.  Children's Somatization Inventory: psychometric properties of the revised form (CSI-24).

Authors:  Lynn S Walker; Joy E Beck; Judy Garber; Warren Lambert
Journal:  J Pediatr Psychol       Date:  2008-09-09

9.  Relationship of clinical severity to packed cell rheology in sickle cell anemia.

Authors:  G Phillips; B Coffey; R Tran-Son-Tay; T R Kinney; E P Orringer; R M Hochmuth
Journal:  Blood       Date:  1991-11-15       Impact factor: 22.113

Review 10.  Sickle cell anemia, the first molecular disease: overview of molecular etiology, pathophysiology, and therapeutic approaches.

Authors:  Martin H Steinberg
Journal:  ScientificWorldJournal       Date:  2008-12-25
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  5 in total

Review 1.  Psychological Predictors of Pain in Children and Adolescents With Sickle Cell Disease: A Scoping Review.

Authors:  Clare Donohoe; Ellen Lavoie Smith
Journal:  J Pediatr Oncol Nurs       Date:  2018-12-19       Impact factor: 1.636

2.  Study protocol for a randomized controlled trial to assess the feasibility of an open label intervention to improve hydroxyurea adherence in youth with sickle cell disease.

Authors:  Arlene Smaldone; Sally Findley; Suzanne Bakken; L Adriana Matiz; Susan L Rosenthal; Haomiao Jia; Sergio Matos; Deepa Manwani; Nancy S Green
Journal:  Contemp Clin Trials       Date:  2016-06-17       Impact factor: 2.226

3.  Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease.

Authors:  Steven K Reader; Laura M Rockman; Katherine M Okonak; Nicole M Ruppe; Colleen N Keeler; Anne E Kazak
Journal:  J Clin Psychol Med Settings       Date:  2020-06

4.  Genetic variants of GCH1 associate with chronic and acute crisis pain in African Americans with sickle cell disease.

Authors:  Nilanjana Sadhu; Ellie H Jhun; Yingwei Yao; Ying He; Robert E Molokie; Diana J Wilkie; Zaijie Jim Wang
Journal:  Exp Hematol       Date:  2018-07-19       Impact factor: 3.084

5.  Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease.

Authors:  Nitya Bakshi; Ines Lukombo; Inna Belfer; Lakshmanan Krishnamurti
Journal:  J Pain Res       Date:  2018-05-08       Impact factor: 3.133

  5 in total

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