Literature DB >> 16536678

Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project.

Donna K McClish1, James L Levenson, Lynne T Penberthy, Susan D Roseff, Viktor E Bovbjerg, John D Roberts, Imoigele P Aisiku, Wally R Smith.   

Abstract

BACKGROUND: Many studies have found gender differences in frequency and intensity of pain. Women often report lower pain thresholds, higher pain ratings, and lower tolerance for pain. People with sickle cell disease (SCD) experience both chronic and acute pain throughout life.
OBJECTIVES: To compare adult men and women with SCD in terms of reported pain, crises, healthcare utilization, and opioid usage.
METHODS: Two hundred twenty-six adults with SCD in Virginia were enrolled in a prospective cohort study of pain and completed daily diaries for 1-6 months. Subjects reported for the previous day their maximum SCD-related pain, distress, and interference (0-9 scale), whether they were in a sickle cell crisis, had unplanned utilization (clinic, emergency room, or hospitalization), or used opioids. Episodes of pain, crisis, or utilization were defined as consecutive days of such. Men and women were compared, using analysis of covariance (ANCOVA), controlling for age, SCD genotype, depression, and education.
RESULTS: There were no significant differences between men and women in the percentage of days subjects experienced pain (men 58.6% vs. women 56.5%) or the number of pain episodes/6 months (7.7 vs. 9.6). Mean pain scores were comparable, when subjects were in crisis (5.5 vs. 5.6) or not (2.5 vs. 2.2). Distress and interference results were similar. Men with the SS genotype reported a higher percentage of days with crisis(18.5% vs. 11.6%) and utilization (5.1% vs. 2.7%) than women with the SS genotype.
CONCLUSIONS: Contrary to many studies of pain, particularly chronic pain, men and women with SCD reported generally similar pain experiences.

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Year:  2006        PMID: 16536678     DOI: 10.1089/jwh.2006.15.146

Source DB:  PubMed          Journal:  J Womens Health (Larchmt)        ISSN: 1540-9996            Impact factor:   2.681


  31 in total

1.  A comparison of analgesic management for emergency department patients with sickle cell disease and renal colic.

Authors:  Matthew P Lazio; Heather H Costello; D Mark Courtney; Zoran Martinovich; Randall Myers; Amy Zosel; Paula Tanabe
Journal:  Clin J Pain       Date:  2010 Mar-Apr       Impact factor: 3.442

2.  Pain site frequency and location in sickle cell disease: the PiSCES project.

Authors:  Donna K McClish; Wally R Smith; Bassam A Dahman; James L Levenson; John D Roberts; Lynne T Penberthy; Imoigele P Aisiku; Susan D Roseff; Viktor E Bovbjerg
Journal:  Pain       Date:  2009-07-23       Impact factor: 6.961

3.  Bayesian analyses demonstrate tissue blood volume is not decreased during acute sickle cell pain episodes: A preliminary study.

Authors:  Maria Perry; Jena Simon; Daniel Gareau; Jeffrey Glassberg
Journal:  Clin Hemorheol Microcirc       Date:  2016       Impact factor: 2.375

4.  Religious coping and hospital admissions among adults with sickle cell disease.

Authors:  Shawn M Bediako; Lakshmi Lattimer; Carlton Haywood; Neda Ratanawongsa; Sophie Lanzkron; Mary Catherine Beach
Journal:  J Behav Med       Date:  2010-09-02

Review 5.  Improving Emergency Department-Based Care of Sickle Cell Pain.

Authors:  Jeffrey A Glassberg
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

6.  Hydroxyurea and acute painful crises in sickle cell anemia: effects on hospital length of stay and opioid utilization during hospitalization, outpatient acute care contacts, and at home.

Authors:  Samir K Ballas; Robert L Bauserman; William F McCarthy; Oswaldo L Castro; Wally R Smith; Myron A Waclawiw
Journal:  J Pain Symptom Manage       Date:  2010-12       Impact factor: 3.612

7.  Sleep Quality, Pain and Self-Efficacy among Community-Dwelling Adults with Sickle Cell Disease.

Authors:  Maxine Adegbola
Journal:  J Natl Black Nurses Assoc       Date:  2015-07

8.  Predictive Ability of Intermittent Daily Sickle Cell Pain Assessment: The PiSCES Project.

Authors:  Wally R Smith; Donna K McClish; James Levenson; Imoigele Aisiku; Bassam Dahman; Viktor E Bovbjerg; Susan Roseff; John Roberts
Journal:  Pain Med       Date:  2018-10-01       Impact factor: 3.750

9.  The impact of a multidisciplinary pain management model on sickle cell disease pain hospitalizations.

Authors:  Amanda M Brandow; Steven J Weisman; Julie A Panepinto
Journal:  Pediatr Blood Cancer       Date:  2010-12-15       Impact factor: 3.167

10.  A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.

Authors:  Lou Ella V Taylor; Nancy A Stotts; Janice Humphreys; Marsha J Treadwell; Christine Miaskowski
Journal:  Pain Manag Nurs       Date:  2011-12-14       Impact factor: 1.929

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