Literature DB >> 20864308

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.

Samir K Ballas1, Robert L Bauserman, William F McCarthy, Oswaldo L Castro, Wally R Smith, Myron A Waclawiw.   

Abstract

CONTEXT: Exploratory findings from the randomized, double-blind, placebo-controlled, multicenter study of hydroxyurea (MSH) in sickle cell anemia (SS). Recurrent acute painful crises may be mild, moderate, or severe in nature and often require treatment at home, in acute care facilities as outpatients, and in the hospital with oral and/or parenteral opioids.
OBJECTIVES: The objectives of this study were to determine the effects of hydroxyurea (HU) on length of stay (LOS) in hospital and opioid utilization during hospitalization, outpatient acute care contacts, and at home.
METHODS: Data from patient diaries, follow-up visit forms, and medical contact forms for the 299 patients enrolled in the MSH were analyzed. Types and dosages of at home, acute care, and in-hospital analgesic usage were explored descriptively.
RESULTS: At-home analgesics were used on 40% of diary days and 80% of two-week follow-up periods, with oxycodone and codeine the most frequently used. Responders to HU used analgesics on fewer days. During hospitalization, 96% were treated with parenteral opioids, with meperidine the most frequently used; oxycodone was the most commonly used oral medication. The average LOS for responders to HU was about two days less than for other groups, and their cumulative time hospitalized during the trial was significantly less than for nonresponders or placebo groups (P<0.022). They also had the lowest doses of parenteral opioids during acute care crises (P=0.015).
CONCLUSION: Beneficial effects of HU include shortening the duration of hospitalization because of acute painful episodes and reducing the net amount of opioid utilization.
Copyright © 2010 U.S. Cancer Pain Relief Committee. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20864308      PMCID: PMC3005988          DOI: 10.1016/j.jpainsymman.2010.03.020

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  42 in total

1.  Why meperidine should not make a comeback in treating patients with sickle cell disease.

Authors:  Mary Ann Howland; Lewis R Goldfrank
Journal:  Ann Emerg Med       Date:  2008-02       Impact factor: 5.721

2.  Use of meperidine as the analgesic of choice in treating pain from acute painful sickle cell crisis.

Authors:  Marshall T Morgan
Journal:  Ann Emerg Med       Date:  2008-02       Impact factor: 5.721

3.  The cost of health care for patients with sickle cell disease.

Authors:  Samir K Ballas
Journal:  Am J Hematol       Date:  2009-06       Impact factor: 10.047

4.  Low frequency of meperidine-associated seizures in sickle cell disease.

Authors:  S Z Nadvi; S Sarnaik; Y Ravindranath
Journal:  Clin Pediatr (Phila)       Date:  1999-08       Impact factor: 1.168

5.  Opioid selection during sickle cell pain crisis and its impact on the development of acute chest syndrome.

Authors:  Iris D Buchanan; Maribel Woodward; George W Reed
Journal:  Pediatr Blood Cancer       Date:  2005-10-15       Impact factor: 3.167

6.  Efficacy of zinc therapy in prevention of crisis in sickle cell anemia: a double blind, randomized controlled clinical trial.

Authors:  V L Gupta; B S Chaubey
Journal:  J Assoc Physicians India       Date:  1995-07

Review 7.  A review of evidence about factors affecting quality of pain management in sickle cell disease.

Authors:  J Elander; K Midence
Journal:  Clin J Pain       Date:  1996-09       Impact factor: 3.442

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

Authors:  Donna K McClish; James L Levenson; Lynne T Penberthy; Susan D Roseff; Viktor E Bovbjerg; John D Roberts; Imoigele P Aisiku; Wally R Smith
Journal:  J Womens Health (Larchmt)       Date:  2006-03       Impact factor: 2.681

9.  Risk factors for hospital readmission within 30 days: a new quality measure for children with sickle cell disease.

Authors:  Melissa J Frei-Jones; Joshua J Field; Michael R DeBaun
Journal:  Pediatr Blood Cancer       Date:  2009-04       Impact factor: 3.167

10.  Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void.

Authors:  Lawrence R Solomon
Journal:  Blood       Date:  2007-10-16       Impact factor: 22.113

View more
  27 in total

1.  A 19-year-old woman with sickle cell disease and pain.

Authors:  Richard Ward; Ewurabena Simpson; Madeleine Verhovsek
Journal:  CMAJ       Date:  2016-02-01       Impact factor: 8.262

Review 2.  Targeting novel mechanisms of pain in sickle cell disease.

Authors:  Huy Tran; Mihir Gupta; Kalpna Gupta
Journal:  Blood       Date:  2017-11-30       Impact factor: 22.113

3.  Review of Medication Therapy for the Prevention of Sickle Cell Crisis.

Authors:  Tanya R Riley; Angelo Boss; Dominique McClain; Treavor T Riley
Journal:  P T       Date:  2018-07

4.  Reply to Ruan X et al: "A comment on pattern of opioid use in sickle cell disease".

Authors:  Jin Han; Santosh L Saraf; Roberto F Machado; Victor R Gordeuk
Journal:  Am J Hematol       Date:  2017-02-07       Impact factor: 10.047

5.  National trends in hospitalizations for sickle cell disease in the United States following the FDA approval of hydroxyurea, 1998-2008.

Authors:  Maureen M Okam; Shimon Shaykevich; Benjamin L Ebert; Alan M Zaslavsky; John Z Ayanian
Journal:  Med Care       Date:  2014-07       Impact factor: 2.983

6.  The association between hydroxyurea treatment and pain intensity, analgesic use, and utilization in ambulatory sickle cell anemia patients.

Authors:  Wally R Smith; Samir K Ballas; William F McCarthy; Robert L Bauserman; Paul S Swerdlow; Martin H Steinberg; Myron A Waclawiw
Journal:  Pain Med       Date:  2011-04-11       Impact factor: 3.750

Review 7.  Targeting novel mechanisms of pain in sickle cell disease.

Authors:  Huy Tran; Mihir Gupta; Kalpna Gupta
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 8.  Optimizing the care model for an uncomplicated acute pain episode in sickle cell disease.

Authors:  Paul Telfer; Banu Kaya
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

9.  A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive Crises.

Authors:  Richard J Lin; Arthur T Evans; Kerri Wakeman; Michelle Unterbrink
Journal:  Hemoglobin       Date:  2015-06-26       Impact factor: 0.849

10.  Updated Mechanisms of Sickle Cell Disease-Associated Chronic pain.

Authors:  Brianna Lutz; Steffen E Meiler; Alex Bekker; Yuan-Xiang Tao
Journal:  Transl Perioper Pain Med       Date:  2015-07-26
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.