Literature DB >> 22891195

Benchmarking pain outcomes for children with sickle cell disease hospitalized in a tertiary referral pediatric hospital.

Abi Vijenthira1, Jennifer Stinson, Jeremy Friedman, Lori Palozzi, Anna Taddio, Dennis Scolnik, Charles Victor, Melanie Kirby-Allen, Fiona Campbell.   

Abstract

BACKGROUND: Painful vaso-occlusive crisis (VOC) is the most common reason for hospitalization in children with sickle cell disease.
OBJECTIVE: To benchmark pain outcomes in sickle cell disease, including process outcomes (eg, pain assessment and documentation practices, pain management interventions) and clinical outcomes (eg, pain intensity over hospital stay), to identify areas for improvement.
METHODS: A retrospective study was conducted on electronic charts of children hospitalized with a primary diagnosis of VOC between July 2007 and August 2008.
RESULTS: A convenience sample of 50 admissions was used. In terms of clinical outcomes, patients presented to the emergency department with an initial median pain intensity of 9⁄10 (interquartile range 8⁄10 to 10⁄10). Forty-three per cent had not used opioids for pain relief at home. The mean (± SD) length of stay was 4.0±2.3 days. For most patients, median scores for highest daily pain intensity remained moderate to high throughout hospitalization, although scores did decrease significantly per day of hospitalization. In terms of process outcomes, pain intensity was assessed according to hospital standards on 25% of days in both the emergency department and the ward. There was no discrepancy between prescribed and administered opioid doses and medication use. In 95% of cases, strong opioid use was in a subtherapeutic or low therapeutic dosage range.
CONCLUSIONS: The results showed three areas to target for improvement: improved pain assessment and documentation using valid pain tools; more aggressive multimodal management for peak VOC pain; and better education and support for pain management at home. Further studies are required to evaluate optimal pain treatment practices.

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Year:  2012        PMID: 22891195      PMCID: PMC3411379          DOI: 10.1155/2012/614819

Source DB:  PubMed          Journal:  Pain Res Manag        ISSN: 1203-6765            Impact factor:   3.037


  25 in total

1.  Guidelines for the management of the acute painful crisis in sickle cell disease.

Authors:  David C Rees; Ade D Olujohungbe; Norman E Parker; Adrian D Stephens; Paul Telfer; Josh Wright
Journal:  Br J Haematol       Date:  2003-03       Impact factor: 6.998

2.  Day case management of sickle pain: 3 years experience in a UK sickle cell unit.

Authors:  J Wright; D Bareford; C Wright; G Augustine; K Olley; L Musamadi; C Dhanda; C Knight
Journal:  Br J Haematol       Date:  2004-09       Impact factor: 6.998

3.  Judging the effectiveness of analgesia for children and adolescents during vaso-occlusive events of sickle cell disease.

Authors:  J E Beyer
Journal:  J Pain Symptom Manage       Date:  2000-01       Impact factor: 3.612

4.  Management 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:  J Pediatr Hematol Oncol       Date:  2003-04       Impact factor: 1.289

5.  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

6.  Patient-controlled analgesia for sickle-cell-related pain.

Authors:  B S Shapiro; D E Cohen; C J Howe
Journal:  J Pain Symptom Manage       Date:  1993-01       Impact factor: 3.612

7.  Treatment of uncomplicated vaso-occlusive crises in children with sickle cell disease in a day hospital.

Authors:  Jean L Raphael; Aditi Kamdar; M Brooke Beavers; Donald H Mahoney; Brigitta U Mueller
Journal:  Pediatr Blood Cancer       Date:  2008-07       Impact factor: 3.167

Review 8.  Chronic-pain medications: equivalence levels and method of quantifying usage.

Authors:  S Masters Steedman; S J Middaugh; W G Kee; D S Carson; R N Harden; M C Miller
Journal:  Clin J Pain       Date:  1992-09       Impact factor: 3.442

9.  Day hospital versus inpatient management of uncomplicated vaso-occlusive crises in children with sickle cell disease.

Authors:  Jean L Raphael; Aditi Kamdar; Tao Wang; Hao Liu; Donald H Mahoney; Brigitta U Mueller
Journal:  Pediatr Blood Cancer       Date:  2008-09       Impact factor: 3.167

10.  Pain in hospitalized children: a prospective cross-sectional survey of pain prevalence, intensity, assessment and management in a Canadian pediatric teaching hospital.

Authors:  Elsa M Taylor; Kristina Boyer; Fiona A Campbell
Journal:  Pain Res Manag       Date:  2008 Jan-Feb       Impact factor: 3.037

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  3 in total

Review 1.  State of the Art Management of Acute Vaso-occlusive Pain in Sickle Cell Disease.

Authors:  Latika Puri; Kerri A Nottage; Jane S Hankins; Doralina L Anghelescu
Journal:  Paediatr Drugs       Date:  2018-02       Impact factor: 3.022

2.  Screening for neuropathic pain in patients with sickle cell disease: is a single assessment scale sufficient?

Authors:  Fabricio Dias Antunes; Cidson Leonardo Silva Junior; Karine Santos Cerqueira; Maira do Livramento Faro; Rosana Cipolotti
Journal:  Orphanet J Rare Dis       Date:  2019-05-14       Impact factor: 4.123

3.  Self-Report for Assessment of Pain and Quality of Life in Children with Sickle Cell Anemia in a Developing Country.

Authors:  Valeska Brito da Cunha; Camila Freitas de Andrade Rodrigues; Thiago Alves Rodrigues; Eduardo José Silva Gomes de Oliveira; João Batista Santos Garcia
Journal:  J Pain Res       Date:  2020-11-30       Impact factor: 3.133

  3 in total

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