Acute pain in adolescents and young adults with sickle cell disease: Delayed and increased opioid dosing following transition to adult care-Reference-Cited by-同舟云学术

Acute pain in adolescents and young adults with sickle cell disease: Delayed and increased opioid dosing following transition to adult care

Published:2017-02-23 Issue:4 Volume:92 Page:E40-E42
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Stehouwer Nathan¹²^ORCID,Edge Preston²,Katie Park Bohyung²,Piccone Connie²³,Little Jane²⁴

Affiliation:

1. Department of Internal Medicine and Pediatrics; University Hospitals Cleveland Medical Center/Rainbow Babies and Children's Hospital; Cleveland Ohio

2. Case Western Reserve University; Cleveland Ohio

3. Division of Hematology and Oncology; Rainbow Babies and Children's Hospital; Cleveland Ohio

4. University Hospitals Seidman Cancer Center; Cleveland Ohio

Funder

Case CAN (Case Children's Access Now)

MEDTAPP Healthcare Access (HCA)

Publisher

Wiley

Subject

Hematology

Reference6 articles.

1. The management of sickle cell pain in the emergency department: a priority for health systems;Po;Clin J Pain.,2013

2. Opioid Analgesic Converter http://www.globalrph.com/narcoticonv.htm 2016

3. Physicians' attitudes and practices in sickle cell disease pain management;Labbe';J Palliat Care.,2005

4. Inpatient management of sickle cell pain: a ‘snapshot’ of current practice;Miller;Am J Hematol.,2012

5. Desai PC Delatore L Hanes D 2015

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