Literature DB >> 30151977

Impact of early analgesia on hospitalization outcomes for sickle cell pain crisis.

Jason Payne1, Inmaculada Aban2, Lee M Hilliard1, Jennifer Madison1, Christina Bemrich-Stolz1, Thomas H Howard1, Amanda Brandow3, Emily Waite1, Jeffrey D Lebensburger1.   

Abstract

BACKGROUND: Painful events are the leading cause of hospitalizations for patients with sickle cell disease. Individualized pain plans targeting patient-specific maximum opioid dosing may shorten hospitalization length and are recommended by national guidelines. Prior to implementing individualized sickle cell pain plans, we tested the hypothesis that a shorter time to achieve a maximum opioid dose would improve hospitalization outcomes. PROCEDURE: Two-year IRB-approved, retrospective study of pediatric patients admitted for vaso-occlusive crisis (VOC). We recorded the emergency department admission time, order entry time for the maximum opioid dose during the hospitalization, and time of discharge orders.  We categorized patients as infrequent if they required <3 admissions for VOC over two years and patients as frequent if they required ≥3 admissions for VOC over two years. To account for multiple admissions, generalized linear modeling was performed.
RESULTS: We identified 236 admissions for acute pain observed in 108 patients. Achieving an earlier maximum opioid dose was significantly associated with shorter length of hospitalization for frequent and infrequent pain patients (both P ≤ 0.0001). As total hospitalization length can be impacted by the time a maximum opioid order was placed, we also analyzed hospitalization length after the maximum opioid order was placed. Frequent pain patients who achieved earlier analgesia had a significantly shorter hospitalization from the time the maximum opioid order was placed (P = 0.03) while no association was found for infrequent pain patients (P = 0.84).
CONCLUSIONS: Early achievement of maximum analgesia improved hospitalization outcomes and warrant further investigation in prospective studies of individualized pain plans.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  outcomes; pain; sickle cell anemia

Mesh:

Substances:

Year:  2018        PMID: 30151977      PMCID: PMC6192851          DOI: 10.1002/pbc.27420

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  20 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.  Opioid doses and acute care utilization outcomes for adults with sickle cell disease: ED versus acute care unit.

Authors:  Robert E Molokie; Chariz Montminy; Corissa Dionisio; Muhammad Ahmen Farooqui; Michel Gowhari; Yingwei Yao; Marie L Suarez; Miriam O Ezenwa; Judith M Schlaeger; Zaijie J Wang; Diana J Wilkie
Journal:  Am J Emerg Med       Date:  2017-07-13       Impact factor: 2.469

3.  Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia.

Authors:  S T Miller; E Wright; M Abboud; B Berman; B Files; C D Scher; L Styles; R J Adams
Journal:  J Pediatr       Date:  2001-12       Impact factor: 4.406

4.  A randomized controlled trial comparing two vaso-occlusive episode (VOE) protocols in sickle cell disease (SCD).

Authors:  Paula Tanabe; Susan Silva; Hayden B Bosworth; Regina Crawford; Judith A Paice; Lynne D Richardson; Christopher N Miller; Jeffrey Glassberg
Journal:  Am J Hematol       Date:  2017-11-10       Impact factor: 10.047

5.  Emergency department management of acute pain episodes in sickle cell disease.

Authors:  Paula Tanabe; Randall Myers; Amy Zosel; Jane Brice; Altaf H Ansari; Julia Evans; Zoran Martinovich; Knox H Todd; Judith A Paice
Journal:  Acad Emerg Med       Date:  2007-03-26       Impact factor: 3.451

6.  Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.

Authors:  Deepika S Darbari; Onyinye Onyekwere; Mehdi Nouraie; Caterina P Minniti; Lori Luchtman-Jones; Sohail Rana; Craig Sable; Gregory Ensing; Niti Dham; Andrew Campbell; Manuel Arteta; Mark T Gladwin; Oswaldo Castro; James G Taylor; Gregory J Kato; Victor Gordeuk
Journal:  J Pediatr       Date:  2011-09-03       Impact factor: 4.406

7.  Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Authors:  S Charache; M L Terrin; R D Moore; G J Dover; F B Barton; S V Eckert; R P McMahon; D R Bonds
Journal:  N Engl J Med       Date:  1995-05-18       Impact factor: 91.245

8.  Do children with sickle cell disease receive disparate care for pain in the emergency department?

Authors:  William T Zempsky; Kristin A Loiselle; Kathleen McKay; Brian H Lee; J Nathan Hagstrom; Neil L Schechter
Journal:  J Emerg Med       Date:  2009-08-22       Impact factor: 1.484

Review 9.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Authors:  Barbara P Yawn; George R Buchanan; Araba N Afenyi-Annan; Samir K Ballas; Kathryn L Hassell; Andra H James; Lanetta Jordan; Sophie M Lanzkron; Richard Lottenberg; William J Savage; Paula J Tanabe; Russell E Ware; M Hassan Murad; Jonathan C Goldsmith; Eduardo Ortiz; Robinson Fulwood; Ann Horton; Joylene John-Sowah
Journal:  JAMA       Date:  2014-09-10       Impact factor: 56.272

10.  Impact of emergency department care on outcomes of acute pain events in children with sickle cell disease.

Authors:  Amanda M Brandow; Mark Nimmer; Timothy Simmons; T Charles Casper; Lawrence J Cook; Corrie E Chumpitazi; J Paul Scott; Julie A Panepinto; David C Brousseau
Journal:  Am J Hematol       Date:  2016-09-03       Impact factor: 10.047

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  6 in total

1.  Improving Pain Assessment Using Vital Signs and Pain Medication for Patients With Sickle Cell Disease: Retrospective Study.

Authors:  Swati Padhee; Gary K Nave; Tanvi Banerjee; Daniel M Abrams; Nirmish Shah
Journal:  JMIR Form Res       Date:  2022-06-23

2.  Developing an emergency department order set to treat acute pain in sickle cell disease.

Authors:  Yves Duroseau; David Beenhouwer; Michael S Broder; Bonnie Brown; Tartania Brown; Sarah N Gibbs; Kaedrea Jackson; Sally Liang; Melanie Malloy; Marie-Laure Romney; Dana Shani; Jena Simon; Irina Yermilov
Journal:  J Am Coll Emerg Physicians Open       Date:  2021-08-07

Review 3.  A Comprehensive Review of the Treatment and Management of Pain in Sickle Cell Disease.

Authors:  Jacob Fiocchi; Ivan Urits; Vwaire Orhurhu; Mariam Salisu Orhurhu; Stephen Giacomazzi; Briggs Hoyt; Alan D Kaye; Rachel J Kaye; Omar Viswanath
Journal:  Curr Pain Headache Rep       Date:  2020-03-21

4.  Lidocaine and Ketamine Infusions as Adjunctive Pain Management Therapy: A Retrospective Analysis of Clinical Outcomes in Hospitalized Patients Admitted for Pain Related to Sickle Cell Disease.

Authors:  Nicolas A Zavala; Randall W Knoebel; Magdalena Anitescu
Journal:  Front Pain Res (Lausanne)       Date:  2022-08-04

5.  Use of Mobile Health Apps and Wearable Technology to Assess Changes and Predict Pain During Treatment of Acute Pain in Sickle Cell Disease: Feasibility Study.

Authors:  Amanda Johnson; Fan Yang; Siddharth Gollarahalli; Tanvi Banerjee; Daniel Abrams; Jude Jonassaint; Charles Jonassaint; Nirmish Shah
Journal:  JMIR Mhealth Uhealth       Date:  2019-12-02       Impact factor: 4.773

Review 6.  Opioid Use in Patients With Sickle Cell Disease During a Vaso-Occlusive Crisis: A Systematic Review.

Authors:  Hadia Arzoun; Mirra Srinivasan; Isra Sahib; Jack Fondeur; Lisbeth Escudero Mendez; Raneem K Hamouda; Lubna Mohammed
Journal:  Cureus       Date:  2022-01-21
  6 in total

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