Literature DB >> 25308571

Shared decision making for hydroxyurea treatment initiation in children with sickle cell anemia.

Lori E Crosby1,2, Lisa M Shook2,3, Russell E Ware2,3,4, William B Brinkman2,5,6.   

Abstract

Clinical trials have demonstrated hydroxyurea's efficacy in improving health outcomes for children with sickle cell anemia (SCA) who have medical complications. New NHLBI clinical guidelines will recommend offering hydroxyurea to young patients regardless of clinical severity. Shared decision making may be an effective approach for implementing this practice change. Decision aids that help patients/parents feel empowered to make this decision and help providers feel comfortable in discussing hydroxyurea as a preventive treatment may facilitate shared discussions between families and providers. We recommend six strategies providers can use to facilitate these discussions while decision aids and tools are being developed. Pediatr Blood Cancer 2015;62:184-185.
© 2014 Wiley Periodicals, Inc. © 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  decision‐making; guidelines; pediatrics; sickle cell anemia; therapeutics

Mesh:

Substances:

Year:  2014        PMID: 25308571      PMCID: PMC5278638          DOI: 10.1002/pbc.25124

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


  10 in total

1.  Shared decision making: really putting patients at the centre of healthcare.

Authors:  A M Stiggelbout; T Van der Weijden; M P T De Wit; D Frosch; F Légaré; V M Montori; L Trevena; G Elwyn
Journal:  BMJ       Date:  2012-01-27

2.  National Institutes of Health Consensus Development Conference statement: hydroxyurea treatment for sickle cell disease.

Authors:  Otis W Brawley; Llewellyn J Cornelius; Linda R Edwards; Vanessa Northington Gamble; Bettye L Green; Charles Inturrisi; Andra H James; Danielle Laraque; Magda Mendez; Carolyn J Montoya; Brad H Pollock; Lawrence Robinson; Aaron P Scholnik; Melissa Schori
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

3.  Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).

Authors:  Winfred C Wang; Russell E Ware; Scott T Miller; Rathi V Iyer; James F Casella; Caterina P Minniti; Sohail Rana; Courtney D Thornburg; Zora R Rogers; Ram V Kalpatthi; Julio C Barredo; R Clark Brown; Sharada A Sarnaik; Thomas H Howard; Lynn W Wynn; Abdullah Kutlar; F Daniel Armstrong; Beatrice A Files; Jonathan C Goldsmith; Myron A Waclawiw; Xiangke Huang; Bruce W Thompson
Journal:  Lancet       Date:  2011-05-14       Impact factor: 79.321

4.  Hydroxyurea in children with sickle cell disease: practice patterns and barriers to utilization.

Authors:  Amanda M Brandow; Danielle L Jirovec; Julie A Panepinto
Journal:  Am J Hematol       Date:  2010-08       Impact factor: 10.047

Review 5.  How I use hydroxyurea to treat young patients with sickle cell anemia.

Authors:  Russell E Ware
Journal:  Blood       Date:  2010-03-11       Impact factor: 22.113

6.  Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

Authors:  T R Kinney; R W Helms; E E O'Branski; K Ohene-Frempong; W Wang; C Daeschner; E Vichinsky; R Redding-Lallinger; B Gee; O S Platt; R E Ware
Journal:  Blood       Date:  1999-09-01       Impact factor: 22.113

7.  Impact of hydroxyurea on clinical events in the BABY HUG trial.

Authors:  Courtney D Thornburg; Beatrice A Files; Zhaoyu Luo; Scott T Miller; Ram Kalpatthi; Rathi Iyer; Phillip Seaman; Jeffrey Lebensburger; Ofelia Alvarez; Bruce Thompson; Russell E Ware; Winfred C Wang
Journal:  Blood       Date:  2012-08-22       Impact factor: 22.113

Review 8.  Decision aids for people facing health treatment or screening decisions.

Authors:  Dawn Stacey; France Légaré; Nananda F Col; Carol L Bennett; Michael J Barry; Karen B Eden; Margaret Holmes-Rovner; Hilary Llewellyn-Thomas; Anne Lyddiatt; Richard Thomson; Lyndal Trevena; Julie H C Wu
Journal:  Cochrane Database Syst Rev       Date:  2014-01-28

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.  Shared decision-making to improve attention-deficit hyperactivity disorder care.

Authors:  William B Brinkman; Jessica Hartl Majcher; Lauren M Poling; Gaoyan Shi; Mike Zender; Heidi Sucharew; Maria T Britto; Jeffery N Epstein
Journal:  Patient Educ Couns       Date:  2013-05-10
  10 in total
  9 in total

1.  The Role of Patient-Physician Communication on the Use of Hydroxyurea in Adult Patients with Sickle Cell Disease.

Authors:  Sarah M Jabour; Sara Beachy; Shayna Coburn; Sophie Lanzkron; Michelle N Eakin
Journal:  J Racial Ethn Health Disparities       Date:  2019-08-13

2.  An Immersive Virtual Reality Curriculum for Pediatric Hematology Clinicians on Shared Decision-making for Hydroxyurea in Sickle Cell Anemia.

Authors:  Francis J Real; Anna M Hood; David Davis; Bradley Cruse; Melissa Klein; Yolanda Johnson; Emily McTate; William B Brinkman; Rogelle Hackworth; Kenyon Hackworth; Charles T Quinn; Lori E Crosby
Journal:  J Pediatr Hematol Oncol       Date:  2022-04-01       Impact factor: 1.289

3.  Targeted Hydroxyurea Education after an Emergency Department Visit Increases Hydroxyurea Use in Children with Sickle Cell Anemia.

Authors:  Lydia H Pecker; Sarah Kappa; Adam Greenfest; Deepika S Darbari; Robert Sheppard Nickel
Journal:  J Pediatr       Date:  2018-06-29       Impact factor: 4.406

4.  Hydroxyurea: Pattern of Use, Patient Adherence, and Safety Profile in Patients with Sickle Cell Disease in Oman.

Authors:  Jimmy Jose; Refaat Abdullah Elsadek; Beena Jimmy; Prasad George
Journal:  Oman Med J       Date:  2019-07

5.  A Multidimensional Electronic Hydroxyurea Adherence Intervention for Children With Sickle Cell Disease: Single-Arm Before-After Study.

Authors:  Susan Creary; Deena Chisolm; Joseph Stanek; Jane Hankins; Sarah H O'Brien
Journal:  JMIR Mhealth Uhealth       Date:  2019-08-08       Impact factor: 4.773

6.  Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial.

Authors:  Anna M Hood; Heather Strong; Cara Nwankwo; Yolanda Johnson; James Peugh; Constance A Mara; Lisa M Shook; William B Brinkman; Francis J Real; Melissa D Klein; Rogelle Hackworth; Sherif M Badawy; Alexis A Thompson; Jean L Raphael; Amber M Yates; Kim Smith-Whitley; Allison A King; Cecelia Calhoun; Susan E Creary; Connie M Piccone; Aimee K Hildenbrand; Steven K Reader; Lynne Neumayr; Emily R Meier; Amy E Sobota; Sohail Rana; Maria Britto; Kay L Saving; Marsha Treadwell; Charles T Quinn; Russell E Ware; Lori E Crosby
Journal:  JMIR Res Protoc       Date:  2021-05-21

7.  Hydroxyurea therapy for children with sickle cell disease: describing how caregivers make this decision.

Authors:  Susan Creary; Susan Zickmund; Diana Ross; Lakshmanan Krishnamurti; Debra L Bogen
Journal:  BMC Res Notes       Date:  2015-08-25

8.  A Retrospective Review to Determine If Children with Sickle Cell Disease Receive Hydroxyurea Monitoring.

Authors:  Susan E Creary; Sarah H O'Brien; Joseph Stanek; Jane S Hankins; Amy Garee; Kyle R Ball; Tina M Andrews; Deena J Chisolm
Journal:  Pediatr Qual Saf       Date:  2017-05-25

9.  Electronically Verified Use of Internet-Based, Multimedia Decision Aids by Adolescents With Type 1 Diabetes and Their Caregivers.

Authors:  Tim Wysocki; Lauren James; Amy Milkes; Alex Taylor; Jessica Pierce; William B Brinkman; Mauri Carakushansky; Judith Ross; Fiona Hirschfeld
Journal:  MDM Policy Pract       Date:  2018-04-18
  9 in total

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