Literature DB >> 27573582

Decreased fetal hemoglobin over time among youth with sickle cell disease on hydroxyurea is associated with higher urgent hospital use.

Nancy S Green1, Deepa Manwani2, Mahvish Qureshi3, Karen Ireland2, Arpan Sinha2, Arlene M Smaldone4,5.   

Abstract

BACKGROUND: Hydroxyurea (HU) induces dose-dependent increased fetal hemoglobin (HbF) for sickle cell disease (SCD). Large deviation from historical personal best (PBest) HbF, a clinic-based version of maximum dose, may identify a subset with suboptimal HU adherence over time. PROCEDURE: Retrospective clinical data from youth ages 10-18 years prescribed HU at two centers were extracted from medical records at three time points: pre-HU initiation, PBest and a recent assessment. Decrease from PBest HbF of 20% or more at recent assessment despite stable dosing was designated as high deviation from PBest. Acute hospital use was compared between 1-year periods, pre-HU and ±6 months for PBest and recent assessment. Groups were compared using descriptive and bivariate nonparametric statistics.
RESULTS: Seventy-five youth, mean HU duration 5.9 years, met eligibility criteria. Mean ages of HU initiation, PBest and recent assessment were 8.0, 10.9 and 13.9 years, respectively. Despite stable dosing, average HbF of 19.5% at PBest overall declined by 31.8% at recent assessment. PBest HbF declined by 11.7 and 40.1% in two groups, the latter comprised 70.7% of the sample, had lower pre-HU and recent HbF and higher dosing. They experienced more urgent hospital use during the year framing recent assessment than during PBest; these findings were supported by sensitivity analysis.
CONCLUSIONS: Decline from PBest HbF is a novel approach to assess HU effectiveness, is common among youth and may represent suboptimal adherence. Larger prospective studies using additional adherence measures are needed to confirm our approach of tracking HbF deviation over time and to define an appropriate cutoff.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  fetal hemoglobin; hydroxyurea; medication adherence; sickle cell disease

Mesh:

Substances:

Year:  2016        PMID: 27573582      PMCID: PMC5072999          DOI: 10.1002/pbc.26161

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


  42 in total

1.  Medication adherence among Latino and non-Latino white children with asthma.

Authors:  Elizabeth L McQuaid; Robin S Everhart; Ronald Seifer; Sheryl J Kopel; Daphne Koinis Mitchell; Robert B Klein; Cynthia A Esteban; Gregory K Fritz; Glorisa Canino
Journal:  Pediatrics       Date:  2012-05-07       Impact factor: 7.124

2.  Adherence to hydroxyurea therapy in children with sickle cell anemia.

Authors:  Courtney D Thornburg; Agustin Calatroni; Marilyn Telen; Alex R Kemper
Journal:  J Pediatr       Date:  2009-11-01       Impact factor: 4.406

3.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

4.  A retrospective study to assess the utility of frequent laboratory monitoring of pediatric patients with sickle cell disease on hydroxyurea.

Authors:  John Nevin; Leann Myers; Ify Osunkwo; Julie Kanter
Journal:  J Pediatr Hematol Oncol       Date:  2014-04       Impact factor: 1.289

5.  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

Review 6.  Adherence to treatment in systemic lupus erythematosus patients.

Authors:  Nathalie Costedoat-Chalumeau; Jacques Pouchot; Gaëlle Guettrot-Imbert; Véronique Le Guern; Gaëlle Leroux; Donata Marra; Nathalie Morel; Jean-Charles Piette
Journal:  Best Pract Res Clin Rheumatol       Date:  2013-06       Impact factor: 4.098

Review 7.  Predictors of self-management in pediatric type 1 diabetes: individual, family, systemic, and technologic influences.

Authors:  Diana Naranjo; Shelagh Mulvaney; Maureen McGrath; Theresa Garnero; Korey Hood
Journal:  Curr Diab Rep       Date:  2014       Impact factor: 4.810

8.  Parent and adolescent distribution of responsibility for diabetes self-care: links to health outcomes.

Authors:  Vicki S Helgeson; Kerry A Reynolds; Linda Siminerio; Oscar Escobar; Dorothy Becker
Journal:  J Pediatr Psychol       Date:  2007-09-10

9.  A tutorial on sensitivity analyses in clinical trials: the what, why, when and how.

Authors:  Lehana Thabane; Lawrence Mbuagbaw; Shiyuan Zhang; Zainab Samaan; Maura Marcucci; Chenglin Ye; Marroon Thabane; Lora Giangregorio; Brittany Dennis; Daisy Kosa; Victoria Borg Debono; Rejane Dillenburg; Vincent Fruci; Monica Bawor; Juneyoung Lee; George Wells; Charles H Goldsmith
Journal:  BMC Med Res Methodol       Date:  2013-07-16       Impact factor: 4.615

10.  Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.

Authors:  Nancy S Green; Katherine L Ender; Farzana Pashankar; Catherine Driscoll; Patricia J Giardina; Craig A Mullen; Lorraine N Clark; Deepa Manwani; Jennifer Crotty; Sergey Kisselev; Kathleen A Neville; Carolyn Hoppe; Sandra Barral
Journal:  PLoS One       Date:  2013-02-07       Impact factor: 3.240

View more
  11 in total

Review 1.  Fetal Hemoglobin Induction by Epigenetic Drugs.

Authors:  Donald Lavelle; James Douglas Engel; Yogen Saunthararajah
Journal:  Semin Hematol       Date:  2018-04-22       Impact factor: 3.851

2.  Greater number of perceived barriers to hydroxyurea associated with poorer health-related quality of life in youth with sickle cell disease.

Authors:  Arlene Smaldone; Deepa Manwani; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2019-04-02       Impact factor: 3.167

Review 3.  Fetal haemoglobin induction in sickle cell disease.

Authors:  Alireza Paikari; Vivien A Sheehan
Journal:  Br J Haematol       Date:  2017-11-16       Impact factor: 6.998

4.  HABIT, a Randomized Feasibility Trial to Increase Hydroxyurea Adherence, Suggests Improved Health-Related Quality of Life in Youths with Sickle Cell Disease.

Authors:  Arlene Smaldone; Sally Findley; Deepa Manwani; Haomiao Jia; Nancy S Green
Journal:  J Pediatr       Date:  2018-03-20       Impact factor: 4.406

5.  Red blood cell transfusion therapy for sickle cell patients with frequent painful events.

Authors:  Lee M Hilliard; Varsha Kulkarni; Bisakha Sen; Cathy Caldwell; Christina Bemrich-Stolz; Thomas H Howard; Amanda Brandow; Emily Waite; Jeffrey D Lebensburger
Journal:  Pediatr Blood Cancer       Date:  2018-08-27       Impact factor: 3.167

6.  End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings.

Authors:  Ann T Farrell; Julie Panepinto; Ankit A Desai; Adetola A Kassim; Jeffrey Lebensburger; Mark C Walters; Daniel E Bauer; Rae M Blaylark; Donna M DiMichele; Mark T Gladwin; Nancy S Green; Kathryn Hassell; Gregory J Kato; Elizabeth S Klings; Donald B Kohn; Lakshmanan Krishnamurti; Jane Little; Julie Makani; Punam Malik; Patrick T McGann; Caterina Minniti; Claudia R Morris; Isaac Odame; Patricia Ann Oneal; Rosanna Setse; Poornima Sharma; Shalini Shenoy
Journal:  Blood Adv       Date:  2019-12-10

7.  HABIT efficacy and sustainability trial, a multi-center randomized controlled trial to improve hydroxyurea adherence in youth with sickle cell disease: a study protocol.

Authors:  Arlene Smaldone; Deepa Manwani; Banu Aygun; Kim Smith-Whitley; Haomiao Jia; Jean-Marie Bruzzese; Sally Findley; Joshua Massei; Nancy S Green
Journal:  BMC Pediatr       Date:  2019-10-15       Impact factor: 2.567

Review 8.  Targeting sickle cell disease root-cause pathophysiology with small molecules.

Authors:  Yogen Saunthararajah
Journal:  Haematologica       Date:  2019-08-08       Impact factor: 9.941

Review 9.  Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective.

Authors:  Rayan Bou-Fakhredin; Lucia De Franceschi; Irene Motta; Maria Domenica Cappellini; Ali T Taher
Journal:  Pharmaceuticals (Basel)       Date:  2022-06-16

10.  Oral tetrahydrouridine and decitabine for non-cytotoxic epigenetic gene regulation in sickle cell disease: A randomized phase 1 study.

Authors:  Robert Molokie; Donald Lavelle; Michel Gowhari; Michael Pacini; Lani Krauz; Johara Hassan; Vinzon Ibanez; Maria A Ruiz; Kwok Peng Ng; Philip Woost; Tomas Radivoyevitch; Daisy Pacelli; Sherry Fada; Matthew Rump; Matthew Hsieh; John F Tisdale; James Jacobberger; Mitch Phelps; James Douglas Engel; Santhosh Saraf; Lewis L Hsu; Victor Gordeuk; Joseph DeSimone; Yogen Saunthararajah
Journal:  PLoS Med       Date:  2017-09-07       Impact factor: 11.069

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.