Literature DB >> 29296801

Pharmacotherapeutical strategies in the prevention of acute, vaso-occlusive pain in sickle cell disease: a systematic review.

Joep W R Sins1,2, David J Mager1,2, Shyrin C A T Davis1, Bart J Biemond2, Karin Fijnvandraat1.   

Abstract

Sickle-cell disease (SCD) is characterized by frequent and painful vaso-occlusive crises (VOCs). Various treatments have been evaluated over the years. However, a clear overview is lacking. The objective of this study was to systematically review all pharmacotherapeutical strategies in the prevention of VOCs beyond hydroxyurea. We performed a systematic literature search (MEDLINE, Embase, CENTRAL). Eligible studies were controlled clinical trials evaluating pharmacotherapeutical interventions targeting the reduction of VOCs in patients with SCD. Primary outcomes were the number or duration of SCD-related pain days, VOCs, or hospital admissions for VOCs. Secondary outcomes included time to first VOC or hospital admission for a VOC. A standardized data extraction sheet was used. The methodological quality of studies was assessed using Cochrane's risk-of-bias tool. A total of 36 studies were included in this review, covering 26 different prophylactic interventions. The most promising interventions for reducing the frequency of either VOCs or hospitalizations were the oral antioxidants l-glutamine and ω-3 fatty acids and the IV antiadhesive agent crizanlizumab. Twenty-three studies did not show any beneficial effect of the intervention under investigation, and 6 studies were either too small or methodologically inadequate to draw conclusions. Because of the heterogeneity of interventions, no meta-analysis was performed. In conclusion, this review identified 3 promising pharmacotherapeutical strategies in the prevention of VOCs in SCD. Importantly, this study highlights the discrepancy between the significant burden of SCD worldwide and the low number of adequate trials performed. This review was registered at PROSPERO (CRD42015025250).

Entities:  

Year:  2017        PMID: 29296801      PMCID: PMC5728463          DOI: 10.1182/bloodadvances.2017007211

Source DB:  PubMed          Journal:  Blood Adv        ISSN: 2473-9529


  76 in total

1.  Inhibition of cell adhesion by anti-P-selectin aptamer: a new potential therapeutic agent for sickle cell disease.

Authors:  Diana R Gutsaeva; James B Parkerson; Shobha D Yerigenahally; Jeffrey C Kurz; Robert G Schaub; Tohru Ikuta; C Alvin Head
Journal:  Blood       Date:  2010-10-06       Impact factor: 22.113

2.  Dietary ω-3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease.

Authors:  Brian T Kalish; Alessandro Matte; Immacolata Andolfo; Achille Iolascon; Olga Weinberg; Alessandra Ghigo; James Cimino; Angela Siciliano; Emilio Hirsch; Enrica Federti; Mark Puder; Carlo Brugnara; Lucia De Franceschi
Journal:  Haematologica       Date:  2015-05-01       Impact factor: 9.941

3.  Piracetam for the treatment of sickle cell disease in children- a double blind test.

Authors:  Mohsen A F El-Hazmi; I Al-Fawaz; A Warsy; A Opawoye; H Taleb; Z Howsawi; A Mohamed; A Wadood Aly; S Refai; P Sugathan; A Rab; H Ahmed; M Abulaban; A Abdulkader; M Farid
Journal:  Saudi Med J       Date:  1998-01       Impact factor: 1.484

4.  Steroid treatment in the prevention of painful episodes in sickle-cell disease.

Authors:  W A Isaacs; C E Effiong; O Ayeni
Journal:  Lancet       Date:  1972-03-11       Impact factor: 79.321

5.  Clinical and biological double-blind-study of ticlopidine in preventive treatment of sickle-cell disease crises.

Authors:  R Cabannes; J Lonsdorfer; J P Castaigne; A Ondo; A Plassard; I Zohoun
Journal:  Agents Actions Suppl       Date:  1984

6.  Antioxidant vitamins C and E supplementation increases markers of haemolysis in sickle cell anaemia patients: a randomized, double-blind, placebo-controlled trial.

Authors:  Martha M Arruda; Grazielle Mecabo; Celso A Rodrigues; Sandra S Matsuda; Iara B Rabelo; Maria S Figueiredo
Journal:  Br J Haematol       Date:  2012-12-29       Impact factor: 6.998

7.  Inefficacy of piracetam in the prevention of painful crises in children and adolescents with sickle cell disease.

Authors:  R C Alvim; M B Viana; M A S Pires; H M O H Franklin; M J Paula; A C Brito; T F Oliveira; P V Rezende
Journal:  Acta Haematol       Date:  2005       Impact factor: 2.195

8.  The contribution of endothelial cell P-selectin to the microvascular flow of mouse sickle erythrocytes in vivo.

Authors:  Stephen H Embury; Neil M Matsui; Sahana Ramanujam; Tanya N Mayadas; Constance T Noguchi; Bhalchandra A Diwan; Narla Mohandas; Anthony T W Cheung
Journal:  Blood       Date:  2004-07-22       Impact factor: 22.113

9.  Effects of pyrimethamine versus proguanil in malarial chemoprophylaxis in children with sickle cell disease: a randomized, placebo-controlled, open-label study.

Authors:  Felicia U Eke; Ifeoma Anochie
Journal:  Curr Ther Res Clin Exp       Date:  2003-09

10.  Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease.

Authors:  Nancy J Wandersee; Jamie L Maciaszek; Katie M Giger; Madelyn S Hanson; Suilan Zheng; YiHe Guo; Barbara Mickelson; Cheryl A Hillery; George Lykotrafitis; Philip S Low; Neil Hogg
Journal:  Blood Cells Mol Dis       Date:  2014-11-25       Impact factor: 3.039

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  13 in total

1.  Realizing effectiveness across continents with hydroxyurea: Enrollment and baseline characteristics of the multicenter REACH study in Sub-Saharan Africa.

Authors:  Patrick T McGann; Thomas N Williams; Peter Olupot-Olupot; George A Tomlinson; Adam Lane; José Luís Reis da Fonseca; Robert Kitenge; George Mochamah; Ham Wabwire; Susan Stuber; Thad A Howard; Kathryn McElhinney; Banu Aygun; Teresa Latham; Brígida Santos; Léon Tshilolo; Russell E Ware
Journal:  Am J Hematol       Date:  2018-01-27       Impact factor: 10.047

Review 2.  Targeting novel mechanisms of pain in sickle cell disease.

Authors:  Huy Tran; Mihir Gupta; Kalpna Gupta
Journal:  Blood       Date:  2017-11-30       Impact factor: 22.113

Review 3.  Measuring success: utility of biomarkers in sickle cell disease clinical trials and care.

Authors:  Ram Kalpatthi; Enrico M Novelli
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

Review 4.  Mast cell-neural interactions contribute to pain and itch.

Authors:  Kalpna Gupta; Ilkka T Harvima
Journal:  Immunol Rev       Date:  2018-03       Impact factor: 12.988

Review 5.  Targeting novel mechanisms of pain in sickle cell disease.

Authors:  Huy Tran; Mihir Gupta; Kalpna Gupta
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 6.  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

7.  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

8.  Crizanlizumab and comparators for adults with sickle cell disease: a systematic review and network meta-analysis.

Authors:  Howard Thom; Jeroen Jansen; Jason Shafrin; Lauren Zhao; George Joseph; Hung-Yuan Cheng; Subhajit Gupta; Nirmish Shah
Journal:  BMJ Open       Date:  2020-09-17       Impact factor: 2.692

9.  Diet and companionship modulate pain via a serotonergic mechanism.

Authors:  Huy Tran; Varun Sagi; Sarita Jarrett; Elise F Palzer; Rajendra D Badgaiyan; Kalpna Gupta
Journal:  Sci Rep       Date:  2021-02-01       Impact factor: 4.379

10.  Profile of crizanlizumab and its potential in the prevention of pain crises in sickle cell disease: evidence to date.

Authors:  Tanya R Riley; Treavor T Riley
Journal:  J Blood Med       Date:  2019-08-30
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