Practical suggestions on intravenous iloprost in Raynaud's phenomenon and digital ulcer secondary to systemic sclerosis: Systematic literature review and expert consensus.


Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 13 01 2018
revised: 27 03 2018
accepted: 29 03 2018
pubmed: 1 5 2018
medline: 24 4 2019
entrez: 1 5 2018
Statut: ppublish

Résumé

Systemic sclerosis (SSc) is an autoimmune chronic disease characterized by vascular impairment, immune dysfunction and collagen deposition. Raynaud's phenomenon (RP) and digital ulcers (DU) are prominent features of SSc. Intravenous (IV) iloprost (ILO), according to the recently updated EULAR recommendations, is indicated for RP after failure of oral therapy. Moreover, IV ILO could be useful in DU healing. IV ILO is currently available mainly on the European market approved for RP secondary to SSc with 3-5 days infusion cycle. Unfortunately, data published varies regarding regimen (dosage, duration and frequency). Up to now, ILO has been studied in small cohorts of patients and in few randomized controlled trials. A systematic review of studies on IV ILO in patients with SSc complicated by DU and RP was performed. Insufficient data were available to perform a meta-analysis according to the GRADE system. We performed a three-stage internet-based Delphi consensus exercise. Three major indications were identified for IV ILO usage in SSc: RP non-responsive to oral therapy, DU healing, and DU prevention. IV ILO should be administered between 0.5 and 2.0ng/kg/min according to patient tolerability with a frequency depending on the indication. Although these suggestions are supported by this expert group to be used in clinical setting, it will be necessary to formally validate the present suggestions in future clinical trials.

Sections du résumé

BACKGROUND BACKGROUND
Systemic sclerosis (SSc) is an autoimmune chronic disease characterized by vascular impairment, immune dysfunction and collagen deposition. Raynaud's phenomenon (RP) and digital ulcers (DU) are prominent features of SSc. Intravenous (IV) iloprost (ILO), according to the recently updated EULAR recommendations, is indicated for RP after failure of oral therapy. Moreover, IV ILO could be useful in DU healing. IV ILO is currently available mainly on the European market approved for RP secondary to SSc with 3-5 days infusion cycle. Unfortunately, data published varies regarding regimen (dosage, duration and frequency). Up to now, ILO has been studied in small cohorts of patients and in few randomized controlled trials.
METHODS METHODS
A systematic review of studies on IV ILO in patients with SSc complicated by DU and RP was performed. Insufficient data were available to perform a meta-analysis according to the GRADE system. We performed a three-stage internet-based Delphi consensus exercise.
RESULTS RESULTS
Three major indications were identified for IV ILO usage in SSc: RP non-responsive to oral therapy, DU healing, and DU prevention. IV ILO should be administered between 0.5 and 2.0ng/kg/min according to patient tolerability with a frequency depending on the indication.
CONCLUSIONS CONCLUSIONS
Although these suggestions are supported by this expert group to be used in clinical setting, it will be necessary to formally validate the present suggestions in future clinical trials.

Identifiants

pubmed: 29706243
pii: S0049-0172(18)30013-1
doi: 10.1016/j.semarthrit.2018.03.019
pii:
doi:

Substances chimiques

Vasodilator Agents 0
Iloprost JED5K35YGL

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

686-693

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Francesca Ingegnoli (F)

Division of Clinical Rheumatology, ASST Pini-CTO, Milano, Italy; Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy. Electronic address: francesca.ingegnoli@unimi.it.

Tommaso Schioppo (T)

Division of Clinical Rheumatology, ASST Pini-CTO, Milano, Italy.

Yannick Allanore (Y)

Paris Descartes University, Cochin Hospital, Rheumatology A department, INSERM U1016, Paris, France.

Roberto Caporali (R)

Division of Rheumatology, University of Pavia, IRCCS S. Matteo Foundation, Pavia, Italy.

Michele Colaci (M)

Rheumatology Unit, University of Modena and Reggio Emilia, Modena, Italy.

Oliver Distler (O)

Department of Rheumatology, University Hospital Zurich, Switzerland.

Daniel E Furst (DE)

Los Angeles, USA UCLA (emeritus); University of Washington, Seattle Wash; University of Florence, Florence, Italy.

Nicolas Hunzelmann (N)

Department of Dermatology, University of Cologne, Cologne, Germany.

Florenzo Iannone (F)

DETO-Section of Rheumathology, Bari, Italy.

Dinesh Khanna (D)

Ann Arbor, University of Michigan, Ann Arbor, Michigan.

Marco Matucci-Cerinic (M)

Department of Experimental and Clinical Medicine, University of Florence & Department of Geriatric Medicine, Division of Rheumatology AOUC, Florence, Italy.

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