Efficacy and safety of long-term treatment with intravenous colchicine for familial Mediterranean fever (FMF) refractory to oral colchicine.
Administration, Intravenous
Administration, Oral
Adult
Colchicine
/ administration & dosage
Diarrhea
/ chemically induced
Familial Mediterranean Fever
/ drug therapy
Female
Humans
Injection Site Reaction
/ etiology
Male
Middle Aged
Myalgia
/ chemically induced
Nausea
/ chemically induced
Time Factors
Treatment Outcome
Tubulin Modulators
/ administration & dosage
Vomiting
/ chemically induced
Adverse events
Colchicine
FMF
Intravenous treatment
Oral colchicine-resistant FMF
Journal
Rheumatology international
ISSN: 1437-160X
Titre abrégé: Rheumatol Int
Pays: Germany
ID NLM: 8206885
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
06
10
2018
accepted:
27
12
2018
pubmed:
4
1
2019
medline:
3
1
2020
entrez:
4
1
2019
Statut:
ppublish
Résumé
Colchicine is the mainstay of treatment for familial Mediterranean fever (FMF). Intravenous (IV) colchicine, administered over several months, has been shown to be effective for FMF patients unresponsive to oral colchicine. The objective of this study was to evaluate the efficacy and safety of long-term IV colchicine treatment in oral colchicine-resistant FMF. We analyzed data of 15 patients with frequent FMF attacks, despite a maximal tolerated dose of oral colchicine (2-3 mg/day), who were treated with weekly IV injections of 1 mg of colchicine for at least 12 months. Treatment efficacy was determined by changes in frequency, duration and severity of FMF attacks. Safety was assessed according to adverse events. The mean duration of IV colchicine treatment was 5.16 ± 2.85 years. Decreases were observed from pre-treatment period in the monthly mean rates of abdominal attacks (from 5.6 ± 3.7 to 1.9 ± 3.3, p = 0.0009), joint attacks (from 6.5 ± 5.1 to 1.6 ± 1.6, p = 0.01) and overall attacks (from 22.3 ± 16.2 to 7.4 ± 5.7, p = 0.002) as well as in the mean duration (from 3.8 ± 1.5 to 2.4 ± 1.1 days per attack, p = 0.008) and severity of attacks (from 9.9 ± 0.3 to 5.7 ± 2.6, on a scale of 0-10, p < 0.05). The rate of adverse events was low, and they were mainly gastrointestinal. No severe or serious adverse events were recorded. Long-term treatment with IV colchicine in patients unresponsive to oral colchicine therapy is effective and safe.
Identifiants
pubmed: 30604205
doi: 10.1007/s00296-018-04237-w
pii: 10.1007/s00296-018-04237-w
doi:
Substances chimiques
Tubulin Modulators
0
Colchicine
SML2Y3J35T
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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