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Achilles tendon complications of fluoroquinolone treatment: a molecule-stratified systematic review and meta-analysis.
Sangiorgio, Alessandro; Sirone, Martina; Adravanti, Federico Maria; Testa, Enrique Adrian; Riegger, Martin; Filardo, Giuseppe.
Afiliación
  • Sangiorgio A; Service of Orthopaedics and Traumatology, Department of Surgery, EOC, Lugano, Switzerland.
  • Sirone M; Service of Orthopaedics and Traumatology, Department of Surgery, EOC, Lugano, Switzerland.
  • Adravanti FM; Service of Orthopaedics and Traumatology, Department of Surgery, EOC, Lugano, Switzerland.
  • Testa EA; 2nd Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
  • Riegger M; Service of Orthopaedics and Traumatology, Department of Surgery, EOC, Lugano, Switzerland.
  • Filardo G; Faculty of Biomedical Sciences, Università della Svizzera Italiana, Lugano, Switzerland.
EFORT Open Rev ; 9(7): 581-588, 2024 Jul 01.
Article en En | MEDLINE | ID: mdl-38949172
ABSTRACT

Purpose:

The association between fluoroquinolone intake and Achilles tendinopathy (AT) or Achilles tendon rupture (ATR) is widely documented. However, it is not clear whether different molecules have the same effect on these complications. The purpose of this study was to document Achilles tendon complications for the most prescribed fluoroquinolones molecules.

Methods:

A literature search was performed on Pubmed, Cochrane, Embase, and Web of Science databases up to April 2023. Inclusion criteria studies of any level of evidence, written in English, documenting the prevalence of AT/ATR after fluoroquinolone consumption and stratifying the results for each type of molecule. The Downs and Black's 'Checklist for Measuring Quality' was used to evaluate the risk of bias.

Results:

Twelve studies investigating 439,299 patients were included (59.7% women, 40.3% men, mean age 53.0 ± 15.6 years). The expected risk of AT/ATR was 0.17% (95% CI 0.15-0.19, standard error (s.e.) 0.24) for levofloxacin, 0.17% (95% CI 0.16-0.19, s.e. 0.20) for ciprofloxacin, 1.40% (95% CI 0.88-2.03, s.e. 2.51) for ofloxacin, and 0.31% (95% CI 0.23-0.40, s.e. 0.77) for the other molecules. The comparison between groups documented a significantly higher AT/ATR rate in the ofloxacin group (P < 0.0001 for each comparison). Levofloxacin and ciprofloxacin showed the same risk (P = n.s.). The included studies showed an overall good quality.

Conclusion:

Ofloxacin demonstrated a significantly higher rate of AT/ATR complications in the adult population, while levofloxacin and ciprofloxacin showed a safer profile compared to all the other molecules. More data are needed to identify other patient and treatment-related factors influencing the risk of musculoskeletal complications.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: EFORT Open Rev Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: EFORT Open Rev Año: 2024 Tipo del documento: Article País de afiliación: Suiza