2014
DOI: 10.4085/1062-6050-49.2.09
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Fluoroquinolones and Tendinopathy: A Guide for Athletes and Sports Clinicians and a Systematic Review of the Literature

Abstract: Fluoroquinolone tendinopathy may not respond well to the current popular eccentric training regimes and may require an alternative, staged treatment approach. Clinicians, athletes, athletic trainers, and their medical support teams should be aware of the need to discuss and possibly discontinue these antibiotics if adverse effects arise.

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Cited by 87 publications
(86 citation statements)
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“…22 The mechanism of action 23 involves the inhibition of bacterial DNA topoisomerase II (gyrase) and topoisomerase IV, which are enzymes involved in untwining bacterial DNA during the replication process. Regrettably, CIP has also been shown to decrease the viability of eukaryotic cells, leading to multiple adverse effects 24,25 , such as tendinopathies 26 and peripheral neuropathy 27,28 , due to a decline in the synthesis of proteins encoded in mitochondrial deoxyribonucleic acid (mtDNA). Analysis of mtDNA from CIP-treated cells revealed the presence of site-specific, double-stranded DNA breaks 29 , which were attributed to inhibition of mitochondrial topoisomerase II activity, functionally and structurally similar to that found in bacteria.…”
Section: Discussionmentioning
confidence: 99%
“…22 The mechanism of action 23 involves the inhibition of bacterial DNA topoisomerase II (gyrase) and topoisomerase IV, which are enzymes involved in untwining bacterial DNA during the replication process. Regrettably, CIP has also been shown to decrease the viability of eukaryotic cells, leading to multiple adverse effects 24,25 , such as tendinopathies 26 and peripheral neuropathy 27,28 , due to a decline in the synthesis of proteins encoded in mitochondrial deoxyribonucleic acid (mtDNA). Analysis of mtDNA from CIP-treated cells revealed the presence of site-specific, double-stranded DNA breaks 29 , which were attributed to inhibition of mitochondrial topoisomerase II activity, functionally and structurally similar to that found in bacteria.…”
Section: Discussionmentioning
confidence: 99%
“…В амбулаторной практике основное значение имеет потенциальная нейротоксичность фторхи-нолонов. Индикатор просудорожной активности, характе-ризующий возбуждающее действие на ЦНС, существует вo всех поколениях этих антибиотиков и проявляется голов-ной болью, головокружением и сонливостью [27]. Одним из наиболее опасных побочных эффектов, связанных с приемом препаратов этой группы, является нарушение ритма, в том числе развитие желудочковых аритмий, а уд-линение интервала QT в настоящее время рассматривается как групповое свойство фторхинолонов [24].…”
Section: © коллектив авторов 2016unclassified
“…Одним из наиболее опасных побочных эффектов, связанных с приемом препаратов этой группы, является нарушение ритма, в том числе развитие желудочковых аритмий, а уд-линение интервала QT в настоящее время рассматривается как групповое свойство фторхинолонов [24]. Еще одним отличительным свойством препаратов этой группы являет-ся развитие в любом возрасте тендинита и возникновение риска разрыва сухожилия, чаще всего ахиллова, что огра-ничивает их применение в пожилом возрасте [27]. Кроме того, фторхинолоны противопоказаны при беременности, кормлении грудью, детям и подросткам до 18 лет.…”
Section: © коллектив авторов 2016unclassified
“…Symptoms may occur hours after started therapy and even after few months after the end of administration. Recovery is significantly slower than after common injury [35]. Similarly doxycycline antibiotics inhibit collagen proteases and reduce mechanical properties of tissue, while on the other hand insulin, estrogen and testosterone -increase collagen production [49,57].…”
Section: Ageing Of the Tendonsmentioning
confidence: 99%