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Diflunisal tolerability in transthyretin cardiac amyloidosis: a single center's experience.
Author: DonnellyJoseph P, HannaMazen, IkramAsad, SamarasChristy, SperryBrett W, ValentJason
Original Abstract of the Article :
Transthyretin (ATTR) amyloidosis is an under-recognized, progressive disease manifesting as cardiomyopathy and/or polyneuropathy. Diflunisal, a nonsteroidal anti-inflammatory drug (NSAID), has demonstrated transthyretin stabilization in vitro and slowing of polyneuropathy progression in the heredita...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://doi.org/10.1080/13506129.2018.1519507
データ提供:米国国立医学図書館(NLM)
Diflunisal Tolerability in Transthyretin Cardiac Amyloidosis
Transthyretin (ATTR) amyloidosis is a complex and often under-recognized disease, affecting both the heart and the nervous system. This study delves into the world of ATTR amyloidosis, specifically focusing on the tolerability of diflunisal, a nonsteroidal anti-inflammatory drug (NSAID), in patients with ATTR cardiac amyloidosis (CA). The researchers investigated the use of diflunisal in a cohort of patients with ATTR-CA, both hereditary and wild-type, hoping to shed light on its potential benefits and adverse effects.
A Promising Approach for Treating ATTR Amyloidosis
The study explores the potential of diflunisal as a therapeutic option for ATTR amyloidosis. The findings suggest that selected patients with ATTR-CA may tolerate diflunisal with limited adverse events. This is a promising development, as diflunisal has previously demonstrated transthyretin stabilization and slowing of polyneuropathy progression in patients with hereditary ATTR amyloidosis. This study expands the potential application of diflunisal to a wider range of ATTR amyloidosis patients, offering a possible treatment strategy for this complex disease.
Navigating the Use of Diflunisal in ATTR Cardiac Amyloidosis
The study highlights the need for careful patient selection and monitoring when considering diflunisal treatment for ATTR-CA. The authors emphasize the importance of a thorough evaluation to identify patients who are most likely to benefit from diflunisal therapy, while minimizing potential risks. Further research is needed to fully understand the long-term effects and optimal dosing strategies for diflunisal in ATTR-CA patients. This study provides valuable insights for clinicians navigating the complex world of ATTR amyloidosis, paving the way for more effective treatment strategies for these patients.
Dr.Camel's Conclusion
This study is like a refreshing oasis in the vast desert of amyloidosis research, offering a potential treatment option for patients with ATTR cardiac amyloidosis. The researchers have unearthed a promising avenue for managing this complex disease, with diflunisal showing potential benefits while minimizing adverse effects. However, like a mirage, further research is needed to solidify the role of diflunisal in the treatment of ATTR-CA and ensure that its use is optimized for each patient.
Date :
- Date Completed 2019-03-11
- Date Revised 2019-03-11
Further Info :
Related Literature
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