Transthyretin Amyloid Cardiomyopathy Treatment - dhritimancmi - Wattpad

Story cover for Transthyretin Amyloid Cardiomyopathy Treatment by dhritimancmi

Transthyretin Amyloid Cardiomyopathy Treatment

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Reads 3
Votes 0
Parts 1
Time <5 mins

amyloidosis anti-inflammatory drugs hereditary nonsteroidal rnai stabilizers therapy transthyretin type wild

While there is no options for Transthyretin Amyloid Cardiomyopathy Treatment, available treatments can help control symptoms and potentially slow disease progression. Treatment options include:


Medications: Diuretics help manage fluid retention. Beta-blockers and ACE inhibitors may help the heart pump more effectively. 

Device-based therapies: A pacemaker or implantable cardioverter defibrillator (ICD) can treat irregular heart rhythms. 

Liver transplantation : For certain types of hereditary ATTR-CM, replacing the liver can stop further production of problematic TTR protein. Considered high-risk with limited longevity benefits.

Tafamidis : The first medication approved by the FDA to treat ATTR-CM. It binds to and stabilizes TTR tetramers to prevent dissociation and amyloid formation. Associated with reduced mortality and cardiovascular hospitalizations.

Inotersen and Patisiran : Two RNA interference drugs approved for hereditary forms that prevent production of problematic TTR protein. Associated with substantial reductions in TTR levels and improved outcomes.

Get more insights on https://www.ukwebwire.com/transthyretin-amyloid-cardiomyopathy-treatment-market-growth-and-trnds-analysis-share-size-demand-forecast//All Rights Reserved

amyloidosis anti-inflammatory drugs hereditary nonsteroidal rnai stabilizers therapy transthyretin type wild

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Tue, Oct 1, 2024

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