Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Prognostic Value of Standard Heart Failure Medication in Patients with Cardiac Transthyretin Amyloidosis
by
Schwarting, Stéphanie K.
, Hegenbart, Ute
, Weiler, Markus
, Schönland, Stefan O.
, Kristen, Arnt V.
, Nagel, Christian
, aus dem Siepen, Fabian
, Hein, Selina
, Hofmann, Eva
, Frey, Norbert
in
ACE inhibitors
/ Adrenergic beta blockers
/ Amyloidosis
/ Biomarkers
/ Biopsy
/ Cardiac patients
/ Cardiomyopathy
/ Cardiovascular disease
/ Comorbidity
/ Coronary heart disease
/ Development and progression
/ Drug therapy
/ Ejection fraction
/ Genotype & phenotype
/ Heart failure
/ Hypertension
/ Medical research
/ Medicine, Experimental
/ Mutation
/ Patient outcomes
/ Scintigraphy
2024
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Prognostic Value of Standard Heart Failure Medication in Patients with Cardiac Transthyretin Amyloidosis
by
Schwarting, Stéphanie K.
, Hegenbart, Ute
, Weiler, Markus
, Schönland, Stefan O.
, Kristen, Arnt V.
, Nagel, Christian
, aus dem Siepen, Fabian
, Hein, Selina
, Hofmann, Eva
, Frey, Norbert
in
ACE inhibitors
/ Adrenergic beta blockers
/ Amyloidosis
/ Biomarkers
/ Biopsy
/ Cardiac patients
/ Cardiomyopathy
/ Cardiovascular disease
/ Comorbidity
/ Coronary heart disease
/ Development and progression
/ Drug therapy
/ Ejection fraction
/ Genotype & phenotype
/ Heart failure
/ Hypertension
/ Medical research
/ Medicine, Experimental
/ Mutation
/ Patient outcomes
/ Scintigraphy
2024
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Prognostic Value of Standard Heart Failure Medication in Patients with Cardiac Transthyretin Amyloidosis
by
Schwarting, Stéphanie K.
, Hegenbart, Ute
, Weiler, Markus
, Schönland, Stefan O.
, Kristen, Arnt V.
, Nagel, Christian
, aus dem Siepen, Fabian
, Hein, Selina
, Hofmann, Eva
, Frey, Norbert
in
ACE inhibitors
/ Adrenergic beta blockers
/ Amyloidosis
/ Biomarkers
/ Biopsy
/ Cardiac patients
/ Cardiomyopathy
/ Cardiovascular disease
/ Comorbidity
/ Coronary heart disease
/ Development and progression
/ Drug therapy
/ Ejection fraction
/ Genotype & phenotype
/ Heart failure
/ Hypertension
/ Medical research
/ Medicine, Experimental
/ Mutation
/ Patient outcomes
/ Scintigraphy
2024
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Prognostic Value of Standard Heart Failure Medication in Patients with Cardiac Transthyretin Amyloidosis
Journal Article
Prognostic Value of Standard Heart Failure Medication in Patients with Cardiac Transthyretin Amyloidosis
2024
Request Book From Autostore
and Choose the Collection Method
Overview
Introduction: Cardiac transthyretin amyloidosis (ATTR) is a progressive, fatal disease leading to heart failure due to accumulation of amyloid fibrils in the interstitial space and may occur as a hereditary (ATTRv) or wild-type (ATTRwt) form. Guidelines recommend the use of ACE inhibitors (ACEis) and beta-blockers (BBs) as heart failure therapy (HFT) in all patients with symptomatic heart failure and reduced ejection fraction, independent of the underlying etiology. However, the prognostic benefit of ACEis and BBs in ATTR has not been elucidated in detail yet. We thus sought to retrospectively investigate the outcome of patients with ATTRwt or ATTRv under HFT. Methods: Medical records of 403 patients with cardiac ATTR (ATTRwt: n = 268, ATTRv: n = 135) were screened for long-term medication as well as clinical, laboratory, electrocardiographic and echocardiographic data. Patients were assessed between 2005 and 2020 at the University Hospital Heidelberg. Kaplan–Meier analysis was used to analyze potential differences in survival among different subgroups. Results: The mean follow-up was 28 months. In total, 43 patients (32%) with ATTRv and 140 patients (52%) with ATTRwt received HFT. Survival was significantly shorter in patients receiving HFT in ATTRv (46 vs. 83 months, p = 0.0007) vs. non-HFT. A significantly better survival was observed in patients with comorbidities (coronary artery disease, arterial hypertension) and HFT among ATTRwt patients (p = 0.004). No significant differences in survival were observed in the other subgroups. Conclusions: Survival analysis revealed a potential benefit of HFT in patients with ATTRwt and cardiac comorbidities such as coronary artery disease and/or arterial hypertension. In contrast, HFT should be used with caution in patients with ATTRv.
MBRLCatalogueRelatedBooks
Related Items
Related Items
This website uses cookies to ensure you get the best experience on our website.