SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Kristen Arnt V.)
 

Sökning: WFRF:(Kristen Arnt V.) > Avoiding misdiagnos...

Avoiding misdiagnosis : expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner

Gertz, Morie (författare)
Adams, David (författare)
Ando, Yukio (författare)
visa fler...
Beirao, Joao Melo (författare)
Bokhari, Sabahat (författare)
Coelho, Teresa (författare)
Comenzo, Raymond L. (författare)
Damy, Thibaud (författare)
Dorbala, Sharmila (författare)
Drachman, Brian M. (författare)
Fontana, Marianna (författare)
Gillmore, Julian D. (författare)
Grogan, Martha (författare)
Hawkins, Philip N. (författare)
Lousada, Isabelle (författare)
Kristen, Arnt V. (författare)
Ruberg, Frederick L. (författare)
Suhr, Ole B. (författare)
Umeå universitet,Avdelningen för medicin
Maurer, Mathew S. (författare)
Nativi-Nicolau, Jose (författare)
Quarta, Candida Cristina (författare)
Rapezzi, Claudio (författare)
Witteles, Ronald (författare)
Merlini, Giampaolo (författare)
visa färre...
 (creator_code:org_t)
2020-09-23
2020
Engelska.
Ingår i: BMC Family Practice. - : BMC. - 1471-2296. ; 21:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Transthyretin amyloidosis (also known as ATTR amyloidosis) is a systemic, life-threatening disease characterized by transthyretin (TTR) fibril deposition in organs and tissue. A definitive diagnosis of ATTR amyloidosis is often a challenge, in large part because of its heterogeneous presentation. Although ATTR amyloidosis was previously considered untreatable, disease-modifying therapies for the treatment of this disease have recently become available. This article aims to raise awareness of the initial symptoms of ATTR amyloidosis among general practitioners to facilitate identification of a patient with suspicious signs and symptoms. Methods These consensus recommendations for the suspicion and diagnosis of ATTR amyloidosis were developed through a series of development and review cycles by an international working group comprising key amyloidosis specialists. This working group met to discuss the barriers to early and accurate diagnosis of ATTR amyloidosis and develop a consensus recommendation through a thorough search of the literature performed using PubMed Central. Results The cardiac and peripheral nervous systems are most frequently involved in ATTR amyloidosis; however, many patients often also experience gastrointestinal and other systemic manifestations. Given the multisystemic nature of symptoms, ATTR amyloidosis is often misdiagnosed as a more common disorder, leading to significant delays in the initiation of treatment. Although histologic evaluation has been the gold standard to confirm ATTR amyloidosis, a range of tools are available that can facilitate early and accurate diagnosis. Of importance, genetic testing should be considered early in the evaluation of a patient with unexplained peripheral neuropathy. Conclusions A diagnostic algorithm based on initial red flag symptoms and manifestations of cardiac or neurologic involvement will facilitate identification by the general practitioner of a patient with clinically suspicious symptoms, enabling subsequent referral of the patient to a multidisciplinary specialized medical center.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Health Care Service and Management, Health Policy and Services and Health Economy (hsv//eng)

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy