PubTransformer

A site to transform Pubmed publications into these bibliographic reference formats: ADS, BibTeX, EndNote, ISI used by the Web of Knowledge, RIS, MEDLINE, Microsoft's Word 2007 XML.

Clinical features of idiopathic restrictive cardiomyopathy: A retrospective multicenter cohort study over 2 decades.

Abstract Idiopathic restrictive cardiomyopathy (RCMP) has not been fully understood because this disease is difficult to diagnose. The present study aimed to assess the clinical profile and outcome of idiopathic RCMP from a multicenter cohort.This investigation is a retrospective study of consecutive patients with idiopathic RCMP at 10 centers in Korea between 1990 and 2010. We evaluated the clinical characteristics of the patients and prognostic factors associated with mortality using multivariate Cox proportional hazards regression analyses.The study included 53 patients (26 men, 49.1%). During a median follow-up of 1.7 years, 17 patients (32.1%) died and 5 patients (9.4%) received a heart transplant. The 5-year survival rate of the overall patients was 64.4% ± 7.8%. In multivariable analyses, the predictors of mortality were tricuspid regurgitation (TR) ≥ moderate (hazard ratio [HR] 32.55, P < .001) and left ventricular end-diastolic diameter (LVEDD) (HR 0.85, P < .001).Idiopathic RCMP showed unfavorable prognosis. Advanced TR and lower LVEDD are independent adverse predictors of mortality in patients with idiopathic RCMP.
PMID
Related Publications

Role of ventricular assist therapy for patients with heart failure and restrictive physiology: Improving outcomes for a lethal disease.

Impact of tricuspid regurgitation after redo valvular surgery on survival in patients with previous mitral valve replacement.

Vena contracta width as a predictor of adverse outcomes in patients with severe isolated tricuspid regurgitation.

Clinical outcome of isolated tricuspid regurgitation.

Prognostic significance of mitral regurgitation and tricuspid regurgitation in patients with left ventricular systolic dysfunction.

Authors

Mayor MeshTerms
Keywords
Journal Title medicine
Publication Year Start




PMID- 28885342
OWN - NLM
STAT- MEDLINE
DA  - 20170908
DCOM- 20170918
LR  - 20170918
IS  - 1536-5964 (Electronic)
IS  - 0025-7974 (Linking)
VI  - 96
IP  - 36
DP  - 2017 Sep
TI  - Clinical features of idiopathic restrictive cardiomyopathy: A retrospective
      multicenter cohort study over 2 decades.
PG  - e7886
LID - 10.1097/MD.0000000000007886 [doi]
AB  - Idiopathic restrictive cardiomyopathy (RCMP) has not been fully understood
      because this disease is difficult to diagnose. The present study aimed to assess 
      the clinical profile and outcome of idiopathic RCMP from a multicenter
      cohort.This investigation is a retrospective study of consecutive patients with
      idiopathic RCMP at 10 centers in Korea between 1990 and 2010. We evaluated the
      clinical characteristics of the patients and prognostic factors associated with
      mortality using multivariate Cox proportional hazards regression analyses.The
      study included 53 patients (26 men, 49.1%). During a median follow-up of 1.7
      years, 17 patients (32.1%) died and 5 patients (9.4%) received a heart
      transplant. The 5-year survival rate of the overall patients was 64.4% +/- 7.8%. 
      In multivariable analyses, the predictors of mortality were tricuspid
      regurgitation (TR) &gt;/= moderate (hazard ratio [HR] 32.55, P &lt; .001) and left
      ventricular end-diastolic diameter (LVEDD) (HR 0.85, P &lt; .001).Idiopathic RCMP
      showed unfavorable prognosis. Advanced TR and lower LVEDD are independent adverse
      predictors of mortality in patients with idiopathic RCMP.
FAU - Hong, Jung Ae
AU  - Hong JA
AD  - aDepartment of Cardiology, Asan Medical Center, University of Ulsan College of
      Medicine bDepartment of Internal Medicine, Seoul National University Hospital
      cDepartment of Internal Medicine, Samsung Medical Center, Sungkyunkwan University
      School of Medicine, Seoul dDepartment of Cardiology, Translational Research
      Center on Aging, Chonnam National University Hospital, Gwangju eDepartment of
      Internal Medicine, Wonju College of Medicine,Yonsei University, Wonju fDepartment
      of Internal Medicine, Kangbuk Samsung Hospital, Seoul gDepartment of Internal
      Medicine, CHA Bundang Medical Center, CHA University school of Medicine, Bundang 
      hDepartment of Cardiology, Sejong General Hospital iDepartment of Cardiovascular 
      Medicine, Gachon University Gil Medical Center, Incheon jDepartment of Internal
      Medicine, Chungbuk National University School of Medicine, Cheongju, Korea.
FAU - Kim, Min-Seok
AU  - Kim MS
FAU - Cho, Min-Su
AU  - Cho MS
FAU - Choi, Hyo In
AU  - Choi HI
FAU - Kang, Duk-Hyun
AU  - Kang DH
FAU - Lee, Sang-Eun
AU  - Lee SE
FAU - Lee, Ga-Yeon
AU  - Lee GY
FAU - Jeon, Eun-Seok
AU  - Jeon ES
FAU - Cho, Jae-Yeong
AU  - Cho JY
FAU - Kim, Kye-Hun
AU  - Kim KH
FAU - Yoo, Byung-Su
AU  - Yoo BS
FAU - Lee, Jong-Young
AU  - Lee JY
FAU - Kim, Won-Jang
AU  - Kim WJ
FAU - Kim, Kyung-Hee
AU  - Kim KH
FAU - Chung, Wook-Jin
AU  - Chung WJ
FAU - Lee, Ju-Hee
AU  - Lee JH
FAU - Cho, Myeong-Chan
AU  - Cho MC
FAU - Kim, Jae-Joong
AU  - Kim JJ
LA  - eng
PT  - Journal Article
PT  - Multicenter Study
PL  - United States
TA  - Medicine (Baltimore)
JT  - Medicine
JID - 2985248R
SB  - AIM
SB  - IM
MH  - Cardiomyopathy, Restrictive/diagnosis/*mortality/physiopathology/*therapy
MH  - Female
MH  - Follow-Up Studies
MH  - Heart Transplantation/statistics &amp; numerical data
MH  - Heart Ventricles/diagnostic imaging
MH  - Humans
MH  - Male
MH  - Middle Aged
MH  - Multivariate Analysis
MH  - Organ Size
MH  - Prognosis
MH  - Proportional Hazards Models
MH  - Republic of Korea
MH  - Retrospective Studies
MH  - Survival Analysis
MH  - Tricuspid Valve Insufficiency/diagnosis/mortality/physiopathology/therapy
EDAT- 2017/09/09 06:00
MHDA- 2017/09/19 06:00
CRDT- 2017/09/09 06:00
AID - 10.1097/MD.0000000000007886 [doi]
AID - 00005792-201709080-00022 [pii]
PST - ppublish
SO  - Medicine (Baltimore). 2017 Sep;96(36):e7886. doi: 10.1097/MD.0000000000007886.