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Mortality in primary and secondary myocarditis.

Publication ,  Journal Article
Pulerwitz, TC; Cappola, TP; Felker, GM; Hare, JM; Baughman, KL; Kasper, EK
Published in: Am Heart J
April 2004

BACKGROUND: Lymphocytic myocarditis presents as a primary disorder or in association with a systemic disease. Whether primary and secondary myocarditis have the same prognosis is unknown. METHODS: Patients (n = 171) referred to the Johns Hopkins Cardiomyopathy service from 1984 to 1998 with newly diagnosed cardiomyopathy were observed for an average of 5.9 years after an original diagnosis of biopsy-proven myocarditis or until reaching the end point of death. Giant-cell myocarditis was excluded from this study. Myocarditis was classified as secondary when a systemic disease was present at the time of presentation; otherwise, myocarditis was classified as primary. Survival rates among patients with primary and secondary myocarditis were compared with Kaplan-Meier analysis and Cox proportional hazard models incorporating clinical variables, including baseline hemodynamics and treatment with immunosuppressive therapy. RESULTS: The mortality rate associated with secondary myocarditis varied substantially depending on the underlying systemic disorder. Peripartum myocarditis, when compared with idiopathic myocarditis, had a reduced mortality rate (relative hazard, 0.23 [0.06-0.98]; P <.05), which was attenuated after controlling for confounding variables (relative hazard, 0.62 [0.13-2.98]; P =.55). In contrast, human immunodeficiency virus myocarditis had a particularly poor prognosis (relative hazard, 6.70 [3.51-12.79]; P <.05), even after controlling for confounding variables. Myocarditis associated with systemic inflammatory disorders showed a trend toward increased mortality rate (relative hazard, 2.46 [0.65-9.38]; P =.19). For both primary and secondary myocarditis, advanced age and pulmonary hypertension were important clinical predictors of death. CONCLUSIONS: The prognosis of patients with secondary myocarditis, when compared with patients with idiopathic myocarditis, seems most affected by the primary disease process.

Duke Scholars

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

April 2004

Volume

147

Issue

4

Start / End Page

746 / 750

Location

United States

Related Subject Headings

  • Survival Rate
  • Scleroderma, Systemic
  • Retrospective Studies
  • Puerperal Disorders
  • Proportional Hazards Models
  • Prognosis
  • Pregnancy Complications
  • Pregnancy
  • Myocarditis
  • Male
 

Citation

APA
Chicago
ICMJE
MLA
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Pulerwitz, T. C., Cappola, T. P., Felker, G. M., Hare, J. M., Baughman, K. L., & Kasper, E. K. (2004). Mortality in primary and secondary myocarditis. Am Heart J, 147(4), 746–750. https://doi.org/10.1016/j.ahj.2003.10.029
Pulerwitz, Todd C., Thomas P. Cappola, G Michael Felker, Joshua M. Hare, Kenneth L. Baughman, and Edward K. Kasper. “Mortality in primary and secondary myocarditis.Am Heart J 147, no. 4 (April 2004): 746–50. https://doi.org/10.1016/j.ahj.2003.10.029.
Pulerwitz TC, Cappola TP, Felker GM, Hare JM, Baughman KL, Kasper EK. Mortality in primary and secondary myocarditis. Am Heart J. 2004 Apr;147(4):746–50.
Pulerwitz, Todd C., et al. “Mortality in primary and secondary myocarditis.Am Heart J, vol. 147, no. 4, Apr. 2004, pp. 746–50. Pubmed, doi:10.1016/j.ahj.2003.10.029.
Pulerwitz TC, Cappola TP, Felker GM, Hare JM, Baughman KL, Kasper EK. Mortality in primary and secondary myocarditis. Am Heart J. 2004 Apr;147(4):746–750.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

April 2004

Volume

147

Issue

4

Start / End Page

746 / 750

Location

United States

Related Subject Headings

  • Survival Rate
  • Scleroderma, Systemic
  • Retrospective Studies
  • Puerperal Disorders
  • Proportional Hazards Models
  • Prognosis
  • Pregnancy Complications
  • Pregnancy
  • Myocarditis
  • Male