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Early Mortality and Cardiorespiratory Failure in Patients with Fibrodysplasia Ossificans Progressiva
Frederick S. Kaplan, MD1; Michael A. Zasloff, MD, PhD2; Joseph A. Kitterman, MD3; Eileen M. Shore, PhD4; Charles C. Hong, MD, PhD5; David M. Rocke, PhD6
1 Department of Orthopaedic Surgery, Hospital of the University of Pennsylvania, Silverstein-2, 3400 Spruce Street, Philadelphia, PA 19104. E-mail address for F.S. Kaplan: Frederick.Kaplan@uphs.upenn.edu
2 Department of Translational Sciences, Georgetown University Medical Center, Washington, DC 20057
3 Department of Pediatrics and Cardiovascular Research Institute, U-503; Box-0734, the University of California at San Francisco, San Francisco, CA 94143-0734
4 Department of Orthopaedic Surgery, University of Pennsylvania School of Medicine, 424 Stemmler Hall, 36th and Hamilton Walk, Philadelphia, PA 19104
5 Departments of Medicine and Pharmacology and Center for Inherited Heart Disease, Vanderbilt University School of Medicine, 2220 Pierce Avenue, 383 Preston Research Building, Nashville, TN 37232
6 Department of Public Health Sciences, University of California at Davis, One Shields Avenue, Davis, CA 95616
The Journal of Bone & Joint Surgery.  2010; 92:686-691  doi:10.2106/JBJS.I.00705
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Abstract

Background: 

Fibrodysplasia ossificans progressiva, a rare genetic disorder of progressive extraskeletal ossification, is the most disabling form of heterotopic ossification in humans. However, little is known about the lifespan or causes of mortality in these patients. We undertook this study to determine the lifespan and causes of mortality in individuals who had fibrodysplasia ossificans progressiva.

Methods: 

We reviewed comprehensive mortality reports from two large registries of patients with fibrodysplasia ossificans progressiva. Together, these registries comprise >90% of all known patients with this condition in the world. We noted the sex, dates of birth and death, and the cause of death for each individual. We verified the cause of death with extensive medical records, when available. We also collected date of birth, current age, and sex information for each living patient member of the International Fibrodysplasia Ossificans Progressiva Association.

Results: 

Sixty deaths (thirty male and thirty female patients) were reported in the fibrodysplasia ossificans progressiva community during a thirty-three-year-period. For all sixty patients, the median age at the time of death was forty years (range, three to seventy-seven years). Data were sufficient to establish the cause of death in forty-eight (80%) of the sixty individuals. The median age at the time of death for the forty-eight patients (twenty-four male and twenty-four female patients) with an established cause of death was also forty years. The median lifespan estimated from the 371 individuals in the international fibrodysplasia ossificans progressiva community who were alive and the sixty who had died was fifty-six years (95% confidence interval, fifty-one to sixty years). The most common causes of death in patients with fibrodysplasia ossificans progressiva were cardiorespiratory failure from thoracic insufficiency syndrome (54%; median age, forty-two years) and pneumonia (15%; median age, forty years).

Conclusions: 

Fibrodysplasia ossificans progressiva is not only an extremely disabling disease but also a condition of considerably shortened lifespan. The most common cause of death in patients with fibrodysplasia ossificans progressiva is cardiorespiratory failure from thoracic insufficiency syndrome.

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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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