Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva

被引:158
作者
Kitterman, JA
Kantanie, S
Rocke, DM
Kaplan, FS
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
[3] Int fibrodysplasia Ossificans Progress Assoc, Winter Springs, FL USA
[4] Univ Calif Davis, Dept Appl Sci, Div Biostat, Davis, CA 95616 USA
[5] Univ Penn, Sch Med, Dept Orthoped Surg, Philadelphia, PA 19104 USA
[6] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
关键词
D O I
10.1542/peds.2005-0469
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. Little is known about diagnostic errors for a disease worldwide. Such errors could alter the disease's natural history, especially if unwarranted interventions cause irreversible harm. Fibrodysplasia ossificans progressiva (FOP), a rare, autosomal dominant genetic disease characterized by episodes of permanent heterotopic ossification of soft tissues, occurs worldwide without racial, ethnic, or geographic predilection. There is no effective treatment, and soft-tissue trauma (eg, biopsies, surgical procedures, intramuscular injections, or mandibular blocks for dental procedures) and viral illnesses are likely to induce episodes of rapidly progressive heterotopic ossification, with resultant permanent loss of motion in the affected area. Accurate diagnoses can be made on the basis of the clinical findings of tumor-like swellings on the head, neck, back, or shoulders and characteristic short great toes with hallux valgus-like malformations and missing interphalangeal joints. On the basis of conversations with numerous individuals with FOP, we suspected that diagnostic errors with FOP are common and often associated with inappropriate and harmful diagnostic and therapeutic procedures. Objective. To document the frequency of diagnostic errors with FOP and complications resulting from misdiagnoses. Design. A questionnaire requesting detailed demographic, diagnostic, and treatment information was sent to all 269 patient-members of the International FOP Association; the sampling frame included > 90% of all known FOP patients worldwide. We received 138 replies (51% response) from 25 countries. The age range was 2 to 71 years; there were 78 female subjects and 60 male subjects. In addition, to assess the availability and adequacy of information about FOP, we reviewed 184 English-language textbooks in relevant specialties published in the past 20 years. Results. Incorrect diagnoses were given initially to 87% of individuals with FOP. This astonishing rate of diagnostic errors occurred worldwide, regardless of ethnicity, geographic background, or misdiagnosing physician's specialty. The most common incorrect diagnosis was cancer (32%). The mean period from the onset of symptoms to correct diagnosis was 4.1 years, and the median number of physicians consulted before the correct diagnosis of FOP was 6. For 67% of patients, unnecessary invasive procedures (biopsies) were performed; 68% received inappropriate therapies. Forty-nine percent of all patients reported permanent loss of mobility resulting from invasive medical interventions that caused posttraumatic ossification. Notably, only 8% of the 184 textbooks that were reviewed contained adequate descriptions of FOP, including the caution that trauma can accelerate the process of heterotopic ossification. Conclusions. Diagnostic errors and inappropriate medical procedures, which may lead to permanent harm, can alter the natural history of a disease. In FOP, the astonishing rates of diagnostic errors and inappropriate invasive medical procedures likely result from lack of physician awareness because of failure of information transfer.
引用
收藏
页码:E654 / E661
页数:8
相关论文
共 37 条
[1]   Paresis of a bone morphogenetic protein-antagonist response in a genetic disorder of heterotopic skeletogenesis [J].
Ahn, J ;
de la Peña, LS ;
Shore, EM ;
Kaplan, FS .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A (04) :667-674
[2]  
[Anonymous], 2000, ERR IS HUMAN BUILDIN, DOI DOI 10.17226/9728
[3]   White paper - Reducing the frequency of errors in medicine using information technology [J].
Bates, DW ;
Cohen, M ;
Leape, LL ;
Overhage, JM ;
Shabot, MM ;
Sheridan, T .
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, 2001, 8 (04) :299-308
[4]   Analysing potential harm in Australian general practice: an incident-monitoring study [J].
Bhasale, AL ;
Miller, GC ;
Reid, SE ;
Britt, HC .
MEDICAL JOURNAL OF AUSTRALIA, 1998, 169 (02) :73-76
[5]   Analysis of the institutional volume-outcome relations for balloon angioplasty and stenting in the stent era in California [J].
Brown, DL .
AMERICAN HEART JOURNAL, 2003, 146 (06) :1071-1076
[6]   THE NATURAL-HISTORY OF HETEROTOPIC OSSIFICATION IN PATIENTS WHO HAVE FIBRODYSPLASIA OSSIFICANS PROGRESSIVA - A STUDY OF 44 PATIENTS [J].
COHEN, RB ;
HAHN, GV ;
TABAS, JA ;
PEEPER, J ;
LEVITZ, CL ;
SANDO, A ;
SANDO, N ;
ZASLOFF, M ;
KAPLAN, FS .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1993, 75A (02) :215-219
[7]  
CONNOR JM, 1982, J MED GENET, V19, P35, DOI 10.1136/jmg.19.1.35
[8]   FIBRODYSPLASIA OSSIFICANS PROGRESSIVA - THE CLINICAL-FEATURES AND NATURAL-HISTORY OF 34 PATIENTS [J].
CONNOR, JM ;
EVANS, DAP .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1982, 64 (01) :76-83
[9]   Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA [J].
de la Peña, LS ;
Billings, PC ;
Fiori, JL ;
Ahn, J ;
Kaplan, FS ;
Shore, EM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (07) :1168-1176
[10]  
de Rijk MC, 2000, NEUROLOGY, V54, pS21