The evolution of the mitochondrial disease diagnostic odyssey

Mitochondrial diseases often require multiple years and clinicians to diagnose. We lack knowledge of the stages of this diagnostic odyssey, and factors that affect it. Our goals are to report the results of the 2018 Odyssey2 (OD2) survey of patients with a medical diagnosis of mitochondrial disease;...

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Veröffentlicht in:Orphanet journal of rare diseases 2023-06, Vol.18 (1), p.157-157, Article 157
Hauptverfasser: Thompson, John L P, Karaa, Amel, Pham, Hung, Yeske, Philip, Krischer, Jeffrey, Xiao, Yi, Long, Yuelin, Kramer, Amanda, Dimmock, David, Holbert, Amy, Gorski, Cliff, Engelstad, Kristin M, Buchsbaum, Richard, Rosales, Xiomara Q, Hirano, Michio
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Sprache:eng
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Zusammenfassung:Mitochondrial diseases often require multiple years and clinicians to diagnose. We lack knowledge of the stages of this diagnostic odyssey, and factors that affect it. Our goals are to report the results of the 2018 Odyssey2 (OD2) survey of patients with a medical diagnosis of mitochondrial disease; and to propose steps to reduce the odyssey going forward, and procedures to evaluate them. Data are from the NIH-funded NAMDC-RDCRN-UMDF OD2 survey (N = 215). The main outcomes are Time from symptom Onset to mitochondrial disease Diagnosis (TOD) and Number of Doctors Seen during this diagnostic process (NDOCS). Expert recoding increased analyzable responses by 34% for final mitochondrial diagnosis and 39% for prior non-mitochondrial diagnosis. Only one of 122 patients who initially saw a primary care physician (PCP) received a mitochondrial diagnosis, compared to 26 of 86 (30%) who initially saw a specialist (p 
ISSN:1750-1172
1750-1172
DOI:10.1186/s13023-023-02754-x