The economic burden of spinal muscular atrophy

被引:35
作者
Armstrong, Edward P. [1 ,2 ]
Malone, Daniel C. [1 ,2 ]
Yeh, Wei-Shi [3 ]
Dahl, Georg J. [4 ]
Lee, Rees L. [5 ]
Sicignano, Nicholas [6 ]
机构
[1] Strateg Therapeut LLC, 11020 N Canada Ridge Dr, Oro Valley, AZ 85737 USA
[2] Univ Arizona, Coll Pharm, Tucson, AZ 85721 USA
[3] Biogen, Weston, MA USA
[4] Naval Med Ctr, Portsmouth, VA USA
[5] Naval Med Res Unit, Dayton, OH USA
[6] Hlth ResearchTx, Trevose, PA USA
关键词
Spinal muscular atrophy; Neuromuscular disease; Muscle disease; SURVIVAL; TYPE-1; EUROPE; CARE;
D O I
10.1080/13696998.2016.1198355
中图分类号
F [经济];
学科分类号
02 ;
摘要
Aim: To evaluate the economic burden of spinal muscular atrophy (SMA).Materials and methods: This study used Department of Defense Military Healthcare System (MHS) data from 2003-2012. Healthcare costs were determined for patients with at least one inpatient or three outpatient claims with a diagnosis of SMA before 18 years of age and who had 6 months of data after first SMA diagnosis or expired within 6 months of initial diagnosis. A comparator cohort was selected using a 3:1 match based on age and gender.Results: A total of 239 individuals with SMA diagnosis met the inclusion criteria along with 717 matched comparator patients. More patients with SMA had hospitalizations (69.5%) compared to the comparator cohort (17.2%, p<0.001). Median total expenditures across all years of data for patients with SMA were $83 652 (25-75th percentile = $29 620-228 754) vs the comparator group of $4329 (25-75(th) percentile = $1229-10 062 (p<0.001)) over an average (SD) of 6.93.6 years. The annualized mean costs of total healthcare expenditures were significantly higher for the SMA cases than the comparison cohort, $47 86288 607 compared to $1861 +/- 6374, respectively (p<0.001). The sub-group of patients with early diagnosis (n=45) had 4.3 +/- 2.9 years of observation with a median cost of $167 921 ($53 349-678 412). Mean age (SD) at first observed SMA diagnosis was 7.5 +/- 6.4 years. Mean (SD) duration of follow-up after initial SMA diagnosis was 4.8 +/- 3.3 years, with a median post-diagnosis cost of $60 213 ($18 229-192 559). The major costs for all patients were outpatient visits [median = $53 152 ($23 902-136 150)], followed by inpatient costs [median = $11 258 ($0-51 987)] and total prescription costs [median = $3167 ($943-13 283)].Limitations: The analysis is limited to the data available and may under-estimate the total cost of SMA.Conclusions: Individuals with SMA have a high degree of morbidity, particularly those diagnosed during infancy. SMA patients have significant medical expenditures and high utilization of healthcare services.
引用
收藏
页码:822 / 826
页数:5
相关论文
共 14 条
[11]   Genetic risk assessment in carrier testing for spinal muscular atrophy [J].
Ogino, S ;
Leonard, DGB ;
Rennert, H ;
Ewens, WJ ;
Wilson, RB .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 110 (04) :301-307
[12]   Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study [J].
Qian, Ying ;
McGraw, Sarah ;
Henne, Jeff ;
Jarecki, Jill ;
Hobby, Kenneth ;
Yeh, Wei-Shi .
BMC NEUROLOGY, 2015, 15
[13]   Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of &gt;72 400 specimens [J].
Sugarman, Elaine A. ;
Nagan, Narasimhan ;
Zhu, Hui ;
Akmaev, Viatcheslav R. ;
Zhou, Zhaoqing ;
Rohlfs, Elizabeth M. ;
Flynn, Kerry ;
Hendrickson, Brant C. ;
Scholl, Thomas ;
Sirko-Osadsa, Deborah Alexa ;
Allitto, Bernice A. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (01) :27-32
[14]   Consensus statement for Standard of Care in Spinal Muscular Atrophy [J].
Wang, Ching H. ;
Finkel, Richard S. ;
Bertini, Enrico S. ;
Schroth, Mary ;
Simonds, Anita ;
Wong, Brenda ;
Aloysius, Annie ;
Morrison, Leslie ;
Main, Marion ;
Crawford, Thomas O. ;
Trela, Anthony .
JOURNAL OF CHILD NEUROLOGY, 2007, 22 (08) :1027-1049