The Natural History of Cardiac and Pulmonary Function Decline in Patients With Duchenne Muscular Dystrophy

被引:47
作者
Roberto, Rolando [1 ]
Fritz, Anto [1 ]
Hagar, Yolanda [2 ]
Boice, Braden [3 ]
Skalsky, Andrew [4 ]
Hwang, Hosun [1 ]
Beckett, Laurel [2 ]
McDonald, Craig [4 ]
Gupta, Munish [1 ]
机构
[1] Univ Calif Davis, Dept Orthoped, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Publ Hlth Sci, Div Biostat, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Sch Med, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Dept Phys Med & Rehabil, Sacramento, CA 95817 USA
关键词
Duchennes Dystrophy; neuromuscular scoliosis; pulmonary function; cardiomyopathy; ADOLESCENT IDIOPATHIC SCOLIOSIS; RESPIRATORY-FUNCTION; SPINAL DEFORMITY; LUNG-FUNCTION; SURGERY; FUSION; PROGRESSION; FIXATION; DISEASES;
D O I
10.1097/BRS.0b013e3181fea1ed
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. Retrospective review of scoliosis progression, pulmonary and cardiac function in a series of patients with Duchenne Muscular Dystrophy (DMD). Objective. To determine whether operative treatment of scoliosis decreases the rate of pulmonary function loss in patients with DMD. Summary of Background Data. It is generally accepted that surgical intervention should be undertaken in DMD scoliosis once curve sizes reach 35 degrees to allow intervention before critical respiratory decline has occurred. There are conflicting reports, however, regarding the effect of scoliosis stabilization on the rate of pulmonary function decline when compared to nonoperative cohorts. Methods. We reviewed spinal radiographs, echocardiograms, and spirometry, hospital, and operative records of all patients seen at our tertiary referral center from July 1, 1992 to June 1, 2007. Data were recorded to Microsoft Excel (Microsoft, Redmond, WA) and analyzed with SAS (SAS Institute, Cary, NC) and R statistical processing software (www.r-project.org). Results. The percent predicted forced vital capacity (PPFVC) decreased 5% per year before operation. The mean PPFVC was 54% (SD = 21%) before operation with a mean postoperative PPFVC of 43% (SD = 14%). Surgical treatment was associated with a 12% decline in PPFVC independent of other treatment variables. PPFVC after operation declined at a rate of 1% per year and while this rate was lower, it was not significantly different than the rate of decline present before operation (P = 0.18). Cardiac function as measured by left ventricular fractional shortening declined at a rate of 1% per year with most individuals exhibiting a left ventricular fractional shortening rate of more than 30 before operation. Conclusion. Operative treatment of scoliosis in DMD using the Luque Galveston method was associated with a reduction of forced vital capacity related to operation. The rate of pulmonary function decline after operation was not significantly reduced when compared with the rate of preoperative forced vital capacity decline.
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收藏
页码:E1009 / E1017
页数:9
相关论文
共 27 条
[1]   Deflazacort treatment of Duchenne muscular dystrophy [J].
Biggar, WD ;
Gingras, M ;
Fehlings, DL ;
Harris, VA ;
Steele, CA .
JOURNAL OF PEDIATRICS, 2001, 138 (01) :45-50
[2]   DUCHENNE MUSCULAR-DYSTROPHY - PATTERNS OF CLINICAL PROGRESSION AND EFFECTS OF SUPPORTIVE THERAPY [J].
BROOKE, MH ;
FENICHEL, GM ;
GRIGGS, RC ;
MENDELL, JR ;
MOXLEY, R ;
FLORENCE, J ;
KING, WM ;
PANDYA, S ;
ROBISON, J ;
SCHIERBECKER, J ;
SIGNORE, L ;
MILLER, JP ;
GILDER, BF ;
KAISER, KK ;
MANDEL, S ;
ARFKEN, C .
NEUROLOGY, 1989, 39 (04) :475-481
[3]  
Galasko C S, 1995, Eur Spine J, V4, P263, DOI 10.1007/BF00301031
[4]   Clinical implications of maximal respiratory pressure determinations for individuals with Duchenne Muscular dystrophy [J].
Hahn, A ;
Bach, JR ;
Delaubier, A ;
RenardelIrani, A ;
Guillon, G ;
Rideau, Y .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1997, 78 (01) :1-6
[5]   CHARACTERIZATION OF DYSTROPHIN IN MUSCLE-BIOPSY SPECIMENS FROM PATIENTS WITH DUCHENNES OR BECKERS MUSCULAR-DYSTROPHY [J].
HOFFMAN, EP ;
FISCHBECK, KH ;
BROWN, RH ;
JOHNSON, M ;
MEDORI, R ;
LOIKE, JD ;
HARRIS, JB ;
WATERSTON, R ;
BROOKE, M ;
SPECHT, L ;
KUPSKY, W ;
CHAMBERLAIN, J ;
CASKEY, CT ;
SHAPIRO, F ;
KUNKEL, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (21) :1363-1368
[6]   PULMONARY-FUNCTION IN DUCHENNE MUSCULAR-DYSTROPHY RELATED TO STAGE OF DISEASE [J].
INKLEY, SR ;
OLDENBURG, FC ;
VIGNOS, PJ .
AMERICAN JOURNAL OF MEDICINE, 1974, 56 (03) :297-306
[7]   EVALUATION OF PULMONARY-FUNCTION IN MUSCULAR-DYSTROPHY PATIENTS REQUIRING SPINAL SURGERY [J].
JENKINS, JG ;
BOHN, D ;
EDMONDS, JF ;
LEVISON, H ;
BARKER, GA .
CRITICAL CARE MEDICINE, 1982, 10 (10) :645-649
[8]   Scoliosis in patients with Duchenne muscular dystrophy [J].
Karol, Lori A. .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2007, 89A :155-162
[9]   EFFECT OF SPINAL SURGERY ON LUNG-FUNCTION IN DUCHENNE MUSCULAR-DYSTROPHY [J].
KENNEDY, JD ;
STAPLES, AJ ;
BROOK, PD ;
PARSONS, DW ;
SUTHERLAND, AD ;
MARTIN, AJ ;
STERN, LM ;
FOSTER, BK .
THORAX, 1995, 50 (11) :1173-1178
[10]   Pulmonary function in adolescent idiopathic scoliosis relative to the surgical procedure [J].
Kim, YJJ ;
Lenke, LG ;
Bridwell, KH ;
Kim, KL ;
Steger-May, K .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2005, 87A (07) :1534-1541