Disordered breathing during sleep in patients with mucopolysaccharidoses

被引:75
作者
Leighton, SEJ
Papsin, B
Vellodi, A
Dinwiddie, R
Lane, R
机构
[1] Great Ormond St Hosp Children NHS Trust, Dept Otolaryngol, London WC1N 3JH, England
[2] Great Ormond St Hosp Children NHS Trust, Metab Unit, London WC1N 3JH, England
[3] Inst Child Hlth, Portex Anaesthesia Intens Therapy & Resp Med Unit, London WC1N 1EH, England
关键词
sleep apnoea; mucopolysaccharidoses; sleep; child;
D O I
10.1016/S0165-5876(01)00417-7
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Obstructive sleep apnoea (OSA) has been reported as a feature of children with mucopolysaccharidoses (MPS). However, the incidence and severity of OSA with respect to disease type is poorly defined. The aim of the present study was to measure objectively the degree of OSA in a group of children with a range of MPS syndromes. Methods: In a cross-sectional study, cardiopulmonary sleep studies were performed during unsedated sleep in 26 children with MPS over a period of 2 years. Scores of OSA severity based upon clinical history and upon objective sleep study data were made in each case and compared. Results: OSA was present in 24/26 patients, and ranged in severity from mild to severe. OSA was most marked in MPS type IH (Hurler syndrome) followed by types IHS (Hurler-Scheie syndrome) and II (Hunter syndrome). Frequent arousals and poor sleep quality, not suspected clinically, were noted in several patients. There was agreement between the clinical and objective scoring systems in only 17/26 patients (65%) with clinical history scores tending to underestimate the most severe cases (5/26 cases) and overestimate the severity in the mild casts (4/26 cases). Conclusions: Obstructive respiratory problems are frequent in MPS patients and there are differences in severity of OSA between the different MPS types. Assessments of the severity of OSA based upon clinical history alone are inadequate. Our results suggest that objective sleep studies are necessary to evaluate these cases, to monitor clinical outcome and to assess the effects of therapeutic intervention. Prospective studies in larger numbers of patients are needed to validate these observations. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:127 / 138
页数:12
相关论文
共 27 条
[11]   BONE-MARROW TRANSPLANTATION IN THE MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-VI) - BIOCHEMICAL AND CLINICAL STATUS 24 MONTHS AFTER TRANSPLANTATION [J].
KRIVIT, W ;
PIERPONT, ME ;
AYAZ, K ;
TSAI, M ;
RAMSAY, NKC ;
KERSEY, JH ;
WEISDORF, S ;
SIBLEY, R ;
SNOVER, D ;
MCGOVERN, MM ;
SCHWARTZ, MF ;
DESNICK, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (25) :1606-1611
[12]  
LEACH J, 1992, ARCH OTOLARYNGOL, V118, P741
[13]   RESOLUTION OF OBSTRUCTIVE SLEEP-APNEA IN HURLER SYNDROME AFTER BONE-MARROW TRANSPLANTATION [J].
MALONE, BN ;
WHITLEY, CB ;
DUVALL, AJ ;
BELANI, K ;
SIBLEY, RK ;
RAMSAY, NKC ;
KERSEY, JH ;
KRIVIT, W ;
BERLINGER, NT .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1988, 15 (01) :23-31
[14]   TRACHEOBRONCHOMALACIA IN HUNTERS SYNDROME [J].
MOREHEAD, JM ;
PARSONS, DS .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1993, 26 (03) :255-261
[15]   AIRWAY-OBSTRUCTION IN HURLER SYNDROME - RADIOGRAPHIC FEATURES [J].
MYER, CM .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1991, 22 (01) :91-96
[16]   SLEEP-APNEA IN SCHEIES SYNDROME [J].
PERKS, WH ;
COOPER, RA ;
BRADBURY, S ;
HORROCKS, P ;
BALDOCK, N ;
ALLEN, A ;
VANTHOFF, W ;
WEIDMAN, G ;
PROWSE, K .
THORAX, 1980, 35 (02) :85-91
[17]   BEHAVIORAL STATES OF NEWBORN-INFANT [J].
PRECHTL, HFR .
BRAIN RESEARCH, 1974, 76 (02) :185-212
[18]   PATHOGENESIS OF UPPER AIRWAY OCCLUSION DURING SLEEP [J].
REMMERS, JE ;
DEGROOT, WJ ;
SAUERLAND, EK ;
ANCH, AM .
JOURNAL OF APPLIED PHYSIOLOGY, 1978, 44 (06) :931-938
[19]  
RUCKENSTEIN MJ, 1991, J OTOLARYNGOL, V20, P177
[20]  
SASAKI CT, 1987, LARYNGOSCOPE, V97, P280