BRONCHOPULMONARY DYSPLASIA - IMPROVEMENT IN LUNG-FUNCTION BETWEEN 7 AND 10 YEARS OF AGE

被引:80
作者
BLAYNEY, M
KEREM, E
WHYTE, H
OBRODOVICH, H
机构
[1] HOSP SICK CHILDREN, DIV NEONATOL, 555 UNIV AVE, TORONTO M5G 1X8, ONTARIO, CANADA
[2] HOSP SICK CHILDREN, DIV CHEST, TORONTO M5G 1X8, ONTARIO, CANADA
关键词
D O I
10.1016/S0022-3476(05)80483-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To evaluate the natural history of bronchopulmonary dysplasia, we studied the same 32 patients at a mean age of 7 and 10 years. The group as a whole had normal height and weight percentiles, and each child grew along his or her established somatic growth curve. Although some children had abnormal values, the group maintained a normal mean total lung capacity and functional residual capacity. The mean residual volume and the residual volume/total lung capacity ratios were elevated at both ages. At age 7 years the 19 patients (59%) who had a forced expiratory volume in 1 second (FEV1) of < 80% had "catch up" improvement by 10 years of age (65 +/- 11% to 72 +/- 16% of predicted value; p < 0.05). All the children who had a normal FEV1 at 7 years of age continued to have a normal FEV1 at age 10 years. Resting single-breath carbon monoxide uptake by the lung was normal when measured at age 10 years. The majority of patients had a positive methacholine challenge test result at both ages, although there was a low incidence of clinically diagnosed asthma. This study demonstrates that patients with bronchopulmonary dysplasia who have normal lung function at age 7 have had normal lung growth and that those with evidence of mild to moderate lung disease have continued lung growth or repair, or both, during their school years.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 19 条
[1]   CHILDHOOD SEQUELAE OF INFANT LUNG-DISEASE - EXERCISE AND PULMONARY-FUNCTION ABNORMALITIES AFTER BRONCHOPULMONARY DYSPLASIA [J].
BADER, D ;
RAMOS, AD ;
LEW, CD ;
PLATZKER, ACG ;
STABILE, MW ;
KEENS, TG .
JOURNAL OF PEDIATRICS, 1987, 110 (05) :693-699
[2]   THE LONG-TERM PULMONARY SEQUELAE OF PREMATURITY - THE ROLE OF FAMILIAL AIRWAY HYPERREACTIVITY AND THE RESPIRATORY-DISTRESS SYNDROME [J].
BERTRAND, JM ;
RILEY, SP ;
POPKIN, J ;
COATES, AL .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (12) :742-745
[3]  
Brody JS, 1986, HDB PHYSL 3, V3, P355
[4]   STANDARDIZATION OF BRONCHIAL INHALATION CHALLENGE PROCEDURES [J].
CHAI, H ;
FARR, RS ;
FROEHLICH, LA ;
MATHISON, DA ;
MCLEAN, JA ;
ROSENTHAL, RR ;
SHEFFER, AL ;
SPECTOR, SL ;
TOWNLEY, RG .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1975, 56 (04) :323-327
[5]   AIRWAY RESPONSIVENESS IN LOW-BIRTH-WEIGHT CHILDREN AND THEIR MOTHERS [J].
CHAN, KN ;
NOBLEJAMIESON, CM ;
ELLIMAN, A ;
BRYAN, EM ;
ABER, VR ;
SILVERMAN, M .
ARCHIVES OF DISEASE IN CHILDHOOD, 1988, 63 (08) :905-910
[6]  
CRAPO RO, 1987, AM REV RESPIR DIS, V135, P1221
[7]   RAPID PLETHYSMOGRAPHIC METHOD FOR MEASURING THORACIC GAS VOLUME - COMPARISON WITH A NITROGEN WASHOUT METHOD FOR MEASURING FUNCTIONAL RESIDUAL CAPACITY IN NORMAL SUBJECTS [J].
DUBOIS, AB ;
BOTELHO, SY ;
BEDELL, GN ;
MARSHALL, R ;
COMROE, JH .
JOURNAL OF CLINICAL INVESTIGATION, 1956, 35 (03) :322-326
[8]   PREMATURITY IS ASSOCIATED WITH ABNORMAL AIRWAY FUNCTION IN CHILDHOOD [J].
GALDESSEBALDT, M ;
SHELLER, JR ;
GROGAARD, J ;
STAHLMAN, M .
PEDIATRIC PULMONOLOGY, 1989, 7 (04) :259-264
[9]   SERIAL DETERMINATION OF PULMONARY-FUNCTION IN INFANTS WITH CHRONIC LUNG-DISEASE [J].
GERHARDT, T ;
HEHRE, D ;
FELLER, R ;
REIFENBERG, L ;
BANCALARI, E .
JOURNAL OF PEDIATRICS, 1987, 110 (03) :448-456
[10]   CARDIORESPIRATORY STATUS IN LONG-TERM SURVIVORS OF PREMATURITY, WITH AND WITHOUT HYALINE-MEMBRANE DISEASE [J].
MACLUSKY, IB ;
STRINGER, D ;
ZARFEN, J ;
SMALLHORN, J ;
LEVISON, H .
PEDIATRIC PULMONOLOGY, 1986, 2 (02) :94-102