Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants with cystic fibrosis

被引：81

作者：

Ranganathan, SC

Bush, A

Dezateux, C

Carr, SB

Hoo, AF

Lum, S

Madge, S

Price, J

Stroobant, J

Wade, A

Wallis, C

Wyatt, H

Stocks, J

机构：

[1] Inst Child Hlth, Intens Therapy & Resp Med Unit, London WC1N 1EH, England

[2] Royal Brompton Hosp, Dept Paediat Resp Med, London SW3 6LY, England

[3] Inst Child Hlth, Ctr Paediat Epidemiol & Biostat, London, England

[4] Royal London Hosp, Dept Child Hlth, London E1 1BB, England

[5] Homerton Univ Hosp, Neonatol Unit, London, England

[6] Great Ormond St Hosp Sick Children, Dept Paediat Resp Med, London WC1N 3JH, England

[7] Kings Coll Hosp London, Dept Child Hlth, London, England

[8] Univ Hosp Lewisham, Dept Child Hlth, London, England

来源：

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE | 2002年 / 166卷 / 10期

关键词：

cystic fibrosis; respiratory function tests; infant; early intervention; forced expiration;

D O I：

10.1164/rccm.2202041

中图分类号：

R4 [临床医学];

学科分类号：

1002 ; 100602 ;

摘要：

Portex Anaesthesia, Intensive Therapy and Respiratory Medicine Unit, Institute of Child Health; Department of Paediatric Respiratory Medicine, Royal Brompton Hospital; Centre for Paediatric Epidemiology and Biostatistics, Institute of Child Health; Department of Child Health, Royal London Hospital; Neonatal Unit, Homerton University Hospital; Department of Paediatric Respiratory Medicine, Great Ormond Street Hospital; Department of Child Health, King's College Hospital; and Department of Child Health, University Hospital Lewisham, London, United Kingdom.

引用

页码：1350 / 1357

页数：8

共 12 条

[1] Effect of airway inflation pressure on forced expiratory maneuvers from raised lung volume in infants
Lum, S
Hoo, AF
Stocks, J
PEDIATRIC PULMONOLOGY, 2002, 33 (02) : 130 - 134
[2] Lung function tests in neonates and infants with chronic lung disease:: Forced expiratory maneuvers
Lum, S
Hülskamp, G
Merkus, P
Baraldi, E
Hofhuis, W
Stocks, J
PEDIATRIC PULMONOLOGY, 2006, 41 (03) : 199 - 214
[3] Airway function in infants newly diagnosed with cystic fibrosis
Ranganathan, SC
Dezateux, C
Bush, A
Carr, SB
Castle, RA
Madge, S
Price, J
Stroobant, J
Wade, A
Wallis, C
Stocks, J
LANCET, 2001, 358 (9297): : 1964 - 1965
[4] Comparison of normal infants and infants with cystic fibrosis using forced expiratory flows breathing air and heliox
Davis, S
Jones, M
Kisling, J
Howard, J
Tepper, RS
PEDIATRIC PULMONOLOGY, 2001, 31 (01) : 17 - 23
[5] PARTIAL EXPIRATORY FLOW-VOLUME LOOPS IN INFANTS WITH CYSTIC-FIBROSIS
BEARDSMORE, CS
AMIT, M
KATZNELSON, D
GODFREY, S
ISRAEL JOURNAL OF MEDICAL SCIENCES, 1983, 19 (09): : 868 - 868
[6] Forced Expiratory Volume in 1 Second Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function
Morgan, Wayne J.
VanDevanter, Donald R.
Pasta, David J.
Foreman, Aimee J.
Wagener, Jeffrey S.
Konstan, Michael W.
JOURNAL OF PEDIATRICS, 2016, 169 : 116 - +
[7] Comparison of normal and cystic fibrosis (CF) infants using forced expiratory flows breathing heliox
Davis, S
Jones, M
Kisling, J
Howard, J
Tepper, RS
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (03) : A504 - A504
[8] Forced Expiratory Volume in 1 Second Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function (vol 169, pg 116, 2016)
Morgan
JOURNAL OF PEDIATRICS, 2018, 197 : 322 - 322
[9] ASSESSMENT OF AIRWAY FUNCTION IN INFANTS WITH CYSTIC FIBROSIS DETECTED THROUGH NEONATAL SCREENING AND BY SYMPTOMS IN ARGENTINA
D'Alessandro, V
Renteria, F.
Prates, S.
Segal, E.
PEDIATRIC PULMONOLOGY, 2009, : 362 - 362
[10] FORCED EXPIRATIONS AGAINST AN EXPIRATORY RESISTANCE IMPROVE MUCUS CLEARANCE AND LUNG-FUNCTION IN CHILDREN WITH CYSTIC-FIBROSIS (CF)
ZACH, MS
OBERWALDNER, B
EVANS, JC
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1986, 133 (04): : A248 - A248

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