Children with pneumonia: how do they present and how are they managed?

被引:47
作者
Clark, Julia E.
Hammal, Donna
Spencer, David
Hampton, Fiona
机构
[1] Newcastle Gen Hosp, Dept Paediat Infect Dis, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[2] Royal Victoria Infirm, SCMS Child Hlth, Sir James Spence Inst, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[3] Freeman Rd Hosp, Dept Resp Paediat, Newcastle Upon Tyne, Tyne & Wear, England
[4] James Cook Univ Hosp, Dept Paediat, Middlesbrough, Cleveland, England
关键词
D O I
10.1136/adc.2006.097402
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: To describe the spectrum of clinical features and management of community acquired pneumonia in the UK. Design: Prospectively recorded clinical details for all children with possible pneumonia and chest x ray ( CXR) changes in 13 hospitals in the North of England between 2001 and 2002. Results: 89% of 711 children presenting to hospital with pneumonia were admitted; 96% received antibiotics, 70% intravenously. 20% had lobar CXR changes, 3% empyema and 4% required intensive care. Respiratory rate (RR), hypoxia and dyspnoea all correlated with each other and prompted appropriate interventions. Admission in children, not infants, was independently associated with RR, oxygen saturation, lobar CXR changes and pyrexia. Neither C-reactive protein, lobar CXR changes or pyrexia were associated with severity. Children over 1 year old with perihilar CXR changes more often had severe disease (p=0.001). Initial intravenous antibiotics were associated with lobar CXR changes in infants and children and with dyspnoea, pyrexia and pleural effusion in children. The presence of pleural effusion increased duration of antibiotic treatment (p < 0.001). Cefuroxime was the most often used intravenous antibiotic in 61%. Oral antibiotics included a penicillin in 258 (46%), a macrolide in 192 (34%) and a cephalosporin in 117 (21%). Infants stayed significantly longer (p < 0.001) as did children with severe disease (p < 0.01), effusions (p=0.005) or lobar CXR changes (p <= 0.001). Conclusions: There is a high rate of intravenous antibiotic administration in hospital admissions for pneumonia. Despite lobar CXR changes not being independently associated with severe disease, initial lobar CXR changes and clinical assessment in children independently influenced management decisions, including admission and route of antibiotics.
引用
收藏
页码:394 / 398
页数:5
相关论文
共 30 条
[1]   Oral amoxicillin versus injectable penicillin for severe pneumonia in children aged 3 to 59 months: a randomised multicentre equivalency study [J].
Addo-Yobo, E ;
Chisaka, N ;
Hassan, M ;
Hibberd, P ;
Lozano, JM ;
Jeena, P ;
MacLeod, WB ;
Maulen, I ;
Patel, A ;
Qazi, S ;
Thea, DM ;
Nguyen, NTV .
LANCET, 2004, 364 (9440) :1141-1148
[2]  
ATKINSON M, 2005, ARCH DIS CHILD S, V90, pA87
[3]   Effectiveness of heptavalent pneumococcal conjugate vaccine in children younger than five years of age for prevention of pneumonia [J].
Black, SB ;
Shinefield, HR ;
Ling, S ;
Hansen, J ;
Fireman, B ;
Spring, D ;
Noyes, J ;
Lewis, E ;
Ray, P ;
Lee, J ;
Hackell, J .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2002, 21 (09) :810-815
[4]  
*BMJ PUBL GROUP, 2005, BNF CHILDREN
[5]  
CHERIAN T, 1988, LANCET, V2, P125
[6]   Rationalised prescribing for community acquired pneumonia: a closed loop audit [J].
Clements, H ;
Stephenson, T ;
Gabriel, V ;
Harrison, T ;
Millar, M ;
Smyth, A ;
Tong, W ;
Linton, CJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 2000, 83 (04) :320-324
[7]   Clinical features, aetiology and outcome of empyema in children in the north east of England [J].
Eastham, KM ;
Freeman, R ;
Kearns, AM ;
Eltringham, G ;
Clark, J ;
Leeming, J ;
Spencer, DA .
THORAX, 2004, 59 (06) :522-525
[8]  
Esposito S, 2001, EUR J CLIN MICROBIOL, V20, P647
[9]   Leptin and the obesity hypoventilation syndrome: a leap of faith? [J].
Fitzpatrick, M .
THORAX, 2002, 57 (01) :1-2
[10]   CLINICAL SIGNS OF PNEUMONIA IN CHILDREN [J].
HARARI, M ;
SHANN, F ;
SPOONER, V ;
MEISNER, S ;
CARNEY, M ;
DECAMPO, J .
LANCET, 1991, 338 (8772) :928-930