Estimation of cancer mortality associated with repetitive computed tomography scanning

被引:134
作者
de Jong, PA
Mayo, JR
Golmohammadi, K
Nakano, Y
Lequin, MH
Tiddens, HAWM
Aldrich, J
Coxson, HO
Sin, DD
机构
[1] Erasmus MC Sophia, Dept Pediat Pulmonol & Allergol, NL-3015 GJ Rotterdam, Netherlands
[2] Erasmus MC Sophia, Dept Pediat Radiol, NL-3015 GJ Rotterdam, Netherlands
[3] St Pauls Hosp, James Hogg iCAPTURE Ctr Cardiovasc & Pulm Res, Vancouver, BC V6Z 1Y6, Canada
[4] Univ British Columbia, Dept Med, Div Pulm, Vancouver, BC V5Z 1M9, Canada
[5] Vancouver Gen Hosp, Dept Radiol, Subdiv Radiat Phys, Vancouver, BC V5Z 1M9, Canada
[6] Univ Alberta, Dept Radiol & Diagnost Imaging, Edmonton, AB, Canada
[7] Shiga Univ Med Sci, Dept Cardiovasc & Resp Med, Shiga, Japan
关键词
cancer mortality; computational model; computed tomography; cystic fibrosis; radiation;
D O I
10.1164/rccm.200505-810OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Low-dose radiation from computed tomography (CT) may increase the risk of certain cancers, especially in children. Objective: We sought to estimate the excess all-cause and cancer-specific mortality, which may be associated with repeated CT scanning of patients with cystic fibrosis (CF). Methods: The radiation dose was calculated for a published CF surveillance CT scanning protocol of biennial CT scans, and the risk per scan was estimated using atom-bomb survivor data. A computational model was developed to calculate the excess mortality in a CF cohort associated with radiation from the CT scan and to evaluate the effects of background survival, scanning interval, and level of CT radiation used. The model assumed that there would be no survival benefits associated with repeated surveillance CT scanning. Results: The average radiation dose for the published CT protocol was 1 mSv. Survival reduction associated with annual scans from age 2 yr until death was approximately 1 mo and 2 yr for CF cohorts, with a median survival of 26 and 50 yr, respectively. Corresponding cumulative cancer mortality was approximately 2 and 13% at age 40 and 65 yr, respectively. Biennial CT scanning reduced all-cause and cumulative cancer mortality by half. Conclusion: Routine lifelong annual CT scans carry a low risk of radiation-induced mortality in CF. However, as the overall survival increases for patients with CF, the risk of radiation-induced mortality may modestly increase. These data indicate that radiation dose must be considered in routine CT imaging strategies for patients with CF, to ensure that benefits outweigh the risks.
引用
收藏
页码:199 / 203
页数:5
相关论文
共 38 条
[11]   Relationship between sputum inflammatory markers, lung function, and lung pathology on high-resolution computed tomography in children with cystic fibrosis [J].
Dakin, CJ ;
Pereira, JK ;
Henry, RL ;
Wang, H ;
Morton, JR .
PEDIATRIC PULMONOLOGY, 2002, 33 (06) :475-482
[12]  
de Jong PA, 2004, EUR RESPIR J, V24, P1071, DOI 10.1183/09031936.04.10099804
[13]   Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis [J].
de Jong, PA ;
Nakano, Y ;
Lequin, MH ;
Mayo, JR ;
Woods, R ;
Paré, PD ;
Tiddens, HAWM .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (01) :93-97
[14]   Pulmonary disease assessment in cystic fibrosis:: Comparison of CT scoring systems and value of bronchial and arterial dimension measurements [J].
de Jong, PA ;
Ottink, MD ;
Robben, SGF ;
Lequin, MH ;
Hop, WCJ ;
Hendriks, JJE ;
Paré, PD ;
Tiddens, HAWM .
RADIOLOGY, 2004, 231 (02) :434-439
[15]  
DEJONG PA, 2005, P AM THORAC SOC, V2, pA576
[16]  
DEJONG PA, 2005, THORAX 1021
[17]   EVOLVING DEMOGRAPHICS OF CYSTIC-FIBROSIS [J].
FIEL, SB ;
FITZSIMMONS, S ;
SCHIDLOW, D .
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 15 (05) :349-355
[18]  
FIEL SB, 2005, P AM THORAC SOC, V2, pA576
[19]   International comparison of median age at death from cystic fibrosis [J].
Fogarty, A ;
Hubbard, R ;
Britton, J .
CHEST, 2000, 117 (06) :1656-1660
[20]   Pathophysiology and management of pulmonary infections in cystic fibrosis [J].
Gibson, RL ;
Burns, JL ;
Ramsey, BW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) :918-951