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. 1989 Feb 25;298(6672):483–487. doi: 10.1136/bmj.298.6672.483

Effects of social class, sex, and region of residence on age at death from cystic fibrosis.

J R Britton 1
PMCID: PMC1835801  PMID: 2495076

Abstract

To determine the time trend in age at death from cystic fibrosis and the independent effects of social class, sex, and region of residence mortality data for England and Wales from 1959 to 1986 were analysed. Median age at death increased from 6 months in 1959 to 17 years in 1986 and was higher in most years from 1970 in male patients (by one to six years) and in social classes with non-manual occupations (by one to 12 years). Independent odds ratios for death above the median age for the year of death (calculated for years from 1974, when regions of residence were coded by regional health authority area) were 1.47 (95% confidence interval 1.16 to 1.87) in male compared with female patients and 2.75 (2.16 to 3.52) in non-manual compared with manual social classes. The independent odds of death at above the median age also varied significantly among regions of residence by a ratio of up to 2.67. Social class, sex, and region of residence are all potential determinants of survival of patients with cystic fibrosis. Social class is particularly likely to confound the effect of management in specialist centres on survival.

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Selected References

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  1. ANDERSEN D. H. Cystic fibrosis of the pancreas. J Chronic Dis. 1958 Jan;7(1):58–90. doi: 10.1016/0021-9681(58)90185-1. [DOI] [PubMed] [Google Scholar]
  2. ANDERSON E. G., LASZLO G., BROWN H. M. A CASE OF MUCOVISCIDOSIS IN AN ADULT. Br J Dis Chest. 1965 Jul;59:173–176. doi: 10.1016/s0007-0971(65)80008-0. [DOI] [PubMed] [Google Scholar]
  3. Allan J. L., Robbie M., Phelan P. D., Danks D. M. The incidence and presentation of cystic fibrosis in Victoria 1955-1978. Aust Paediatr J. 1980 Dec;16(4):270–273. doi: 10.1111/j.1440-1754.1980.tb01314.x. [DOI] [PubMed] [Google Scholar]
  4. Corey M., Levison H., Crozier D. Five- to seven-year course of pulmonary function in cystic fibrosis. Am Rev Respir Dis. 1976 Dec;114(6):1085–1092. doi: 10.1164/arrd.1976.114.6.1085. [DOI] [PubMed] [Google Scholar]
  5. Corey M., McLaughlin F. J., Williams M., Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41(6):583–591. doi: 10.1016/0895-4356(88)90063-7. [DOI] [PubMed] [Google Scholar]
  6. DOOLEY R. R., GUILMETTE F., LEUBNER H., PATTERSON P. R., SHWACHMAN H., WEIL C. Cystic fibrosis of the pancreas with varying degrees of pancreatic insufficiency. AMA J Dis Child. 1956 Oct;92(4):347–368. doi: 10.1001/archpedi.1956.02060030341004. [DOI] [PubMed] [Google Scholar]
  7. Dynesen H., Flensborg E. W. Prognosen for cystisk fibrose i Danmark 1945-1974. Betydning af centraliseret kontrol og behandling. Ugeskr Laeger. 1978 Feb 27;140(9):463–470. [PubMed] [Google Scholar]
  8. George L., Norman A. P. Life tables for cystic fibrosis. Arch Dis Child. 1971 Apr;46(246):139–143. doi: 10.1136/adc.46.246.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hill D. J., Martin A. J., Davidson G. P., Smith G. S. Survival of cystic fibrosis patients in South Australia. Evidence that cystic fibrosis centre care leads to better survival. Med J Aust. 1985 Sep 16;143(6):230–232. doi: 10.5694/j.1326-5377.1985.tb122953.x. [DOI] [PubMed] [Google Scholar]
  10. Huang N. N., Macri C. N., Girone J., Sproul A. Survival of patients with cystic fibrosis. Am J Dis Child. 1970 Oct;120(4):289–295. doi: 10.1001/archpedi.1970.02100090063002. [DOI] [PubMed] [Google Scholar]
  11. Hudson I., Phelan P. D. Are sex, age at diagnosis, or mode of presentation prognostic factors for cystic fibrosis? Pediatr Pulmonol. 1987 Sep-Oct;3(5):288–297. doi: 10.1002/ppul.1950030503. [DOI] [PubMed] [Google Scholar]
  12. KARLISH A. J., TARNOKY A. L. Mucoviscidosis as a factor in chronic lung disease in adults. Lancet. 1960 Sep 3;2(7149):514–515. doi: 10.1016/s0140-6736(60)91542-7. [DOI] [PubMed] [Google Scholar]
  13. McPartlin J. F., Dickson J. A., Swain V. A. Meconium ileus. Immediate and long-term survival. Arch Dis Child. 1972 Apr;47(252):207–210. doi: 10.1136/adc.47.252.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Penketh A. R., Wise A., Mearns M. B., Hodson M. E., Batten J. C. Cystic fibrosis in adolescents and adults. Thorax. 1987 Jul;42(7):526–532. doi: 10.1136/thx.42.7.526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Phelan P. D., Allan J. L., Landau L. I., Barnes G. L. Improved survival of patients with cystic fibrosis. Med J Aust. 1979 Apr 7;1(7):261–263. doi: 10.5694/j.1326-5377.1979.tb112071.x. [DOI] [PubMed] [Google Scholar]
  16. Phelan P., Hey E. Cystic fibrosis mortality in England and Wales and in Victoria, Australia 1976-80. Arch Dis Child. 1984 Jan;59(1):71–73. doi: 10.1136/adc.59.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pogue R. E., Warwick W. J. Cystic fibrosis. A new challenge to internal medicine. Minn Med. 1969 Sep;52(9):1551–1555. [PubMed] [Google Scholar]
  18. Stern R. C., Boat T. F., Doershuk C. F., Tucker A. S., Primiano F. P., Jr, Matthews L. W. Course of cystic fibrosis in 95 patients. J Pediatr. 1976 Sep;89(3):406–411. doi: 10.1016/s0022-3476(76)80537-9. [DOI] [PubMed] [Google Scholar]
  19. Tomashefski J. F., Christoforidis A. J., Abdullah A. K. Cystic fibrosis in young adults: an overlooked diagnosis, with emphasis on pulmonary function and radiological patterns. Chest. 1970 Jan;57(1):28–36. doi: 10.1378/chest.57.1.28. [DOI] [PubMed] [Google Scholar]
  20. Warwick W. J., Pogue R. E., Gerber H. U., Nesbitt C. J. Survival patterns in cyctic fibrosis. J Chronic Dis. 1975 Dec;28(11-12):609–622. doi: 10.1016/0021-9681(75)90074-0. [DOI] [PubMed] [Google Scholar]
  21. Wilmott R. W., Tyson S. L., Dinwiddie R., Matthew D. J. Survival rates in cystic fibrosis. Arch Dis Child. 1983 Oct;58(10):835–836. doi: 10.1136/adc.58.10.835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Wilmott R. W., Tyson S. L., Matthew D. J. Cystic fibrosis survival rates. The influences of allergy and Pseudomonas aeruginosa. Am J Dis Child. 1985 Jul;139(7):669–671. doi: 10.1001/archpedi.1985.02140090031019. [DOI] [PubMed] [Google Scholar]
  23. Wood R. E., Boat T. F., Doershuk C. F. Cystic fibrosis. Am Rev Respir Dis. 1976 Jun;113(6):833–878. doi: 10.1164/arrd.1976.113.6.833. [DOI] [PubMed] [Google Scholar]

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