#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Position and yield of colonoscopy within the faecal occult bleeding test (FOBT) based screening program


Authors: J. Špičák 1;  P. Štirand 1;  P. Drastich 1;  M. Beneš 1;  T. Hucl 1;  P. Wohl 1;  V. Nosek 3;  Š. Suchánek 2;  M. Řehoř 3;  O. Urban 4;  M. Zavoral 2
Authors‘ workplace: Klinika hepatogastroenterologie, IKEM, Praha2Interní klinika, ÚVN Praha3Endoskopické oddělení, Nemocnice Jablonec nad Nisou4Interní oddělení, Vítkovická nemocnice, a. s., Ostrava 1
Published in: Gastroent Hepatol 2011; 65(4): 181-188
Category: Endoscopy: Original Article

Overview

Introduction, aim of the study: Colorectal carcinoma is one of the most serious malignancies. Screening may reduce its incidence as well as mortality by up to tens of percents. Each region should optimise screening with respect to the specific conditions. This prospective multicenter study aimed to provide an overview of colorectal neoplasia detection and assess the potential of colonoscopy and the screening program.

Results:
We assessed 3,400 subsequent colonoscopies performed between 2009 and 2010. In four centres the caecum and the terminal ileum were reached in 89 to 93% and in 73 to 87% of patients, respectively. Both values were significantly higher than during the 2005/2006 study. The incidence of advanced neoplasia in the age categories up to 40, 40–45, 45–50 and over 50 years was 0.9%, 4.4%, 12% and 38.1%, respectively. The most frequent location of advanced neoplasia was the rectosigmoid followed by the colon ascendens and the caecum. Only slightly over 50% of advanced neoplasia were potentially within the reach of a sigmoidoscope. In the group aged > 40 years, we assessed 2,126 colonoscopies. 564 (26.5%) were indicated within the screening. Women involved in the screening accounted for 43.4%; the incidence of advanced neoplasia was 15.5% in women and 19.1% in men. In the screened patients with positive family history, the incidence of advanced neoplasia equalled 4.3%, while it was 32.6% in the other patients. Within the screening, the incidence of advanced neoplasia was 21.2% after positive FOBT, 13.1% in primary colonoscopies and 7.4% after negative FOBT. The average age at the time of screening colono­scopies was 50 years, 58 years with diagnostic colonoscopies, 45 years with positive family history screening and 52 years with negative family history screening.

Conclusion:
The ratio of screening colonoscopies and symptomatic indications was approximately 1 to 4 in patients aged > 40 years and did not change in 4 years. The ability to reach the caecum as well as the terminal ileum increased. The detection of colorectal carcinoma and its precursors was extraordinarily high in all the subgroups. A relatively high proportion of advanced neoplasia was localised beyond the potential reach of the sigmoidoscope. Male patients prevail in the ­screening and there is a high proportion of patients with positive family history. The low yield of screening with positive family history can be explained by significantly lower age. They probably come for the examination earlier as they are informed about the risk.

Key words:
colorectal cancer – screening – colonoscopy – faecal occult blood test (FOBT) – family history


Sources

1. Brenner H, Hoffmeister M, Brenner G et al. Expected reduction of colorectal cancer incidence within 8 years after introduction of the German screening colonoscopy programe“ estimates based on 1 ,875, 708 screening colonoscopies. Eur J Cancer 2009; 45(11): 2027–2032.

2. Adler A, Roll S, Marowski B et al. Appropriateness of colonoscopy in the era of colorectal cancer screening: a prospective, multicenter study in a private-practice setting (Berlin Colonoscopy Project 1, BECOP 1). Dis Colon Rectum 2007; 50(10): 1628–1638.

3. Maar C. Increasing Public Acceptance for CRC Screening through Public Relation Campaigns and Networking. Z Gastroenterol 2008; 46 (Suppl 1): S35–S37.

4. Rex DK. Quality in colonoscopy: caecal intubation first, then what? Am J Gastroenterol 2006; 101(4): 732–734.

5. Johnson DA, Gurney MS, Volpe RJ et al. A Prospective Study of the Prevalence of Colonic Neoplasms in Asymptomatic Patiens with an Age-related Risk. Am J Gastroenterol 1990; 85(8): 969–974.

6. Rex DK, Khan AM, Shah P et al. Screening Colonoscopy in Asymptomatic Average-Risk African Americans. Gastrointest Endosc 2000; 51(5): 524–527.

7. Prajappati DN, Saeian K, Binion DG et al. Volume and yield of screening colonoscopy at a tertiary medical center after change in medicare reimbursement. Am J Gastroenterol 2003; 98(1): 194–199.

8. Imperiale TF, Ranshoff DF, Itzkowitcz SH et al. Fecal DNA versus Faecal Occult Blood for Colorectal Cancer Screening in an Average-risk Population. N Engl J Med 2004; 351(26): 2704–2714.

9. Pickhardt PJ, Choi JR, Hwang I et al. Nonadenomatous Polyps at CT colonography: Prevalence, Size Distribution, and Detection Rates. Radiology 2004; 232(3): 784–790.

10. Regula J, Rupinski M, Kraszewska E et al. Colonoscopy in Colorectal-Cancer Screening for Detection of Advanced Neoplasia. N Engl J Med 2006; 355(18): 1863–1872.

11. Kim DH, Pickhardt PJ, Taylor AJ et al. CT Colonography versus Colonoscopy for the Detection of Advanced Neoplasia. N Engl J Med 2007; 357(14): 1403–1412.

12. Frič P, Zavoral M, Dvořáková H et al. An adapter program of colorectal cicer screening – 7 years experience and cost-benenfit analysis. Hepatogastroenterology 1994; 5: 413–416.

13. Suchánek Š, Zavoral M, Majek O et al. National colorectal cicer screening programme in the Czech Republic. Gut 2010; 59, suppl. III:A84.

14. Špičák J, Štirand P, Drastich P et al. Postavení a výtěžnost koloskopie v rámci screeningového programu založeného na testu na okultní krvácení (TOK) ve stolici. Čes a Slov Gastroent a Hepatol 2010; 64(6): 4–9.

15. Bond JH. Colon polyps and cancer. Endoscopy 2003; 35(1): 27–35.

16. Atkin W, Kralj-Hans I, Wardle J et al. Colorectal cancer screening. Randomised trial of flexible sigmoidoscopy. BMJ 2010; 341: c4618.

17. Dušek L, Mužík J, Kubásková M et al. Epidemiologie zhoubných nádorů v České republice (online), Masarykova universita. http//www.svod.cz.

18. Brenner H, Hoffmeister M, Ardt V et al. Gender diferences in colorectal cancer: implications for age at initiation of screening. British Journal of Cancer 2007; 96(5): 828–831.

19. Nguyen SP, Bent S, Chen Y-H et al. Gender as a risk factor for advanced neoplasia and colorectal cancer: a systematic review and metaanalysis. Clin Gastroenhterol Hepatol 2009; 7(6): 676–681.

20. Hoffmeister M, Schmitz S, Karmrodt E et al. Male sex and smoking have a larger impact on the prevalence of colorectal neoplasia than family history of colorectal cancer. Clin Gastroenterol Hepatol 2010; 8(10): 870–876.

21. Armelao F, Paternolli C, Franceschini G et al. Colonoscopic finding in first-degree relatives of patients with colorectal cancer: a population-based screening program. Gastrointest Endosc 2011; 73(3): 527–534.

Labels
Paediatric gastroenterology Gastroenterology and hepatology Surgery

Article was published in

Gastroenterology and Hepatology

Issue 4

2011 Issue 4

Most read in this issue
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#