Identifikation von Personen mit familiärem oder hereditärem Darmkrebsrisiko mittels eines Fragebogens zur Familienanamnese

Katalinic, Alexander; Raspe, H; Waldmann, Annika

doi:10.1055/s-0028-1109469

Cited by 8 publications

(8 citation statements)

References 13 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Taking this questionnaire as a basis, Katalinic et al . found a prevalence of 8.2% of persons at increased risk in Germany in the age group of 30–54 years and 6.7% in the age group of 30–49 years respectively (Katalinic et al . 2009).…”

Section: Discussionmentioning

confidence: 99%

“…The simple three-question instrument about family history of CRC was developed to screen for individuals with an increased risk for familial or hereditary CRC. Taking this questionnaire as a basis, Katalinic et al found a prevalence of 8.2% of persons at increased risk in Germany in the age group of 30-54 years and 6.7% in the age group of 30-49 years respectively (Katalinic et al 2009). In our study, at t1, the prevalence of increased risk was 16% in both age groups and therefore highly increased compared with the German general population.…”

Section: Discussionmentioning

confidence: 99%

“…Katalinic et al . previously estimated the potential of early detection of CRC in persons with familial or hereditary risk with this questionnaire by projection (Katalinic et al . 2009).…”

Section: Introductionmentioning

confidence: 99%

“…Given a 10% prevalence of persons with a familial risk in the German general population and a maximum knowledge of all tumour cases in kindred, a total of 5.7% of all Germans in the age group 30–49 years would be classified as familial risk persons (7.2% in the age group 30–54 years). If the questionnaire was used on a population‐based level and the participation rate was 35%, approximately 542 000 persons in the age group 30–49 years (816 000 in the age group 30–54 years) would be classified as having a familial or hereditary risk for CRC (Katalinic et al . 2009).…”

Section: Introductionmentioning

confidence: 99%

“…Amsterdam criteria as well as Bethesda guidelines are diagnostic guidelines to identify individuals with familial or hereditary risk (Rodriguez-Bigas et al 1997 Comments regarding the meaning of 'Yes'-answers are provided for users. Katalinic et al previously estimated the potential of early detection of CRC in persons with familial or hereditary risk with this questionnaire by projection (Katalinic et al 2009). Given a 10% prevalence of persons with a familial risk in the German general population and a maximum knowledge of all tumour cases in kindred, a total of 5.7% of all Germans in the age group 30-49 years would be classified as familial risk persons (7.2% in the age group 30-54 years).…”

Section: Introductionmentioning

confidence: 99%

See 4 more Smart Citations

Does a screening questionnaire for familial and hereditary colorectal cancer risk work in a health insurance population?

Pieper¹,

Kolankowska²,

Jöckel³

2012

European Journal of Cancer Care

View full text Add to dashboard Cite

The aim of our study was to evaluate actual prevalence, uptake and first experiences with a questionnaire developed for early detection of colorectal cancer (CRC) in persons with familial/hereditary risk. A cross sectional study in an insurance population aged 30-54 years was conducted. Subjects with ICD-10 codes C00 to C97 and D37 to D48 were excluded. A standardised questionnaire was sent to 12,139 subjects. Three months later, subjects with a reported family history were followed by a second questionnaire. An additional telephone survey was performed to validate responses. Nineteen per cent met the inclusion criteria (mean age 45 ± 7 years, 38% men). Three hundred and seventy-three subjects (16%) were followed by a second questionnaire. Of these, 248 (66%) returned. Forty-four per cent were already aware of their increased risk of developing CRC. Awareness was associated with knowledge of CRC. One hundred subjects (41%) reported that they had informed their general practitioner (GP) or gastroenterologist. A colonoscopy or stool test was recommended to 92. Subjects who found out about their increased risk for the first time, reported significantly less frequent physician contact (GP: 20% vs. 34%, gastroenterologist: 8% vs. 21%). Results indicate that there is a need for a structured, person at risk-adapted, statutory early detection program.

show abstract

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

“…Katalinic et al . previously estimated the potential of early detection of CRC in persons with familial or hereditary risk with this questionnaire by projection (Katalinic et al . 2009).…”

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 3 more Smart Citations

Does a screening questionnaire for familial and hereditary colorectal cancer risk work in a health insurance population?

Pieper¹,

Kolankowska²,

Jöckel³

2012

European Journal of Cancer Care

View full text Add to dashboard Cite

show abstract

Colon cancer in rapidly developing countries: review of the lifestyle, dietary, consanguinity and hereditary risk factors

Bener

2010

Oncol Rev

View full text Add to dashboard Cite

Colon cancer rates are rising dramatically in once low incidence nations. These nations are undergoing rapid economic development and are known as ''nations in transition'' (NIT). This review identifies some of the most common etiological risk factors of colon cancer in these nations and evaluates the existing epidemiological evidence. The main risk factors which were found to be prevalent in NIT include: lifestyle factors such as physical inactivity, obesity and abdominal adiposity, alcohol consumption and cigarette smoking; dietary factors such as fatty food and red meat consumption. Protective factors included white meat and fiber consumption. Several studies found to have significantly higher rates of colon cancer among the young population (\40 years old). There appears to be a quantitative and qualitative increase in risk to relatives of patients diagnosed at a young age compared with those diagnosed later in life, at least part of which is likely to be the result of a hereditary susceptibility. Close relatives of patients with colon cancer are at an increased risk of developing a colon cancer. Close relatives of early onset cases warrant more intensive endoscopic screening and at an earlier age than relatives of patients diagnosed at older ages. Furthermore, these suggest the existence of genetic predispositions in these nations which need to be investigated further and have implications for screening programs. In conclusion, public health awareness campaigns promoting prevention of modifiable risk factors and screening initiatives with guidelines suited to the age-specific incidence rates of NIT are needed very urgently.

show abstract

Vorsorge bei familiärem Risiko für das kolorektale Karzinom – FARKOR-Studie – eine kritische Stellungnahme

2024

Z Gastroenterol

View full text Add to dashboard Cite

Identifikation von Personen mit familiärem oder hereditärem Darmkrebsrisiko mittels eines Fragebogens zur Familienanamnese

Abstract: If the questionnaire is used on a population-based level and the participation rate is 35 %, approximately 542 000 persons in the age group 30 - 49 years (816 000 in the age group 30 - 54 years) will be classified as having a familial or hereditary risk for colorectal cancer.

Cited by 8 publications

References 13 publications

Does a screening questionnaire for familial and hereditary colorectal cancer risk work in a health insurance population?

Does a screening questionnaire for familial and hereditary colorectal cancer risk work in a health insurance population?

Colon cancer in rapidly developing countries: review of the lifestyle, dietary, consanguinity and hereditary risk factors

Vorsorge bei familiärem Risiko für das kolorektale Karzinom – FARKOR-Studie – eine kritische Stellungnahme

Contact Info

Product

Resources

About