Evidence map›Paper›PMID 27696385›Full record

ArticleClinical genetics2017

Evaluation of a population-based approach to familial colorectal cancer.

P S Parfrey, E Dicks, O Parfrey, P J McNicholas, H Noseworthy, M O Woods, C Negriin, J Green

Abstract read
In one paragraph

Article in Clinical genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

P S ParfreyThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
E DicksThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
O ParfreyThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
P J McNicholasThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
H NoseworthyThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
M O WoodsThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
C NegriinThe Clinical Epidemiology Unit, Memorial University, St Johns, Newfoundland, Canada.
J GreenDiscipline of Genetics, Health Sciences Centre, Memorial University, St Johns, Newfoundland, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As Newfoundland has the highest rate of familial colorectal cancer (CRC) in the world, we started a population-based clinic to provide colonoscopic and Lynch syndrome (LS) screening recommendations to families of CRC patients based on family risk. Of 1091 incident patients 51% provided a family history. Seventy-two percent of families were at low or intermediate-low risk of CRC and colonoscopic screening recommendations were provided by letter. Twenty-eight percent were at high and intermediate-high risk and were referred to the genetic counsellor, but only 30% (N = 48) were interviewed by study end. Colonoscopy was recommended more frequently than every 5 years in 35% of families. Lower family risk was associated with older age of proband but the frequency of screening colonoscopy recommendations varied across all age groups, driven by variability in family history. Twenty-four percent had a high MMR predict score for a Lynch syndrome mutation, and 23% fulfilled the Provincial Program criteria for LS screening. A population-based approach in the provision of colonoscopic screening recommendations to families at risk of CRC was limited by the relatively low response rate. A family history first approach to the identification of LS families was inefficient.

Indexed as

Mass ScreeningAgedColonoscopyColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisFemaleGenetic CounselingGenetic Predisposition to DiseaseHumansMaleNewfoundland and LabradorTreatment Refusalcolonoscopic screeningfamilial colorectal cancerLynch syndrome screeningpopulation-based

Identifiers

PMID27696385
PMCPMC5413826

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.