Incorporating faecal haemoglobin measurement using the faecal immunochemical test (FIT) in the referral, triage and prioritisation pathway for patients with colorectal symptoms
Incorporating faecal haemoglobin (FHb) measurement using the faecal immunochemical test (FIT) in the investigation pathway for patients with colorectal symptoms may improve access to colonoscopy for those at greatest risk of significant disease. To derive a colorectal symptom pathway incorporating s...
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Veröffentlicht in: | New Zealand medical journal 2023-07, Vol.136 (1578), p.55-76 |
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description | Incorporating faecal haemoglobin (FHb) measurement using the faecal immunochemical test (FIT) in the investigation pathway for patients with colorectal symptoms may improve access to colonoscopy for those at greatest risk of significant disease.
To derive a colorectal symptom pathway incorporating standard clinical and FIT data to guide referral, triage, and prioritisation of cases in New Zealand.
Diagnostic accuracy of FIT to rule out colorectal cancer (CRC) was determined by meta-analysis. Thereafter, the risk of CRC after FIT was estimated for common clinical presentations by Bayesian methodology, using a specifically collated retrospective cohort of symptomatic cases. A symptom/FIT pathway was developed iteratively following multi-disciplinary engagement.
Eighteen studies were included in meta-analysis. The sensitivity and specificity for CRC were 89.0% (95%CI 87.0-90.9%) and 80.1% (95%CI 77.7-82.4%) respectively, at a FHb threshold of >10mcg haemoglobin per gram stool, and 95.7% (95%CI 93.2-97.7%) and 60.5% (95%CI 53.8-67.0%) respectively, at the limit of detection. The final pathway was 97% sensitive for CRC, compared with 90% for the current direct access criteria, and requires 47% fewer colonoscopies. Estimated prevalence of CRC among those declined investigation was 0.23%.
Incorporating FIT in the new patient symptomatic pathway as presented appears feasible, safe, and allows for resources to be targeted to those at greatest risk of disease. Further work is needed to ensure equity for Māori if this pathway were introduced nationally. |
doi_str_mv | 10.26635/6965.5966 |
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To derive a colorectal symptom pathway incorporating standard clinical and FIT data to guide referral, triage, and prioritisation of cases in New Zealand.
Diagnostic accuracy of FIT to rule out colorectal cancer (CRC) was determined by meta-analysis. Thereafter, the risk of CRC after FIT was estimated for common clinical presentations by Bayesian methodology, using a specifically collated retrospective cohort of symptomatic cases. A symptom/FIT pathway was developed iteratively following multi-disciplinary engagement.
Eighteen studies were included in meta-analysis. The sensitivity and specificity for CRC were 89.0% (95%CI 87.0-90.9%) and 80.1% (95%CI 77.7-82.4%) respectively, at a FHb threshold of >10mcg haemoglobin per gram stool, and 95.7% (95%CI 93.2-97.7%) and 60.5% (95%CI 53.8-67.0%) respectively, at the limit of detection. The final pathway was 97% sensitive for CRC, compared with 90% for the current direct access criteria, and requires 47% fewer colonoscopies. Estimated prevalence of CRC among those declined investigation was 0.23%.
Incorporating FIT in the new patient symptomatic pathway as presented appears feasible, safe, and allows for resources to be targeted to those at greatest risk of disease. Further work is needed to ensure equity for Māori if this pathway were introduced nationally.</description><identifier>ISSN: 1175-8716</identifier><identifier>EISSN: 1175-8716</identifier><identifier>DOI: 10.26635/6965.5966</identifier><identifier>PMID: 37414077</identifier><language>eng</language><publisher>New Zealand: Pasifika Medical Association Group (PMAG)</publisher><subject>Accuracy ; Bayes Theorem ; Colonoscopy ; Colorectal cancer ; Colorectal Neoplasms - diagnosis ; Datasets ; Early Detection of Cancer - methods ; Feces - chemistry ; Gastroenterology ; Hemoglobin ; Hemoglobins - analysis ; Humans ; Inflammatory bowel disease ; Maori People ; Medical diagnosis ; Meta-analysis ; New Zealand ; Occult Blood ; Patients ; Primary care ; Referral and Consultation ; Retrospective Studies ; Sensitivity and Specificity ; Triage</subject><ispartof>New Zealand medical journal, 2023-07, Vol.136 (1578), p.55-76</ispartof><rights>PMA.</rights><rights>Copyright New Zealand Medical Association (NZMA) Jul 7, 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37414077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Falvey, James</creatorcontrib><creatorcontrib>Frampton, Christopher M A</creatorcontrib><creatorcontrib>Gearry, Richard B</creatorcontrib><creatorcontrib>Hudson, Ben</creatorcontrib><creatorcontrib>Whiteley, Lucinda</creatorcontrib><title>Incorporating faecal haemoglobin measurement using the faecal immunochemical test (FIT) in the referral, triage and prioritisation pathway for patients with colorectal symptoms</title><title>New Zealand medical journal</title><addtitle>N Z Med J</addtitle><description>Incorporating faecal haemoglobin (FHb) measurement using the faecal immunochemical test (FIT) in the investigation pathway for patients with colorectal symptoms may improve access to colonoscopy for those at greatest risk of significant disease.
To derive a colorectal symptom pathway incorporating standard clinical and FIT data to guide referral, triage, and prioritisation of cases in New Zealand.
Diagnostic accuracy of FIT to rule out colorectal cancer (CRC) was determined by meta-analysis. Thereafter, the risk of CRC after FIT was estimated for common clinical presentations by Bayesian methodology, using a specifically collated retrospective cohort of symptomatic cases. A symptom/FIT pathway was developed iteratively following multi-disciplinary engagement.
Eighteen studies were included in meta-analysis. The sensitivity and specificity for CRC were 89.0% (95%CI 87.0-90.9%) and 80.1% (95%CI 77.7-82.4%) respectively, at a FHb threshold of >10mcg haemoglobin per gram stool, and 95.7% (95%CI 93.2-97.7%) and 60.5% (95%CI 53.8-67.0%) respectively, at the limit of detection. The final pathway was 97% sensitive for CRC, compared with 90% for the current direct access criteria, and requires 47% fewer colonoscopies. Estimated prevalence of CRC among those declined investigation was 0.23%.
Incorporating FIT in the new patient symptomatic pathway as presented appears feasible, safe, and allows for resources to be targeted to those at greatest risk of disease. Further work is needed to ensure equity for Māori if this pathway were introduced nationally.</description><subject>Accuracy</subject><subject>Bayes Theorem</subject><subject>Colonoscopy</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - diagnosis</subject><subject>Datasets</subject><subject>Early Detection of Cancer - methods</subject><subject>Feces - chemistry</subject><subject>Gastroenterology</subject><subject>Hemoglobin</subject><subject>Hemoglobins - analysis</subject><subject>Humans</subject><subject>Inflammatory bowel disease</subject><subject>Maori People</subject><subject>Medical diagnosis</subject><subject>Meta-analysis</subject><subject>New Zealand</subject><subject>Occult Blood</subject><subject>Patients</subject><subject>Primary care</subject><subject>Referral and Consultation</subject><subject>Retrospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Triage</subject><issn>1175-8716</issn><issn>1175-8716</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkc1u1TAQhSMEoqWw4QGQJTYFcYt_YjtZoorClSqxKeto4kxuXMV2sB1V9636iDi0RYjVzMifz7HnVNVbRi-4UkJ-Vq2SF7JV6ll1ypiWu0Yz9fyf_qR6ldItpVzKlr6sToSuWU21Pq3u996EuIQI2foDGQENzGQCdOEwh9564hDSGtGhz2RNG5QnfAKtc6sPZkJntzFjyuT8an_zgZSbGxdxxBhh_kRytHBAAn4gS7Qh2mxTMQ2eLJCnOziSMcStt8UpkTubJ2LCHCKaXKTT0S05uPS6ejHCnPDNYz2rfl59vbn8vrv-8W1_-eV6ZwSjedfTsaaDlgIUN02tTa8bXveG8hoBTNPjYKAt5wZ6ynHUXLWDANarhkuhR3FWnT_oLjH8Wsu_OmeTwXkGj2FNHW-E5FpK3Rb0_X_obVijL6_bKM14LSgv1McHysSQUtlLV9bgIB47Rrs_OXZbjt2WY4HfPUquvcPhL_oUnPgNIVOb2Q</recordid><startdate>20230707</startdate><enddate>20230707</enddate><creator>Falvey, James</creator><creator>Frampton, Christopher M A</creator><creator>Gearry, Richard B</creator><creator>Hudson, Ben</creator><creator>Whiteley, Lucinda</creator><general>Pasifika Medical Association Group (PMAG)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AYAGU</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20230707</creationdate><title>Incorporating faecal haemoglobin measurement using the faecal immunochemical test (FIT) in the referral, triage and prioritisation pathway for patients with colorectal symptoms</title><author>Falvey, James ; Frampton, Christopher M A ; Gearry, Richard B ; Hudson, Ben ; Whiteley, Lucinda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-b0f40d753a62c847cb7824bc024eaac8bedca9753cab02ef7269d3a1b682537f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Accuracy</topic><topic>Bayes Theorem</topic><topic>Colonoscopy</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - diagnosis</topic><topic>Datasets</topic><topic>Early Detection of Cancer - methods</topic><topic>Feces - chemistry</topic><topic>Gastroenterology</topic><topic>Hemoglobin</topic><topic>Hemoglobins - analysis</topic><topic>Humans</topic><topic>Inflammatory bowel disease</topic><topic>Maori People</topic><topic>Medical diagnosis</topic><topic>Meta-analysis</topic><topic>New Zealand</topic><topic>Occult Blood</topic><topic>Patients</topic><topic>Primary care</topic><topic>Referral and Consultation</topic><topic>Retrospective Studies</topic><topic>Sensitivity and Specificity</topic><topic>Triage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Falvey, James</creatorcontrib><creatorcontrib>Frampton, Christopher M A</creatorcontrib><creatorcontrib>Gearry, Richard B</creatorcontrib><creatorcontrib>Hudson, Ben</creatorcontrib><creatorcontrib>Whiteley, Lucinda</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Australia & New Zealand Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>New Zealand medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Falvey, James</au><au>Frampton, Christopher M A</au><au>Gearry, Richard B</au><au>Hudson, Ben</au><au>Whiteley, Lucinda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incorporating faecal haemoglobin measurement using the faecal immunochemical test (FIT) in the referral, triage and prioritisation pathway for patients with colorectal symptoms</atitle><jtitle>New Zealand medical journal</jtitle><addtitle>N Z Med J</addtitle><date>2023-07-07</date><risdate>2023</risdate><volume>136</volume><issue>1578</issue><spage>55</spage><epage>76</epage><pages>55-76</pages><issn>1175-8716</issn><eissn>1175-8716</eissn><abstract>Incorporating faecal haemoglobin (FHb) measurement using the faecal immunochemical test (FIT) in the investigation pathway for patients with colorectal symptoms may improve access to colonoscopy for those at greatest risk of significant disease.
To derive a colorectal symptom pathway incorporating standard clinical and FIT data to guide referral, triage, and prioritisation of cases in New Zealand.
Diagnostic accuracy of FIT to rule out colorectal cancer (CRC) was determined by meta-analysis. Thereafter, the risk of CRC after FIT was estimated for common clinical presentations by Bayesian methodology, using a specifically collated retrospective cohort of symptomatic cases. A symptom/FIT pathway was developed iteratively following multi-disciplinary engagement.
Eighteen studies were included in meta-analysis. The sensitivity and specificity for CRC were 89.0% (95%CI 87.0-90.9%) and 80.1% (95%CI 77.7-82.4%) respectively, at a FHb threshold of >10mcg haemoglobin per gram stool, and 95.7% (95%CI 93.2-97.7%) and 60.5% (95%CI 53.8-67.0%) respectively, at the limit of detection. The final pathway was 97% sensitive for CRC, compared with 90% for the current direct access criteria, and requires 47% fewer colonoscopies. Estimated prevalence of CRC among those declined investigation was 0.23%.
Incorporating FIT in the new patient symptomatic pathway as presented appears feasible, safe, and allows for resources to be targeted to those at greatest risk of disease. Further work is needed to ensure equity for Māori if this pathway were introduced nationally.</abstract><cop>New Zealand</cop><pub>Pasifika Medical Association Group (PMAG)</pub><pmid>37414077</pmid><doi>10.26635/6965.5966</doi><tpages>22</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Accuracy Bayes Theorem Colonoscopy Colorectal cancer Colorectal Neoplasms - diagnosis Datasets Early Detection of Cancer - methods Feces - chemistry Gastroenterology Hemoglobin Hemoglobins - analysis Humans Inflammatory bowel disease Maori People Medical diagnosis Meta-analysis New Zealand Occult Blood Patients Primary care Referral and Consultation Retrospective Studies Sensitivity and Specificity Triage |
title | Incorporating faecal haemoglobin measurement using the faecal immunochemical test (FIT) in the referral, triage and prioritisation pathway for patients with colorectal symptoms |
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