Controversy surrounding recommendations for supplemental screening (ultrasound and magnetic resonance screening) in women with dense breasts exists, as the long-term benefits from these additional modalities may not outweigh the harms. This study aimed to examine factors associated with supplemental screening intentions following a hypothetical breast density notification in a population of women who have not been routinely notified. Australian women of breast screening age participated in an online randomised experimental study where they were presented with one of two breast density notifications (with or without health literacy-sensitive information) and asked their screening intentions. After adjusting for covariates in multivariable analyses, women in both groups (n = 940) who indicated higher levels of breast cancer worry, had private health insurance, had a family history of breast cancer, and had a greater number of times previously attending mammography screening had higher intentions for supplemental screening. Understanding women's supplemental screening intentions following notification of dense breasts has important implications for health systems with breast screening considering the impacts of widespread notification. Personal, clinical and psychological factors should be considered when discussing both the benefits and harms of supplemental screening with women with dense breasts.
{"title":"Factors associated with women's supplemental screening intentions following dense breast notification in an online randomised experimental study.","authors":"Brooke Nickel, Hankiz Dolan, Nehmat Houssami, Erin Cvejic, Meagan Brennan, Jolyn Hersch, Melanie Dorrington, Angela Verde, Lisa Vaccaro, Kirsten McCaffery","doi":"10.1177/09691413221125320","DOIUrl":"https://doi.org/10.1177/09691413221125320","url":null,"abstract":"<p><p>Controversy surrounding recommendations for supplemental screening (ultrasound and magnetic resonance screening) in women with dense breasts exists, as the long-term benefits from these additional modalities may not outweigh the harms. This study aimed to examine factors associated with supplemental screening intentions following a hypothetical breast density notification in a population of women who have not been routinely notified. Australian women of breast screening age participated in an online randomised experimental study where they were presented with one of two breast density notifications (with or without health literacy-sensitive information) and asked their screening intentions. After adjusting for covariates in multivariable analyses, women in both groups (n = 940) who indicated higher levels of breast cancer worry, had private health insurance, had a family history of breast cancer, and had a greater number of times previously attending mammography screening had higher intentions for supplemental screening. Understanding women's supplemental screening intentions following notification of dense breasts has important implications for health systems with breast screening considering the impacts of widespread notification. Personal, clinical and psychological factors should be considered when discussing both the benefits and harms of supplemental screening with women with dense breasts.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 2","pages":"92-95"},"PeriodicalIF":2.9,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9656202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221122014
Patricia Fitzpatrick, Helen Byrne, Fidelma Flanagan, Ann O'Doherty, Alissa Connors, Aideen Larke, Risteard O'Laoide, Yvonne Williams, Therese Mooney
Objective and setting: Accurate monitoring of interval cancers is important both for quality improvement and education and is a key parameter of breast screening quality assurance. Issues in relation to communication regarding interval cervical cancer in the Irish cervical screening programme were found, prompting interval cancer process review in all cancer screening programmes. An international survey to examine international consensus on interval breast cancer audit processes was conducted to inform Irish processes.
Methods: A survey of 24 international population-based breast screening programmes was done to determine which undertook audit of interval breast cancer; if yes, they were asked (1) how they undertake audit, (2) if they obtain individual consent for audit and inform women of audit results, and (3) if disclosure of audit results occurs.
Results: Response was 71% (17/24). Of these, 71% (12/17) have a programmatic audit process to calculate the interval cancer rate (ICR). Of these, ten also carry out radiological reviews, three using a blinded review. Two inform patients that audit is taking place; two provide choice to be in the audit; nine state that routine screening consent covers audit. For two of the five that have an open disclosure policy for medical incidents, this policy applies to screening interval cancers. One other country/region has an open disclosure policy for category 3 interval cancers only. Five have legal protection for interval cancers arising in the screened population.
Conclusion: While consistency in providing aggregate programmatic audits exists, there is no consistent approach to individual interval cancer reviews or results disclosure.
{"title":"Interval cancer audit and disclosure in breast screening programmes: An international survey.","authors":"Patricia Fitzpatrick, Helen Byrne, Fidelma Flanagan, Ann O'Doherty, Alissa Connors, Aideen Larke, Risteard O'Laoide, Yvonne Williams, Therese Mooney","doi":"10.1177/09691413221122014","DOIUrl":"https://doi.org/10.1177/09691413221122014","url":null,"abstract":"<p><strong>Objective and setting: </strong>Accurate monitoring of interval cancers is important both for quality improvement and education and is a key parameter of breast screening quality assurance. Issues in relation to communication regarding interval cervical cancer in the Irish cervical screening programme were found, prompting interval cancer process review in all cancer screening programmes. An international survey to examine international consensus on interval breast cancer audit processes was conducted to inform Irish processes.</p><p><strong>Methods: </strong>A survey of 24 international population-based breast screening programmes was done to determine which undertook audit of interval breast cancer; if yes, they were asked (1) how they undertake audit, (2) if they obtain individual consent for audit and inform women of audit results, and (3) if disclosure of audit results occurs.</p><p><strong>Results: </strong>Response was 71% (17/24). Of these, 71% (12/17) have a programmatic audit process to calculate the interval cancer rate (ICR). Of these, ten also carry out radiological reviews, three using a blinded review. Two inform patients that audit is taking place; two provide choice to be in the audit; nine state that routine screening consent covers audit. For two of the five that have an open disclosure policy for medical incidents, this policy applies to screening interval cancers. One other country/region has an open disclosure policy for category 3 interval cancers only. Five have legal protection for interval cancers arising in the screened population.</p><p><strong>Conclusion: </strong>While consistency in providing aggregate programmatic audits exists, there is no consistent approach to individual interval cancer reviews or results disclosure.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"36-41"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/79/a7/10.1177_09691413221122014.PMC9925906.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9299735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413231154697
{"title":"Thanks to reviewers.","authors":"","doi":"10.1177/09691413231154697","DOIUrl":"https://doi.org/10.1177/09691413231154697","url":null,"abstract":"","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"51"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9229648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221122055
Erika Marina Solla Negrao, Cesar Cabello, Livia Conz, Edmundo Carvalho Mauad, Luiz Carlos Zeferino, Diama Bhadra Vale
Objectives: To evaluate the performance of breast cancer screening and early diagnosis during the pandemic, compared to the pre-pandemic period.Setting: The public referral centre for screening in Campinas, São Paulo State, Brazil.
Methods: This is an audit study of performance screening and diagnostic indicators. Two periods were analysed: 2019, the pre-COVID period, and 2020, the COVID period. All women who underwent mammography in these periods were included. Indicators were compared between periods, and the US Breast Cancer Surveillance Consortium benchmarks were used as a reference.
Results: A comparison between the periods shows a reduction of 57.4% in screening and 4.4% in diagnosis using mammography. Cancer detection rate per 1000 screening mammograms dropped from 4.62 to 2.83 (p = 0.031), while it increased from 84.43 to 89.36 in diagnosis mammograms (p = 0.701), higher than the reference (34.4, p < 0.001). With regard to diagnosis, the proportion of minimal cancers was reduced (p = 0.005) and was lower than the reference (40.0%, p < 0.001), along with the proportion of node-negative invasive cancers (p < 0.001). The mean size of invasive tumours was similar in the two periods (32.50 mm and 33.40 mm, p = 0.808) but larger than the reference value (16.50 mm, p < 0.001). Recall rate was lower in the COVID period (22.55% vs. 27.37%, p = 0.015).
Conclusion: The COVID pandemic caused an overall decrease in breast screening and detection of breast cancer cases, although the reduction in number of diagnosis mammograms performed was minimal. Tumour mean size was large in both periods, the pandemic highlighting a previous profile of detection at an advanced stage.
{"title":"The impact of the COVID-19 pandemic on breast cancer screening and diagnosis in a Brazilian metropolitan area.","authors":"Erika Marina Solla Negrao, Cesar Cabello, Livia Conz, Edmundo Carvalho Mauad, Luiz Carlos Zeferino, Diama Bhadra Vale","doi":"10.1177/09691413221122055","DOIUrl":"https://doi.org/10.1177/09691413221122055","url":null,"abstract":"<p><strong>Objectives: </strong>To evaluate the performance of breast cancer screening and early diagnosis during the pandemic, compared to the pre-pandemic period.<b>Setting:</b> The public referral centre for screening in Campinas, São Paulo State, Brazil.</p><p><strong>Methods: </strong>This is an audit study of performance screening and diagnostic indicators. Two periods were analysed: 2019, the pre-COVID period, and 2020, the COVID period. All women who underwent mammography in these periods were included. Indicators were compared between periods, and the US Breast Cancer Surveillance Consortium benchmarks were used as a reference.</p><p><strong>Results: </strong>A comparison between the periods shows a reduction of 57.4% in screening and 4.4% in diagnosis using mammography. Cancer detection rate per 1000 screening mammograms dropped from 4.62 to 2.83 (p = 0.031), while it increased from 84.43 to 89.36 in diagnosis mammograms (p = 0.701), higher than the reference (34.4, p < 0.001). With regard to diagnosis, the proportion of minimal cancers was reduced (p = 0.005) and was lower than the reference (40.0%, p < 0.001), along with the proportion of node-negative invasive cancers (p < 0.001). The mean size of invasive tumours was similar in the two periods (32.50 mm and 33.40 mm, p = 0.808) but larger than the reference value (16.50 mm, p < 0.001). Recall rate was lower in the COVID period (22.55% vs. 27.37%, p = 0.015).</p><p><strong>Conclusion: </strong>The COVID pandemic caused an overall decrease in breast screening and detection of breast cancer cases, although the reduction in number of diagnosis mammograms performed was minimal. Tumour mean size was large in both periods, the pandemic highlighting a previous profile of detection at an advanced stage.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"42-46"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922643/pdf/10.1177_09691413221122055.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10814865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221132674
Daniel Satgé, Motoi Nishi
Dear Editors, Current guidelines for breast cancer screening in women with intellectual disability (WIDs) do not differ from those for women in the general population. However, research suggests that WIDs are younger and have more advanced disease at breast cancer diagnosis than women in the general population. Three studies conducted in France showed breast cancer appearing earlier (Table 1). A hospital survey in central France included 11 breast cancer cases in WIDs discovered at a mean age of 55.6 years, 7 years earlier than in the control cohort (62.4 years). Five of the 11 malignancies (45%) were discovered in women before the age of 50. The cases in WIDs however were at a more advanced stage than in the control cohort (American Joint Committee on Cancer: AJCC1, OR=3.2, p=0.010). A study including 1519 randomly selected institutions dedicated to disabled adults across the whole of France identified 13 breast cancer cases in WIDs (with age known). These were diagnosed at a mean age of 47.8 years, 15 years earlier than in the French population during the corresponding period, and eight (61%) were in women under 50 years at diagnosis. The third was a population-based study conducted in the south of France which analyzed breast cancers in 21 WIDs. The mean age at diagnosis was 7 years earlier (54.7 years vs 61.8 years) than for controls in the regional Cancer Registry. Seven tumors (33%) were diagnosed before 50 years of age. There was also a trend to greater tumor volume (more advanced T stage) (Jacot et al., article submitted). A literature search conducted by one of us (MN) on Japanese publication sources, using “Japan Medical Abstract Society” (ICHUSHI) which includes medical conference reports, with key words “breast cancer” and “intellectual disability” yielded five articles and abstracts published 2003–2018.Thefive Japanesewomen concerned were aged 38–61 (mean 46.6). According to the data of “Cancer Statistics”, Cancer Information Service, National Cancer Center, Japan (National Cancer Registry, Ministry of Health, Labor and Welfare)” in recent years (2016–2018), the mean age at diagnosis of female breast cancer in Japan is 62.4 years. Three of the five WIDs were younger than 50 years at diagnosis. In a US nationwide study of data collected during 2010, 384 breast cancers among 602 reproductive cancers in WIDs were treated almost seven years earlier, at a mean age of 61, compared to 67.8 years for women without intellectual disability. Mass screening is a precious opportunity to treat breast cancer early in WIDs. First, breast cancer which has a similar incidence compared to women in the general population is the most frequent malignancy in WIDs. Second, WIDs have greater risk factors such as being more frequently overweight or obese, less involved in physical exercise, more frequently nulliparous and rarely breast feeding. Third, many WIDs do not practice breast self-palpation and have difficulties expressing their pain and symptoms. Fou
{"title":"Age at breast cancer screening in women with intellectual disability.","authors":"Daniel Satgé, Motoi Nishi","doi":"10.1177/09691413221132674","DOIUrl":"https://doi.org/10.1177/09691413221132674","url":null,"abstract":"Dear Editors, Current guidelines for breast cancer screening in women with intellectual disability (WIDs) do not differ from those for women in the general population. However, research suggests that WIDs are younger and have more advanced disease at breast cancer diagnosis than women in the general population. Three studies conducted in France showed breast cancer appearing earlier (Table 1). A hospital survey in central France included 11 breast cancer cases in WIDs discovered at a mean age of 55.6 years, 7 years earlier than in the control cohort (62.4 years). Five of the 11 malignancies (45%) were discovered in women before the age of 50. The cases in WIDs however were at a more advanced stage than in the control cohort (American Joint Committee on Cancer: AJCC1, OR=3.2, p=0.010). A study including 1519 randomly selected institutions dedicated to disabled adults across the whole of France identified 13 breast cancer cases in WIDs (with age known). These were diagnosed at a mean age of 47.8 years, 15 years earlier than in the French population during the corresponding period, and eight (61%) were in women under 50 years at diagnosis. The third was a population-based study conducted in the south of France which analyzed breast cancers in 21 WIDs. The mean age at diagnosis was 7 years earlier (54.7 years vs 61.8 years) than for controls in the regional Cancer Registry. Seven tumors (33%) were diagnosed before 50 years of age. There was also a trend to greater tumor volume (more advanced T stage) (Jacot et al., article submitted). A literature search conducted by one of us (MN) on Japanese publication sources, using “Japan Medical Abstract Society” (ICHUSHI) which includes medical conference reports, with key words “breast cancer” and “intellectual disability” yielded five articles and abstracts published 2003–2018.Thefive Japanesewomen concerned were aged 38–61 (mean 46.6). According to the data of “Cancer Statistics”, Cancer Information Service, National Cancer Center, Japan (National Cancer Registry, Ministry of Health, Labor and Welfare)” in recent years (2016–2018), the mean age at diagnosis of female breast cancer in Japan is 62.4 years. Three of the five WIDs were younger than 50 years at diagnosis. In a US nationwide study of data collected during 2010, 384 breast cancers among 602 reproductive cancers in WIDs were treated almost seven years earlier, at a mean age of 61, compared to 67.8 years for women without intellectual disability. Mass screening is a precious opportunity to treat breast cancer early in WIDs. First, breast cancer which has a similar incidence compared to women in the general population is the most frequent malignancy in WIDs. Second, WIDs have greater risk factors such as being more frequently overweight or obese, less involved in physical exercise, more frequently nulliparous and rarely breast feeding. Third, many WIDs do not practice breast self-palpation and have difficulties expressing their pain and symptoms. Fou","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"47-48"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10718106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221139960
Takeshi Takahashi
Of the guidelines (for men at average and high risk) listed in their table, the US Preventive Services Task Force (USPSTF) recommendations are made solely by public health physicians, while others are made mainly by urologists. In the US, the 2012 USPSTF’s Grade D recommendation (not recommended) was strongly opposed by the American Urological Association (AUA), claiming that PSA screening reduces cancer mortality. After being upgraded to Grade C in 2018, the AUA endorsed it and other guidelines have been adapted accordingly. However, in practice, information provided by hospitals to patients tends to have nuances in favor of PSA screening. In Europe, the European Association of Urology (EAU) recommends PSA screening, arguing that it reduces cancer mortality and that the risk-adapted strategy has solved the problem. Since prostate cancer is a cancer of the elderly, the risk of death from other causes is overwhelmingly higher than that from cancer. Improvements in cancer-specific mortality have no benefit unless overall survival (OS) changes. If only the cause of death changes and the length of life remains the same, there is no need for early detection and treatment. In the UK, attempts to encourage PSA screening of high-risk populations, such as men of Black race, have been criticized. The prostate cancer mortality rate of 5.4 per 10,000 may become 10.8 in the high-risk group, but we don’t know how the screening group mortality rate would change, from 4.3 per 10,000 (according to USPSTF summary), and there would be no change in the OS. Higher risk does not necessarily mean greater benefit from screening. In addition, it is known that the mortality rate of prostate cancer is extremely low in Asians. Screening is less and less relevant, and the benefit, if any, will be even smaller. Urologists do not adequately understand the recommendations of public health physicians. One of the reasons why there is no PSA screening program in the UK is that the National Health Service, made up of many public health physicians, respects the fact that there is insufficient evidence of its efficacy and cost-effectiveness. The USPSTF does not recommend publically funded screening. Grade C recommendations are for private insurance coverage. In other words, in the US, you should be well informed, be convinced, pay, and take responsibility for the consequences yourself. The UK and Canada have public medical insurance and no PSA screening. In Japan, a group of public health physicians published a guideline in 2009 that is nearly identical to the 2018 USPSTF statement. Urologists were initially members of the group and involved in the development of the guideline, but they resigned because they were unhappy with the content and have since developed their own, recommending PSA screening for all age groups and almost identical to the 2012 AUA comments. Even after the AUA approved the USPSTF statement in 2018, it has yet to be revised. The prostate cancer mortality among J
{"title":"Public health perspective on prostate-specific antigen screening: Implications of overdiagnosis and differences in health insurance systems across countries.","authors":"Takeshi Takahashi","doi":"10.1177/09691413221139960","DOIUrl":"https://doi.org/10.1177/09691413221139960","url":null,"abstract":"Of the guidelines (for men at average and high risk) listed in their table, the US Preventive Services Task Force (USPSTF) recommendations are made solely by public health physicians, while others are made mainly by urologists. In the US, the 2012 USPSTF’s Grade D recommendation (not recommended) was strongly opposed by the American Urological Association (AUA), claiming that PSA screening reduces cancer mortality. After being upgraded to Grade C in 2018, the AUA endorsed it and other guidelines have been adapted accordingly. However, in practice, information provided by hospitals to patients tends to have nuances in favor of PSA screening. In Europe, the European Association of Urology (EAU) recommends PSA screening, arguing that it reduces cancer mortality and that the risk-adapted strategy has solved the problem. Since prostate cancer is a cancer of the elderly, the risk of death from other causes is overwhelmingly higher than that from cancer. Improvements in cancer-specific mortality have no benefit unless overall survival (OS) changes. If only the cause of death changes and the length of life remains the same, there is no need for early detection and treatment. In the UK, attempts to encourage PSA screening of high-risk populations, such as men of Black race, have been criticized. The prostate cancer mortality rate of 5.4 per 10,000 may become 10.8 in the high-risk group, but we don’t know how the screening group mortality rate would change, from 4.3 per 10,000 (according to USPSTF summary), and there would be no change in the OS. Higher risk does not necessarily mean greater benefit from screening. In addition, it is known that the mortality rate of prostate cancer is extremely low in Asians. Screening is less and less relevant, and the benefit, if any, will be even smaller. Urologists do not adequately understand the recommendations of public health physicians. One of the reasons why there is no PSA screening program in the UK is that the National Health Service, made up of many public health physicians, respects the fact that there is insufficient evidence of its efficacy and cost-effectiveness. The USPSTF does not recommend publically funded screening. Grade C recommendations are for private insurance coverage. In other words, in the US, you should be well informed, be convinced, pay, and take responsibility for the consequences yourself. The UK and Canada have public medical insurance and no PSA screening. In Japan, a group of public health physicians published a guideline in 2009 that is nearly identical to the 2018 USPSTF statement. Urologists were initially members of the group and involved in the development of the guideline, but they resigned because they were unhappy with the content and have since developed their own, recommending PSA screening for all age groups and almost identical to the 2012 AUA comments. Even after the AUA approved the USPSTF statement in 2018, it has yet to be revised. The prostate cancer mortality among J","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"49-50"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10718646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221117685
Anas Almatrafi, Owen Thomas, Matthew Callister, Rhian Gabe, Rebecca J Beeken, Richard Neal
Objective: Comorbidity is associated with adverse outcomes for all lung cancer patients, but its burden is less understood in the context of screening. This review synthesises the prevalence of comorbidities among lung cancer screening (LCS) candidates and summarises the clinical recommendations for screening comorbid individuals.
Methods: We searched MEDLINE, EMBASE, EBM Reviews, and CINAHL databases from January 1990 to February 2021. We included LCS studies that reported a prevalence of comorbidity, as a prevalence of a particular condition, or as a summary score. We also summarised LCS clinical guidelines that addressed comorbidity or frailty for LCS as a secondary objective for this review. Meta-analysis was used with inverse-variance weights obtained from a random-effects model to estimate the prevalence of selected comorbidities.
Results: We included 69 studies in the review; seven reported comorbidity summary scores, two reported performance status, 48 reported individual comorbidities, and 12 were clinical guideline papers. The meta-analysis of individual comorbidities resulted in an estimated prevalence of 35.2% for hypertension, 23.5% for history of chronic obstructive pulmonary disease (COPD) (10.7% for severe COPD), 16.6% for ischaemic heart disease (IHD), 13.1% for peripheral vascular disease (PVD), 12.9% for asthma, 12.5% for diabetes, 4.5% for bronchiectasis, 2.2% for stroke, and 0.5% for pulmonary fibrosis.
Conclusions: Comorbidities were highly prevalent in LCS populations and likely to be more prevalent than in other cancer screening programmes. Further research on the burden of comorbid disease and its impact on screening uptake and outcomes is needed. Identifying individuals with frailty and comorbidities who might not benefit from screening should become a priority in LCS research.
{"title":"The prevalence of comorbidity in the lung cancer screening population: A systematic review and meta-analysis.","authors":"Anas Almatrafi, Owen Thomas, Matthew Callister, Rhian Gabe, Rebecca J Beeken, Richard Neal","doi":"10.1177/09691413221117685","DOIUrl":"https://doi.org/10.1177/09691413221117685","url":null,"abstract":"<p><strong>Objective: </strong>Comorbidity is associated with adverse outcomes for all lung cancer patients, but its burden is less understood in the context of screening. This review synthesises the prevalence of comorbidities among lung cancer screening (LCS) candidates and summarises the clinical recommendations for screening comorbid individuals.</p><p><strong>Methods: </strong>We searched MEDLINE, EMBASE, EBM Reviews, and CINAHL databases from January 1990 to February 2021. We included LCS studies that reported a prevalence of comorbidity, as a prevalence of a particular condition, or as a summary score. We also summarised LCS clinical guidelines that addressed comorbidity or frailty for LCS as a secondary objective for this review. Meta-analysis was used with inverse-variance weights obtained from a random-effects model to estimate the prevalence of selected comorbidities.</p><p><strong>Results: </strong>We included 69 studies in the review; seven reported comorbidity summary scores, two reported performance status, 48 reported individual comorbidities, and 12 were clinical guideline papers. The meta-analysis of individual comorbidities resulted in an estimated prevalence of 35.2% for hypertension, 23.5% for history of chronic obstructive pulmonary disease (COPD) (10.7% for severe COPD), 16.6% for ischaemic heart disease (IHD), 13.1% for peripheral vascular disease (PVD), 12.9% for asthma, 12.5% for diabetes, 4.5% for bronchiectasis, 2.2% for stroke, and 0.5% for pulmonary fibrosis.</p><p><strong>Conclusions: </strong>Comorbidities were highly prevalent in LCS populations and likely to be more prevalent than in other cancer screening programmes. Further research on the burden of comorbid disease and its impact on screening uptake and outcomes is needed. Identifying individuals with frailty and comorbidities who might not benefit from screening should become a priority in LCS research.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"3-13"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/30/e3/10.1177_09691413221117685.PMC9925896.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9299241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221149640
Nicholas J Wald, Stephen W Duffy, Allan Hackshaw
Despite being documented it is not widely recognized that important causal risk factors of potential significance in the primary prevention of disease usually make poor screening tests. This arises because the quantitative association between causal risk factors and disease is usually too small for the risk factor to be a useful screening test. Two examples are the measurement of serum cholesterol as a screening test for heart attacks and blood pressure measurement as a screening test for stroke. While these risk factors are the drivers of heart attacks and strokes throughout the world, when considered as screening tests, they typically have detection rates (sensitivities) for a 5% false positive rate (DR5) of no more than 15% to 20%. Even non-causal risk factors have been invoked as screening tests when their screening performance is poor, for example, coronary calcification as a possible test for coronary heart disease. There is a numerical relationship between measures widely used in investigating causal risk factors such as relative risk or odds ratios and measures of screening performance such as the DR5. A web-based Risk–Screening Converter is available on the Medical Screening Society website (https://www.medicalscreeningsociety.com/rsc.asp). The Risk–Screening Converter converts measures identified as risk factors in epidemiological studies which have a Gaussian distribution into measures of screening performance of potential tests and vice versa. The Converter can be used to determine whether measures such as the odds ratio across the highest and lowest quintile groups of a risk factor are large enough to be considered as a screening test. For example, the Risk–Screening Converter can be used to show that cholesterol is not a good screening test for ischaemic heart disease. In a study of the concentration of total cholesterol in men with a future ischaemic heart disease event the odds ratio between the highest and lowest quintile groups of the distribution of serum total cholesterol was approximately 3.3, similar to the results from other studies. When this odds ratio is entered into the Risk–Screening Converter (see Figure 1) an estimated DR5 of 11.2% is obtained showing that serum cholesterol measurement in adults is not a good screening test for ischaemic heart disease despite it being widely used for this purpose. The Converter has been used in a study to assess the incremental value of polygenic risk scores (PRS) over traditional risk factor scores in the prediction of coronary heart disease events. The study used the results from five cohorts. The cohort with the most discriminatory PRS reported an odds ratio of 4.51 between the highest and lowest quintile groups of the distribution of PRS. The Converter was used in the study to show that this odds ratio corresponds to a false positive rate of 77.1% at a 90% detection rate (FPR90), which is equivalent to a DR5 of 13.5%. The Converter shows that adding a PRS to traditional risk scor
{"title":"The Risk-Screening Converter.","authors":"Nicholas J Wald, Stephen W Duffy, Allan Hackshaw","doi":"10.1177/09691413221149640","DOIUrl":"https://doi.org/10.1177/09691413221149640","url":null,"abstract":"Despite being documented it is not widely recognized that important causal risk factors of potential significance in the primary prevention of disease usually make poor screening tests. This arises because the quantitative association between causal risk factors and disease is usually too small for the risk factor to be a useful screening test. Two examples are the measurement of serum cholesterol as a screening test for heart attacks and blood pressure measurement as a screening test for stroke. While these risk factors are the drivers of heart attacks and strokes throughout the world, when considered as screening tests, they typically have detection rates (sensitivities) for a 5% false positive rate (DR5) of no more than 15% to 20%. Even non-causal risk factors have been invoked as screening tests when their screening performance is poor, for example, coronary calcification as a possible test for coronary heart disease. There is a numerical relationship between measures widely used in investigating causal risk factors such as relative risk or odds ratios and measures of screening performance such as the DR5. A web-based Risk–Screening Converter is available on the Medical Screening Society website (https://www.medicalscreeningsociety.com/rsc.asp). The Risk–Screening Converter converts measures identified as risk factors in epidemiological studies which have a Gaussian distribution into measures of screening performance of potential tests and vice versa. The Converter can be used to determine whether measures such as the odds ratio across the highest and lowest quintile groups of a risk factor are large enough to be considered as a screening test. For example, the Risk–Screening Converter can be used to show that cholesterol is not a good screening test for ischaemic heart disease. In a study of the concentration of total cholesterol in men with a future ischaemic heart disease event the odds ratio between the highest and lowest quintile groups of the distribution of serum total cholesterol was approximately 3.3, similar to the results from other studies. When this odds ratio is entered into the Risk–Screening Converter (see Figure 1) an estimated DR5 of 11.2% is obtained showing that serum cholesterol measurement in adults is not a good screening test for ischaemic heart disease despite it being widely used for this purpose. The Converter has been used in a study to assess the incremental value of polygenic risk scores (PRS) over traditional risk factor scores in the prediction of coronary heart disease events. The study used the results from five cohorts. The cohort with the most discriminatory PRS reported an odds ratio of 4.51 between the highest and lowest quintile groups of the distribution of PRS. The Converter was used in the study to show that this odds ratio corresponds to a false positive rate of 77.1% at a 90% detection rate (FPR90), which is equivalent to a DR5 of 13.5%. The Converter shows that adding a PRS to traditional risk scor","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"1-2"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10710996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01DOI: 10.1177/09691413221123131
Bontha V Babu, Yogita Sharma, Parikipandla Sridevi, Shaily B Surti, Manoranjan Ranjit, Deepa Bhat, Jatin Sarmah, Godi Sudhakar
Objective: To describe the development and implementation of a population-based screening programme for sickle cell disease (SCD) implemented in 12 SCD-endemic and tribal-dominated primary/community health centres (PHCs/CHCs) across six districts of India.
Setting: India reports a huge burden of SCD, especially among indigenous (tribal) communities. However, there is no state-led SCD programme in many places, and systematic screening is absent. This situation necessitates developing a model of population screening.
Methods: This programme was meant to screen all people and was carried out in three tiers. The first tier was a symptomatic survey carried out by community health workers. Regular health workers then screened those referred by sickle cell solubility test at sub-health centres as the second tier. The third tier was confirmation by haemoglobin electrophoresis at PHCs/CHCs. Communities were mobilised and prepared to accept the screening. Capacity building of health facilities was ensured through training and supply of equipment and material.
Results: Initial observation based on six months' data revealed that out of the 110,754 tribal population of 12 PHCs/CHCs, 8418 (7.6%) were identified in the symptomatic survey. Subsequently, 9416 people, including the above 8418, underwent the solubility test, and 2607 (27.7%) were found to be positive. Of these, 1978 (78.9%) underwent electrophoresis. About 64.2% were found to be positive for sickle haemoglobin (233 (18.4%) SCD and 1036 (81.6%) SCD trait).
Conclusions: The study demonstrates the feasibility of establishing a population-based screening programme in the primary health care system. It is easy to implement in tribal habitations as part of the proposed national SCD/haemoglobinopathies programme.
{"title":"Feasibility of population-based screening of sickle cell disease through the primary health care system in tribal areas of India.","authors":"Bontha V Babu, Yogita Sharma, Parikipandla Sridevi, Shaily B Surti, Manoranjan Ranjit, Deepa Bhat, Jatin Sarmah, Godi Sudhakar","doi":"10.1177/09691413221123131","DOIUrl":"https://doi.org/10.1177/09691413221123131","url":null,"abstract":"<p><strong>Objective: </strong>To describe the development and implementation of a population-based screening programme for sickle cell disease (SCD) implemented in 12 SCD-endemic and tribal-dominated primary/community health centres (PHCs/CHCs) across six districts of India.</p><p><strong>Setting: </strong>India reports a huge burden of SCD, especially among indigenous (tribal) communities. However, there is no state-led SCD programme in many places, and systematic screening is absent. This situation necessitates developing a model of population screening.</p><p><strong>Methods: </strong>This programme was meant to screen all people and was carried out in three tiers. The first tier was a symptomatic survey carried out by community health workers. Regular health workers then screened those referred by sickle cell solubility test at sub-health centres as the second tier. The third tier was confirmation by haemoglobin electrophoresis at PHCs/CHCs. Communities were mobilised and prepared to accept the screening. Capacity building of health facilities was ensured through training and supply of equipment and material.</p><p><strong>Results: </strong>Initial observation based on six months' data revealed that out of the 110,754 tribal population of 12 PHCs/CHCs, 8418 (7.6%) were identified in the symptomatic survey. Subsequently, 9416 people, including the above 8418, underwent the solubility test, and 2607 (27.7%) were found to be positive. Of these, 1978 (78.9%) underwent electrophoresis. About 64.2% were found to be positive for sickle haemoglobin (233 (18.4%) SCD and 1036 (81.6%) SCD trait).</p><p><strong>Conclusions: </strong>The study demonstrates the feasibility of establishing a population-based screening programme in the primary health care system. It is easy to implement in tribal habitations as part of the proposed national SCD/haemoglobinopathies programme.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"28-35"},"PeriodicalIF":2.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10708534","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-01Epub Date: 2022-08-29DOI: 10.1177/09691413221109999
Omar Ali, Sunnia Gupta, Kate Brain, Kate J Lifford, Shantini Paranjothy, Sunil Dolwani
Objective: Colorectal cancer (CRC) is the third most common cancer and the second largest cause of cancer-related death worldwide. Current CRC screening in various countries involves stool-based faecal immunochemical testing (FIT) and/or colonoscopy, yet public uptake remains sub-optimal. This review assessed the literature regarding acceptability of alternative CRC screening modalities compared to standard care in average-risk adults.
Method: Systematic searches of MEDLINE, EMBASE, CINAHL, Cochrane and Web of Science were conducted up to February 3rd, 2022. The alternative interventions examined were computed tomography colonography, flexible sigmoidoscopy, colon capsule endoscopy and blood-based biomarkers. Outcomes for acceptability were uptake, discomfort associated with bowel preparation, discomfort associated with screening procedure, screening preferences and willingness to repeat screening method. A narrative data synthesis was conducted.
Results: Twenty-one studies met the inclusion criteria. Differences between intervention and comparison modalities in uptake did not reach statistical significance in most of the included studies. The findings do suggest FIT as being more acceptable as a screening modality than flexible sigmoidoscopy. There were no consistent significant differences in bowel preparation discomfort, screening procedure discomfort, screening preference and willingness to repeat screening between the standard care and alternative modalities.
Conclusion: Current evidence comparing standard colonoscopy and stool-based CRC screening with novel modalities does not demonstrate any clear difference in acceptability. Due to the small number of studies available and included in each screening comparison and lack of observed differences, further research is needed to explore factors influencing acceptability of alternative CRC modalities that might result in improvement in population uptake within different contexts.
{"title":"Acceptability of alternative technologies compared with faecal immunochemical test and/or colonoscopy in colorectal cancer screening: A systematic review.","authors":"Omar Ali, Sunnia Gupta, Kate Brain, Kate J Lifford, Shantini Paranjothy, Sunil Dolwani","doi":"10.1177/09691413221109999","DOIUrl":"10.1177/09691413221109999","url":null,"abstract":"<p><strong>Objective: </strong>Colorectal cancer (CRC) is the third most common cancer and the second largest cause of cancer-related death worldwide. Current CRC screening in various countries involves stool-based faecal immunochemical testing (FIT) and/or colonoscopy, yet public uptake remains sub-optimal. This review assessed the literature regarding acceptability of alternative CRC screening modalities compared to standard care in average-risk adults.</p><p><strong>Method: </strong>Systematic searches of MEDLINE, EMBASE, CINAHL, Cochrane and Web of Science were conducted up to February 3<sup>rd</sup>, 2022. The alternative interventions examined were computed tomography colonography, flexible sigmoidoscopy, colon capsule endoscopy and blood-based biomarkers. Outcomes for acceptability were uptake, discomfort associated with bowel preparation, discomfort associated with screening procedure, screening preferences and willingness to repeat screening method. A narrative data synthesis was conducted.</p><p><strong>Results: </strong>Twenty-one studies met the inclusion criteria. Differences between intervention and comparison modalities in uptake did not reach statistical significance in most of the included studies. The findings do suggest FIT as being more acceptable as a screening modality than flexible sigmoidoscopy. There were no consistent significant differences in bowel preparation discomfort, screening procedure discomfort, screening preference and willingness to repeat screening between the standard care and alternative modalities.</p><p><strong>Conclusion: </strong>Current evidence comparing standard colonoscopy and stool-based CRC screening with novel modalities does not demonstrate any clear difference in acceptability. Due to the small number of studies available and included in each screening comparison and lack of observed differences, further research is needed to explore factors influencing acceptability of alternative CRC modalities that might result in improvement in population uptake within different contexts.</p>","PeriodicalId":51089,"journal":{"name":"Journal of Medical Screening","volume":"30 1","pages":"14-27"},"PeriodicalIF":2.6,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/dd/e4/10.1177_09691413221109999.PMC9925898.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10722760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}