Evaluating HIV Clinical Care Quality in Massachusetts Sites Supported through...JSI
This presentation was produced by Jeanne Day, MPH; Nancy Reinhalter, RN; Joseph Musolino; Joseph Rego; Amy Flynn; Katelyn Flaherty Dore; Ashley Hatcher, as part of the HIV/AIDS Clinical Quality Assurance Project. For more information about the project, visit: http://www.jsi.com/JSIInternet/USHealth/project/display.cfm?ctid=na&cid=na&tid=40&id=21641
The Department of Internal Medicine celebrates our 75th successful year, and the conclusion of FY2019 with a highlights presentation. For higher quality images and better view-ability, please download the file.
Dolores Steinwall, the president of the Lymphedema Association of Ontario (LAO), introduced the webinar about lymphedema. Ann DiMenna, a physiotherapist and director of LAO, then discussed the lymphatic system, signs and risks of lymphedema, and treatment methods like manual lymph drainage, compression therapy, and exercise. Over 400,000 Canadians are affected by lymphedema resulting from cancer treatment, injuries, or other causes. The LAO aims to support those living with lymphedema and raise awareness.
This document evaluates the utilization of Low Acuity Pathway (LAP) protocols by paramedics in rural and regional NSW Ambulance services. It finds that while LAP protocols were recorded in 14.26% of low acuity cases, the non-transport rate was only 16.8% and LAP protocols were recorded in less than 1% of total cases. Extended care paramedics had higher non-transport rates than standard paramedics using LAP protocols. The study concludes that LAP protocols are underutilized in rural areas similarly to metropolitan areas, and further research is needed on specialized paramedic models for low acuity care.
One in five women who survive breast cancer will develop lymphoedema of the upper body at some point in their life. Following breast surgery, women are recommended to follow strategies to minimise their lymphoedema risk (e.g., limiting exposure of the at-risk arm to trauma). Adherence to these strategies is typically less than optimal.
This document summarizes research on quality of life for bladder cancer patients. Quantitative studies found that muscle-invasive bladder cancer patients reported worse quality of life and more symptoms than non-muscle-invasive patients. Both groups experienced problems with urinary and sexual symptoms. Qualitative interviews found patients endorsed having a navigator to help with treatment, monitoring, and managing symptoms. Future research plans include developing a bladder cancer navigation intervention and studying quality of life and distress over time. The goal is to improve survivorship care through tailored interventions.
R frank jones assessing the african american urology experience during traini...zmrogers
This document summarizes a presentation given to the R. Frank Jones Urologic Society on diversity in urology. It discusses the history of African Americans in medicine, highlights pioneers like Richard Francis Jones, and reviews data on diversity among urology residents and faculty. It also presents strategies to improve the "urologic pipeline" for African Americans, such as partnering with undergraduate institutions that have high numbers of African American medical school applicants and creating pipeline programs like summer research opportunities. The goal is to continue attracting more African Americans to urology given changing US demographics and reduce health disparities.
Don't miss our upcoming webinars! Subscribe today.
In this webinar:
1) Attendees will be provided with an overview of the drug approval and reimbursement processes.
2) People will be taken through a review of the updated CADTH patient group/clinician input processes.
3) Everyone will have a better understanding of how the processes are connected and flow into one another.
View the YouTube video here: https://youtu.be/-Bv9DZvSITk
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Evaluating HIV Clinical Care Quality in Massachusetts Sites Supported through...JSI
This presentation was produced by Jeanne Day, MPH; Nancy Reinhalter, RN; Joseph Musolino; Joseph Rego; Amy Flynn; Katelyn Flaherty Dore; Ashley Hatcher, as part of the HIV/AIDS Clinical Quality Assurance Project. For more information about the project, visit: http://www.jsi.com/JSIInternet/USHealth/project/display.cfm?ctid=na&cid=na&tid=40&id=21641
The Department of Internal Medicine celebrates our 75th successful year, and the conclusion of FY2019 with a highlights presentation. For higher quality images and better view-ability, please download the file.
Dolores Steinwall, the president of the Lymphedema Association of Ontario (LAO), introduced the webinar about lymphedema. Ann DiMenna, a physiotherapist and director of LAO, then discussed the lymphatic system, signs and risks of lymphedema, and treatment methods like manual lymph drainage, compression therapy, and exercise. Over 400,000 Canadians are affected by lymphedema resulting from cancer treatment, injuries, or other causes. The LAO aims to support those living with lymphedema and raise awareness.
This document evaluates the utilization of Low Acuity Pathway (LAP) protocols by paramedics in rural and regional NSW Ambulance services. It finds that while LAP protocols were recorded in 14.26% of low acuity cases, the non-transport rate was only 16.8% and LAP protocols were recorded in less than 1% of total cases. Extended care paramedics had higher non-transport rates than standard paramedics using LAP protocols. The study concludes that LAP protocols are underutilized in rural areas similarly to metropolitan areas, and further research is needed on specialized paramedic models for low acuity care.
One in five women who survive breast cancer will develop lymphoedema of the upper body at some point in their life. Following breast surgery, women are recommended to follow strategies to minimise their lymphoedema risk (e.g., limiting exposure of the at-risk arm to trauma). Adherence to these strategies is typically less than optimal.
This document summarizes research on quality of life for bladder cancer patients. Quantitative studies found that muscle-invasive bladder cancer patients reported worse quality of life and more symptoms than non-muscle-invasive patients. Both groups experienced problems with urinary and sexual symptoms. Qualitative interviews found patients endorsed having a navigator to help with treatment, monitoring, and managing symptoms. Future research plans include developing a bladder cancer navigation intervention and studying quality of life and distress over time. The goal is to improve survivorship care through tailored interventions.
R frank jones assessing the african american urology experience during traini...zmrogers
This document summarizes a presentation given to the R. Frank Jones Urologic Society on diversity in urology. It discusses the history of African Americans in medicine, highlights pioneers like Richard Francis Jones, and reviews data on diversity among urology residents and faculty. It also presents strategies to improve the "urologic pipeline" for African Americans, such as partnering with undergraduate institutions that have high numbers of African American medical school applicants and creating pipeline programs like summer research opportunities. The goal is to continue attracting more African Americans to urology given changing US demographics and reduce health disparities.
Don't miss our upcoming webinars! Subscribe today.
In this webinar:
1) Attendees will be provided with an overview of the drug approval and reimbursement processes.
2) People will be taken through a review of the updated CADTH patient group/clinician input processes.
3) Everyone will have a better understanding of how the processes are connected and flow into one another.
View the YouTube video here: https://youtu.be/-Bv9DZvSITk
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Physician density may correlate to worse urologic cancer outcomes according to a study examining cancer mortality rates. The study analyzed cancer mortality rate data from the CDC and found significantly higher renal cancer mortality rates in areas with low physician density. Additionally, there was a negative association between median family income and bladder and renal cancer mortality rates. The study compared counties with the highest and lowest mortality rates for prostate, bladder, and renal cancers and found those with high rates had significantly lower physician population densities and higher rates of residents without health insurance compared to low mortality rate counties.
This document discusses cancer in older adults and the use of comprehensive geriatric assessment (CGA) to evaluate older cancer patients. It makes three key points:
1. CGA can help oncologists define "elderly" cancer patients and evaluate them for treatment. Factors like frailty, comorbidities, and functional status are more important than age alone.
2. CGA has prognostic value, as it can identify risk factors for toxicity from chemotherapy and predict patient outcomes. Frail older patients have higher risks of adverse events.
3. CGA tools have been developed that use factors like frailty, blood pressure, liver/kidney function to predict risks of severe toxicity and categorize
This document discusses the experience of the Saskatchewan Cancer Agency Patient Family Advisory Council (PFAC) in involving patients and families in health technology assessment. It begins by providing background on the Saskatchewan Cancer Agency and its establishment of the PFAC to ensure patient- and family-centered care. The PFAC initially focused on tangible accomplishments but realized more meaningful engagement required challenging assumptions. Over time, as trust was built, the PFAC felt comfortable questioning staff and asking them to present as guests rather than feeling represented. This helped clarify roles for change and idea implementation, as some staff were unclear on how patient input affected decision-making.
1) Native Hawaiians experience higher rates of certain cancers compared to other ethnic groups in Hawaii. They also face cultural, geographic, and health literacy barriers to participation in clinical trials.
2) Effective strategies to increase Native Hawaiian enrollment in clinical trials have included education programs for physicians and communities, partnerships between organizations, and support services for patients.
3) Current research is using focus groups to better understand attitudes that may affect clinical trial participation among Native Hawaiians in order to further improve representation.
A national approach to improve the quality of Aftercare for survivors of TYA cancer - End of Treatment Summaries / Care Plans
Dr Helen Jenkinson, Consultant Paediatric Oncologist
on behalf of the NCSI steering group
Event held in London on Wednesday 9 October with the Teenage and Young Adult (TYA) Centre Champions and our Clinical Leads to share learning, good practice examples, the successes, challenges and barriers to implementing:
Treatment summaries
End of treatment care plans
Increased self-management for TYAs after cancer treatment
The output from the meeting will be to define what support NHS IQ can provide locally to assist TYA teams in order to make progress with their implementation plans.
This literature review covers three topics: pneumonia, lung cancer, and pulmonary fibrosis. For pneumonia, it summarizes that the declines in childhood pneumonia hospitalizations observed after the introduction of PCV7 vaccines were sustained over a decade. It also found substantial reductions in adult pneumonia hospitalizations. For lung cancer, it discusses findings from several large randomized controlled trials that low-dose CT screening detects more early-stage lung cancers compared to chest radiography and tends to result in a stage shift toward earlier diagnoses. For pulmonary fibrosis, it reviews that the natural history can vary significantly, from complete resolution to progressive fibrosis leading to respiratory failure.
Theo Georghiou and Dr Jessica Sheringham: Data and Colorectal Cancer, 30 June...Nuffield Trust
This document summarizes a study that analyzed linked primary care, hospital, and cancer registry data to examine diagnostic pathways for colorectal cancer patients in North East London. The study found that it was feasible to link these routine data sources. Analysis at the population level identified factors associated with emergency presentations, such as late cancer stage and fewer GP visits. Examination of individual pathways showed diversity in healthcare use prior to diagnosis and identified cases for further audit.
Stm functional showdeck mockup v2 w refsmonkmartinez
1. The study examined rates of hematopoietic stem cell transplantation (HCT) for leukemia, lymphoma, and multiple myeloma between 1997-2002 using data from the Center for International Blood and Marrow Transplant Registry and SEER cancer registry.
2. It found that Caucasians were more likely than African Americans to receive HCT, including autologous, HLA identical sibling, and unrelated donor HCT.
3. Men were slightly more likely than women to receive HCT overall, but this difference was only significant for autologous HCT.
Don't miss our upcoming webinars. Subscribe today!
This presentation will highlight the promising new therapeutic strategies in the treatment of gliomas, with a focus on trials or therapies that will soon be available for Canadian patients.
View the YouTube video: https://youtu.be/ibbEuvSF7xY
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Weight loss among patients with Head and Neck Cancer at St Vincent's Hospital...Cancer Institute NSW
Patients with Squamous cell carcinoma (SCC) of the Head and Neck (H&N) are often treated with curative intent using treatment protocols placing them at high risk of nutritional decline. Recently released COSA guidelines recommend that prophylactic enteral feeding should be considered for T4 upper aerodigestive tract tumours undergoing concurrent chemoradiotherapy. Evidence is yet to identify optimal method of nutrition intervention and timing across all tumour stages in this population.
JMCP 2016 Access to new meds for hep C in Medicaid membersKimberly Lenz
This document summarizes a study that evaluated access to new hepatitis C virus (HCV) treatment medications among Medicaid patients in Massachusetts. The study found that only 5.1% of MassHealth members with HCV had their healthcare provider submit a prior authorization request for treatment with sofosbuvir or simeprevir. Patients who had a treatment request were more likely to be older, have advanced liver disease or have been recently treated for HCV, and less likely to have a substance use disorder. Nearly all (90%) of treatment requests were approved. The results suggest that while the Medicaid program did not restrict access, other factors like provider prioritization and patient barriers influenced who received treatment.
Don't miss our upcoming webinars: Subscribe today!
In this webinar:
Dr. Krista Noonan is a medical oncologist specializing in thoracic and genitourinary malignancies at BC Cancer, Surrey Centre. Her research interests focus on thoracic and genitourinary malignancies and health services research. On Thursday, February 27, join Dr. Noonan as she: - Reviews the advancements in systemic therapy in lung cancer over the past decade - Highlights how the advancements in systemic therapy have dramatically improved quality of life and length of life.
View the video: https://youtu.be/3DaUwQ8ab44
To learn more about CCSN, visit us at survivornet.ca
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
5th Annual Early Age Onset Colorectal Cancer Summit - Session II: Family History Ascertainment in the US - What Steps are Needed to Improve the Well Documented Less Than Optimal Status of this Situation?
Don't miss our upcoming webinars! Subscribe today!
In April, CCSN virtually met with MPPs throughout Ontario to discuss our COVID-19 and Cancer Care - Wave 2 Survey. During these meetings, we discussed the difficulty cancer patients and pre-diagnosis patients have had with accessing cancer services during the pandemic and the importance of ensuring the cancer patients receive their 1st and 2nd vaccine doses in a timely manner.
In this webinar, CCSN's Public Policy Analyst Conrad will begin by sharing some of the highlights from our meetings with Ontario MPPs. He will then turn things over to our patient advocates and they will share some of their reflections from our meetings as well as their own experiences with accessing cancer care during the pandemic. Lastly, Conrad will take a closer look at the Ontario data from our survey.
View the YouTube video: https://youtu.be/05u4i89WFfQ
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Don't miss our upcoming webinars! Subscribe today!
In this webinar:
In May-June, 2020, the Canadian Cancer Survivor Network (CCSN) commissioned Leger to conduct a national survey to evaluate the impact that COVID-19 has had on cancer patients, survivors, pre-diagnosis patients, and caregivers. The results of our first survey revealed that the pandemic response has triggered another public health crisis - the postponement and cancellation of essential cancer tests, procedures, and treatments.
CCSN commissioned Leger for a second survey in December, 2020 to evaluate the impact that the suspension of cancer services during the first wave is currently having on those who have been affected by cancer.
Join CCSN and Leger as we present the results of the COVID-19 and Cancer Care Disruption in Canada Survey - Wave 2 and hear from members of the cancer community about how the pandemic has directly impacted them.
View the YouTube video: https://youtu.be/qN4Hq7OtBys
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
The document discusses barriers to minority patient enrollment in cancer clinical trials. It conducted a systematic literature review on barriers and found that minority populations experience systemic, institutional, and individual barriers. It also reviewed physician cultural sensitivity training programs and found they are insufficient. The document created a presentation on how patient navigators can help address these barriers by informing patients about clinical trials and assisting with the enrollment process. It recommends developing a community health worker/patient navigator program to recruit minority patients from community centers and guide them through cancer treatment and clinical trial enrollment at hospitals.
Project ECHO aims to expand access to specialty healthcare for common and complex diseases in rural and underserved areas through its teleECHO model. It uses videoconferencing and case-based learning to train primary care providers to safely and effectively treat diseases like hepatitis C. Evaluations show providers gain clinical skills and patients achieve similar treatment outcomes to specialty clinics. The model has been successfully implemented for over a dozen disease areas.
2014 Palmetto Care Connections Annual Meeting Presentationkfp1956
This document discusses remote patient monitoring and its role in addressing challenges in the current healthcare system. It outlines how remote patient monitoring can help transform care delivery from a volume-based model to a value-based model. It provides examples of remote patient monitoring programs that have demonstrated reductions in hospitalizations, emergency room visits, and costs through improved management of chronic conditions. The document concludes that remote patient monitoring presents opportunities to support new care delivery models and reimbursement approaches that focus on quality and value over volume.
CUPS presentation 2 from Sept 2017 CACHC conferencecachc
This document summarizes a community-based program called Connect 2 Care (C2C) that provides intensive case management for socially vulnerable patients in Calgary who frequently use emergency departments and acute care services. The program is a partnership between Calgary Urban Project Society (CUPS) health clinics, Alpha House shelters, and local hospitals. Early evaluation data shows C2C is successfully housing clients, connecting them to primary care, and reducing acute care use. The program aims to scale up its model across Calgary and Alberta to better support this high-needs population through care coordination and addressing social determinants of health.
Physician density may correlate to worse urologic cancer outcomes according to a study examining cancer mortality rates. The study analyzed cancer mortality rate data from the CDC and found significantly higher renal cancer mortality rates in areas with low physician density. Additionally, there was a negative association between median family income and bladder and renal cancer mortality rates. The study compared counties with the highest and lowest mortality rates for prostate, bladder, and renal cancers and found those with high rates had significantly lower physician population densities and higher rates of residents without health insurance compared to low mortality rate counties.
This document discusses cancer in older adults and the use of comprehensive geriatric assessment (CGA) to evaluate older cancer patients. It makes three key points:
1. CGA can help oncologists define "elderly" cancer patients and evaluate them for treatment. Factors like frailty, comorbidities, and functional status are more important than age alone.
2. CGA has prognostic value, as it can identify risk factors for toxicity from chemotherapy and predict patient outcomes. Frail older patients have higher risks of adverse events.
3. CGA tools have been developed that use factors like frailty, blood pressure, liver/kidney function to predict risks of severe toxicity and categorize
This document discusses the experience of the Saskatchewan Cancer Agency Patient Family Advisory Council (PFAC) in involving patients and families in health technology assessment. It begins by providing background on the Saskatchewan Cancer Agency and its establishment of the PFAC to ensure patient- and family-centered care. The PFAC initially focused on tangible accomplishments but realized more meaningful engagement required challenging assumptions. Over time, as trust was built, the PFAC felt comfortable questioning staff and asking them to present as guests rather than feeling represented. This helped clarify roles for change and idea implementation, as some staff were unclear on how patient input affected decision-making.
1) Native Hawaiians experience higher rates of certain cancers compared to other ethnic groups in Hawaii. They also face cultural, geographic, and health literacy barriers to participation in clinical trials.
2) Effective strategies to increase Native Hawaiian enrollment in clinical trials have included education programs for physicians and communities, partnerships between organizations, and support services for patients.
3) Current research is using focus groups to better understand attitudes that may affect clinical trial participation among Native Hawaiians in order to further improve representation.
A national approach to improve the quality of Aftercare for survivors of TYA cancer - End of Treatment Summaries / Care Plans
Dr Helen Jenkinson, Consultant Paediatric Oncologist
on behalf of the NCSI steering group
Event held in London on Wednesday 9 October with the Teenage and Young Adult (TYA) Centre Champions and our Clinical Leads to share learning, good practice examples, the successes, challenges and barriers to implementing:
Treatment summaries
End of treatment care plans
Increased self-management for TYAs after cancer treatment
The output from the meeting will be to define what support NHS IQ can provide locally to assist TYA teams in order to make progress with their implementation plans.
This literature review covers three topics: pneumonia, lung cancer, and pulmonary fibrosis. For pneumonia, it summarizes that the declines in childhood pneumonia hospitalizations observed after the introduction of PCV7 vaccines were sustained over a decade. It also found substantial reductions in adult pneumonia hospitalizations. For lung cancer, it discusses findings from several large randomized controlled trials that low-dose CT screening detects more early-stage lung cancers compared to chest radiography and tends to result in a stage shift toward earlier diagnoses. For pulmonary fibrosis, it reviews that the natural history can vary significantly, from complete resolution to progressive fibrosis leading to respiratory failure.
Theo Georghiou and Dr Jessica Sheringham: Data and Colorectal Cancer, 30 June...Nuffield Trust
This document summarizes a study that analyzed linked primary care, hospital, and cancer registry data to examine diagnostic pathways for colorectal cancer patients in North East London. The study found that it was feasible to link these routine data sources. Analysis at the population level identified factors associated with emergency presentations, such as late cancer stage and fewer GP visits. Examination of individual pathways showed diversity in healthcare use prior to diagnosis and identified cases for further audit.
Stm functional showdeck mockup v2 w refsmonkmartinez
1. The study examined rates of hematopoietic stem cell transplantation (HCT) for leukemia, lymphoma, and multiple myeloma between 1997-2002 using data from the Center for International Blood and Marrow Transplant Registry and SEER cancer registry.
2. It found that Caucasians were more likely than African Americans to receive HCT, including autologous, HLA identical sibling, and unrelated donor HCT.
3. Men were slightly more likely than women to receive HCT overall, but this difference was only significant for autologous HCT.
Don't miss our upcoming webinars. Subscribe today!
This presentation will highlight the promising new therapeutic strategies in the treatment of gliomas, with a focus on trials or therapies that will soon be available for Canadian patients.
View the YouTube video: https://youtu.be/ibbEuvSF7xY
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Weight loss among patients with Head and Neck Cancer at St Vincent's Hospital...Cancer Institute NSW
Patients with Squamous cell carcinoma (SCC) of the Head and Neck (H&N) are often treated with curative intent using treatment protocols placing them at high risk of nutritional decline. Recently released COSA guidelines recommend that prophylactic enteral feeding should be considered for T4 upper aerodigestive tract tumours undergoing concurrent chemoradiotherapy. Evidence is yet to identify optimal method of nutrition intervention and timing across all tumour stages in this population.
JMCP 2016 Access to new meds for hep C in Medicaid membersKimberly Lenz
This document summarizes a study that evaluated access to new hepatitis C virus (HCV) treatment medications among Medicaid patients in Massachusetts. The study found that only 5.1% of MassHealth members with HCV had their healthcare provider submit a prior authorization request for treatment with sofosbuvir or simeprevir. Patients who had a treatment request were more likely to be older, have advanced liver disease or have been recently treated for HCV, and less likely to have a substance use disorder. Nearly all (90%) of treatment requests were approved. The results suggest that while the Medicaid program did not restrict access, other factors like provider prioritization and patient barriers influenced who received treatment.
Don't miss our upcoming webinars: Subscribe today!
In this webinar:
Dr. Krista Noonan is a medical oncologist specializing in thoracic and genitourinary malignancies at BC Cancer, Surrey Centre. Her research interests focus on thoracic and genitourinary malignancies and health services research. On Thursday, February 27, join Dr. Noonan as she: - Reviews the advancements in systemic therapy in lung cancer over the past decade - Highlights how the advancements in systemic therapy have dramatically improved quality of life and length of life.
View the video: https://youtu.be/3DaUwQ8ab44
To learn more about CCSN, visit us at survivornet.ca
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
5th Annual Early Age Onset Colorectal Cancer Summit - Session II: Family History Ascertainment in the US - What Steps are Needed to Improve the Well Documented Less Than Optimal Status of this Situation?
Don't miss our upcoming webinars! Subscribe today!
In April, CCSN virtually met with MPPs throughout Ontario to discuss our COVID-19 and Cancer Care - Wave 2 Survey. During these meetings, we discussed the difficulty cancer patients and pre-diagnosis patients have had with accessing cancer services during the pandemic and the importance of ensuring the cancer patients receive their 1st and 2nd vaccine doses in a timely manner.
In this webinar, CCSN's Public Policy Analyst Conrad will begin by sharing some of the highlights from our meetings with Ontario MPPs. He will then turn things over to our patient advocates and they will share some of their reflections from our meetings as well as their own experiences with accessing cancer care during the pandemic. Lastly, Conrad will take a closer look at the Ontario data from our survey.
View the YouTube video: https://youtu.be/05u4i89WFfQ
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
Don't miss our upcoming webinars! Subscribe today!
In this webinar:
In May-June, 2020, the Canadian Cancer Survivor Network (CCSN) commissioned Leger to conduct a national survey to evaluate the impact that COVID-19 has had on cancer patients, survivors, pre-diagnosis patients, and caregivers. The results of our first survey revealed that the pandemic response has triggered another public health crisis - the postponement and cancellation of essential cancer tests, procedures, and treatments.
CCSN commissioned Leger for a second survey in December, 2020 to evaluate the impact that the suspension of cancer services during the first wave is currently having on those who have been affected by cancer.
Join CCSN and Leger as we present the results of the COVID-19 and Cancer Care Disruption in Canada Survey - Wave 2 and hear from members of the cancer community about how the pandemic has directly impacted them.
View the YouTube video: https://youtu.be/qN4Hq7OtBys
Follow CCSN on social media:
Twitter - https://twitter.com/survivornetca
Facebook - https://www.facebook.com/CanadianSurvivorNet
Instagram: https://www.instagram.com/survivornet_ca/
Pinterest - https://www.pinterest.com/survivornetwork
The document discusses barriers to minority patient enrollment in cancer clinical trials. It conducted a systematic literature review on barriers and found that minority populations experience systemic, institutional, and individual barriers. It also reviewed physician cultural sensitivity training programs and found they are insufficient. The document created a presentation on how patient navigators can help address these barriers by informing patients about clinical trials and assisting with the enrollment process. It recommends developing a community health worker/patient navigator program to recruit minority patients from community centers and guide them through cancer treatment and clinical trial enrollment at hospitals.
Project ECHO aims to expand access to specialty healthcare for common and complex diseases in rural and underserved areas through its teleECHO model. It uses videoconferencing and case-based learning to train primary care providers to safely and effectively treat diseases like hepatitis C. Evaluations show providers gain clinical skills and patients achieve similar treatment outcomes to specialty clinics. The model has been successfully implemented for over a dozen disease areas.
2014 Palmetto Care Connections Annual Meeting Presentationkfp1956
This document discusses remote patient monitoring and its role in addressing challenges in the current healthcare system. It outlines how remote patient monitoring can help transform care delivery from a volume-based model to a value-based model. It provides examples of remote patient monitoring programs that have demonstrated reductions in hospitalizations, emergency room visits, and costs through improved management of chronic conditions. The document concludes that remote patient monitoring presents opportunities to support new care delivery models and reimbursement approaches that focus on quality and value over volume.
CUPS presentation 2 from Sept 2017 CACHC conferencecachc
This document summarizes a community-based program called Connect 2 Care (C2C) that provides intensive case management for socially vulnerable patients in Calgary who frequently use emergency departments and acute care services. The program is a partnership between Calgary Urban Project Society (CUPS) health clinics, Alpha House shelters, and local hospitals. Early evaluation data shows C2C is successfully housing clients, connecting them to primary care, and reducing acute care use. The program aims to scale up its model across Calgary and Alberta to better support this high-needs population through care coordination and addressing social determinants of health.
CSHGP Operations Research Findings_David Shankin_5.8.14CORE Group
The project aimed to improve maternal and child health in rural Honduras by establishing community-based health units (UCOS) staffed by volunteers. An evaluation found that the UCOS model significantly improved six coverage indicators, such as the proportion of the target population served. It also improved some outcomes, like the number of women receiving prenatal care. Costs to clients were much lower than using existing facilities. The Ministry of Health recognized benefits but recommended further testing the model. ChildFund continues supporting some initial UCOS sites and expanding the approach.
Cheshire and Wirral Best Practice event - 8 NovemberInnovation Agency
The document outlines plans for developing integrated care communities across South Cheshire and Vale Royal. Key points include:
- The formation of 5 care community teams to provide coordinated, patient-centered care across the region.
- Initial priority projects include developing the care community teams, improving GP out-of-hours care, and musculoskeletal physiotherapy.
- Achievements so far include aligning staff to the 5 communities, implementing rapid response services, and beginning multidisciplinary team meetings.
- Future goals involve strengthening primary care partnerships, expanding social care support, and using data to better manage patient risk levels.
The document discusses population-based screening for non-communicable diseases (NCDs) like diabetes, hypertension, and cancers in India. It notes that NCDs are a leading cause of death and outlines the roles that ASHAs, ANMs, medical officers, and other staff play in screening communities and referring individuals to health facilities for diagnosis and treatment. The goal of population-based screening is to establish a sustainable system for early detection and management of NCDs to improve health outcomes and quality of life.
Aaron Brizell - ECO 17: Transforming care through digital healthInnovation Agency
Presentation by Aaron Brizell, Population Health Programme Manager, Wirral University Teaching Hospital NHS Foundation Trust: The benefits of system-wide population health and analytics at ECO 17: Transforming care through digital health on Tuesday 4 December at Lancaster University, Lancaster
A Mixed Method Study Evaluating an Innovative Care Model for Rural Outpatient...DataNB
The care model in Saint John, New Brunswick, supports outpatient mastectomies and lumpectomies, the primary treatments for non-metastatic breast cancer. Given the geographic distribution of the province, many patients travel long distances to receive surgical care at regional hospitals. These patients may face: i) a stressful trip home post-surgery, ii) expensive hotel accommodations; or iii) medically unnecessary hospital stays. Therefore, the Breast Health Program partnered with Delta Hotels by Marriott in Saint John to create the “Delta Oasis” program that offers rural outpatient breast surgery patients and their families’ free accommodations and extramural care. The present study used a mixed-methods approach to investigate patients’ experiences with this program. We found that the program yielded positive benefits for patients, including reduced stress and discomfort associated with travel, and for the Delta Hotels, such as increased customer loyalty and word-of-mouth advertising (i.e., incentives to continue offering the program). Furthermore, there are significant financial implications associated with the Delta Oasis program that could yield health system savings; hotel accommodations are five times less costly than traditional hospital stays for breast surgery perioperative care. The Delta Oasis program is a beneficial alternative to inpatient care that is often not medically necessary for breast cancer surgery. Thanks to the innovative partnership between Saint John’s Breast Health Program and Delta Brunswick Hotel, the Delta Oasis program generates zero cost to the provincial healthcare system. Establishing funding partners and adapting this service to other types of low-risk surgery could bring forth added health system savings.
Dr Jeremy Veillard: High Use in the Health Sector in Canada, 30 June 2014Nuffield Trust
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Transportation cost and retention in hiv care in rural Haiti
1. Transportation cost and
retention in HIV care in Haiti
Leonard Sowah, MBChB, MPH
Assistant Professor of Medicine
University of Maryland School of Medicine
2. Acknowledgements
• Dr. Christa Desiral – who helped with data
collection
• Miss Blaise – Who was very helpful with our
data collection
• Dr. Ivy Mwangi – Who gave advice on data
analysis
• Regine – Who helped in data collection
3. Background
• HIV infection has been shown to
disproportionately affect economically
disadvantaged individuals
• Studies in most resource limited settings and
even in developed world suggest that
transportation cost can affect HIV treatment
outcomes
4. Background
• Even in the US studies done in Southern USA suggest that
cost of transportation may affect retention in HIV clinic1
• Studies done in Sub-Saharan Africa using qualitative data
suggests that patients have to make difficult decisions to
make it to clinic appointment2
• In one study on loss to follow-up in Uganda a participant
stated; “sometimes I have to do without maybe salt,
paraffin, kerosene, so that I can get transportation to come
here2
• There is a strong correlation between compliance to clinic
appointment and failure of treatment
1. Sherer R, Stieglitz K, Narra J, et al. HIV multidisciplinary teams work: support services improve access to and retention in HIV primary care. AIDS care.
2002;14(S1):31-44.
2. Tuller DM, Bangsberg DR, Senkungu J, Ware NC, Emenyonu N, Weiser SD. Transportation costs impede sustained adherence and access to HAART in a clinic
population in southwestern Uganda: a qualitative study. AIDS and Behavior. 2010;14(4):778-784.
5. Background
• Cost of HIV care however increases
significantly if patients fail first line regimens
• HIV treatment interruptions therefore
significantly affect the stability and economic
indices of the health system1
• Losina et al calculated that treatment
interruption on average reduces life-expectancy
by 4.67 years2
1. Sanders D, Sambo A. AIDS in Africa: the implications of economic recession and structural adjustment. Health Policy and
Planning. 1991;6(2):157-165.
Losina E, Touré H, Uhler LM, et al. Cost-effectiveness of preventing loss to follow-up in HIV treatment programs: a Cote
d'Ivoire appraisal. PLoS medicine. 2009;6(10):e1000173.
6. Study Rational
Aim
• To determine if the cost of transportation
predicts loss to follow up in HIV Care
• Study Hypothesis
– Patients living in locations with transportation cost
greater than $2 are more likely to be lost to care
– Patients living in locations that require two or
more public transport trips to travel to clinic
would be more likely to be lost to care
7. Study Rational
• We also considered other variables such
as:
– Age of patient
– Sex
– Milot residents vrs non-residents
– Residence in proposed clinic catchment area
– Enrolment CD4 count
8. Study Setting
• Hopital Sacre Coeur de Milot, HIV Clinic
• Located in Northern Haiti 12 miles southwest
of Cap Haitien
• There are several other HIV treatment sites in
the area
• Clinic offers transportation assistance to
patients however policy on assistance has
gone through multiple revisions
10. Study Population
• All patients enrolled in clinic prior to
December 31st, 2006
• Exclusion Criteria
– Patients < 18 yrs of age as at December 31st 2006
– Patients without any form of address information
in Medical Record
– Patients resident in locales outside the Northern
Department
12. Patient Enrollment Chart
599 individuals enrolled in clinic from
November 2004 – December 2006
53 individuals with age <18yrs
by year end 2006 excluded
546 adult patients
439 adults > 18 years old with
addresses remaining
107 individuals without
addresses excluded
29 individuals resident outside
of the Northern Department
excluded
Final sample of 410 adult patients
13. Study Methods
• Retrospective cohort design
• Data collection was by chart review of patients
enrolled from November 2004 – December 31st,
2006
• Social workers were interviewed to obtain
information on clinic policies on patient
enrolment follow-up and patient support
• Data was analyzed using Cox’s proportional
hazards regression to determine independent
predictors of being lost to follow-up.
14. Municipality Cost of two-way Taxi
Data on (Haitien Transportation Gourde)
Costs
Cost of two-way
taxi (US Dollar)
Distance in Miles
to Milot
Milot 40.00 0.94
Cap Haitien 40.00 0.94 11.24
Grande Riviere du Nord 80.00 1.88 3.63
Plaine du Nord 80.00 1.88 5.46
Quartier Morin 80.00 1.88 7.58
Limonade 80.00 1.88 8.03
Dondon 240.00 5.65 6.73
Limbe 90.00 2.12 15.21
Acul du Nord 100.00 2.35 9.16
Bahon 140.00 3.29 14.06
Borgne 280.00 6.59 30.06
Bas Limbe 200.00 4.71 19.16
Ranquitte 240.00 5.65 18.75
Sainte Raphael 240.00 5.65 14.61
Pignon 380.00 8.94 24.98
Pilate 340.00 8.00 25.24
15. Table showing distribution of patients by various covariates and adjusted
and unadjusted hazard ratios with age groups up to 60yr and above
16. Table showing unadjusted and adjusted hazards of
loss to follow by cost of transportation and distance
with age as two categories.
18. Kaplan-Meier curves of retention by transportation cost
and number of trips
All p-values are calculated by the log-rank test with the null hypothesis that the
retention for the two groups are equal
20. Summary of Results
• The four year retention rates for patients from
communities with < $2 transportation cost is
81.9% cf 68.9% for those > $2
• Individuals from communities requiring more
than $2 for two way transportation costs are
1.91 times as likely to be lost to care in 48
mths (p-value – 0.02)
21. Summary of Results
• Younger patients aged < 30 yrs were 3 times
as likely to be lost to care in 48 mths
compared to older patients (p-value – 0.001)
• Individuals living in Milot did not have
significantly better retention in clinic
compared to all other patients
• Male patients were 1.7 times as likely to be
lost to care compared to their female
counterparts (p-value – 0.02)
22. Summary of Results
• Patients with CD4 counts less than 200 at time
of enrolment are 1.68 times more likely to be
lost to care after 48 mths (p-value 0.02)
• Male patients were 1.5 times more likely to
come from places with transportation cost >
$2 (p-value – 0.16)
• Mean transportation cost for females $1.36
(SD: 0.94), males $ 1.67 (SD:1.74)
23. Discussion
• Are patients with transportation cost > $2 who do
not show up in clinic lost to care or just
transferred to another facility?
• Why are younger patients < 30 yrs 3 times more
likely to be lost to care?
• Why are men more likely to come from places
with higher transportation costs?
• Why are some patients coming from places like
Hinche 40 miles, Borgne 30 miles and Pilate 25
miles?
24. Study Team
• Leonard Sowah1, MD,
MPH
• Franck Turenne2, MD
• Ulrike Buchwald1, MD
• Nephtalie Mesidor2, MD
• Guesly Delva1, MD
• Camille Dessaigne3, MS
• Anthony Edozien1, MD
• Harold Previl4, MD
• Devang Patel1, MD
• Robert Redfield1, MD
• Anthony Amoroso1, MD
• Institutions
– Institute of Human
Virology, Baltimore
MD1,
– Université Notre
Dame d’Haiti, Port
au Prince, Haiti2,
– University of
Miami, Miami FL3,
– Hopital Sacre
Coeur, Milot, Haiti4
Distances to Milot were obtained from www.distancecalculator.globalfeed.com on 6/22/2014 using the lower value of estimated travel/road distance
Data on transportation cost was obtained from clinic social worker estimates of transportation cost from the different localities within the Northern department and converted into US dollars using 2010 Haitian Gourde US dollar exchange rate
The adjusted hazard ratio was after adjusting for age as 5 different age groups, sex and enrollment CD4 greater or less than 200 cells/µl.