This document describes a study conducted at a resident clinic to reduce inappropriate Pap testing. The researchers implemented an intervention where they created a dedicated "Pap clinic" with a specific EMR template highlighting cervical cancer screening guidelines. In a pilot study before the intervention, 17% of Pap tests were inappropriate. After the intervention, the rate of inappropriate Pap tests significantly decreased to 1.7%. The intervention was effective at improving adherence to Pap testing guidelines. However, the study had limitations like a small sample size. Overall, the results suggest creating dedicated clinics and EMR templates can help reduce over-screening in primary care settings.
This study analyzed data from 10 randomized controlled trials testing post-discharge care management programs for heart failure patients. It found that programs using multidisciplinary teams and in-person communication significantly reduced hospital readmissions and readmission days compared to routine care. However, programs relying only on telephone follow-up did not significantly reduce hospital use. The study concludes that payers should incentivize hospitals to adopt chronic care management programs shown to effectively reduce hospital utilization, which could lower costs for programs like Medicare that cover many patients with chronic illnesses.
While clinical trials represent leading cancer research, less than 5% of cancer patients enroll due to a lack of awareness and resources. Physicians have little time to enroll patients, and patients and doctors have misconceptions about clinical trials. Molecular targeted trials, based on genetic markers, require less patients than traditional trials to produce meaningful results. Unlike traditional trials, targeted trials do not use placebos and allow switching to tested drugs if beneficial. While complex genetic profiling is required for targeted trials, they provide more personalized treatment with fewer side effects than chemotherapy. Focusing clinical trial searches on predefined molecular markers can help patients find more suitable targeted trials.
This study assessed adherence to recommendations for follow-up imaging made in emergency abdominal ultrasound examinations. Of 1404 exams, recommendations were made in 329 reports (23.4%), totaling 355 recommendations. Adherence was 52.9%, defined as the recommended study being performed. Adherence was influenced by factors like ultrasound findings being abnormal versus normal, the organ system/pathology involved, and whether findings matched clinical suspicion. Addressing these factors could improve adherence and continuity of patient care.
The document discusses diagnostic error in healthcare. It begins by noting that inaccurate diagnoses, incorrect treatments, and lack of diagnoses contribute to unnecessary costs, inefficiency, and patient dissatisfaction. Improving diagnostic accuracy can help achieve quality, control costs, and increase patient satisfaction. The document then discusses:
- The high incidence of diagnostic errors, which result in tens of thousands of deaths per year and enormous financial tolls.
- Evidence that diagnostic errors commonly cause patient harm and occur across primary care, inpatient, and outpatient settings.
- An innovative solution of independent virtual second opinions to address diagnostic errors by improving accuracy and ensuring appropriate treatment.
The document summarizes 15 research articles that evaluated the accuracy of the Confusion Assessment Method for the ICU (CAM-ICU) in identifying delirium in adult ICU patients compared to practitioner judgment. The majority of studies were quasi-experimental and found that the CAM-ICU more accurately identified delirium than practitioner judgment alone. However, the CAM-ICU had lower sensitivity than specificity, so it could potentially under-identify delirium. The studies concluded that while the CAM-ICU is currently the most accurate tool, it should be used along with practitioner judgment until a screening tool with higher sensitivity is developed.
Webinar: Oncology Trial Recruitment: Challenging Indications and Challenging ...Medpace
Medpace experts discuss how to overcome oncology recruitment challenges for clinical trials for specific populations, indications, and challenging studies.
1) The document discusses improving outcomes and endpoints in cancer trials by better defining what is important to measure, making endpoints more understandable for patients, and advancing endpoints to reflect changes in trial design and treatments.
2) It notes that endpoints need to show clinically relevant benefits to patients, and that improvements in trial design should be accompanied by improvements in available endpoints.
3) Stakeholders including clinicians, patients, and regulators must work together to determine the best approach for research that ensures accountability and optimizes the use of resources.
Implementing a shared care model to prevent liver cancer and improve chronic ...Cancer Institute NSW
Hepatocellular cancer (HCC) is among the top 10 causes of cancer death in Australia, with ~80% of cases attributable to chronic viral hepatitis. Although 60-80% of HCCs are preventable by antiviral therapies, multiple barriers exist in the diagnostic and treatment continuum. Chronic hepatitis B (CHB) is the main cause for rising HCC rates in Western Sydney, where the greatest burden of disease is among people born in hepatitis B endemic countries.
This study analyzed data from 10 randomized controlled trials testing post-discharge care management programs for heart failure patients. It found that programs using multidisciplinary teams and in-person communication significantly reduced hospital readmissions and readmission days compared to routine care. However, programs relying only on telephone follow-up did not significantly reduce hospital use. The study concludes that payers should incentivize hospitals to adopt chronic care management programs shown to effectively reduce hospital utilization, which could lower costs for programs like Medicare that cover many patients with chronic illnesses.
While clinical trials represent leading cancer research, less than 5% of cancer patients enroll due to a lack of awareness and resources. Physicians have little time to enroll patients, and patients and doctors have misconceptions about clinical trials. Molecular targeted trials, based on genetic markers, require less patients than traditional trials to produce meaningful results. Unlike traditional trials, targeted trials do not use placebos and allow switching to tested drugs if beneficial. While complex genetic profiling is required for targeted trials, they provide more personalized treatment with fewer side effects than chemotherapy. Focusing clinical trial searches on predefined molecular markers can help patients find more suitable targeted trials.
This study assessed adherence to recommendations for follow-up imaging made in emergency abdominal ultrasound examinations. Of 1404 exams, recommendations were made in 329 reports (23.4%), totaling 355 recommendations. Adherence was 52.9%, defined as the recommended study being performed. Adherence was influenced by factors like ultrasound findings being abnormal versus normal, the organ system/pathology involved, and whether findings matched clinical suspicion. Addressing these factors could improve adherence and continuity of patient care.
The document discusses diagnostic error in healthcare. It begins by noting that inaccurate diagnoses, incorrect treatments, and lack of diagnoses contribute to unnecessary costs, inefficiency, and patient dissatisfaction. Improving diagnostic accuracy can help achieve quality, control costs, and increase patient satisfaction. The document then discusses:
- The high incidence of diagnostic errors, which result in tens of thousands of deaths per year and enormous financial tolls.
- Evidence that diagnostic errors commonly cause patient harm and occur across primary care, inpatient, and outpatient settings.
- An innovative solution of independent virtual second opinions to address diagnostic errors by improving accuracy and ensuring appropriate treatment.
The document summarizes 15 research articles that evaluated the accuracy of the Confusion Assessment Method for the ICU (CAM-ICU) in identifying delirium in adult ICU patients compared to practitioner judgment. The majority of studies were quasi-experimental and found that the CAM-ICU more accurately identified delirium than practitioner judgment alone. However, the CAM-ICU had lower sensitivity than specificity, so it could potentially under-identify delirium. The studies concluded that while the CAM-ICU is currently the most accurate tool, it should be used along with practitioner judgment until a screening tool with higher sensitivity is developed.
Webinar: Oncology Trial Recruitment: Challenging Indications and Challenging ...Medpace
Medpace experts discuss how to overcome oncology recruitment challenges for clinical trials for specific populations, indications, and challenging studies.
1) The document discusses improving outcomes and endpoints in cancer trials by better defining what is important to measure, making endpoints more understandable for patients, and advancing endpoints to reflect changes in trial design and treatments.
2) It notes that endpoints need to show clinically relevant benefits to patients, and that improvements in trial design should be accompanied by improvements in available endpoints.
3) Stakeholders including clinicians, patients, and regulators must work together to determine the best approach for research that ensures accountability and optimizes the use of resources.
Implementing a shared care model to prevent liver cancer and improve chronic ...Cancer Institute NSW
Hepatocellular cancer (HCC) is among the top 10 causes of cancer death in Australia, with ~80% of cases attributable to chronic viral hepatitis. Although 60-80% of HCCs are preventable by antiviral therapies, multiple barriers exist in the diagnostic and treatment continuum. Chronic hepatitis B (CHB) is the main cause for rising HCC rates in Western Sydney, where the greatest burden of disease is among people born in hepatitis B endemic countries.
The document discusses how patients can find, select, and shape clinical trials in order to identify research that is most beneficial. It emphasizes that patients should: understand their treatment options and scientific landscape; carefully evaluate trial design and motivations; and recognize that various stakeholders have competing interests. The goal is not just increasing the number of trials, but improving trial quality so they answer patients' needs. Patients are encouraged to engage with research groups long-term to help guide trial design toward options that offer meaningful benefit.
This document discusses patient engagement in drug development. It defines patients as those with or at risk of a medical condition, along with their families and caregivers. Patient engagement is described as a bi-directional relationship built on principles like partnership and transparency. The document outlines how patients are experts on their disease based on factors like symptoms, quality of life, and treatment experiences. It traces the evolution of patient engagement through different versions of PDUFA (Prescription Drug User Fee Act) and guidance documents from the FDA. The role of patients is described as continuous throughout the drug development lifecycle, from helping design clinical trials to aiding in data interpretation. Different levels of engagement are identified, from being a study participant to leading research
Predictors of MDT review and the impact on lung cancer survival for HNELHD re...Cancer Institute NSW
Review by a Multidisciplinary Team (MDT) has been shown to lead to increased rates of surgical resection, radiotherapy, chemotherapy and timeliness of care. Most recently, the Victorian lung cancer patterns of care study have found that MDT review is an independent predictor of lung cancer survival.
2018 Genetic Testing Assessment: These slides discuss issues associated with genetic testing interpretation. All who order genetic testing should be familiar with these recent publications.
This research poster presentation examines the impact of increased protein intake on pressure ulcer prevalence in nursing home patients aged 65 and older with Braden Scale scores between 15-18. The study aims to decrease pressure ulcer rates by providing an extra 30g of protein in a daily smoothie to the sample population. Skin assessments using the Braden Scale will be conducted before and after the 6-week intervention to evaluate changes in pressure ulcer risk levels. The poster outlines the background, PICO question, literature review supporting the benefits of protein supplementation, methods of implementation, and plans for data analysis to determine if the intervention is effective in reducing pressure ulcer prevalence.
This study assessed the efficacy of using SMS reminders to improve adherence to a 6-dose antimalarial treatment in Zambia. The study involved 96 participants who were randomized into an intervention group that received SMS reminders or a control group. Adherence was measured using electronic monitors on medication bottles. The results found no significant difference in adherence rates between the groups, with both showing adherence over 65%. The study identifies limitations and implications for further research on using mHealth to improve malaria treatment adherence.
No 3 tue 0800 clanon tue universal testing atlanta kac pro 2CDC NPIN
Routine HIV screening is a proven, cost-effective public health intervention that can help stop the spread of AIDS in the U.S. Screening allows for earlier diagnosis and better health outcomes. While some argue HIV screening requires special procedures due to its stigma and history, opt-out screening models have shown to significantly reduce patient anxiety about testing and normalize HIV testing. Most Americans believe HIV screening should be treated like other routine health screenings.
This document describes a pilot study that evaluated the impact of including a pharmacist in the transitions of care process for patients discharged from an inpatient family medicine service. Key findings include:
- A pharmacist called patients within 2-7 days of discharge and documented any interventions in the electronic medical record. This reduced medication errors and delays in initiating new medications.
- A physician questionnaire found that including the pharmacist improved quality of care, reduced medication errors and prior authorization delays, and saved physician time with medication reconciliation.
- The readmission and emergency department visit rates during the 6 month pilot period were lower than the previous 6 months, suggesting the pharmacist interventions may have prevented readmissions.
This document provides an overview of precision medicine and pharmacogenomics. It discusses barriers to implementing pharmacogenomic testing, key medical settings and patient populations to target, and considerations for integrating test results into clinical workflows. Evidence is presented showing pharmacogenomic testing can reduce adverse drug reactions and alter prescribing. The document emphasizes engaging patients and generating more evidence of the clinical value and economic benefits of pharmacogenomic testing.
Evaluation of comorbid autoimmune diseases among patients and family members enrolled in the Alopecia
Areata Registry, Biobank & Clinical Trials Network.
This document describes a randomized controlled trial that tested the effectiveness of the Cancer Screening Office Systems (Cancer SOS) intervention at increasing cancer screening rates among patients at primary care clinics serving disadvantaged populations.
The intervention included a cancer screening checklist and color-coded stickers to track screening tests. Eight clinics were randomized to the intervention or control group. Screening rates for mammograms, Pap smears, and fecal occult blood tests were compared before and 12 months after the intervention.
The results showed that the intervention significantly increased screening rates for mammograms and fecal occult blood tests compared to the control group, after adjusting for baseline differences. There was also a trend toward increased Pap smear screening. The intervention
This study surveyed pharmacists in Minnesota to identify gaps between the information resources taught in school and those available in practice. The survey assessed which resources pharmacists have access to and use most frequently in their workplace. Results showed pharmacists have the most access to and use Drug Facts and Comparisons, Micromedex, Pharmacists Letter, and UpToDate most frequently. Factors like reputation, accuracy, ease of use, and cost influence which resources pharmacists choose. Rural pharmacists had less access than urban pharmacists, suggesting interventions are needed to broaden rural pharmacists' access to evidence-based resources.
This study examined the impact of passive and active electronic medical record alerts on referrals to physical therapy and medication management for elderly patients at high risk of falls. The study found that a passive alert showing fall prevention resources had little impact on physical therapy referrals. However, an active alert identifying high-risk medications was associated with increased response to the passive alert and led to more medication reviews and discontinuations. The results suggest that active alerts may be more effective than passive alerts at prompting clinician action to address fall risk factors.
1) Drug development involves multiple phases of clinical trials in humans (phases I-IV) to test dosing, safety and efficacy in an increasing number of patients before regulatory approval and market access.
2) Patient involvement in clinical research is important to ensure trials address patient priorities and perspectives on risk/benefit, endpoints, and trial design elements like inclusion criteria.
3) Key elements of a clinical trial protocol include type of comparisons, randomization, blinding, endpoints, inclusion/exclusion criteria, schedule of events, informed consent process, and patient reported outcomes.
Results of an Online Survey of Stakeholders Regarding Barriers and Solutions ...John Reites
The survey found that the most significant barrier to clinical trial recruitment according to stakeholders was finding patients who meet eligibility criteria. The next most significant barriers were insufficient staff time for recruitment activities, followed by the length and complexity of consent forms, and protocol requirements other than eligibility criteria. Suggestions to overcome barriers included broadening eligibility criteria, improving planning, using effective recruitment methods and technology, simplifying processes, and improving staff support. Most stakeholders were optimistic that national recruitment rates would increase over the next 5-10 years if effective partnerships were formed between sectors like patient advocates, researchers, sponsors, and regulators.
Our main involvement with your clinical research recruitment program concludes with processing the responses to your mailer. As our staff members direct the respondents to your site, you can begin conducting final interviews to complete the clinical trial recruitment process.
Cancer patients’ experiences in one tertiary referral emergency department (E...Cancer Institute NSW
The demand on Australian EDs has increased by an average of 4.2% each year while the cancer incidence rate has doubled since 1991. Many patients with cancer present to EDs but may be better managed using alternative healthcare models.
This document discusses challenges in interpreting health-related quality of life (HRQOL) findings across cancer clinical trials. Two hypothetical trials that tested the same treatment showed conflicting HRQOL results. This was because the trials may have assessed different HRQOL areas, endpoints, handling of missing data, and analysis populations. To address this, international collaboration is needed to set standards for HRQOL analyses in cancer trials. This would help ensure HRQOL questions, designs, analyses and interpretations are consistent across trials.
This document discusses challenges in using Bayesian and decision analysis approaches for regulating medical products. It notes issues like subjectivity in choosing priors, controlling type I error rates, and the need for legal availability of prior information. Promising areas for using prior information include pediatric trials, rare diseases, safety, and expedited access programs. Bayesian adaptive designs allow interim analyses to optimize sample size and model-based likelihoods. Decision analysis can make benefit-risk determinations more explicit through tools like influence diagrams and considering patient preferences. The highest value of Bayesian approaches is in accounting for external evidence, using flexible trial designs, modeling likelihoods, developing transparent decision rules based on factors like medical need and patient perspectives.
Valuing the EQ-5D-Y Using a Discrete Choice Experiment: Do Adult and Adolesce...Office of Health Economics
Slides from a presentation OHE's Koonal Shah gave at the PROMs research conference on June 20th, 2018. The subject of the presentation was valuing the EQ-5D-Y using a discrete choice experiment: do adult and adolescent preferences differ?
1. The document discusses standard quizzing rules for a secret quiz including long connect questions at the end that provide additional points. The quiz master's decision is final.
2. It then provides a series of quotes criticizing the Iran nuclear deal and lists the various terrorist groups it claims will benefit from funds released to Iran.
3. Several multiple choice questions then test knowledge of individuals and organizations involved in recent events.
The document discusses how patients can find, select, and shape clinical trials in order to identify research that is most beneficial. It emphasizes that patients should: understand their treatment options and scientific landscape; carefully evaluate trial design and motivations; and recognize that various stakeholders have competing interests. The goal is not just increasing the number of trials, but improving trial quality so they answer patients' needs. Patients are encouraged to engage with research groups long-term to help guide trial design toward options that offer meaningful benefit.
This document discusses patient engagement in drug development. It defines patients as those with or at risk of a medical condition, along with their families and caregivers. Patient engagement is described as a bi-directional relationship built on principles like partnership and transparency. The document outlines how patients are experts on their disease based on factors like symptoms, quality of life, and treatment experiences. It traces the evolution of patient engagement through different versions of PDUFA (Prescription Drug User Fee Act) and guidance documents from the FDA. The role of patients is described as continuous throughout the drug development lifecycle, from helping design clinical trials to aiding in data interpretation. Different levels of engagement are identified, from being a study participant to leading research
Predictors of MDT review and the impact on lung cancer survival for HNELHD re...Cancer Institute NSW
Review by a Multidisciplinary Team (MDT) has been shown to lead to increased rates of surgical resection, radiotherapy, chemotherapy and timeliness of care. Most recently, the Victorian lung cancer patterns of care study have found that MDT review is an independent predictor of lung cancer survival.
2018 Genetic Testing Assessment: These slides discuss issues associated with genetic testing interpretation. All who order genetic testing should be familiar with these recent publications.
This research poster presentation examines the impact of increased protein intake on pressure ulcer prevalence in nursing home patients aged 65 and older with Braden Scale scores between 15-18. The study aims to decrease pressure ulcer rates by providing an extra 30g of protein in a daily smoothie to the sample population. Skin assessments using the Braden Scale will be conducted before and after the 6-week intervention to evaluate changes in pressure ulcer risk levels. The poster outlines the background, PICO question, literature review supporting the benefits of protein supplementation, methods of implementation, and plans for data analysis to determine if the intervention is effective in reducing pressure ulcer prevalence.
This study assessed the efficacy of using SMS reminders to improve adherence to a 6-dose antimalarial treatment in Zambia. The study involved 96 participants who were randomized into an intervention group that received SMS reminders or a control group. Adherence was measured using electronic monitors on medication bottles. The results found no significant difference in adherence rates between the groups, with both showing adherence over 65%. The study identifies limitations and implications for further research on using mHealth to improve malaria treatment adherence.
No 3 tue 0800 clanon tue universal testing atlanta kac pro 2CDC NPIN
Routine HIV screening is a proven, cost-effective public health intervention that can help stop the spread of AIDS in the U.S. Screening allows for earlier diagnosis and better health outcomes. While some argue HIV screening requires special procedures due to its stigma and history, opt-out screening models have shown to significantly reduce patient anxiety about testing and normalize HIV testing. Most Americans believe HIV screening should be treated like other routine health screenings.
This document describes a pilot study that evaluated the impact of including a pharmacist in the transitions of care process for patients discharged from an inpatient family medicine service. Key findings include:
- A pharmacist called patients within 2-7 days of discharge and documented any interventions in the electronic medical record. This reduced medication errors and delays in initiating new medications.
- A physician questionnaire found that including the pharmacist improved quality of care, reduced medication errors and prior authorization delays, and saved physician time with medication reconciliation.
- The readmission and emergency department visit rates during the 6 month pilot period were lower than the previous 6 months, suggesting the pharmacist interventions may have prevented readmissions.
This document provides an overview of precision medicine and pharmacogenomics. It discusses barriers to implementing pharmacogenomic testing, key medical settings and patient populations to target, and considerations for integrating test results into clinical workflows. Evidence is presented showing pharmacogenomic testing can reduce adverse drug reactions and alter prescribing. The document emphasizes engaging patients and generating more evidence of the clinical value and economic benefits of pharmacogenomic testing.
Evaluation of comorbid autoimmune diseases among patients and family members enrolled in the Alopecia
Areata Registry, Biobank & Clinical Trials Network.
This document describes a randomized controlled trial that tested the effectiveness of the Cancer Screening Office Systems (Cancer SOS) intervention at increasing cancer screening rates among patients at primary care clinics serving disadvantaged populations.
The intervention included a cancer screening checklist and color-coded stickers to track screening tests. Eight clinics were randomized to the intervention or control group. Screening rates for mammograms, Pap smears, and fecal occult blood tests were compared before and 12 months after the intervention.
The results showed that the intervention significantly increased screening rates for mammograms and fecal occult blood tests compared to the control group, after adjusting for baseline differences. There was also a trend toward increased Pap smear screening. The intervention
This study surveyed pharmacists in Minnesota to identify gaps between the information resources taught in school and those available in practice. The survey assessed which resources pharmacists have access to and use most frequently in their workplace. Results showed pharmacists have the most access to and use Drug Facts and Comparisons, Micromedex, Pharmacists Letter, and UpToDate most frequently. Factors like reputation, accuracy, ease of use, and cost influence which resources pharmacists choose. Rural pharmacists had less access than urban pharmacists, suggesting interventions are needed to broaden rural pharmacists' access to evidence-based resources.
This study examined the impact of passive and active electronic medical record alerts on referrals to physical therapy and medication management for elderly patients at high risk of falls. The study found that a passive alert showing fall prevention resources had little impact on physical therapy referrals. However, an active alert identifying high-risk medications was associated with increased response to the passive alert and led to more medication reviews and discontinuations. The results suggest that active alerts may be more effective than passive alerts at prompting clinician action to address fall risk factors.
1) Drug development involves multiple phases of clinical trials in humans (phases I-IV) to test dosing, safety and efficacy in an increasing number of patients before regulatory approval and market access.
2) Patient involvement in clinical research is important to ensure trials address patient priorities and perspectives on risk/benefit, endpoints, and trial design elements like inclusion criteria.
3) Key elements of a clinical trial protocol include type of comparisons, randomization, blinding, endpoints, inclusion/exclusion criteria, schedule of events, informed consent process, and patient reported outcomes.
Results of an Online Survey of Stakeholders Regarding Barriers and Solutions ...John Reites
The survey found that the most significant barrier to clinical trial recruitment according to stakeholders was finding patients who meet eligibility criteria. The next most significant barriers were insufficient staff time for recruitment activities, followed by the length and complexity of consent forms, and protocol requirements other than eligibility criteria. Suggestions to overcome barriers included broadening eligibility criteria, improving planning, using effective recruitment methods and technology, simplifying processes, and improving staff support. Most stakeholders were optimistic that national recruitment rates would increase over the next 5-10 years if effective partnerships were formed between sectors like patient advocates, researchers, sponsors, and regulators.
Our main involvement with your clinical research recruitment program concludes with processing the responses to your mailer. As our staff members direct the respondents to your site, you can begin conducting final interviews to complete the clinical trial recruitment process.
Cancer patients’ experiences in one tertiary referral emergency department (E...Cancer Institute NSW
The demand on Australian EDs has increased by an average of 4.2% each year while the cancer incidence rate has doubled since 1991. Many patients with cancer present to EDs but may be better managed using alternative healthcare models.
This document discusses challenges in interpreting health-related quality of life (HRQOL) findings across cancer clinical trials. Two hypothetical trials that tested the same treatment showed conflicting HRQOL results. This was because the trials may have assessed different HRQOL areas, endpoints, handling of missing data, and analysis populations. To address this, international collaboration is needed to set standards for HRQOL analyses in cancer trials. This would help ensure HRQOL questions, designs, analyses and interpretations are consistent across trials.
This document discusses challenges in using Bayesian and decision analysis approaches for regulating medical products. It notes issues like subjectivity in choosing priors, controlling type I error rates, and the need for legal availability of prior information. Promising areas for using prior information include pediatric trials, rare diseases, safety, and expedited access programs. Bayesian adaptive designs allow interim analyses to optimize sample size and model-based likelihoods. Decision analysis can make benefit-risk determinations more explicit through tools like influence diagrams and considering patient preferences. The highest value of Bayesian approaches is in accounting for external evidence, using flexible trial designs, modeling likelihoods, developing transparent decision rules based on factors like medical need and patient perspectives.
Valuing the EQ-5D-Y Using a Discrete Choice Experiment: Do Adult and Adolesce...Office of Health Economics
Slides from a presentation OHE's Koonal Shah gave at the PROMs research conference on June 20th, 2018. The subject of the presentation was valuing the EQ-5D-Y using a discrete choice experiment: do adult and adolescent preferences differ?
1. The document discusses standard quizzing rules for a secret quiz including long connect questions at the end that provide additional points. The quiz master's decision is final.
2. It then provides a series of quotes criticizing the Iran nuclear deal and lists the various terrorist groups it claims will benefit from funds released to Iran.
3. Several multiple choice questions then test knowledge of individuals and organizations involved in recent events.
El documento resume una visita de campo a la troncal 7 para identificar los tipos de drenaje existentes. Se describen 6 puntos diferentes a lo largo de la vía, incluyendo las características y estado de los drenajes. La mayoría se encuentran en deterioro debido a falta de mantenimiento, aunque algunos están en mejor estado. En general, el documento enfatiza la importancia de los drenajes para canalizar agua y extender la vida útil de la vía.
1. The document describes an upcoming quiz competition with 7 rounds of questions on various topics.
2. It provides details of the different rounds - written, connect, buzzer, audience questions.
3. Sample questions are provided from the different rounds on topics like science, history, and current events.
I apologize, I do not have enough context to determine what the image represents. Could you please provide some additional information about the image or question?
The document provides the questions and answers for a quiz. It includes questions about topics like Greek mythology, Dante's Inferno, the Watergate scandal, Ludwig van Beethoven, folk songs, film review websites, Tasmanian devils, carousels, gestures of respect, video games, restaurants recreating movie sets, fictional African mountains, Spanish regions, national anthems, NASA engineers, places related to the JFK assassination, countercultures, Henry David Thoreau's Walden, memorials to Princess Diana, and a Paolo Veronese painting.
El documento define el outsourcing como la transferencia de ciertos procesos complementarios de una empresa a terceros para reducir costos y enfocarse en las actividades principales. Algunas razones comunes para usar outsourcing son reducir gastos, evitar funciones no esenciales, y acceder a capacidades especializadas. Áreas comunes para outsourcing incluyen call centers, fabricación, y servicios de seguridad.
Quiz Meet Quiz: General Quiz conducted by Karthik on 25th September, 2016.
Disclaimer: All questions are original. Any resemblance whatsoever to other questions of similar kind is purely coincidental.
The document provides information about an intra-college quiz competition with 20 multiple choice questions. It includes questions about logos, songs, people, definitions, restaurants, events, phobias, inventions, and more. The top 6 teams that correctly answer the most questions will qualify for the finals round of the competition.
The document provides instructions for a quiz with 20 questions and 5 potential tiebreaker questions marked with stars. It notes there will be partial points on some questions and emphasizes being nice. The quizmaster's decision is final. It then lists several trivia questions about various topics, asking for references, names, or terms to fill in blanks.
Prelims for Gen quiz made for Splash'16, annual cultural fest of Lady Hardinge Medical College, Delhi. Mains at http://www.slideshare.net/alchemistprithvi/cognitio-the-gen-quiz-finals
The document appears to be a quiz related to drugs, music, and pop culture. It contains 22 multiple choice questions testing knowledge about:
1) The meaning behind LSD blotters commemorating "Bicycle Day"
2) The controversial album cover artwork for Load by Metallica
3) The erotic graphic novel by Melinda Gebbie depicting fictional characters from Alice in Wonderland and Peter Pan.
It concludes by identifying an Indian April Fools' joke claiming the first ever live action film of the comic character Savita Bhabhi.
Finance and Economics Quiz Finals held at MIT Manipal by ESOMSandeep Rao
Finance and Economics Quiz Finals held on the 28th of October 2016 for the Economics Society of Manipal by Sandeep Rao, Abhishek Batni and Rijul Kapoor
This document contains details about a 20 question quiz being conducted. It provides information about the number of questions, marks allocation, tie-breaking rules, and criteria to advance to the final round. It then presents 20 multiple choice questions on topics ranging from Indian food, literature, sports, history, and more. For each question, the relevant information is presented followed by multiple choice answers to select from.
This document contains 8 multiple choice questions about business and finance concepts like ploughing back of profits, capital gearing, bank overdrafts, shares, watered capital, operating leverage, net present value, and dividends. For each question there is a multiple choice answer option listed as the correct response.
This document summarizes 5 research studies that will impact clinical practice for academic family physicians. It discusses studies on appropriate use of antithrombotic medication in atrial fibrillation patients, the association between neighborhood walkability and rates of overweight/obesity/diabetes, predictors of frequent primary care visits among older patients, differences in patient experience survey responses based on survey delivery method, and a randomized trial on oral/topical antibiotics for infected eczema in children. The document analyzes the research questions, methods, findings and implications of each study.
The study found that 17% of Pap tests ordered in their resident clinic were inappropriate based on USPSTF guidelines. They created an intervention called the "Pap Clinic" which used an EMR template to guide decision making and patient discussions about cervical cancer screening guidelines. After implementing this clinic, they found a statistically significant decrease in inappropriate Pap tests, from 17% pre-intervention to 1.7% post-intervention. While the results were promising, the study had limitations including a small sample size and potential for selection bias. The intervention showed that templates in EMRs have potential to improve adherence to screening guidelines.
This document discusses criteria and considerations for screening diseases. It defines screening as the presumptive identification of unrecognized disease or defect through tests or procedures in apparently healthy individuals. Some key points:
- Important criteria for screening a disease include having a recognizable early asymptomatic period, a known natural history, available effective treatment, and evidence that early detection reduces mortality and morbidity.
- Screening tests should be reasonably quick, easy, inexpensive, safe, and have acceptable sensitivity, specificity, and positive predictive value.
- Cut-off points for positive screening tests involve balancing factors like disease prevalence and severity, and impacts of false positives versus false negatives.
- Validity and accuracy of screening tests depend on their
This document discusses experimental studies and randomized clinical trials. It defines clinical trials as medical research studies conducted with human subjects to evaluate new interventions. Randomized clinical trials are described as the gold standard for comparing an intervention to a placebo or control group by randomly assigning subjects to each. The basic steps of a randomized clinical trial are outlined as drawing up a protocol, selecting study populations, randomizing subjects, administering the intervention, follow up, and assessment of outcomes. Advantages include providing evidence of causality, while disadvantages include cost and sample size requirements. Methods to reduce bias like randomization and blinding are also described.
This document summarizes six research studies that will impact family medicine practice. The studies include: 1) decreased STI screening rates in young women after changes to cervical cancer guidelines, 2) reduced cervical dysplasia in adolescent girls receiving the HPV vaccine, 3) potential cost savings of a universal public drug plan in Canada, 4) using an online smoking cessation program to increase medication use, 5) unintended effects of wait time policies on medical education, and 6) increasing potentially inappropriate bupropion prescriptions suggesting misuse. The document provides an overview of each study's question, methods, findings, and implications for academic and clinical practice.
1 prof james bently cervical cancer screening 2014Tariq Mohammed
This document discusses options for cervical cancer screening including visual inspection with acetic acid (VIA), cervical cytology, HPV testing, and combinations of tests. It reviews the strengths and limitations of different screening methods and highlights priorities for efficient, low-cost screening in low-resource settings. Optimal screening may involve initial HPV testing at age 35 with reflex cytology for positives and cytology follow-up of negatives before longer rescreening intervals.
1 prof james bently cervical cancer screening 2014Tariq Mohammed
This document discusses options for cervical cancer screening including visual inspection with acetic acid (VIA), cervical cytology, HPV testing, and combinations of tests. It reviews the strengths and limitations of different screening methods and highlights priorities for efficient, low-cost screening in low-resource settings. Optimal screening may involve initial HPV testing at age 35 with reflex cytology for positives and cytology follow-up of negatives before longer interval rescreening.
Critical appraisal of randomized clinical trialsSamir Haffar
The document discusses key concepts in randomized clinical trials (RCTs), including:
1) RCTs are considered the gold standard for evaluating the effectiveness of interventions due to their ability to minimize bias through randomization and blinding.
2) Proper randomization aims to create comparable treatment and control groups, conceal allocation to prevent bias, and may involve simple, stratified or blocked methods.
3) Blinding (masking) of participants, investigators and assessors can decrease observation bias and is important for RCT validity, though full blinding is not always possible.
4) Intention-to-treat analysis includes all randomized patients to preserve comparable groups and prevent bias from non-compliance.
bevacizumab chemotherapy treatment of metastastic colorectal cancer metasta...Мандухай Г.
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MedicReS
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February 13-14, 2017
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1. Intervention to Reduce Inappropriate
Papanicolaou Testing in a Resident
Clinic
L. Kyle Horton MD, MBA
Samantha H. H. Hudson MD, Meng
Denise L. Borden MD
Arpita Aggarwal MD, MS
2. Slide 2
Disclosure Statement
Speaker: Kyle Horton MD, MBA
Co-Investigators from VCU Internal Medicine:
Samantha H. H. Hudson MD, Meng
Denise L. Borden MD
Arpita Aggarwal MD
Contributors to Pilot Study
Ajay Patil DO
Amy Anderson DO, MPH
Neither the speaker nor any co-investigators have any relevant disclosures
to make.
3. Slide 3
Background
• Guideline-inconsistent cancer screening is
prevalent
-Yabroff et al survey regarding Papanicolaou
testing published in Annals 2006 to 2007
*Internists only guideline-consistent 27.5% of
time
-Yabroff et al regarding colorectal cancer
screening
*Only 19.1% of providers guideline-consistent
Yabroff et al. Ann Int Med. 2009; 151: 602-611
Yabroff et al. J Gen Intern Med. 2010; 10.1007
4. Slide 4
VCU IM Resident Clinic
• Internal Medicine and Med/Peds Residents
-Continuity clinic 1/2 day per week
• Diverse Population
– Urban and Rural
– Largely underserved
– Often under- or non-insured
5. Slide 5
Over-screening for Cervical Cancer
• Noted over-screening for cervical cancer in our
resident clinic
• Conflicting Guidelines
-American College of Obstetrics and Gynecology
(ACOG)
-United States Preventive Services Task Force
(USPSTF)
-American Cancer Society (ACS)
• Residents have varied training/backgrounds
-Family Medicine, Internal Medicine, and OB/Gyn
7. Slide 7
Aim
Aim: Design and implement an intervention to
improve
-Understanding of guidelines
-Adherence to guidelines
Goal: achieve 95% adherence to USPSTF
cervical cancer screening guidelines
8. Slide 8
Intervention Plan
• Created a “Pap Clinic” held 1/2 day per week
-For focused Women’s Health Visits
-Created an Electronic Medical Record
Template Note
*Highlights relevant Gyn history
*Incorporates the USPSTF guidelines
*Includes a follow-up plan for further
screening
9. Slide 9
Methods
• Pilot Study-229 charts assessed for
appropriateness
• Implemented the “Pap Clinic”
• Retrospectively reviewed 119 charts from
“Pap Clinic”
• Univariate and bivariate analyses: means,
Fisher exact, and ANOVA tests
• SAS 9.2 statistical software
• P-value <0.05 was considered statistically
significant
10. Slide 10
Demographics
Pilot Post-Intervention
Age
Average 51.4 50.8
Inappropriate 60.3 73.5
Race
African-American 69.9% 68.9%
Caucasian 28.4% 30.3%
Other 1.7% 0.8%
Insurance
Medicare 32.3% 38.7%
Private 22.7% 11.8%
Indigent 26.2% 30.3%
Self-Pay 15.3% 10.9%
Other 3.5% 8.4%
11. Slide 11
Results
Pre-Intervention vs. Post-Intervention
17.0% Inappropriate
(229 Total Patients)
1.7% Inappropriate
(119 Total Patients)
Statistically significant decrease in inappropriate Paps
(Fisher Exact Test p<0.0001)
Inappropriate
Appropriate
12. Slide 12
Limitations
• Results may lack generalizability
-Interns more easily molded by intervention
• May reflect selection bias to referred patients
• Small sample size post-intervention
• Too early to assess for overall effect
-Not all of current residents rotated through
the “Pap Clinic”
-Still 16.8% inappropriate referrals
13. Slide 13
Conclusions
• Creating a clinic for focused women’s health visits
using an electronic medical record template was
effective at reducing inappropriate Pap testing
• The Future: Data re-analysis for broader efficacy
once all trainees have rotated through the clinic
• Implication: creating electronic medical record
templates and focusing women’s health visits may
prove to be an effective way to improve compliance
with Pap testing guidelines in primary care
14. Slide 14
Questions?
THE WALL STREET JOURNAL 2/15/2011
“Questioning the Need For Routine Pelvic Exam”
By Melinda Beck
“Of all the indignities that women endure in their
lives, one of the most dreaded is the routine
pelvic exam.”
-Based on commentary Journal of Women’s
Health
-Article makes reference to the new ACOG
guidelines recommending Pap every 2 years
for women age 21 to 30 and 3 years 30 for
older
Editor's Notes
As background, there has been much attention recently devoted to the fact that guideline-inconsistent cancer screening is prevalent.
A survey published in Annals regarding Pap testing found that despite physician commitment to guidelines, a very low percentage of providers were guideline consistent in their recommendations across clinical vignettes.
-Internists were only guideline consistent across all vignettes for Pap screening 27.5% of the time
This problem was also evident in recent research regarding colorectal cancer screening
-Investigators noted both overuse and underuse of screening with only 19.1% of providers guideline consistent recommendations across all colorectal cancer screening modalities
With the recent research and attention to guidelines, we turned to our own internal medicine resident clinic at the VCU ambulatory care center pictured to the right.
The VCU internal medicine resident clinic is staffed by both internal medicine and med/peds residents who maintain their own patient panel and see patients 1/2 day per week.
Patients served come from both urban and rural settings throughout a broad distance in southern Virginia
Patients are largely medically underserved and often under or non-insured
With regard to our own clinic and adherence to cancer screening guidelines, we noted a tendency to over-screen patients for cervical cancer.
Much of the confusion about cervical cancer screening stems from the multiple sources of often conflicting guidelines.
The principle sources of Pap testing guidelines include the American College of Obstetrics and Gynecology as well as the U.S. Preventive Services Task Force and the American Cancer Society. The conflicting recommendations from these three sources often contribute to confusion among providers.
Residents are likely aware of all three of the major sources of guidelines based on their medical school training. The fact that students are trained in pap testing on family medicine, internal medicine, and OB/gyn rotations renders them especially vulnerable
Suspecting that our residents were vulnerable to confusion about cervical cancer screening and noting a tendency toward overscreening in our own clinic, we began a retrospective chart review including 229 patients who underwent Pap testing between February of 2004 and December of 2009. Appropriateness of Pap tests was based on USPSTF guidelines for cervical cancer screening
On the left, you’ll note that we conducted inappropriate pap tests 17% of the time (n=39; mean age 60.3, SD +/- 10.3 years). On the right you’ll see that out of the inappropriate tests, 79.5% were performed on women post hysterectomy for a non-malignant cause, 12.9% on women &gt; age 65 without risk factors, and 7.7% on women &gt; age 65 who also had a hysterectomy for non-malignant cause.
Our aim was to design and implement an intervention to improve residents understanding of guidelines and their adherence to guidelines with regard to the appropriate use of Pap testing.
We hypothesized that we would achieve 95% adherence to USPSTF cervical cancer screening guidelines
Our intervention plan created a “Pap Clinic” held 1/2 day per week, staffed by 2 interns, a women’s health resident, and an attending.
Essential components to the plan for our clinic were to allow for focused women’s health visits and to design an appropriate electronic medical record template to help with these focused visits
Key components to the electronic medical record template
Highlights relevant GYN history to prompt the questions needed to ascertain appropriateness of a Pap smear (repetitively and methodically collect the necessary information to determine if pap testing is appropriate
2. Incorporates a brief version of the USPSTF guidelines themselves (visual reminder of guidelines repetitively)
3. Interns were advised to include in their plan why they did/did not perform Pap testing and a recommendation regarding the appropriate interval for screening to inform the referring providers
In our pilot study, 229 charts were reviewed for appropriateness of Pap testing with a result of 17% inappropriate testing.
Instituted the Pap Clinic
Subsequently, we reviewed 119 charts from our “Pap Clinic” between February 2009 and July 2010
Criteria for appropriateness were the same pre and post-intervention
We conducted univariate and bivariate analyses with means, Fisher exact, and ANOVA tests
We used SAS 9.2 statistical software and a p-value &lt;0.05 was considered statistically significant
Demographic information was collected during the pilot study and post-intervention to analyze for differences with regard to age, race, and insurance status. You’ll note that there were no significant differences between the initial study group and the post-intervention characteristics.
Note that the average age was not substantially different between our pilot study patients and the post-intervention group.
Similarly, the ethnic breakdown of patients was not significantly different with the majority of patients being African-American
Finally, the percentage insured by either medicare or private insurance was not substantially different (55% vs. 50.5%)
You’ll remember that in our pilot study, 17% of Pap tests performed in our clinic were inappropriate by USPSTF guidelines with the vast majority (79.5%) done on women who were post-hysterectomy for benign reasons.
On the right hand side of the screen, you’ll see that post-intervention there was a statistically significant decrease in inappropriate Paps based on USPSTF guidelines. We were able to achieve our goal 95% adherence to USPSTF guidelines with only 1.7% inappropriate tests, both of which were performed on women. Both of the inappropriate tests in our post-intervention group were done on patients who were too old and post-hysterectomy for benign reasons.
Results may lack generalizability both in terms of the demographics and complexity of our patient population (majority are african american and underinsured), as well results may be more robust in the setting of medical education because interns are more easily molded by intervention than experienced practitioners
Both of these facts may mean that results are not generalizable to other clinics and practice settings
Our post-intervention data is subject to selection bias in that only Pap smears performed in the Pap clinic were analyzed post-intervention
We may be over-estimating our intervention effect size based on our small sample size post-intervention. Given the simplicity of our intervention, we were willing to over-estimate our treatment effect size and tolerate a large Type I error
It is still too early to assess for the overall effect of our intervention. At present, the first interns to rotate through the Pap Clinic are still second years.
-Note that we still have 16.8% inappropriate referral