Three key themes emerged from the analysis of organizational culture aspects that impact hospital discharge: 1) A fragmented interface between hospitals and primary care with an inward focus on hospital care and lack of awareness of community needs; 2) Undervaluing of administrative discharge tasks compared to clinical work; and 3) A lack of reflection on discharge processes and opportunities for improvement. Nine categories further described barriers such as insufficient communication, task burdens, and negative attitudes. The study suggests organizational culture, including how hospital providers value discharge handovers and community outreach, is critical to effective transitions of care.
This document introduces patient engagement and participation in healthcare. It describes the spectrum of engagement from passive compliance to active co-design of care and systems. Common manifestations include seeking health information, contributing to care plans, and engaging in advocacy. Technology enables greater engagement through online resources, communication tools, and data generation. Benefits include improved outcomes, safety, and experiences for both patients and clinicians. However, cultural and systemic barriers still limit progress toward ideals of full partnership and co-production.
This document summarizes a session at the 2015 CADTH conference on engaging patients in defining value and drug development. It provides an overview of the session which included panels discussing defining value from the patient perspective and models of patient engagement. It also summarizes some of the key points discussed, such as the need to include patient perspectives throughout the drug development process to better measure what is meaningful to patients and alternative approaches to patient engagement like patient and community engagement researchers. The document advocates that embedding meaningful patient measures can help weight evidence from the patient perspective.
Perspectives on Transitional Care for Vulnerable Older Patients A Qualitative...Austin Publishing Group
Transitional care for vulnerable older patients is optimal if, on top of the organization of transitional care, these patients and their informal caregivers have trust in the professionals involved. Regarding the challenge of organizing increasingly complex transitional care for vulnerable older patients, the focus should shift towards optimizing trust.
Listening to the Patient - Leveraging Direct-to-Patient Data Collection to Sh...John Reites
This document discusses how engaging patients directly through online surveys can provide valuable input to clinical trial design and improve the likelihood of study success.
In two case studies, patients provided feedback that (1) resulted in adjusting patient reported outcome survey cutoff scores, expanding the eligible patient pool ten-fold, and (2) encouraged investigators to approach patients about postmortem research by indicating they were comfortable discussing such issues. Direct engagement of over 250 patient assessments has supported development of study protocols, feasibility calculations, and recruitment plans. Involving patients early in the design process through digital technologies can help address recruitment challenges and optimize trials.
1) A meta-analysis of survey data from over 21,000 patients with chronic conditions found several key factors that influence patient interest and participation in clinical trials.
2) Health condition, age, gender, treatment satisfaction, awareness of new treatments, and the patient-physician relationship were found to impact a patient's likelihood of interest in clinical trials.
3) In addition to interest, prior clinical trial participation, health condition, treatment satisfaction, and concerns about cost also predicted a patient's actual likelihood of enrolling in future clinical trials if eligible.
Rabica Shahid has over 6 years of experience as a clinical research coordinator. She holds an MD from Windsor University School of Medicine and an advanced diploma in biotechnology from Centennial College. Her experience includes coordinating clinical trials, scheduling participants, reviewing protocols, obtaining informed consent, and ensuring compliance. She is proficient in EMR systems and has experience in various clinical settings including family medicine, internal medicine, OB/GYN, and others. Her future goals are to provide compassionate care using her skills and knowledge, cultivate leadership in her field, and continue expanding her knowledge through research.
Predicting Patient Interest and Participation in Clinical TrialsNassim Azzi, MBA
- A meta-analysis of survey data from over 21,000 patients with chronic conditions found several key factors that influence patient interest and participation in clinical trials.
- Health condition, age, gender, dissatisfaction with current treatment, patient-physician engagement, concerns about costs, and awareness of new treatments in development were significant predictors of interest in clinical trials.
- Additionally, having previously participated in a clinical trial, especially for one's own health condition, was a strong indicator that a patient would be willing to participate in future clinical research if eligible.
4.epidemiology tutorial (realtioonship of epidemiology biostatistics & dph ) ...Tin Myo Han
Showing relationship between Epidemiology, Bio-statistics and Dental public health activities for 4th year dental students
to get more understanding on why they need to do students' research project and how to apply it!
This document introduces patient engagement and participation in healthcare. It describes the spectrum of engagement from passive compliance to active co-design of care and systems. Common manifestations include seeking health information, contributing to care plans, and engaging in advocacy. Technology enables greater engagement through online resources, communication tools, and data generation. Benefits include improved outcomes, safety, and experiences for both patients and clinicians. However, cultural and systemic barriers still limit progress toward ideals of full partnership and co-production.
This document summarizes a session at the 2015 CADTH conference on engaging patients in defining value and drug development. It provides an overview of the session which included panels discussing defining value from the patient perspective and models of patient engagement. It also summarizes some of the key points discussed, such as the need to include patient perspectives throughout the drug development process to better measure what is meaningful to patients and alternative approaches to patient engagement like patient and community engagement researchers. The document advocates that embedding meaningful patient measures can help weight evidence from the patient perspective.
Perspectives on Transitional Care for Vulnerable Older Patients A Qualitative...Austin Publishing Group
Transitional care for vulnerable older patients is optimal if, on top of the organization of transitional care, these patients and their informal caregivers have trust in the professionals involved. Regarding the challenge of organizing increasingly complex transitional care for vulnerable older patients, the focus should shift towards optimizing trust.
Listening to the Patient - Leveraging Direct-to-Patient Data Collection to Sh...John Reites
This document discusses how engaging patients directly through online surveys can provide valuable input to clinical trial design and improve the likelihood of study success.
In two case studies, patients provided feedback that (1) resulted in adjusting patient reported outcome survey cutoff scores, expanding the eligible patient pool ten-fold, and (2) encouraged investigators to approach patients about postmortem research by indicating they were comfortable discussing such issues. Direct engagement of over 250 patient assessments has supported development of study protocols, feasibility calculations, and recruitment plans. Involving patients early in the design process through digital technologies can help address recruitment challenges and optimize trials.
1) A meta-analysis of survey data from over 21,000 patients with chronic conditions found several key factors that influence patient interest and participation in clinical trials.
2) Health condition, age, gender, treatment satisfaction, awareness of new treatments, and the patient-physician relationship were found to impact a patient's likelihood of interest in clinical trials.
3) In addition to interest, prior clinical trial participation, health condition, treatment satisfaction, and concerns about cost also predicted a patient's actual likelihood of enrolling in future clinical trials if eligible.
Rabica Shahid has over 6 years of experience as a clinical research coordinator. She holds an MD from Windsor University School of Medicine and an advanced diploma in biotechnology from Centennial College. Her experience includes coordinating clinical trials, scheduling participants, reviewing protocols, obtaining informed consent, and ensuring compliance. She is proficient in EMR systems and has experience in various clinical settings including family medicine, internal medicine, OB/GYN, and others. Her future goals are to provide compassionate care using her skills and knowledge, cultivate leadership in her field, and continue expanding her knowledge through research.
Predicting Patient Interest and Participation in Clinical TrialsNassim Azzi, MBA
- A meta-analysis of survey data from over 21,000 patients with chronic conditions found several key factors that influence patient interest and participation in clinical trials.
- Health condition, age, gender, dissatisfaction with current treatment, patient-physician engagement, concerns about costs, and awareness of new treatments in development were significant predictors of interest in clinical trials.
- Additionally, having previously participated in a clinical trial, especially for one's own health condition, was a strong indicator that a patient would be willing to participate in future clinical research if eligible.
4.epidemiology tutorial (realtioonship of epidemiology biostatistics & dph ) ...Tin Myo Han
Showing relationship between Epidemiology, Bio-statistics and Dental public health activities for 4th year dental students
to get more understanding on why they need to do students' research project and how to apply it!
Medical Research - Cultural concerns, Truth telling & Conflict of interestPratik Parikh
The document summarizes key topics from Pratik Umesh Parikh's seminar on medical research methodology and biostatistics. It discusses cultural concerns in medical research, including how language and religion can create barriers. It also covers the importance of truth telling in medical care, managing conflicts of interest, and references several sources that informed the seminar topics.
Module 2: Evidence-Based Dental Public HealthKelley Minars
The updated version of this tutorial is available here: http://www.slideshare.net/uthsclib/module-2-evidencebased-dental-public-health-1724938
Module 2 of the Oral Health Tutorial, a production of UT HSC Libraries.
This module focuses on evidence-based dental health. View this tutorial to learn how to define evidence-based dental public health, learn effective retrieval strategy, be able to critique the literature and apply it to public health dental practice.
This tutorial is copyright Lara Sapp and Julie Gaines. Uploaded with permission.
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.
This document discusses the rise of evidence-based health care over the last decade. Key points:
- Evidence-based health care aims to minimize problems like overuse, underuse and misuse of treatments by basing clinical practice closely on scientific research evidence.
- During the 1990s, the concepts of evidence-based health care spread widely and began influencing health policymakers, providers and researchers.
- Advances have been made in managing and disseminating research findings through initiatives like the Cochrane Collaboration and clinical practice guidelines.
- However, integrating research evidence into everyday clinical practice remains a challenge and some critics argue evidence-based practice could stifle innovation.
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.
Mosio's Clinical Trial Patient Recruitment and Retention Ebook (First Edition)Mosio
The first edition of Mosio's patient recruitment and retention ebook contains 68 tips and examples from clinical research industry professionals on ways to improve efforts to recruit, retain and engage clinical trial patients.
To get access to a free download of the 2nd Edition, visit http://www.mosio.com/prebook
For more information on how you can improve patient engagement while increasing workflow efficiencies in communicating with study participants using two-way text messaging, please visit us at http://www.mosio.com
Best Practices in Clinical Study RecruitmentCTSI at UCSF
This document discusses best practices in clinical study recruitment and retention. It covers:
1) Recruitment practices such as performing initial analyses of study design and site-specific factors, planning and budgeting for screen failures and protocol changes, and implementing a staged communication plan.
2) Retention practices like ensuring participants are well-informed, understanding their needs, and keeping communication open.
3) A proposed Participant Recruitment Service at UCSF to centralize recruitment efforts through activities like recruitment analysis, direct mailings to patient cohorts, and developing recruitment materials and resources.
Implement a Direct-to-Patient Approach to Increase Patient Engagement and Ret...John Reites
Article by MM&M (Medical, Marketing & Media) on 25 Mar 2015 with John Reites discussing direct-to-patient approaches to conduct innovation research models that increase engagement and retention.
Weblink: http://www.mmm-online.com/pharmaceutical/implement-a-direct-to-patient-approach-to-increase-patient-engagement-and-retention/article/405443/
Gorter et al TRACE main paper BMJ Open May 2015Oksana Hlyva
This study assessed the use, utility, and impact of two transition interventions - the Youth KIT organizational tool and an online transition mentor - for 50 youth with chronic health conditions transitioning to adult healthcare over 4 years. Most youth used the medical section of the Youth KIT and some engaged with the online mentor. Perceived utility of the interventions was modest. Youth set goals in multiple life domains and goal achievement increased over time. However, the quantitative and qualitative evidence showed the interventions alone were insufficient for empowering youth in transition. Tailored, integrated supports involving both pediatric and adult healthcare systems are needed.
Recruitment & Retention Plan: A Sample Strategy PresentationMarwah Zagzoug, PhD
The document outlines a trial enrollment strategy and patient recruitment plan for a clinical trial comparing ZOCOR and Lipitor in patients with high cholesterol. The trial is currently under-enrolled, with only 2 patients enrolled out of a goal of 10. Various recruitment methods like advertising and outreach are proposed to boost enrollment. Barriers to recruitment and retention like patient burden and lack of communication are identified, along with strategies to improve participation like transportation assistance and regular contact with patients.
This document summarizes a presentation about the Patient Centered Outcomes Research Institute (PCORI) and its methods. It discusses how PCORI funds research to help patients make informed healthcare decisions by producing high-quality evidence. Key points include that PCORI research must be patient-centered, compare at least two alternatives, and use outcomes that matter to patients. It also outlines PCORI's research portfolio, methodology standards, and application review process.
A presentation showcasing some of the patient recruitment challenges that I encountered as a recruitment manager as well as some of the strategies -- DIGITAL ADVERTISING -- I used to overcome them.
This document discusses key considerations for patient recruitment in clinical investigations. It outlines that recruitment is crucial for study success and validity. Factors that influence recruitment include study design elements like eligibility criteria, experimental procedures, and follow up requirements. Proper investigator and site selection also impact recruitment. Close management and monitoring by the sponsoring company can help address recruitment challenges. Various recruitment methods like advertising must be done appropriately.
Code of ethics and legal practices has been very old element in the professional management of the doctor’s behaviour. The ethical practices or code shows a commitment to act with honesty in extreme situations. At the time patients seek medical treatment they are not just entering a normal social relationship, they often feel vulnerable but required to share and expose important aspects of their lives. Codes of ethical conducts provide some tangible safety to both doctors and patients in such circumstances. In the below report, the researcher is explaining ethical, legal and
professional guidelines and principles for health care as well as its implications in the healthcare sector of the United Kingdom. After reading this report, the reader would be able to understand how healthcare adopts ethical practices at the workplace and ensures protection of patients in their medical treatment.
Patient recruitment & retention is highlighted as the key factor in ensuring study success, the area of patient retention in clinical trials is often overlooked. Retention of patients throughout the life of a clinical trial is however extremely vital from scientific as well as economic point of view. Poor recruitment & retention negatively impacts on the overall evaluable data for regulatory submissions. Dropped participants must be replaced which incurs further expenditures and time delays. Subject dropout rates are estimated to range from 15-40% of enrolled participants in clinical trials.
Clinical trials are necessary for medical research. Producing new medicines to the market depends on the strength of research organizations and drug companies to test and verify their work vigorously through their Clinical Trials, but finding people willing to participate is notoriously tricky.
Best strategies for successful recruitment and retentionTrialJoin
Best strategies for successful recruitment and retention for clinical research studies
Contact info@trialjoin.com for more information about patient recruitment help, obtaining new studies or help with site management.
Recruitment Metrics from a Direct-to-Patient Approach to Enroll Patients in a...John Reites
1) Researchers recruited patients into a diabetes practice-based research network using a direct-to-patient recruitment approach which involved mailing eligible patients and allowing them to enroll online or by phone.
2) Over 10 months, 78 practice sites mailed letters to 31,181 patients, resulting in 2,183 patients (7%) enrolling in the study by accessing the website or calling.
3) The enrolled patients represent an average of 27 patients per site. Baseline surveys were completed by 96% of enrolled patients. Physician and office administrator survey completion rates were 73% and 76% respectively.
Pejman Ferdowsian is a medical doctor seeking a new position. He has over 10 years of experience in various medical specialties including family medicine, internal medicine, surgery, obstetrics/gynecology, pathology, pediatrics, psychiatry, and interventional radiology. He has worked in clinical settings in the US and Canada. Pejman has strong communication, research, and analysis skills. He is currently involved in ongoing medical research and professional development.
This document summarizes a research study that used the Intervention Mapping framework to develop a guiding framework for improving patient discharge from hospitals to primary care. The study conducted interviews and focus groups with patients, families, and providers to identify barriers to effective discharge. Key issues included lack of communication between hospital and primary care providers, incomplete discharge information, and lack of patient understanding. The study then defined desired outcomes, specific performance objectives, and change objectives needed to address the identified barriers. Finally, the study selected evidence-based methods and strategies to achieve the change objectives, such as discharge templates, medication reconciliation, and teach-back techniques. The resulting framework provides guidance for interventions to improve patient handovers between hospital and primary care.
Hesselink et al. BMC Health Services Research 2014, 14389ht.docxpooleavelina
Hesselink et al. BMC Health Services Research 2014, 14:389
http://www.biomedcentral.com/1472-6963/14/389
RESEARCH ARTICLE Open Access
Improving patient discharge and reducing
hospital readmissions by using Intervention
Mapping
Gijs Hesselink1*, Marieke Zegers1, Myrra Vernooij-Dassen1,2,3, Paul Barach4,5,6, Cor Kalkman4, Maria Flink7,8,
Gunnar Öhlén9,10, Mariann Olsson7,8, Susanne Bergenbrant11, Carola Orrego12, Rosa Suñol12, Giulio Toccafondi13,
Francesco Venneri13, Ewa Dudzik-Urbaniak14, Basia Kutryba14, Lisette Schoonhoven1, Hub Wollersheim1
and on behalf of the European HANDOVER Research Collaborative
Abstract
Background: There is a growing impetus to reorganize the hospital discharge process to reduce avoidable
readmissions and costs. The aim of this study was to provide insight into hospital discharge problems and
underlying causes, and to give an overview of solutions that guide providers and policy-makers in improving
hospital discharge.
Methods: The Intervention Mapping framework was used. First, a problem analysis studying the scale, causes, and
consequences of ineffective hospital discharge was carried out. The analysis was based on primary data from 26
focus group interviews and 321 individual interviews with patients and relatives, and involved hospital and
community care providers. Second, improvements in terms of intervention outcomes, performance objectives and
change objectives were specified. Third, 220 experts were consulted and a systematic review of effective discharge
interventions was carried out to select theory-based methods and practical strategies required to achieve change
and better performance.
Results: Ineffective discharge is related to factors at the level of the individual care provider, the patient, the
relationship between providers, and the organisational and technical support for care providers. Providers can
reduce hospital readmission rates and adverse events by focusing on high-quality discharge information, well-
coordinated care, and direct and timely communication with their counterpart colleagues. Patients, or their carers,
should participate in the discharge process and be well aware of their health status and treatment. Assessment by
hospital care providers whether discharge information is accurate and understood by patients and their community
counterparts, are important examples of overcoming identified barriers to effective discharge. Discharge templates,
medication reconciliation, a liaison nurse or pharmacist, regular site visits and teach-back are identified as effective
and promising strategies to achieve the desired behavioural and environmental change.
Conclusions: This study provides a comprehensive guiding framework for providers and policy-makers to improve
patient handover from hospital to primary care.
Keywords: Patient handoff, Patient discharge, Patient readmission, Intervention mapping, Adverse events
* Correspondence: [email protected]
1Radboud University Medical Center, Sc ...
Medical Research - Cultural concerns, Truth telling & Conflict of interestPratik Parikh
The document summarizes key topics from Pratik Umesh Parikh's seminar on medical research methodology and biostatistics. It discusses cultural concerns in medical research, including how language and religion can create barriers. It also covers the importance of truth telling in medical care, managing conflicts of interest, and references several sources that informed the seminar topics.
Module 2: Evidence-Based Dental Public HealthKelley Minars
The updated version of this tutorial is available here: http://www.slideshare.net/uthsclib/module-2-evidencebased-dental-public-health-1724938
Module 2 of the Oral Health Tutorial, a production of UT HSC Libraries.
This module focuses on evidence-based dental health. View this tutorial to learn how to define evidence-based dental public health, learn effective retrieval strategy, be able to critique the literature and apply it to public health dental practice.
This tutorial is copyright Lara Sapp and Julie Gaines. Uploaded with permission.
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.
This document discusses the rise of evidence-based health care over the last decade. Key points:
- Evidence-based health care aims to minimize problems like overuse, underuse and misuse of treatments by basing clinical practice closely on scientific research evidence.
- During the 1990s, the concepts of evidence-based health care spread widely and began influencing health policymakers, providers and researchers.
- Advances have been made in managing and disseminating research findings through initiatives like the Cochrane Collaboration and clinical practice guidelines.
- However, integrating research evidence into everyday clinical practice remains a challenge and some critics argue evidence-based practice could stifle innovation.
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.
Mosio's Clinical Trial Patient Recruitment and Retention Ebook (First Edition)Mosio
The first edition of Mosio's patient recruitment and retention ebook contains 68 tips and examples from clinical research industry professionals on ways to improve efforts to recruit, retain and engage clinical trial patients.
To get access to a free download of the 2nd Edition, visit http://www.mosio.com/prebook
For more information on how you can improve patient engagement while increasing workflow efficiencies in communicating with study participants using two-way text messaging, please visit us at http://www.mosio.com
Best Practices in Clinical Study RecruitmentCTSI at UCSF
This document discusses best practices in clinical study recruitment and retention. It covers:
1) Recruitment practices such as performing initial analyses of study design and site-specific factors, planning and budgeting for screen failures and protocol changes, and implementing a staged communication plan.
2) Retention practices like ensuring participants are well-informed, understanding their needs, and keeping communication open.
3) A proposed Participant Recruitment Service at UCSF to centralize recruitment efforts through activities like recruitment analysis, direct mailings to patient cohorts, and developing recruitment materials and resources.
Implement a Direct-to-Patient Approach to Increase Patient Engagement and Ret...John Reites
Article by MM&M (Medical, Marketing & Media) on 25 Mar 2015 with John Reites discussing direct-to-patient approaches to conduct innovation research models that increase engagement and retention.
Weblink: http://www.mmm-online.com/pharmaceutical/implement-a-direct-to-patient-approach-to-increase-patient-engagement-and-retention/article/405443/
Gorter et al TRACE main paper BMJ Open May 2015Oksana Hlyva
This study assessed the use, utility, and impact of two transition interventions - the Youth KIT organizational tool and an online transition mentor - for 50 youth with chronic health conditions transitioning to adult healthcare over 4 years. Most youth used the medical section of the Youth KIT and some engaged with the online mentor. Perceived utility of the interventions was modest. Youth set goals in multiple life domains and goal achievement increased over time. However, the quantitative and qualitative evidence showed the interventions alone were insufficient for empowering youth in transition. Tailored, integrated supports involving both pediatric and adult healthcare systems are needed.
Recruitment & Retention Plan: A Sample Strategy PresentationMarwah Zagzoug, PhD
The document outlines a trial enrollment strategy and patient recruitment plan for a clinical trial comparing ZOCOR and Lipitor in patients with high cholesterol. The trial is currently under-enrolled, with only 2 patients enrolled out of a goal of 10. Various recruitment methods like advertising and outreach are proposed to boost enrollment. Barriers to recruitment and retention like patient burden and lack of communication are identified, along with strategies to improve participation like transportation assistance and regular contact with patients.
This document summarizes a presentation about the Patient Centered Outcomes Research Institute (PCORI) and its methods. It discusses how PCORI funds research to help patients make informed healthcare decisions by producing high-quality evidence. Key points include that PCORI research must be patient-centered, compare at least two alternatives, and use outcomes that matter to patients. It also outlines PCORI's research portfolio, methodology standards, and application review process.
A presentation showcasing some of the patient recruitment challenges that I encountered as a recruitment manager as well as some of the strategies -- DIGITAL ADVERTISING -- I used to overcome them.
This document discusses key considerations for patient recruitment in clinical investigations. It outlines that recruitment is crucial for study success and validity. Factors that influence recruitment include study design elements like eligibility criteria, experimental procedures, and follow up requirements. Proper investigator and site selection also impact recruitment. Close management and monitoring by the sponsoring company can help address recruitment challenges. Various recruitment methods like advertising must be done appropriately.
Code of ethics and legal practices has been very old element in the professional management of the doctor’s behaviour. The ethical practices or code shows a commitment to act with honesty in extreme situations. At the time patients seek medical treatment they are not just entering a normal social relationship, they often feel vulnerable but required to share and expose important aspects of their lives. Codes of ethical conducts provide some tangible safety to both doctors and patients in such circumstances. In the below report, the researcher is explaining ethical, legal and
professional guidelines and principles for health care as well as its implications in the healthcare sector of the United Kingdom. After reading this report, the reader would be able to understand how healthcare adopts ethical practices at the workplace and ensures protection of patients in their medical treatment.
Patient recruitment & retention is highlighted as the key factor in ensuring study success, the area of patient retention in clinical trials is often overlooked. Retention of patients throughout the life of a clinical trial is however extremely vital from scientific as well as economic point of view. Poor recruitment & retention negatively impacts on the overall evaluable data for regulatory submissions. Dropped participants must be replaced which incurs further expenditures and time delays. Subject dropout rates are estimated to range from 15-40% of enrolled participants in clinical trials.
Clinical trials are necessary for medical research. Producing new medicines to the market depends on the strength of research organizations and drug companies to test and verify their work vigorously through their Clinical Trials, but finding people willing to participate is notoriously tricky.
Best strategies for successful recruitment and retentionTrialJoin
Best strategies for successful recruitment and retention for clinical research studies
Contact info@trialjoin.com for more information about patient recruitment help, obtaining new studies or help with site management.
Recruitment Metrics from a Direct-to-Patient Approach to Enroll Patients in a...John Reites
1) Researchers recruited patients into a diabetes practice-based research network using a direct-to-patient recruitment approach which involved mailing eligible patients and allowing them to enroll online or by phone.
2) Over 10 months, 78 practice sites mailed letters to 31,181 patients, resulting in 2,183 patients (7%) enrolling in the study by accessing the website or calling.
3) The enrolled patients represent an average of 27 patients per site. Baseline surveys were completed by 96% of enrolled patients. Physician and office administrator survey completion rates were 73% and 76% respectively.
Pejman Ferdowsian is a medical doctor seeking a new position. He has over 10 years of experience in various medical specialties including family medicine, internal medicine, surgery, obstetrics/gynecology, pathology, pediatrics, psychiatry, and interventional radiology. He has worked in clinical settings in the US and Canada. Pejman has strong communication, research, and analysis skills. He is currently involved in ongoing medical research and professional development.
This document summarizes a research study that used the Intervention Mapping framework to develop a guiding framework for improving patient discharge from hospitals to primary care. The study conducted interviews and focus groups with patients, families, and providers to identify barriers to effective discharge. Key issues included lack of communication between hospital and primary care providers, incomplete discharge information, and lack of patient understanding. The study then defined desired outcomes, specific performance objectives, and change objectives needed to address the identified barriers. Finally, the study selected evidence-based methods and strategies to achieve the change objectives, such as discharge templates, medication reconciliation, and teach-back techniques. The resulting framework provides guidance for interventions to improve patient handovers between hospital and primary care.
Hesselink et al. BMC Health Services Research 2014, 14389ht.docxpooleavelina
Hesselink et al. BMC Health Services Research 2014, 14:389
http://www.biomedcentral.com/1472-6963/14/389
RESEARCH ARTICLE Open Access
Improving patient discharge and reducing
hospital readmissions by using Intervention
Mapping
Gijs Hesselink1*, Marieke Zegers1, Myrra Vernooij-Dassen1,2,3, Paul Barach4,5,6, Cor Kalkman4, Maria Flink7,8,
Gunnar Öhlén9,10, Mariann Olsson7,8, Susanne Bergenbrant11, Carola Orrego12, Rosa Suñol12, Giulio Toccafondi13,
Francesco Venneri13, Ewa Dudzik-Urbaniak14, Basia Kutryba14, Lisette Schoonhoven1, Hub Wollersheim1
and on behalf of the European HANDOVER Research Collaborative
Abstract
Background: There is a growing impetus to reorganize the hospital discharge process to reduce avoidable
readmissions and costs. The aim of this study was to provide insight into hospital discharge problems and
underlying causes, and to give an overview of solutions that guide providers and policy-makers in improving
hospital discharge.
Methods: The Intervention Mapping framework was used. First, a problem analysis studying the scale, causes, and
consequences of ineffective hospital discharge was carried out. The analysis was based on primary data from 26
focus group interviews and 321 individual interviews with patients and relatives, and involved hospital and
community care providers. Second, improvements in terms of intervention outcomes, performance objectives and
change objectives were specified. Third, 220 experts were consulted and a systematic review of effective discharge
interventions was carried out to select theory-based methods and practical strategies required to achieve change
and better performance.
Results: Ineffective discharge is related to factors at the level of the individual care provider, the patient, the
relationship between providers, and the organisational and technical support for care providers. Providers can
reduce hospital readmission rates and adverse events by focusing on high-quality discharge information, well-
coordinated care, and direct and timely communication with their counterpart colleagues. Patients, or their carers,
should participate in the discharge process and be well aware of their health status and treatment. Assessment by
hospital care providers whether discharge information is accurate and understood by patients and their community
counterparts, are important examples of overcoming identified barriers to effective discharge. Discharge templates,
medication reconciliation, a liaison nurse or pharmacist, regular site visits and teach-back are identified as effective
and promising strategies to achieve the desired behavioural and environmental change.
Conclusions: This study provides a comprehensive guiding framework for providers and policy-makers to improve
patient handover from hospital to primary care.
Keywords: Patient handoff, Patient discharge, Patient readmission, Intervention mapping, Adverse events
* Correspondence: [email protected]
1Radboud University Medical Center, Sc ...
This document discusses patient satisfaction in healthcare. It begins by introducing patient satisfaction as a concept that considers a patient's needs, expectations of care, and healthcare experiences. Several theories of patient satisfaction are mentioned. The literature review highlights factors that can affect patient satisfaction, including provider characteristics like communication skills and patient characteristics like socioeconomic status. Ensuring patient satisfaction is important for compliance, care-seeking behaviors, and quality improvement. The document then describes a study conducted in Pakistan that assessed patient satisfaction in an outpatient department, finding high satisfaction with doctors, facilities, and a willingness to return. It recommends further studies in other care settings and obtaining ongoing patient feedback.
Evaluating the Effectiveness of Communityand Hospital MedicaBetseyCalderon89
Evaluating the Effectiveness of Community
and Hospital Medical Record Integration
on Management of Behavioral Health
in the Emergency Department
Stephanie Ngo, MD
Mohammad Shahsahebi, MD, MBA
Sean Schreiber, MSED, LPC
Fred Johnson, MBA
Mina Silberberg, PhD
Abstract
This study evaluated the correlation of an emergency department embedded care coordinator
with access to community and medical records in decreasing hospital and emergency
department use in patients with behavioral health issues. This retrospective cohort study
presents a 6-month pre-post analysis on patients seen by the care coordinator (n=524). Looking
at all-cause healthcare utilization, care coordination was associated with a significant median
decrease of one emergency department visit per patient (p G 0.001) and a decrease of 9.5 h in
emergency department length of stay per average visit per patient (pG0.001). There was no
significant effect on the number of hospitalizations or hospital length of stay. This intervention
demonstrated a correlation with reducing emergency department use in patients with behavioral
health issues, but no correlation with reducing hospital utilization. This under-researched
approach of integrating medical records at point-of-care could serve as a model for better
emergency department management of behavioral health patients.
Address correspondence to Mohammad Shahsahebi, MD, MBA, Department of Community and Family Medicine, Duke
University, Durham, NC, USA. Phone: (919) 342-8845; Email: [email protected]
Stephanie Ngo, MD, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Fred Johnson, MBA, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Mina Silberberg, PhD, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Mohammad Shahsahebi, MD, MBA, Northern Piedmont Community Care, Durham, NC, USA. Phone: (919) 342-8845;
Email: [email protected]
Fred Johnson, MBA, Northern Piedmont Community Care, Durham, NC, USA.
Sean Schreiber, MSED, LPC, Alliance Behavioral Health, Raleigh, NC, USA.
Journal of Behavioral Health Services & Research, 2017. 651–658. c)2017 National Council for Behavioral Health. DOI
10.1007/s11414-017-9574-7
Evaluating the effectiveness of community NGO ET AL. 651
Introduction
Background
Patients with behavioral health issues often require more resource-intensive care and are more
likely to be frequent users of health services.1–7 Brennan et al. found that patients with at least one
primary psychiatric visit to the emergency department (ED) were 4.6 times more likely than those
without a primary psychiatric visit to be classified as high utilizers of health services overall, and
that on average, high utilizers with a primary psychiatric visit had a significantly higher number of
ED visits than non-psychiatric high utilizers.7
Furthermore, Bboarding^ of patients with behavioral health issues has become a serious problem
for patients who requi ...
This document discusses outcomes research, which seeks to understand the end results of healthcare practices and interventions. It describes two agencies, the Agency for Healthcare Research and Quality and the Patient-Centered Outcomes Research Institute, that focus on outcomes research and fund studies to increase healthcare effectiveness. Both agencies emphasize measures like quality of life and patient preferences. The document also discusses positive and negative impacts of outcomes research, how it assesses elements of health important to patients, and how researchers have developed ways to broadly measure health status.
This document discusses outcomes research, which seeks to understand the end results of healthcare practices and interventions. It describes two agencies, the Agency for Healthcare Research and Quality and the Patient-Centered Outcomes Research Institute, that focus on outcomes research and fund studies to increase healthcare effectiveness. Both agencies emphasize measures like quality of life and patient preferences. The document also outlines some positive and negative impacts of outcomes research, and stresses the importance of using broader health status measures that go beyond just physical health outcomes.
ABSTRACT Handover, or the communication of patient information be.docxransayo
ABSTRACT: Handover, or the communication of patient information between clinicians, is a fundamental component of health care. Psychiatric settings are dynamic environments relying on timely and accurate communication to plan care and manage risk. Crisis assessment and treatment teams are the primary interface between community and mental health services in many Australian and international health services, facilitating access to assessment, treatment, and admission to hospital. No previous research has investigated the handover between crisis assessment and treatment teams and inpatient psychiatric units, despite the importance of handover to care planning. The aim of the present study was to identify the nature and types of information transferred during these handovers, and to explore how these guides initial care planning. An observational, exploratory study design was used. A 20-item handover observation tool was used to observe 19 occasions of handover. A prospective audit was undertaken on clinical documentation arising from the admission. Clinical information, including psychiatric history and mental state, were handed over consistently; however, information about consumer preferences was reported less consistently. The present study identified a lack of attention to consumer preferences at handover, despite the current focus on recovery-oriented models for mental health care, and the centrality of respecting consumer preferences within the recovery paradigm.
INTRODUCTION Handover is the transfer of verbal and written communication of patient information between members of the health-care team. It is integral to the practice of all healthcare clinicians (Millar & Sands 2012). The Australian Commission for Safety and Quality in Health Care (ACSQHC 2011) recognizes the importance of handover in the continuum of health care, and acknowledges that information transferred between clinicians during the handover can directly affect the quality of care delivered to patients. Poor-quality handover practice has been linked to a number of unfavourable patient outcomes, including increased hospital stays, consumer dissatisfaction, delays in treatment, and other adverse clinical outcomes (Hill & Nyce 2010; Manser & Foster 2011; Siemsen et al. 2012; World Health Organization Collaborating Centre for Patient Safety
Solution
s (WHOCCPSS) 2007). In the present study, we report on the findings of a study that investigated handover between the crisis assessment and treatment team (CATT) and the inpatient psychiatric unit (IPU).
There is little in the published literature that reports on handover practices in acute psychiatric settings, and no previous research that has specifically investigated handover between the CATT and the IPU. The lack of studies in this area is concerning, given that in Australia and internationally, CATT service models are in wide use to facilitate community access to psychiatric assessment and care for people who are experien.
This study investigated the quality and safety of discharge prescriptions from mental health hospitals in the UK. The researchers found that:
1) 20.8% of discharge prescriptions contained at least one prescribing error, with an overall error rate of 5.08% of prescribed items. Nearly three-quarters of errors were considered clinically relevant.
2) Increasing numbers of medications prescribed (polypharmacy) and prescriptions written by GP Trainees and Core/Specialist Trainees were associated with higher rates of prescribing errors.
3) Over 70% of prescriptions contained clerical errors, most commonly related to specifying who should continue prescribing medications. Over 67% of prescriptions requiring communication
DN 703 Identifying a Target Population Research Paper.docxwrite5
The target population is adult patients who return to the emergency department within 72 hours of being discharged. This population often returns due to an inability to understand discharge instructions and access follow-up care. The paper will analyze the cultural, psychosocial, environmental, and demographic factors of this population and propose an intervention involving nurses providing detailed discharge explanations and ensuring effective communication through the use of interpreters if needed. It will also discuss developing a discharge checklist and establishing reliable post-discharge contact to address patient concerns without returning to the emergency department.
DN 703 Unit 8 Identifying a Target Population.docxwrite5
This document discusses identifying a target population for a DNP project aimed at reducing emergency department readmissions. The target population is identified as the adult population who have been discharged from the emergency department without proper education or instructions, often due to language barriers. Cultural, psychosocial, environmental, and demographic factors of this target population are analyzed. The document also outlines an intervention strategy of providing patient education and a discharge checklist to improve understanding and reduce unnecessary returns to the emergency department. An implementation plan, expected outcomes, and evaluation strategy for the project are required to address this issue.
By administering assessments and analyzing the results, targeted aTawnaDelatorrejs
By administering assessments and analyzing the results, targeted and individualized interventions can be determined to best serve the needs of students with disabilities. The actual implementation of the interventions provides teachers opportunities to collect data and gauge the effectiveness of the interventions in addressing documented student needs. Teachers can also gain important skills and knowledge on how to best advocate for practical classroom interventions. Teachers will also be able to collaborate with colleagues and families in mentoring students to take ownership of learning strategies.
Allocate at least 2 hours in the field to support this field experience,
Part 1: Assessment and Interventions
Select at least one student to whom you will administer the informal RTI assessment created in Clinical Field Experience A. Score the assessment and share the results with the student to increase understanding of his or her strengths and areas for improvement.
Collaborate with the certified special education teacher and the student to develop 2-3 interventions based on the student assessment data to support the student’s progress in the classroom. In addition, detail one intervention that can be incorporated at home with family support.
Use any remaining field experience hours to assist the teacher in providing instruction and support to the class.
Part 2: Reflection
In 250-500 words, summarize and reflect upon the following:
· Describe each intervention, including teacher, student, and family roles, where applicable.
· Your experiences administering the assessment, analyzing the results, and providing the student feedback on his or her performance.
· Explain how you expect the interventions you developed to meet the needs of the student, incorporating his or her assessment results in your response.
· Explain how you will use your findings in your future professional practice.
APA format is not required, but solid academic writing is expected.
This assignment uses a rubric. Review the rubric prior to beginning the assignment to become familiar with the expectations for successful completion.
You are required to submit this assignment to LopesWrite. A link to the LopesWrite technical support articles is located in Class Resources if you need assistance.
6
Annotated Bibliography
Student’s Name
Course
Instructor’s name.
Institutional Affiliation
October 7, 2021.
Annotated Bibliography
Ali, H., Ibrahem, S. Z., Al Mudaf, B., Al Fadalah, T., Jamal, D., & El-Jardali, F. (2018). Baseline assessment of patient safety culture in public hospitals in Kuwait. BMC Health Services Research, 18(1). https://doi.org/10.1186/s12913-018-2960-x
The researchers conducted a cross-sectional study in 16 public hospitals in Kuwait using the Hospital Survey on Patient Safety Culture (HSOPSC). The study aimed to assess patient safety culture in public hospitals as perceived by hospital staff and relate the findings similar to regional and international ...
This document summarizes a transitional care workgroup meeting held on July 12, 2013. The meeting included introductions and presentations on transitional care evidence and measuring patient-centered outcomes. Participants discussed a vignette about a patient being discharged from the hospital to identify questions patients would have about participating in a new transitional care program. The group's objectives were to understand transitional care broadly and narrow the topic by prioritizing important questions from multiple stakeholder perspectives. Breakout sessions allowed for submitted questions and discussion of proposed research topics. The meeting concluded with recapping next steps and welcoming further input.
MHA6999 SEMINAR IN HEALTHCARE CASES-- WEEK 2 LECTURE, DISCUSSION, DioneWang844
MHA6999 SEMINAR IN HEALTHCARE CASES-- WEEK 2 LECTURE, DISCUSSION, AND PROJECT INSTRUCTIONS
Page | 1
Quality
Nearly fifteen years ago, the Institute of Medicine published the “To Err Is Human” report, which exposed the substantial impact of medical errors in the US healthcare system and called for a dramatic system change, including an improved understanding of those errors (McCarthy, Tuiskula, Driscoll, & Davis, 2017). Medical errors are considered to be failure to achieve the original goal or plan of action, and these errors may range from a patient falls to a mistake in the operating room. Not only do medical errors cause harm to the patient and jeopardize the patient’s trust, but they also cause a financial strain for the health system (“To Err is Human,” 1999). One of the contributing factors to medical errors is the lack of effective communication between doctors who are treating the same patient. This results in healthcare providers overprescribing medications for patients as well as increases the possibility of a patient having unnecessary tests or procedures performed. The report’s four-tiered approach includes:
· Focusing on creating a stronger foundation of education on patient safety
· Mandating a nationwide reporting system to encourage timely reporting of errors
· Increasing the standards of performance for healthcare providers
· Taking advantage of the security that safety systems offer (“To Err is Human,” 1999)
Creating a strong educational foundation for patient safety is most important. Healthcare personnel are much more likely to actively participate in reporting systems, encourage one another to perform at a higher level, and take advantage of safety systems when they are well educated on patient safety and the implications of medical errors. The reporting system seems to provide the least amount of impact on patient safety as they can result in losing patient trust in certain healthcare systems. The healthcare system as a whole has made progress in establishing a safe environment for patients when they are in need of care.
Challenges for Patient Safety and Steps for Improvement
Despite continuing evidence of problems in patient safety and gaps between the care that patients receive and the evidence about what they should receive, efforts to improve quality in healthcare show mostly inconsistent and patchy results.
Tap each image to know more.
Data Collection and Monitoring Systems
This always takes much more time and energy than anyone anticipates. It is worth investing heavily in data from the outset. Assess local systems, train people, and have quality assurance.
Tribalism and Lack of Staff Engagement
Overcoming a perceived lack of ownership and professional or disciplinary boundaries can be very difficult. Clarify who owns the problem and solution, agree roles and responsibilities at the outset, work to common goals, and use shared language.
Convince People That There's a Problem
Use hard data to secure emotional e ...
The document describes the development of a transitional care program called C-TraIn for uninsured and Medicaid patients at Oregon Health & Science University. Key steps included engaging institutional leaders, performing a needs assessment of 116 inpatients, and convening stakeholder work groups. The needs assessment found that many patients lacked access to primary care and faced barriers to medication access. This informed the design of C-TraIn, which includes elements such as a transitional care nurse, pharmacy consultations, 30 days of medications for uninsured patients, and linkages to community medical homes. An economic analysis estimated potential cost savings from reducing readmissions, which helped gain institutional support and funding to implement and study the program.
PCOMS and an Acute Care Inpatient Unit: Quality Improvement and Reduced Readm...Barry Duncan
High psychiatric readmission rates continue while evidence suggests that care is not perceived by patients as “patient centered.” Research has focused on aftercare strategies with little attention to the inpatient treatment itself as an intervention to reduce readmission rates. Quality improvement strategies based on patient-centered care may offer an alternative. We evaluated outcomes and readmission rates using a benchmarking methodology with a naturalistic data set from an inpatient psychiatric facility (N 2,247) that used a quality-improvement strategy called systematic patient feedback. A systematic patient feedback system, the Partners for Change Outcome Management System (PCOMS), was used. Overall pre-post effect sizes were d 1.33 and d 1.38 for patients diagnosed with a mood
disorder. These effect sizes were statistically equivalent to RCT benchmarks for feedback and depression.
Readmission rates were 6.1% (30 days), 9.5% (60 days), and 16.4% (180 days), all lower than national benchmarks. We also found that patients who achieved clinically significant treatment outcomes were less likely to be readmitted. We tentatively suggest that a focus on real-time patient outcomes as well as care that is “patient centered” may provide lower readmission rates.
Jeff Grever - Culminating Project Poster - FINALJeff Grever
- The document discusses a study that evaluated placing hyperlinks on secure healthcare websites to increase registration in a clinical research volunteer registry called ResearchMatch.
- Results showed unique visitors to the community participation webpage increased over 1000% after adding a hyperlink to OSUMyChart, and new ResearchMatch registrations from Ohio residents near the study site increased 56-70%.
- The study suggests strategically placing hyperlinks on secure websites in a healthcare context can increase interest in clinical research participation and registrations in online volunteer registries.
The panel convened by the National Patient Safety Foundation to discuss the current state of patient safety 15 years after the seminal IOM report To Err Is Human identified several key points:
1) While awareness of patient safety issues has increased, progress has been slower than anticipated and the scale of improvement has been limited.
2) A total systems approach is needed to move beyond reactive, piecemeal interventions to prioritizing safety culture, developing the science of safety, and ensuring coordination across the care continuum and settings.
3) Specific recommendations include establishing safety leadership, centralized oversight, common safety metrics, increased research funding, addressing safety across all care settings, supporting the healthcare workforce, partnering with patients and families, and optim
PROs and PROMs Understanding Patient Reported Outcome Measuresijtsrd
In the ever evolving landscape of healthcare, the quest for patient centeredness has transcended mere rhetoric to become a fundamental cornerstone, fundamentally altering the dynamics of clinical decision making. This shift represents a seismic departure from traditional healthcare paradigms, where the patients voice was often relegated to the periphery. Now, it stands as an imperative, a guiding principle that necessitates the active integration of patient perspectives into the very fabric of clinical decision making processes. Sushma K. V | Dr. Ashwini P S | Sneha John "PROs & PROMs: Understanding Patient-Reported Outcome Measures" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-8 | Issue-1 , February 2024, URL: https://www.ijtsrd.com/papers/ijtsrd62413.pdf Paper Url: https://www.ijtsrd.com/other-scientific-research-area/other/62413/pros-and-proms-understanding-patientreported-outcome-measures/sushma-k-v
This document summarizes a presentation about communication experiences of children with cerebral palsy in health care settings and the potential for technologies to improve engagement. It discusses parent feedback wanting involvement in decision making and consideration of broader impacts. Using technologies like PCEHR and decision aids may help provide better evidence and access to information. Clinical implications discussed include involving parents and children in goal setting and information sharing. Future research directions explored uptake of PCEHR, health impacts of technologies, and communicative environments in health settings.
This document discusses trends and issues in nursing. It outlines how nursing will shift from hospitals to homes and communities, with a focus on prevention and patient outcomes. Nurses will be primary care providers for diverse services. There will also be challenges relating to ethics, costs, access, and quality of care. Globalization will bring opportunities and challenges as the work environment emphasizes cost-effectiveness and quality. The roles and responsibilities of nurses are changing as health care transitions to more community-based, evidence-based, and interdisciplinary models of care.
Pediatric heart failure can be life-threatening and lead to frequent readmissions. The article discusses the complex factors that contribute to high readmission rates for children with heart failure, including lack of care coordination and continuity. It recommends 10 strategies to improve communication during care transitions and reduce readmissions, such as creating common metrics to track outcomes, recognizing this as a complex adaptive challenge, and engaging clinicians in leadership and redesigning care processes. The goal is to improve outcomes and reduce costs through more coordinated, patient-centered care for this vulnerable population.
This document summarizes a study that assessed current practices in teaching life support competencies in healthcare. The study conducted surveys to: 1) Identify life support courses provided in UK hospitals and required by professional bodies, 2) Describe curriculum content and teaching methods of popular in-hospital courses, 3) Examine fidelity of implementation of courses in England. The study found that most NHS hospitals provide adult life support courses, with the Resuscitation Council UK Advanced Life Support course most common. Many hospitals also provide in-house courses. Recognition and management of pre-arrest deterioration are now widely taught. While life support training is provided in all medical schools, approaches vary and pre-arrest management courses are less common. Only a
This document provides a summary of a human factors analysis conducted of the Pediatric Blood & Marrow Transplantation Unit (PBMTU) at Duke University Hospital. The analysis was conducted over several months in late 2006 and early 2007 by a multi-disciplinary team from Aptima, Inc. The team conducted over 50 interviews and observations to identify stress points and potential failures within the PBMTU system. The analysis utilized several human factors techniques including interviews, observations, modeling, and assessment of the clinical microsystem framework. The report details the assessments and provides recommendations in each area of the framework to improve safety, quality of care, staff retention and the unit's ability to serve more patients.
This section discusses team training research and makes recommendations for improving team training in medical contexts. It summarizes that while some team training programs for healthcare professionals have shown promise, such as Anesthesia Crisis Resource Management (ACRM) training and MedTeams training, the evidence supporting their effectiveness in enhancing patient safety is still limited. It recommends developing a theoretical model of medical team performance, continuing to learn from the broader science of team performance and training, identifying core competencies for effective medical teamwork through consensus, and leveraging proven instructional strategies from team training research. The overall aim is to provide a strategy for further investigating how team training can help the medical community improve patient safety.
The document summarizes a study conducted by the Florida Patient Safety Network on establishing a Patient Safety Authority in Florida. Key points:
- The study was mandated by the Florida legislature in response to Senate Bill 2-D from 2003 to evaluate creating a statewide Patient Safety Authority.
- The Authority would be responsible for activities and functions to improve patient safety and quality of care in health facilities and among practitioners.
- The study examined options for the Authority to directly perform safety functions, or contract with or partner with university patient safety centers.
- The Network coordinated its efforts with various stakeholders and academic medical centers across the state to conduct a comprehensive review and provide recommendations.
The Telluride Interdisciplinary Roundtable met in 2005 and 2006 to design a comprehensive patient safety curriculum for medical students. The group developed 11 specific curricular elements and identified challenges to implementation. A patient safety curriculum was successfully developed over two years. Future meetings focused on evaluating pilots of the curriculum in medical schools and developing new ideas. Continued collaboration between professions will help create a standardized longitudinal patient safety curriculum.
- Management interventions can be divided into targeted service interventions with narrow effects and generic service interventions that have diffuse effects like policy interventions.
- For targeted service interventions, measuring changes in clinical processes is often more cost-effective than measuring patient outcomes in evaluations.
- Clinical processes are not usually suitable primary endpoints for evaluations of policy and generic service interventions because their effects are too diffuse.
- Multiple clinical processes are consolidated into a small number of patient outcomes, which are the default primary endpoints for policy and generic service intervention evaluations.
- When a policy or generic service intervention is inexpensive and plausible effects on patient outcomes are difficult to detect, effects can still be studied at earlier process levels in Donabedian's causal chain model
This document describes a 9-step framework for evaluating the expected cost-effectiveness of a service intervention at the design stage. It applies this framework to evaluate an intervention to improve clinical handovers between hospital and community care.
The key steps are: 1) Identifying endpoints and grouping them, 2) Estimating baseline risks, 3) Eliciting expected effectiveness from experts, 4) Assigning utility values to endpoint groups, 5) Costing the intervention, 6) Estimating healthcare costs of adverse events, 7) Calculating health benefits, 8) Determining cost-effectiveness, and 9) Conducting sensitivity analysis.
When applied to a handover improvement intervention, literature suggested adverse events follow 19%
The document summarizes a systematic review of 36 randomized controlled trials that tested interventions to improve handovers of patients from hospitals to primary care. The majority (69.4%) of studies found statistically significant effects favoring the intervention, and most (94.4%) interventions were multicomponent. Effective interventions included medication reconciliation, electronic tools to facilitate discharge summaries, discharge planning involving both hospital and primary care providers, electronic discharge notifications, and Web-based access to discharge information for primary care physicians. The review found interventions often reduced hospital use, improved continuity of care, and enhanced patient status after discharge. However, the heterogeneity of interventions and outcomes made firm conclusions difficult to draw.
This document is a business reply card from Jones & Bartlett Learning requesting a review copy of the book "Case Studies in Patient Safety: Foundations for Core Competencies". It provides instructions for qualified instructors to request a complimentary review copy for course adoption consideration by filling out their contact and course details on the pre-paid reply card or online. The book contains 24 first-person accounts of preventable health care errors told from the patient's perspective to illustrate lessons learned and strategies for preventing future errors.
- 15-year-old Lewis Blackman underwent elective surgery for pectus excavatum (sunken chest) at an academic medical center.
- In the days following surgery, Lewis experienced worsening abdominal pain but nurses dismissed it as constipation and insisted he walk more.
- His condition deteriorated over several hours but nurses were busy preparing for an inspection and did not take his worsening vital signs seriously.
- It was not until Lewis said "It's going black" that a cardiac code was called, but he could not be resuscitated and died 31 hours after reporting the abdominal pain.
This document discusses improving quality and safety in healthcare systems through an improvement science approach. It provides three key building blocks for developing a "high reliability organization":
1) Establishing a culture devoted to quality with trust, constructive error management, and zero tolerance for unsafe practices.
2) Implementing clear responsibility and accountability through defined care pathways, outcome measurement, and bottom-up process improvement.
3) Optimizing and standardizing processes through evidence-based standard operating procedures and scrutiny of variations.
Measurement of outcomes is also discussed as crucial for continuous improvement towards being "better than the rest." Engaging all levels is emphasized as fundamental to achieving reliable performance.
This document discusses the potential role of national health insurance in creating a safe, affordable, and high-quality healthcare system in the Bahamas. It begins by outlining the government's vision of transforming healthcare to be the safest and most effective in the region. It then discusses some of the current challenges in the Bahamian healthcare system, including a lack of coordination, increasing costs, and workforce issues. The document also reviews international healthcare system rankings and compares mortality rates between public and private patients in Bahamian hospitals. Overall, the document examines how a national health insurance system could help address issues in the current healthcare system and better serve the needs of Bahamians.
Yes, we're ready to go on bypass.
Perfusionist: Yes, I'm ready for bypass.
Surgeon: Okay, let's go on bypass.
Hospital B
Surgeon: Heparin please.
Anaesthetist: Heparin going in now. *administers heparin*
Perfusionist: Heparin level is therapeutic, I'm ready for bypass.
Surgeon: Okay, let's go on bypass.
Learning: Explicit verbal confirmation of key steps improves safety.
Catchpole K, 2011, in press
Human Factors in Healthcare
l Design of equipment, tasks, jobs, and environments
l Understanding human
More from Wayne State University School of Medicine (15)