IPCHS

Contents tagged: patient outreach

Aug. 30, 2016 Europe Practice

Reorienting the model of care, Creating an enabling environment

Identifying high-risk chronic patients for targeted primary care intervention in Veneto, Italy

Adjusted Clinical Groups were introduced in primary care as a means to proactively target patients at high risk for chronic disease with personalized health interventions and preventive services; when designing the initiative, leaders sought out existing solutions from abroad which could be adapted for application in Veneto; gradual implementation of the initiative through a three-phase pilot project allowed time to explore, verify and refine activities before scaling up across Veneto; services were reoriented to become more proactive, nurses were awarded additional responsibilities related to patient outreach and patients’ own role in their care was increased; Veneto's existing strong data collection system was essential for allowing predictive risk modelling using Adjusted Clinical Groups. The initiative capitalized on the “goldmine” of data already being collected for administrative purposes.

adjusted clinical groups, at-risk populations, patient outreach, predictive risk modelling, preventive care

Sept. 6, 2016 Europe Practice

Engaging and empowering people and communities, Reorienting the model of care, Coordinating services within and across sectors

Implementing targeted cancer screening programmes in the Czech Republic

The Ministry of Health developed a national cancer screening programme to increase population uptake of existing screening services. Through this programme, health insurance companies proactively send at-risk enrolees personalized invitations to participate in cancer screenings; strong Ministerial leadership provided an overarching direction for the initiative, promoting alignment across key stakeholders; use of available data helped identify key problems and supported tailoring of activities to meet observed gaps in service delivery; national information campaigns, run through various media channels, supported efforts by educating the public on the importance of cancer screenings; the initiative prioritized a proactive approach to addressing cancer mortality, promoting a shift away from the reliance on reactive service provision.

at-risk populations, cancer, health insurers, patient outreach, screening

Sept. 7, 2016 Europe Practice

Engaging and empowering people and communities, Reorienting the model of care, Coordinating services within and across sectors

Strengthening cancer screening in Montenegro

In 2008, the Government of Montenegro released the National Cancer Control Plan. Responding to recommendations proposed by the Plan, the Institute of Public Health developed a comprehensive cancer screening programme for colorectal cancer. Following successful piloting, the colorectal cancer screening programme is now being expanded to cover other priority cancers; partnerships with stakeholders outside of the health sector provided access to technologies and tools for engaging the public. Text messaging was the main tool used for outreach; moving from a reactive to a proactive approach was important for reaching and engaging the target population and increasing uptake of screenings; a strong information system supported a data-driven initiative design, facilitated implementation and enabled monitoring and evaluation.

cancer, m-health, national cancer plan, patient outreach, screening

Feb. 10, 2020 Africa Publication

Engaging and empowering people and communities, Coordinating services within and across sectors, Creating an enabling environment

Giving patients a voice: implementing patient and public involvement to strengthen research in sub-Saharan Africa

Patient and public involvement (PPI) is recognised as a valuable tool in improving the quality and relevance of research. Defined as "research being carried out "with" or "by" members of the public rather than "to", "about" or "for" them", PPI is a method of involving patients and the public in the design, conduct and dissemination of research and services that affect them, providing for a more democratic approach and patient empowerment.

empower patients, improve the quality of care, patient involvement, patient outreach, public sector, quality of health care