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The importance of addressing patients' perspectives to assess the value of medical interventions is currently widely recognised, particularly in situations where only the patient has direct knowledge of treatment benefit or where no agreed upon biomarkers exist [ 2- 4].
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Given that beneficence and non-maleficence are both addressing patient interest and wellbeing, but from two opposing perspectives, this observation could be explained by the PTs focusing more on preventing the harm that errors mean for the patient.
Furthermore, the application of ICF-oriented instrume.gs, e.g. the Rehabilitation Problem-Solving Form (RPS-Form) [ 27], which is a patient-centred evaluation tool, addresses the patients' perspective and their needs in rehabilitation.
Addressing the patient perspective is perceived as an essential step to enhance patient participation, to build agreement through a critical exchange between doctors and patients, and finally to contribute to patients' satisfaction [ 28, 29].
We can therefore conclude that although there is only partial coverage in validated instruments of all PHC attributes best addressed by patient perspective and relevant for health reform evaluation, the core attributes are well covered.
Understanding patients' perspectives and addressing cultural barriers to care are important for ensuring effective communication and diabetes control [ 20- 22].
The measure is expected to address six areas of reform: integrating patients' perspectives into the regulatory process, modernizing clinical trials, fostering the future of science, investing in advancing research, incentivizing the development of new drugs and devices for unmet medical needs and supporting digital medicine.
We hope that patients' perspectives will be a call to action to address the obstacles identified in the pathway to MDR-TB treatment initiation.
This article has paid attention to the accounts of adults with mitochondrial disease, and builds on the limited literature addressing the perspectives of patients and families.
Grunfeld and Earle (2010) note that there is little research on patients' perspectives concerning models of survivorship care [ 29], and our study begins to address this gap, by illuminating patients' concerns about and experiences of primary care follow-up.
Matrix tabulation of interventions and patients' perspectives identified a range of priorities raised by people infected with HIV-1 that were not addressed in evaluated interventions.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com