Impact of BACIS Program on Quality of Care

This chapter presents the methodology for measuring the system's impact on the quality of care. The system's impact on the quality of care was measured through a compliance review using the standards of care set in the maternal health guidelines. In the framework for development of clinical practice guideline-based decision support systems, the compliance review is part of the section on evaluation. The compliance review addresses the following objectives: measurement of compliance with processes of care at the study clinic before introduction of the BACIS program, measurement of improvements in compliance after the introduction of the BACIS program, and a qualitative review undertaken in order to understand the reasons for non-compliance.

2018 ◽  
Vol 158 (3) ◽  
pp. 427-431 ◽  
Author(s):  
Helene J. Krouse ◽  
Charles (Charlie) W. Reavis ◽  
Robert J. Stachler ◽  
David O. Francis ◽  
Sarah O’Connor

This plain language summary for patients serves as an overview in explaining hoarseness (dysphonia). The summary applies to patients in all age groups and is based on the 2018 “Clinical Practice Guideline: Hoarseness (Dysphonia) (Update).” The evidence-based guideline includes research to support more effective identification and management of patients with hoarseness (dysphonia). The primary purpose of the guideline is to improve the quality of care for patients with hoarseness (dysphonia) based on current best evidence.


In this chapter, the framework from Chapter 6 on design and development of clinical practice guideline-based decision support systems is used to review the design and development of the BACIS program. The data for carrying out the review of the BACIS program is drawn from three main sources. These are interviews of the health practitioners participating in the BACIS program study, a document review, as well as from observations made by the author during the study in his engagement with study participants during the stages of system development and piloting. In the evaluation, a review of requirements analysis is carried out, as per the framework elaborated in Chapter 6. Then a review of the systems features is also carried out after it.


2020 ◽  
Vol 41 (1) ◽  
pp. 165-170
Author(s):  
Rajendra Gyawali ◽  
Melinda Toomey ◽  
Fiona Stapleton ◽  
Lisa Dillon ◽  
Barbara Zangerl ◽  
...  

2020 ◽  
Vol 3 (5) ◽  
pp. e205535 ◽  
Author(s):  
Melissa C. Brouwers ◽  
Karen Spithoff ◽  
Kate Kerkvliet ◽  
Pablo Alonso-Coello ◽  
Jako Burgers ◽  
...  

2021 ◽  
Vol 9 (7) ◽  
pp. e002552
Author(s):  
Matthew D Galsky ◽  
Arjun V Balar ◽  
Peter C Black ◽  
Matthew T Campbell ◽  
Gail S Dykstra ◽  
...  

A number of immunotherapies have been developed and adopted for the treatment of urothelial cancer (encompassing cancers arising from the bladder, urethra, or renal pelvis). For these immunotherapies to positively impact patient outcomes, optimal selection of agents and treatment scheduling, especially in conjunction with existing treatment paradigms, is paramount. Immunotherapies also warrant specific and unique considerations regarding patient management, emphasizing both the prompt identification and treatment of potential toxicities. In order to address these issues, the Society for Immunotherapy of Cancer (SITC) convened a panel of experts in the field of immunotherapy for urothelial cancer. The expert panel developed this clinical practice guideline (CPG) to inform healthcare professionals on important aspects of immunotherapeutic treatment for urothelial cancer, including diagnostic testing, treatment planning, immune-related adverse events (irAEs), and patient quality of life (QOL) considerations. The evidence- and consensus-based recommendations in this CPG are intended to give guidance to cancer care providers treating patients with urothelial cancer.


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