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Exploring the Implementation of the Chronic Care Model in Systemic Sclerosis Management

Exploring the Implementation of the Chronic Care Model in Systemic Sclerosis Management

Introduction

As Special Education Directors, our primary role is to ensure that all students receive the support they need to thrive in their educational environment. This includes understanding and implementing research findings that can improve the quality of care and support provided to students with chronic conditions. A recent study titled "Patient Assessment Chronic Illness Care (PACIC) and its associations with quality of life among Swiss patients with systemic sclerosis: a mixed methods study" offers insights that can be applied to enhance care models, particularly for rare diseases like systemic sclerosis (SSc).

Understanding the Chronic Care Model (CCM)

The Chronic Care Model (CCM) is a widely adopted framework designed to improve the management of chronic illnesses. It emphasizes productive interactions between proactive healthcare teams and informed patients. The model includes six core elements: community resources, health systems, self-management support, delivery-system design, decision support, and clinical information systems. These elements aim to enhance patient outcomes and reduce healthcare costs.

Key Findings from the Study

The study employed a mixed methods design to evaluate the implementation of CCM elements in the care of Swiss patients with systemic sclerosis. It used the Patient Assessment of Chronic Illness Care (PACIC) tool to assess patient experiences. The findings revealed a mean PACIC score of 3.0/5.0, indicating that care was not fully aligned with the CCM. Notably, the study identified significant gaps in goal setting, tailoring, and problem-solving counseling.

Implications for Practitioners

For practitioners working with students with chronic conditions, the study highlights the importance of implementing CCM elements to improve care quality. Key areas for improvement include:

Encouraging Further Research

The study underscores the need for further research to explore the implementation of CCM elements in rare disease care. Practitioners are encouraged to engage in research initiatives that investigate innovative care models and their impact on patient outcomes. By contributing to the body of knowledge, practitioners can help shape more effective care strategies for students with chronic conditions.

Conclusion

Incorporating the findings from the PACIC study into practice can enhance the quality of care for students with systemic sclerosis and other chronic conditions. By focusing on personalized care, problem-solving counseling, and self-management support, practitioners can create a more supportive and effective educational environment for these students.

To read the original research paper, please follow this link: Patient Assessment Chronic Illness Care (PACIC) and its associations with quality of life among Swiss patients with systemic sclerosis: a mixed methods study.


Citation: Kocher, A., Simon, M., Dwyer, A. A., Blatter, C., Bogdanovic, J., Künzler-Heule, P., Villiger, P. M., Dan, D., Distler, O., Walker, U. A., & Nicca, D. (2023). Patient Assessment Chronic Illness Care (PACIC) and its associations with quality of life among Swiss patients with systemic sclerosis: a mixed methods study. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-022-02604-2
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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