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January 10.2026
2 Minutes Read

Surgeons Weigh In: What Maryland's All-Payer Model Means for Healthcare

Maryland's All-Payer Model healthcare cost illustration.

Understanding Maryland's Unique All-Payer Model

Maryland’s All-Payer Model stands out as a revolutionary healthcare endeavor, launching in 2014 with the ambitious goal of standardizing hospital payments across public and private insurers. This initiative aimed to control costs while enhancing patient care by establishing a set price for patients regardless of their insurance coverage. Over the years, the model has evolved to encompass total healthcare spending across all payers, thereby impacting various facets of healthcare delivery.

Surgeons' Experience and Perspectives on the Model

Recent findings from a study assessing surgeons' experiences highlight a high level of awareness among Maryland’s surgical community about the All-Payer Model. A striking 71.5% of surgeons reported a solid understanding of how the model influences patient outcomes. However, this understanding appears to be somewhat superficial, as many surgeons expressed concerns about the model's limited impact on clinical decision-making and referral management. For instance, only 17.0% felt the model had aided in managing referrals effectively.

Key Insights from the Survey

The researchers implemented a comprehensive survey, targeting 121 surgeons and achieving a 65% response rate. The results revealed a mixed bag of opinions: while 77.2% of surgeons recognized the model's significance on their practice, only 38.8% recalled receiving adequate information about the model from their institutions. Peer discussions emerged as a significant source of information, yet the lack of formal communication hindered surgeons' engagement with the model’s benefits.

Challenges and Opportunities in the Implementation

Surgeons highlighted notable challenges with the implementation of the All-Payer Model. Issues such as communication gaps and lack of involvement in the design and execution of the model were prevalent. Despite acknowledging the move towards centralized complex care management, many believed the reimbursement structure still felt tethered to traditional fee-for-service models. As a result, critical aspects like reducing preventable hospital use and unplanned readmissions remained largely unaddressed.

Future Trajectories for Maryland's Healthcare Landscape

Moving forward, it's vital for policymakers to consider the value of engaging surgeons in discussions about healthcare payment reforms. As noted by study authors, the sustainability of quality improvements relies on bridging communication gaps and aligning incentives for clinicians. By fostering collaboration among surgeons and healthcare administrators, the foundations for successful healthcare delivery can be reinforced.

Conclusion: The Road Ahead

While Maryland's All-Payer Model exhibits promising approaches to healthcare reimbursement, the experiences and insights of its surgical community reveal significant areas for improvement. For the model to truly enhance patient care and streamline complex surgical processes, systemic changes in communication and involvement are essential. Understanding and addressing the concerns of surgeons will be pivotal for the model’s ongoing success in reshaping the Maryland healthcare landscape.

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02.24.2026

Why Reducing RA Medication Might Increase Flares: Patient Insights

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02.23.2026

FDA Approves Acalabrutinib and Venetoclax Combination: A Game Changer for CLL Patients

Update Acalabrutinib and Venetoclax: A New Era for CLL Treatment The recent approval of the combination treatment of acalabrutinib and venetoclax by the FDA marks a significant step forward for patients diagnosed with chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL). This innovative pairing not only offers hope for effective management but represents a shift towards a more targeted therapy approach. Understanding the FDA Approval On February 19, 2026, the FDA gave its green light for this combination, establishing it as the first all-oral, fixed-duration regimen for treating adult patients with CLL/SLL. The approval stems from the promising outcomes seen in the AMPLIFY clinical trial, which demonstrated that patients on this combination therapy experienced a statistically significant improvement in progression-free survival (PFS) compared to traditional chemotherapy options like fludarabine combined with cyclophosphamide and rituximab (FCR) or bendamustine with rituximab (BR). A Closer Look at the AMPLIFY Trial The AMPLIFY trial involved adult participants with untreated CLL without a specific genetic mutation (del(17p) or TP53). Researchers highlighted that patients receiving acalabrutinib and venetoclax had a remarkably better median PFS – a crucial measure in oncology as it reflects the length of time patients live without the cancer worsening. While the median PFS was not reached in the treatment arm, those on conventional therapy had a median PFS of 47.6 months, showcasing the potential effectiveness of this new combination therapy. Benefits of a New Treatment Paradigm Dr. Jennifer Brown, one of the principal investigators in the study, emphasized that traditional continuous therapies for CLL often lead to treatment fatigue and other burdensome side effects over time. The new acalabrutinib plus venetoclax regimen circumvents this issue by being a fixed-duration therapy, thus simplifying treatment timelines and reducing long-term toxicity. Such an approach empowers healthcare providers to tailor treatments to meet individual patient goals effectively. The Safety Profile: What Patients Should Know While the efficacy of acalabrutinib and venetoclax is a highlight, understanding the safety profile associated with these medications remains essential. In the AMPLIFY trial, serious adverse reactions were reported in 25% of the treatment group, though many experienced side effects milder than those associated with chemotherapy. Familiarizing patients and healthcare providers with these risks, which include opportunistic infections and cardiovascular issues, enhances informed decision-making in treatment plans. Future Directions in CLL Treatment This FDA approval is a vital indicator of the shifts happening in the management of CLL, underscoring a movement towards precision medicine. With ongoing research and development, we can expect further innovations that could alter the landscape of treatment for blood cancers. With the clinical success of acalabrutinib and venetoclax, there lies significant opportunity for the oncology community to explore similar combination therapies aimed at improving patient outcomes. In conclusion, as we observe advancements like the FDA approval of acalabrutinib with venetoclax, it invites optimism for both current and future patients battling CLL. Patients and families navigating this complex journey benefit greatly from being informed about such developments, facilitating conversations with healthcare providers about treatment options tailored to their unique circumstances.

02.21.2026

Lipedema is Now Recognized as a Chronic Disease: A Paradigm Shift in Care

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