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Blue Cross denies coverage for Alzheimer's drug Lekimbi amid safety concerns


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Blue Cross denies coverage for Alzheimer's drug Lekimbi amid safety concerns
In a recent meeting of the Alzheimer’s Disease and Dementia Advisory Council, significant discussions centered around the new Alzheimer’s drug, Lekimbi, and its implications for Arkansas residents. The council examined the drug's approval process and its potential impact on patients suffering from mild cognitive impairment and mild dementia.

The meeting highlighted that Lekimbi is currently covered for an initial approval duration of three months, requiring six doses of infusion. However, the drug must be prescribed by a geriatrician or neurologist, and there are strict authorization requirements, including documented evidence of beta amyloid presence and cognitive testing.

Jill Johnson, a clinical pharmacist with extensive experience, provided insights into the drug's effectiveness. While Lekimbi has shown some ability to slow the progression of Alzheimer’s, the results indicate that the difference is minimal—only 0.45 points on a clinical scale, which is below the threshold that patients can perceive as beneficial. Johnson emphasized that although the drug is statistically significant, it does not provide a noticeable improvement in patients' daily lives.

Concerns were also raised regarding the safety of Lekimbi. Adverse reactions, including infusion reactions and amyloid-related imaging abnormalities (ARIA), were discussed. The data revealed that patients receiving Lekimbi experienced higher rates of edema and hemorrhaging compared to those on placebo, raising questions about the drug's overall safety profile.

In contrast, Medicaid representatives confirmed that the program would cover Lekimbi, aligning with federal guidelines for FDA-approved drugs. This decision could provide crucial access for many patients who might benefit from the treatment.

As the council continues to evaluate the implications of Lekimbi, the discussions reflect a broader commitment to addressing the needs of Alzheimer’s patients in Arkansas. The outcomes of these deliberations will play a vital role in shaping future healthcare policies and ensuring that residents have access to effective treatments.

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