Momentum to address prior authorization challenges
April 05, 2026
One tactic that insurance companies use to help contain costs is to require providers to seek approvals before actually performing specific operations (a practice known as prior authorization). It is not difficult to imagine how this practice can go wrong. KFF Health News published an article about one family's struggle with an insurer's delayed approval. The article notes "His family didn't expect the procedure to eradicate the cancer, but they hoped it would buy him more time and improve his quality of life." and that "The insurer said the procedure wasn't medically necessary and that it was considered 'experimental and investigational.'" When the insurer finally did reverse course, "Within one week of the reversal in late May, Eric Tennant was hospitalized. His health continued to decline, and by midsummer he was no longer considered a suitable candidate for the procedure." Notably, the procedure in question (histotripsy) "was a less expensive alternative to chemotherapy, which his insurer had already authorized."
The main question in this context is: who gets to decide whether the insurance company should authorize a procedure? The insurer authorized chemotherapy, but apparently, the family opted not to continue that treatment. Should the insurer be allowed to deny the histotripsy treatment, even if medical experts believe it would help? It appears that enough of the public has tired of challenges with the practice of prior authorization that "By late 2025, 48 other states, in addition to the District of Columbia and Puerto Rico, already had some form of a prior authorization law — or laws — on the books." For the state in question for this article (West Virginia), the new law seems rather limited in scope. Presumably, if patients and providers continue to face challenges with prior authorization, stronger regulation will be considered.