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Why We Love Committees

Daily Remedy by Daily Remedy
July 31, 2022
in Contrarian
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Why We Love Committees

Confident diverse group of hospital administrators sit down to discuss important issues withe healthcare professionals.

Healthcare loves committees. We have them everywhere. Seemingly, every bureaucratic organization in healthcare is administered through a loose conglomerate of individuals held together under the aegis of a committee.

Most never question why it is this way. We just accept it as tradition, like the sanctity of the clinical exam. We know of better ways to do things, but we still do it. But the concept of the committee is more telling than just healthcare’s deference to tradition. It reveals much about how we think in healthcare.

We think in groups, and the most dominant voice in the room influences the group the most. The idea being clinical medicine is egalitarian, so the strongest clinical minds should have the most sway. This makes sense if a committee is reviewing patient diagnosis, but it makes less sense for less clinical matters.

When discussing whether to add a new facility or to break ground on a new hospital, the talking points are not only clinical, but economic. The manner in which we make these decisions should differ from in how most we make clinical decisions. Yet, they are not.

They are grander extensions of the same committee design. Inevitably, the most dominant voices soon become the only voice and all others fall in line. This is how bureaucracies form in healthcare. Committees grow in size and scope, but the fundamental means of decision-making remain the same. So the same voice grows louder.

Whereas before the loudest voice had the strongest clinical acumen, now the loudest voice has the greatest sway. But the mechanisms of checks and balances get lost along the way. Bureaucracies exist for those in positions of power to exert it without being held liable.

In small clinical committees, if you are right or wrong, then you know it immediately. The effects of the decision are apparent. But for larger committees, the effects of the decision are less pronounced. It is difficult to say whether building the new hospital was the right decision.

This is because most decisions are not simply right or wrong. They depend on the context in which we decide. There is a science to this, the theory of committee decision-making. Mostly relegated to theoretical business and economic classes, the study of group decisions is not commonly applied in healthcare.

We like our tried-and-true model of loose committees with loose agendas. But as healthcare becomes more economic, the ability to make decisions becomes paramount. We cannot make clinical decisions the way we make economic ones. We have to learn when and how to optimize the decision-making process.

This is where the science of group decisions comes into play. We must frame how we derive consensus on decisions relative to the decisions being made. This starts with committee design. Different decisions are processed and discussed in group settings in different ways. It depends on the subject expertise of the committee members and the subject being discussed.

Financial committees should handle matters differently than clinical ones. And those who comprise one committee should not be on the other. This would require a certain level of delegation, divvying the decision-making among different groups.

But healthcare, for all its growth, remains beholden to its roots. And at its root lies the sole physician lording over all clinical decisions. We can discuss paternalism as subject expertise. We can even cover it up through the veneer of bureaucracy. But even underground, the roots make their presence known.

So committees retain their original structure, a loose mix of individuals in which the most dominant voice becomes the principal decision-making. And the more healthcare scales, the most pervasive those select voices become.

This is why healthcare loves committees so much.

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Daily Remedy

Dr. Jay K Joshi serves as the editor-in-chief of Daily Remedy. He is a serial entrepreneur and sought after thought-leader for matters related to healthcare innovation and medical jurisprudence. He has published articles on a variety of healthcare topics in both peer-reviewed journals and trade publications. His legal writings include amicus curiae briefs prepared for prominent federal healthcare cases.

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Videos

This conversation focuses on debunking myths surrounding GLP-1 medications, particularly the misinformation about their association with pancreatic cancer. The speaker emphasizes the importance of understanding clinical study designs, especially the distinction between observational studies and randomized controlled trials. The discussion highlights the need for patients to critically evaluate the sources of information regarding medication side effects and to empower themselves in their healthcare decisions.

Takeaways
GLP-1 medications are not linked to pancreatic cancer.
Peer-reviewed studies debunk misinformation about GLP-1s.
Anecdotal evidence is not reliable for general conclusions.
Observational studies have limitations in generalizability.
Understanding study design is crucial for evaluating claims.
Symptoms should be discussed in the context of clinical conditions.
Not all side effects reported are relevant to every patient.
Observational studies can provide valuable insights but are context-specific.
Patients should critically assess the relevance of studies to their own experiences.
Engagement in discussions about specific studies can enhance understanding

Chapters
00:00
Debunking GLP-1 Medication Myths
02:56
Understanding Clinical Study Designs
05:54
The Role of Observational Studies in Healthcare
Debunking Myths About GLP-1 Medications
YouTube Video DM9Do_V6_sU
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BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

by Daily Remedy
February 15, 2026
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Can lowering tau biology translate into a clinically meaningful slowing of decline in people with early symptomatic Alzheimer’s disease? That is the practical question behind BIIB080, an intrathecal antisense therapy designed to reduce production of tau protein by targeting the tau gene transcript. In a phase 1b program originally designed for safety and dosing, investigators later examined cognitive, functional, and global outcomes as exploratory endpoints. The clinical question matters because current disease-modifying options primarily target amyloid, while tau pathology tracks...

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