Doctor
Visits as Data Points
The Patient Centered Research Institute (PCORI)announced Tuesday how it
would move forward on that mission: spend $68 million to fund a network of
health-care systems that cover as many as 12 million patients. The idea is to
use all the doctor visits that already happen — and all the treatments that
doctors prescribe — to figure out which ones do best for a certain type of
patient.
Sarah Kliff, “Under
Obamacare Program, doctor visits would become data points, “ Washington Post, April 23, 2012
Data Point Definition
If you haven’t heard, this is the age of Big Data. The reasoning behind Big Data goes like this: Big Data is impersonal. Big Data has no bias. Big Data is objective. Big Data is easily collectiable. Big Data is measurable. Therefore, Big Data is good.
Never mind that medicine is personal, confidential. subjective, and an Art. With computers, artificial intelligence, and public funding, medicine has become a measurable, manageable Science. Big Data is King.
Big Data can now, and with precision, define where we shop, what we buy, when and where we buy, and who we elect. Big Data can define what kind and the best of care we
receive, and, ultimately, to what doctors and hospitals we go. Those doctors and hospitals presumably will be the
ones with the best outcomes and with no personal self-interests, income, or revenue axes to grind.
Here is how the Washington Post explains
the Obama administration's Big Data program,
“The Affordable
Care Act created the Patient Centered
Research Outcomes Institute (PCORI) to support comparative
effectiveness research, studies that identify the most effective treatments
when a whole array of options might be available."
"PCORI announced
Tuesday how it would move forward on that mission: spend $68 million to fund a
network of health-care systems that cover as many as 12 million patients. The
idea is to use all the doctor visits that already happen — and all the
treatments that doctors prescribe — to figure out which ones do best for a
certain type of patient.”
Two
Big Obstacles with the Big Data Outcome Program – Patients and Doctors
At a recent
meeting of 500 patients at which the program was explained and patients were
asked if it would be OK if their data was used, two patients raised their hand in affirmation and
approval.
Doctors aren’t
any happier with the idea. In a local
health system, doctors are asked to
wheel around or carry a laptop to enter patient data at the point of care, or “data
point,” If you prefer. I am aware of two doctors who have left the system
because they were uncomfortable with entering data in front of patients. Said one to me, “I was trained to take care
of people, not to being a computer technician and data entry clerk.”
Tweet: Patients
and doctors are uncomfortable with using computers at the point of care to
gather data on the efficacy of personal care and outcomes.
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