US proposes ‘new rules’ to increase organ transplants

‘Over 20 die every day’

WASHINGTON, Dec 18, (AP): The US government is overhauling parts of the nation’s transplant system to make sure organs from the dead no longer go to waste – and to make it easier for the living to donate.

The rules proposed Tuesday aim to ease an organ shortage so severe that more than 113,000 Americans linger on the transplant waiting list – and about 20 die each day.

Part of the reason: An Associated Press analysis recently found some of the groups that collect organs at death secure donors at half the rate of others, missed opportunities that could have saved lives. But the government currently has little way to directly compare organ collection agencies and force poor performers to improve.

“No life-saving organ should go to waste,” Medicare chief Seema Verma said in announcing stricter standards to hold those agencies more accountable.

At the same time, the administration also aims to spur more living donors by allowing them to be reimbursed for lost wages and child care or elder care expenses incurred during their hospitalization and recovery.

“When an American wishes to become a living donor, we don’t believe their financial situation should limit their generosity,” said Health and Human Services Secretary Alex Azar, whose father received a kidney transplant from a living donor.

Kidneys

The rules come after President Donald Trump in July ordered a revamping of care for kidney disease, including spurring transplants of kidneys and other organs. The proposals are open for public comment for 60 days. Transplant advocates praised the move.

“Patients are dying, and they deserve better,” Jennifer Erickson, a former Obama administration staffer who worked on transplant policy, said of the crackdown on “organ procurement organizations,” or OPOs.

And the association that represents those organ collection groups pledged to work with Medicare, which regulates the nonprofits, to implement the tougher standards.

The new rules are “an opportunity to drive meaningful changes that will increase the availability of organs for transplant and save more lives,” Kelly Ranum, CEO of Louisiana’s OPO and president of the association, said in a statement.

Today, the country is divided into 58 zones, each assigned an OPO to essentially be a matchmaker – rapidly collecting organs from willing donors at death and getting them to the right transplant center, even if a hospital calls with a potential donor at 3 am. It’s hard to tell how well they do the job. They self-report to the government success rates without any way to tell how many potential donations were left behind, or why. And current rules give little incentive for retrieving less-thanperfect organs, such as those from older donors.

“For countless patients, an imperfect organ is better than no organ at all,” Verma said.

Under the proposal, Medicare will calculate each OPO’s donation and transplantation rates using federal death records that show the entire pool of potential donors each has to draw from – anyone 75 or younger who dies in a hospital of conditions that wouldn’t automatically preclude donation.

For the first time, that would allow Medicare to rank OPO performance. Verma promised yearly evaluations, saying any organ agency that didn’t do as well as the top quarter of their competitors would be pushed to improve.

“This is a great first step,” said Greg Segal of the advocacy group Organize, whose father waited five years for a heart transplant. “Now the government needs to implement the rule as strongly and quickly as possible.”

Verma estimated the change could spark another 5,000 transplants a year. A 2017 study by University of Pennsylvania researchers had estimated that a better-functioning system could yield as many as 28,000 additional organs.

Deceased donors make up most transplants but people lucky enough to receive a kidney or part of a liver from a living donor not only cut their wait, but those organs tend to survive longer. Yet fewer than 7,000 of the 36,529 transplants performed last year were from living donors.

Currently, the transplant recipient’s insurance pays the donor’s medical bills. But donors are out of work for weeks recuperating and not all employers allow some form of paid time off. The new proposal aims to ease that economic hurdle; still to be determined is exactly who will qualify.

Also: LOUISVILLE, Ky:

A cut to the tax coal companies pay to fund a trust for sick miners will cost taxpayers at least $15 billion by 2050, according to a new report from a national watchdog group.

An excise tax rate on mined coal that funds the Black Lung Disability Trust Fund expired at the beginning of 2019 due to inaction by Congress. That led to a reduction in the amount coal companies pay into the fund, which pays benefits and medical bills for miners diagnosed with black lung disease.

“By failing to extend the excise tax, Congress is shifting billions of dollars in liabilities from coal companies to taxpayers,” said Autumn Hanna, vice-president of Taxpayers for Common Sense. The Washington-based group released a report on Tuesday that said the fund’s debt could be as high as $26 billion by 2050.

The US Department of Labor earlier this year confirmed to The Associated Press that a funding shortfall in the Black Lung Trust Fund would be covered by borrowing from the US Treasury.

A excise tax rate of $1.10 per ton of underground mined coal was cut by more than half to about 50 cents in the new year. The fund took in about $450 million in revenue in fiscal year 2017.

The cut came as a surge of black lung disease scars miners’ lungs at younger ages than ever.