WHO cautious on Covid-19 plasma as US issues emergency authorisation

Author: AP/Reuters/Web Desk

The World Health Organisation on Monday was cautious about endorsing the use of recovered Covid-19 patients’ plasma to treat those who are ill, saying evidence it works remains “low quality” even as the United States issued emergency authorisation for such therapies.

So-called convalescent plasma, which has long been used to treat diseases, has emerged as the latest political flashpoint in the race to find therapies for Covid-19.

The US Food & Drug Administration (FDA) on Sunday authorised its use after President Donald Trump blamed the agency for impeding the roll-out of vaccines and therapeutics for political reasons.

The technique involves taking antibody-rich plasma from patients who have recovered from Covid-19 and giving it to those who are suffering from severe active infections in hopes they will recover more quickly.

Soumya Swaminathan, WHO chief scientist, said only a few clinical trials of convalescent plasma have produced results, and the evidence, at least so far, has not been convincing enough to endorse it beyond use as an experimental therapy. While a few trials have shown some benefit, she said, they have been small and their data, so far, inconclusive.

“At the moment, it’s still very low-quality evidence,” Swaminathan told a news conference. “So we recommend that convalescent plasma is still an experimental therapy, it should continue to be evaluated in well-designed randomised clinical trials.”

Evidence is conflicting: One Chinese study showed plasma from people who have recovered from coronavirus failed to make a difference in hospitalised patients, while another, pooled analysis showed it can lower the risk of death.

One challenge, Swaminathan added, was plasma’s variability, since it is drawn from many different people, producing a product that is less-standardised than monoclonal antibodies crafted in the lab.

World Health Organisation senior adviser Bruce Aylward added that beyond plasma’s efficacy, there were also potential safety risks that must be vetted.

“There are a number of side effects,” Aylward said, ranging from mild fevers to severe lung injuries or circulatory overload. “For that reason, the clinical trial results are extremely important.”

The US National Institutes of Health this month announced it was giving several million dollars toward a mid-stage convalescent plasma trial.

Share
Leave a Comment

Recent Posts

  • Business

CDNS attains Rs 600 billion mark in annual savings target

The Central Directorate of National Savings (CDNS) has accomplished a target of Rs 600 billion…

6 hours ago
  • Business

777 planes can land at Faisalabad airport after expansion: Airport manager

About 777 planes could land at Faisalabad International Airport after the expansion of its runway…

6 hours ago
  • Business

Gold prices up by Rs2,100 per tola

The price of 24 karat per tola gold increased by Rs 2,100 and was sold…

6 hours ago
  • Business

Industry leaders push for sustainable policies through collaboration

The government needs to establish long-term and sustainable policies in consultation with the real stakeholders…

6 hours ago
  • Business

Value-added textile export industry be top priority of govt: PHMA

The value-added export-oriented textile industry should be given the top priority of the government, providing…

6 hours ago
  • Business

FRIA wants special incentives for cash-strapped small industry

The Ferozepur Road Industrial Association (FRIA) has asked the government to announce soft financing with…

6 hours ago