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Rare Disease Patients Suffer As CoEs Under-Utilise Funds, Shows Data

Five out of 12 Centres of Excellence (COEs) formed to treat patients suffering from rare diseases have utilised less than 35 per cent of the funds allotted to them by the Centre over the last three years, according to patient advocacy groups and data from a reply given in Parliament.  

These centres were created under the National Policy for Rare Disease (NPRD) in 2021.

According to data accessed by Business Standard, the maximum fund utilisation was seen at Institute of Postgraduate Medical Education and Research (IPGMER), Kolkata at 93.65 per cent. The next in the chart was King Edward Medical Hospital, Mumbai at 93.55 per cent.

But five institutes at the bottom have spent less than 35 per cent of the fund allotted to them. (see the chart).

Hyderabad-based Centre for DNA Fingerprinting & Diagnostics with Nizam’s Institute of Medical Sciences stands last in the list with only 4.53 per cent funds utilisation. Followed by Delhi’s Maulana Azad Medical College at 17.62 per cent.

According to a reply given by the health ministry in Parliament, as of February this year these centres have utilised only 48% of around Rs 109 crore disbursed in the last three years.

COEs are institutions identified by the central government to actively treat patients suffering from rare diseases. Currently, 12 such centres have a quota of 2,420 rare disease patients from six categories across three groups. 

“While the government has set up CoEs to treat patients with rare diseases, patients with Group 3a conditions are still experiencing inordinate delay in procedural formalities across these centres,” a member associated with an advocacy group for patients with Group 3a conditions said.  

According to the rare disease policy enacted in 2021, Group 3a includes conditions such as Lysosomal Storage Disorders (LSD’s) for which definitive treatment is available but challenges are to make optimal patient selection for benefit, very high cost, and lifelong therapy. 

“There are currently around 454 eligible rare disease patients with LSD’s such as Pompe disease, Fabry disease, Mucopolysaccharidosis (MPS) type I and type II in India, to be put on immediate life-saving therapy as per the National Policy for Rare Diseases 2021,” the member added. 

The human cost

According to data available on the government’s digital portal for crowdfunding and voluntary donations for patients of rare diseases, more than 300 out of 454 LSD patients currently eligible for funding under Group 3a are not getting any treatment in CoEs. 

Currently, only 98 LSD patients are on government-approved treatment.

“The delay in the commencement of the treatment process and uncertainties around sustainable funding of Group 3a disorders are turning fatal, with around 28 of these 454 patients reported to have lost their lives in the last few months awaiting treatment support,” an official said.

The groups have asked the government to direct CoEs to ensure efficient utilisation of funds provisioned by the ministry. 

This comes after several caregivers and advocacy groups for patients with 3a conditions had written a letter to Union Health Minister JP Nadda last month, citing the inordinate delays being faced by patients eligible for treatment under the NPRD.   

The letter had stated that several patients across the CoEs have been put off life-saving therapies after the one-time support of Rs 50 lakh was exhausted.

Missing urgency

“No urgency being shown by centres,” a distressed parent said.

A Delhi-based parent, whose six-year old child is diagnosed with MPS-2, said that he has been waiting to get the child on-boarded at the ministry’s designated CoE for treatment, despite his child being eligible to be put on life-saving therapy as per the guidelines of the NPRD. 

“My child deserves to lead a near-normal life and I urge the government to intervene in the matter to save the lives of hundreds of other children as well,” he added. 

Similarly, a Hyderabad-based parent of an eight-year old Pompe disease patient said that while his child is eligible for Enzyme Replacement Therapy (ERT) with the available Rs 50 lakh funding, he is still running from pillar to post.

“My child could be saved if he gets regular ERT sessions. But I do not see any urgency by the hospital despite available funds. We are in distress as we are concerned about our kid’s life, his health is deteriorating,” he added.  

Highlighting the need to ensure timely treatment for patients with Group 3a disorders, a medical expert said that patients with LSD’s are largely young children and the delay in medical treatment could lead to life-threatening complications. 

“These diseases have therapies approved by the Drugs Controller General of India (DCGI) and are available in India with proven clinical outcomes, as well as available government funding. Despite this, it is disappointing to see patients waiting for the inevitable,” he said.

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