HEALTH-E NEWS

TB patients still shunned by families

By Amy Green for Health-e news 25 March 2019
Caption
Patients participating in TB Day at Khayelitsha's Site B clinic in Cape Town, South Africa on 24 March 2011. (Photo by Gallo Images/Foto24/Lulama Zenzile)

Despite South Africa being the only country in the world to make a new TB drug available to all who have drug-resistant TB, many TB patients are still avoided by their families.

It felt like my entire family just dumped me in the hospital to die,” remembered mother-of-two Nomasonto Lubisi from eMalahleni in Mpumalanga after being diagnosed with multidrug-resistant TB (MDR-TB).

Shortly after her diagnosis in December 2017, Lubisi was admitted to a provincial hospital and placed on a treatment regimen consisting of a cocktail of potent drugs.

One of these medicines was bedaquiline, the first anti-TB drug developed in almost half a century. This makes Lubisi one of just 28,700 people on the planet with access to the life-saving drug. More than two-thirds of these patients are in South Africa, which is one of a number of reasons the country has received widespread praise for its anti-TB policies.

But Lubisi didn’t feel that fortunate:

My family were scared of getting TB from me and made me live in isolation before I went to hospital. I was in there a year and they didn’t visit me, not even once.”

In light of her experience, the words uttered by Deputy President David Mabuza barely a week ago ring hollow.

Our people need not feel bad about getting TB,” he said, speaking at the launch of a TB prevention initiative in Durban.

For as long we breathe, we can contract TB because this disease is an airborne disease. There is also no need to ill-treat people with TB. As we said, anyone can get it. Let us not stigmatise people with TB, instead let us help them get the treatment and get cured.”

In 2018, the government decided to introduce bedaquiline as the first-line option for treatment of patients with resistant forms of TB, which, up until that point, had entailed two years of toxic treatment that causes permanent hearing loss in up to a third of patients. To make matters worse, only about half the patients who managed to finish this gruelling prescription were cured.

In contrast, a bedaquiline-based regimen cures up to 80% of patients, according to new evidence published in March 2019 in New England Journal of Medicine.

However, South Africa remains the first and only nation to have implemented the superior and more tolerable regimen.

South Africa’s leadership in rolling out novel tuberculosis therapeutics should stand as an inspiration for all of us who aim to end tuberculosis, which will only be possible if innovation is embraced,” Doctor’s Without Borders’ (MSF) Anja Reuter noted in 2018 in The Lancet Respiratory Medicine journal.

Earlier in 2019 Health Minister Aaron Motsoaledi reiterated that an estimated 160,000 people are ill with TB in South Africa, but are not on treatment, and termed them “missing patients”.

Ingrid Schoeman, a TB survivor and dietitian with the local organisation TB Proof, said that this is precisely why it is not enough to introduce new drugs, as the stigma surrounding the disease prevents many of these patients from going to health facilities and testing for TB.

Imagine how lonely it must be to be sick and fear losing your friends, your job or relationships because you got sick with TB. TB stigma causes people to avoid seeking health care and, without treatment, you cannot be cured,” she said.

And the source of discrimination endured by those with TB isn’t just from families, friends or even strangers. Many South Africans complain that some health workers are an added hurdle to accessing TB care.

Twenty-four-year-old Siphiwe Buthelezi, also from Mpumalanga, is being treated for MDR-TB, but his treatment has been threatened on more than one occasion due to fear.

At times if I couldn’t get my treatment when I was supposed to. I wouldn’t get it because I was afraid that the nurses will shout at me because that’s what happened before,” he said.

Buthelezi has “struggled a lot to take my treatment because I do not have a strong support system on my side and then the problem caused by the poor attitudes from nurses to me as a patient”.

South Africa is also dropping the ball on other seemingly-simple anti-TB tools, particularly when it comes to preventing the spread of the illness.

According to Dr Neil Schluger, a TB expert from international organisation Vital Strategies, “the scope of South Africa’s TB problem is just enormous”.

To its credit, the country has been enthusiastic and a world leader in adopting new TB technologies and tools… but infection control programmes (not everywhere, but in most facilities) are lacking,” he said.

These include the availability of protective masks for health workers, proper ventilation systems and handling of TB specimens.

But for patients like 51-year-old Andries Maille from Barberton in Mpumalanga, while it is “good” that politicians are talking about TB stigma, he wondered if anything would change for ordinary South Africans.

Currently undergoing MDR-TB treatment, the miner told Health-e News he had witnessed “people not seeking professional help for TB because of the stigma and discrimination they experience in society”. Maille said:

If I didn’t get the support I have from my family I wouldn’t have been able to accept that I have MDR-TB. I probably would have died before I even got diagnosed.” DM

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