InnoHEALTH magazine Volume 4 issue 1 | Page 51

saliva is another cause of worry which takes a physical, emotional and mental toll on the patient. Since most infected individuals begin to feel better after a few weeks of treatment and the length and side-effects of the drug treatment are arduous, many patients stop the treatment prematurely or skip doses. Rampant patient non-compliance when it comes to completion of anti-TB therapy is one of the main factors for the emergence of a more severe form of the disease, one which is resistance to common drugs! This is a big reason for TB reactivation and the continued prevalence of this disease even though it is completely curable in most cases. Drug resistance in TB has been known since the first antibiotics to treat this disease were put into place. An increasingly larger repertoire of drug resistant strains necessitated and increasingly larger arsenal of drugs to treat the disease. As of today, TB strains resistant to one of the first line of four antibiotics are called resistant strains. Strains resistant to two first line antibiotics are called multi-drug resistant strains of TB or MDR-TB. These are treated with a second line of antibiotics, consisting of fluoroquinolones (levofloxacin, moxifloxacin and gatifloxacin) or injectable drugs such as amikacin, kanamycin and streptomycin. More recently, a third category of strains labelled Extensively drug resistant- or XDR-TB has been described with resistance to a fluoroquinolone and at least one of three injectable drugs. A total of 12 drugs are approved today, each of which individually and in combination are used to treat these three categories of TB, MDR-TB and XDR-TB. However, a little characterized fourth type of strain, dubbed totally drug resistant- or TDR- TB has been reported in India, Italy, Iran and South Africa. These strains are completely resistant to all known anti- TB medication and given the airborne and infectious nature of the disease, are ticking time bombs of catastrophe. NEWER STRATEGIES IN TB HEALTHCARE The emergence of drug resistance, the persistently high rate of TB incidence 52 Volume 4 | Issue 1 | January-March 2019 and TB mortality and the challenges associated with patient non-compliance demand improved methods to detect TB with high accuracy, newer drugs to treat resistant forms of TB and increased awareness of the disease. Bedaquiline and delamanid are two new drugs for TB that have shown promising results in clinical trials after nearly 40 years of failed attempts. These two drugs have received approval for use in the treatment of MDR- and XDR-TB. Additionally, a new drug combination involving bedaquiline, pretomanid and linezolid is reported to have successfully treated XDR-TB in six months with a lower mortality rate than current treatments. However, these new treatment regimens are yet to enter mainstream clinical practice, with further and larger clinical trials needed to make an accurate cost-benefit analysis of these strategies. LOOKING TO THE FUTURE Although the current situation of TB in India and worldwide looks bleak, the global TB incidence is falling at the rate of 2% per year. According to WHO, this rate needs to increase to 5% to achieve the WHO Global Plan to End TB milestones of reaching 90% of all people with TB through national TB programmes, reaching atleast 90% of vulnerable high- risk population through affordable treatment and achieve atleast 90% success in the treatment of all people diagnosed with TB. Achieving both WHO and RNTCP milestones will require a concerted effort by policymakers, healthcare providers, TB researchers, patients and the general public. What we need today is increased public spending on healthcare to make TB therapy affordable and accessible, improvement of research funding and infrastructure and stronger public awareness campaigns to disseminate the reality and requirements of ending TB. Over just the past two centuries, TB is estimated to have killed 1 billion people, which is more than the number of people killed due to AIDS, cholera, influenza, plague and smallpox combined! It is time we take the initiative and responsibility to help the millions that are suffering from this deadly disease. Vignesh Narayan is a scientist and science writer at the Indian Institute of Science who currently studies the molecular biology of the TB pathogen Mycobacterium tuberculosis in an attempt to understand how the bacterium senses and responds to its environment and develop new drugs and drug targets to combat the disease.