The antibiotic resistance is now common place throughout the globe. Two highly problematic antibiotic resistant
infections are those produced by multi-drug resistant Mycobacterium tuberculosis (MDRTB) and methicillin resistant Staphylococcus aureus (MRSA). Although
vancomycin is useful for therapy of MRSA, there is now evidence that resistance to this antibiotic is taking place. Intracellular
infections of MRSA are very difficult to manage and are recurrent especially when invasive prosthetic devices are employed. This mini-review provides cogent evidence that both intracellular MDRTB and intracellular MRSA can be killed by concentrations of the non-antibiotic
phenothiazine,
Thioridazine, at concentrations in the medium that are below those present in the plasma of patients treated with this agent. Although
thioridazine has been claimed to cause arrhythmias and even
sudden death, the frequencies of these episodes are rare and when present, they are related to the patients underlying cardiac status as opposed to the direct effect of the agent itself. The authors do not suggest that
thioridazine be used indiscriminately for MDRTB or intracellular
infections produced by MRSA. However, there are circumstances where there are no alternative forms of therapy and the patient faces an unfavourable prognosis. For these highly selective and controlled situations, the use of
thioridazine in the manner employed for the therapy of psychosis is recommended (compassionate therapy).