HAIs are among the top 5 urgent public health threats in the US due to the high recurrence rates of infections following standard antibiotic treatments. Specifically, Clostridioides difficile infections (CDI), the high recurrence rates with first-line antibiotics which underscores the need for new treatments. Introducing targeted therapies could significantly improve CDI management. While the long-term effects of these therapies are still uncertain, expanding the treatment options for C difficile gives healthcare professionals more ways to treat the infection, aiming ultimately to reduce patient distress.
Due to its lower recurrence risk, the microbiome-preserving antibiotic Fidaxomicin is advised as the primary treatment for C difficile infection. The effectiveness of fecal microbiota transplants (FMT) in managing recurrent CDI has paved the way for defined microbiome biotherapeutics, which provide a safer and more regulated option to complement antibiotic treatment. Considering the link between antibiotic-induced disruption of the gut microbiota and C difficile recurrence, upcoming therapies focus on minimizing reliance on antibiotics for managing the infection.
The infection encompasses fidaxomicin, vancomycin, and metronidazole. Fidaxomicin, recognized for its narrow spectrum activity, has been shown to better preserve the intestinal microbiome compared to vancomycin, offering similar rates of clinical cure but with a reduced risk of C difficile recurrence. The standard course of fidaxomicin treatment is 200 mg every 12 hours for 10 days, it is advised as the primary therapy for initial episodes of non-severe CDI, as well as for severe and severe-complicated/refractory cases. In situations where fidaxomicin is unavailable, vancomycin, 125 mg every 6 hours for 10 days, serves as a substitute. Metronidazole is no longer recommended as a first-line treatment for CDI. Metronidazole is still used as a primary treatment in several countries due to the cost and accessibility of alternative medications.
