4.2 Article

The Role of Phage Therapy in Burn Wound Infections Management: Advantages and Pitfalls

Journal

JOURNAL OF BURN CARE & RESEARCH
Volume 43, Issue 2, Pages 336-342

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jbcr/irab175

Keywords

-

Funding

  1. FCT - Fundacao para a Ciencia e Tecnologia, I.P., within CINTESIS, RD Unit [UIDB/4255/2020]

Ask authors/readers for more resources

This systematic review addresses the general characteristics of bacteriophages, their activity compared to conventional antibiotics, their effectiveness against biofilms, administration methods, and their use in burn wound infections. Although recognized for its potential value in modern wound care, specific aspects need to be considered, including the lack of consensus on therapeutic guidelines/regulatory policies and laboratory support that can predict efficacy.
Burn wound infections are often the source of bacteria responsible for systemic infections, including bloodstream infections and pneumonia that ultimately can result in multisystem organ failure and death. Any rapid change in the burn wound appearance or the clinical condition of the burn patient may herald burn wound infection or sepsis. The revival of phage therapy, either in single mode or in combination with conventional antibiotics may represent a valuable alternative, to treat specific bacterial infections such as burn wound infections, including those caused by multidrug-resistant organisms. This systematic review addresses the: 1) general characteristics of bacteriophages; 2) activity of bacteriophages vs conventional antibiotics; 3) activity of bacteriophages against biofilms; 4) bacteriophage administration; and 5) use of bacteriophages in burn wound infections. Although several scientific organizations/societies recognized that phage therapy could be of key value in modern wound care, specific aspects are critical for a burn surgeon and might represent pitfalls discouraging phage therapy adoption in burn wound management; in particular, the unavailability of consensual therapeutic guidelines/regulatory policies and the lack of laboratorial support that might be predictive of its efficacy. The availability of a product/formulation convenient to use, with adequate stability and shelf half-life is also a key condition.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available