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WOUND CARE COURSE: NEVER TOO LATE- part 2
Dr. Khadijah Nordin
• What is biofilm?
• How biofilm form?
• What are the function of biofilm?
• How biofilm affected in wound healing?
• Did you know there are some criteria that are suggestive that the
wound may have biofilm?
• How to diagnose wound with biofilm?
• How to treat biofilm?
• Planktonic cells
 defined as “free flowing bacteria in suspension”
• Biofilm
which is defined as “a structured community of bacterial cells enclosed in a
self-produced polymeric matrix (extracellular polymeric substance-EPS) and
adherent to an inert (non living thing) or living surface
 EPS is composed of proteins, polysaccharides, anionic and cationic ions and extracellular
DNA (eDNA) among other micro and macro components
are reported to be composed of 10–20% microorganisms and 80–90%
extracellular material
present in most chronic wounds and are likely to be located both on the
surface and in deeper wound layers, but may not be present uniformly across
or within the wound
response to them are associated with delayed wound healing.
Biofilms in chronic wounds are likely to be more established or mature .
The biofilm structure may promote the presence of anaerobic bacteria
The microbiota of chronic wounds is often polymicrobial; however, wound
biofilms may consist of single or multiple bacterial species .
Microbial diversity in a wound (planktonic and biofilms) can be influenced by
location and wound characteristics .
Biofilms in wounds may progress to contain fewer, more dominant species over
time but more research is needed to verify this
Biofilms are more tolerant to the host immune response and can evade
phagocytosis due to community defenses
Biofilm formation
Biofilm in wound
Biofilm affected wound healing
• Biofilms are thought to play a key role delayed wound healing and
are believed to be found in the majority of chronic wounds.
• Biofilms trigger a chronic inflammatory response in a wound which is
an attempt to rid the wound of the biofilms.
• This response results in large numbers of neutrophils and
macrophages grouping around the biofilms.
• Neutrophils and macrophages secrete high levels of reactive oxygen
species (ROS) and proteases to help to break down the attachments
between the wound tissue and the biofilms.
• The problem is that the ROS and proteases injure normal granulating
tissue and impact proteins and immune cells which then results in
delayed wound healing and the wound seemingly ‘stuck’ in a
prolonged inflammatory wound healing phase.
Did you know there are some criteria that are
suggestive that the wound may have biofilm?
• Failure of appropriate antibiotic treatment;
• Recalcitrance to appropriate antimicrobial treatment;
• Recurrence of delayed healing on cessation of antibiotic treatment;
• Delayed healing in spite of optimal wound management and health
support;
• Increased exudate/moisture;
• Low level chronic inflammation
How to diagnose wound with biofilm?
• There are currently no routine diagnostic tests available to confirm
biofilm presence
• Wound biofilms are difficult to visualize macroscopically and slough,
debris, and exudate may be visually mistaken for biofilm by
clinicians/healthcare professionals
• Tissue biopsies are more reliable than swabs to reveal biofilms in
wounds. However, routine culture techniques do not necessarily
identify biofilm presence.
Biofilm treatment strategy
Biofilms should be considered in the treatment of poorly healing wound
Antibiofilm strategies should continue to be used until the wound bed is
visibly clean, displaying healthy granulation tissue, and/or on a healing
Debridement is one of the most important treatment strategies against
biofilms, but does not remove all biofilm, and therefore cannot be used
alone—this is one of the critical principles of wound bed preparation
(tissue, infection/inflammation, moisture balance, and edge of wound)
Systemic antibiotics cannot eradicate a wound biofilm; therefore,
antibiotic stewardship must be considered with controlled use to help
manage planktonic bacteria, acute infection, and prevention of associated
systemic infections
When considering topical antiseptics, those that are known to have
antibiofilm properties are preferred
Prevention and treatment of biofilms should be considered in early
surgical wounds when there is a high risk of surgical site infection and
dehiscence (open colorectal surgery, cesarean section, and major
joint replacement serve as examples)
Biofilm treatments may be aligned across different types of chronic
wounds, as similar dominant microflora are usually implicated—
assuming the wound-specific factors are addressed with other
treatment strategies
Antibiofilm Agents
Short Term
Lactoferrin
Xylitol
Gallium
Farnasol
Deferoxamine
EDTA
Dispersin B
Fatty Acid Gel
Nitric Oxide
Long Term
Quorum Sensing
Inhibitor
RNA III Inhibitory Peptide
Furanones
Autoinducer
Biofilm Based Wound Care
Debridement- Frequent and aggressive
Selective biocides
Silver, Iodosorb, Hydrofera Blue
Antibiofilm Agents
Lactoferrin, Xylitol, Farnasol
Plant Products, Fatty Acid Gel
Antibiotics
Adjunct
Strong and long
Multiple Concurrent Strategies
Thank you

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Biofilm

  • 1. WOUND CARE COURSE: NEVER TOO LATE- part 2 Dr. Khadijah Nordin
  • 2.
  • 3. • What is biofilm? • How biofilm form? • What are the function of biofilm? • How biofilm affected in wound healing? • Did you know there are some criteria that are suggestive that the wound may have biofilm? • How to diagnose wound with biofilm? • How to treat biofilm?
  • 4.
  • 5. • Planktonic cells  defined as “free flowing bacteria in suspension” • Biofilm which is defined as “a structured community of bacterial cells enclosed in a self-produced polymeric matrix (extracellular polymeric substance-EPS) and adherent to an inert (non living thing) or living surface  EPS is composed of proteins, polysaccharides, anionic and cationic ions and extracellular DNA (eDNA) among other micro and macro components are reported to be composed of 10–20% microorganisms and 80–90% extracellular material present in most chronic wounds and are likely to be located both on the surface and in deeper wound layers, but may not be present uniformly across or within the wound response to them are associated with delayed wound healing.
  • 6. Biofilms in chronic wounds are likely to be more established or mature . The biofilm structure may promote the presence of anaerobic bacteria The microbiota of chronic wounds is often polymicrobial; however, wound biofilms may consist of single or multiple bacterial species . Microbial diversity in a wound (planktonic and biofilms) can be influenced by location and wound characteristics . Biofilms in wounds may progress to contain fewer, more dominant species over time but more research is needed to verify this Biofilms are more tolerant to the host immune response and can evade phagocytosis due to community defenses
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 17.
  • 18. • Biofilms are thought to play a key role delayed wound healing and are believed to be found in the majority of chronic wounds. • Biofilms trigger a chronic inflammatory response in a wound which is an attempt to rid the wound of the biofilms. • This response results in large numbers of neutrophils and macrophages grouping around the biofilms. • Neutrophils and macrophages secrete high levels of reactive oxygen species (ROS) and proteases to help to break down the attachments between the wound tissue and the biofilms. • The problem is that the ROS and proteases injure normal granulating tissue and impact proteins and immune cells which then results in delayed wound healing and the wound seemingly ‘stuck’ in a prolonged inflammatory wound healing phase.
  • 19.
  • 20.
  • 21. Did you know there are some criteria that are suggestive that the wound may have biofilm? • Failure of appropriate antibiotic treatment; • Recalcitrance to appropriate antimicrobial treatment; • Recurrence of delayed healing on cessation of antibiotic treatment; • Delayed healing in spite of optimal wound management and health support; • Increased exudate/moisture; • Low level chronic inflammation
  • 22. How to diagnose wound with biofilm? • There are currently no routine diagnostic tests available to confirm biofilm presence • Wound biofilms are difficult to visualize macroscopically and slough, debris, and exudate may be visually mistaken for biofilm by clinicians/healthcare professionals • Tissue biopsies are more reliable than swabs to reveal biofilms in wounds. However, routine culture techniques do not necessarily identify biofilm presence.
  • 23. Biofilm treatment strategy Biofilms should be considered in the treatment of poorly healing wound Antibiofilm strategies should continue to be used until the wound bed is visibly clean, displaying healthy granulation tissue, and/or on a healing Debridement is one of the most important treatment strategies against biofilms, but does not remove all biofilm, and therefore cannot be used alone—this is one of the critical principles of wound bed preparation (tissue, infection/inflammation, moisture balance, and edge of wound) Systemic antibiotics cannot eradicate a wound biofilm; therefore, antibiotic stewardship must be considered with controlled use to help manage planktonic bacteria, acute infection, and prevention of associated systemic infections
  • 24. When considering topical antiseptics, those that are known to have antibiofilm properties are preferred Prevention and treatment of biofilms should be considered in early surgical wounds when there is a high risk of surgical site infection and dehiscence (open colorectal surgery, cesarean section, and major joint replacement serve as examples) Biofilm treatments may be aligned across different types of chronic wounds, as similar dominant microflora are usually implicated— assuming the wound-specific factors are addressed with other treatment strategies
  • 25.
  • 26.
  • 27. Antibiofilm Agents Short Term Lactoferrin Xylitol Gallium Farnasol Deferoxamine EDTA Dispersin B Fatty Acid Gel Nitric Oxide Long Term Quorum Sensing Inhibitor RNA III Inhibitory Peptide Furanones Autoinducer
  • 28. Biofilm Based Wound Care Debridement- Frequent and aggressive Selective biocides Silver, Iodosorb, Hydrofera Blue Antibiofilm Agents Lactoferrin, Xylitol, Farnasol Plant Products, Fatty Acid Gel Antibiotics Adjunct Strong and long Multiple Concurrent Strategies
  • 29.

Editor's Notes

  1. The first step is the attachment of the bacterial cells to the selected abiotic or biotic surface. Bacteria usually adhere to a conditioning film typically composed of organic molecules (e.g. nutrients, salivary proteins, large macromolecules) that can promote the adherence of bacteria to the surface. Initial attachment is mediated through weak reversible van der Waals interactions between the cell surface and the substratum, which can lead to stronger adhesion receptor mediated attachment (25). Bacterial cell surface structures such as flagella, fimbriae, LPS, and exopolysaccharides participate in irreversible interactions. These can be dipole, hydrogen, ionic, or hydrophobic. The second step corresponds to the development of micro-colonies promoted by the growth and division of the first attached cells (primary colonizers). The micro-colonies progressively enlargeand coalesce to form the first layer of cells covering the surface. When multiple layers of cells pile up on the surface, the third step of the formation is obtained, indicated by the presence of a mature biofilm characterized by the presence of macro-colonies surrounded by water channels that help distribute nutrients and signaling molecules. Finally, to survive when nutrients become limited, or simply to spread and colonize to other niches, some biofilm cells can detach individually or in clumps. In general, biofilm dispersion occurs in response to environmental changes and is dependent on growing conditions