USE OF WOUND ANTISEPTICS IN ANTISEPTICS IN PRACTICE

20 10月 2023
Author :  

MANAGING THE CHALLENGES AND RISKS OF INFECTION IN WOUND CARE

USE OF DIFFERENT ANTISEPTICS IN PRACTICE

WOUND CLEANSING AND TIPS FOR BEST PRACTICE

GUIDANCE AND PATHWAYS FOR ANTISEPTIC USE

THE IMPORTANCE OF AN ANTIMICROBIAL STEWARDSHIP-FOCUSED APPROACH

EXPERT PANEL

Harikrishna K. R. Nair (Chair), Professor and Head of the Wound Care Unit, Department of Internal Medicine, Kuala Lumpur Hospital, Malaysia

Beata Mrozikiewicz-Rakowska, President of the Polish Wound Management Association, Department of Endocrinology, Medical Centre of Postgraduate Education, Warsaw, Poland

Debora Sanches Pinto, Assistant Physician, Division of Plastic Surgery and Burns, University of São Paulo Faculty of Medicine Clinics Hospital, São Paulo, Brazil

Ewa K. Stuermer, Professor, Surgical Head of the Comprehensive Wound Center, Head of Translational Research, Department for Vascular Medicine, University Hospital Hamburg-Eppendorf, Hamburg, Germany

Johannes Matiasek, Associate Professor and Specialist in Plastic, Reconstructive and Aesthetic Surgery, Medizin am Kärntner Ring, Vienna, Austria

Johanna Sander, Head of Advanced Wound Care, 2 Military Hospital, Cape Town, South Africa

José Luis Lázaro-Martínez, Professor, The Complutense University of Madrid; Clinical Director, Complutense University Podiatric Clinic; Head of Diabetic Foot Unit, University Podiatric Clinic, Madrid, Spain

Karen Ousey, Professor of Skin Integrity, Director for the Institute of Skin Integrity and Infection Prevention, University of Huddersfield, United Kingdom

Ojan Assadian, Medical Director, Hospital Wiener Neustadt, Austria; Professor Emeritus, University of Huddersfield, United Kingdom

Paul J. Kim, Medical Director, University of Texas Southwestern Medical Center; Professor, Department of Plastic Surgery and Orthopaedic Surgery, University of Texas Southwestern, United States

Steven L. Percival, Professor (Honorary), University of Manchester, United Kingdom; CEO and Director, Biofilm Centre, 5D Health Protection Group Ltd, Liverpool, United Kingdom

PUBLISHED BY: Wounds International 108 Cannon Street London EC4N 6EU, UK

Tel: + 44 (0)20 7627 1510 该Email地址已收到反垃圾邮件插件保护。要显示它您需要在浏览器中启用JavaScript。 www.woundsinternational.com

© Wounds International, 2023

The meeting and this document have been supported by B Braun, Bactiguard, Schülke and Urgo Medical.

The views in this document do not necessarily reflect those of the sponsors.

How to cite this document: Nair HKR et al (2023) International Consensus Document: Use of wound antiseptics in practice. Wounds International. Available online at www.woundsinternational. com

FOREWORD

      Prevention, detection, treatment and management of wound infection remains a paramount concern for clinicians worldwide. Wound infection is a complex manifestation in which microorganisms outcompete the host immune system (Haalboom et al, 2019), and it is considered to be one of the most common and serious challenges hindering the wound healing process (Mota et al, 2021). Chronically infected wounds are associated with significant physical, emotional and economic burdens, and these are increasing due to an ageing population and rising prevalence of comorbidities (Zhu et al, 2022). Therefore, clinicians need to take a proactive approach to ensure the effective and sustainable management of wound infection in clinical practice.

      The use of antiseptics to prevent and treat wound infection is increasingly being explored, due to the rapid spread of antimicrobial resistance (AMR) and rising emergence of multidrug resistant bacteria, such as Staphylococcus aureus (Barrigah-Benissan et al, 2022). Early and judicious use of topical antimicrobial agents, such as antiseptics, may have an important role to play in limiting biofilm formation, including limiting regrowth and spread of infection (Schultz et al, 2017). Furthermore, advocating for the responsible use of antibiotics to preserve their effectiveness for generations to come is crucial.

      To address these issues, an international group of experts convened for an online meeting in August 2023 to develop this international consensus document, focusing on the use of antiseptics in practice for the prevention and treatment of wound infection.

This consensus document aims to:

■ Address the challenges and risks of infection in wound care

■ Consider experiences and practice around the world

■ Provide an overview of the different antiseptics used in practice

■ Focus on cleansing alongside antisepsis

■ Provide guidance on the use of antiseptics in practice

■ Reaffirm the importance of an antimicrobial stewardship-focused approach.

      The guidance in this document aims to shed light on the potential benefits of using antiseptics to prevent and treat wound infection, alongside practical guidance on how to use them safely and effectively in clinical practice. There needs to be an environment that fosters behavioural change with a focus on sharing best practice, to ensure that infection prevention practices are being followed and interdisciplinary working is embraced.

Harikrishna K. R. Nair (Chair)

      Identifying wound infection can be challenging, and this is especially the case in chronic wounds and in patients with dark skin tones, where infection may not present with the same clinical signs and symptoms as it does in acute wounds or light skin tones (Rutter, 2018). Chronic wound infection delays the healing process, and it has a significant burden on healthcare systems with implications for practice, including increased pain and reduced quality of life (Falcone et al, 2021). It is important to note that chronic wounds always have a bacterial burden which does not necessarily require action in order for the wound to heal. Regardless, early and accurate detection of wound infection is essential, so that appropriate treatment can be selected in a timely manner to prevent development of further complications. Likewise, an ability to correctly rule out infection prevents the unnecessary use of antibiotics (Lipsky et al, 2016; Haalboom et al, 2019), and clinician experience can play a major role in the detection of infection.

Defining wound infection and related terms

      It is clear that properly defined terminology is essential, and definitions can provide guidance and help with communication. However, it is difficult to define wound infection, and existing literature reviews have shown that infection is not defined very well in general. In particular, there is some confusion regarding the difference between contamination, colonisation, a wound infected with a biofilm and an infected wound. According to the International Wound Infection Institute (IWII, 2022), wound infection is defined as ‘the invasion of a wound by proliferating microorganisms to a level that invokes a local and/or systemic response in the host’. In contrast, biofilms are complex polymicrobial communities – attached either to each other or to a surface and become encased within an extracellular polymeric substance – that can increase the likelihood of a wound becoming infected and can prevent wound closure (Wolcott et al, 2016; Kadam et al, 2019). Once microbes reach a critical level, which depends on microbial consortium synergy as well as microbial numbers, there is potential for a biofilm-infiltrated wound to deteriorate to clinical infection (Alves et al, 2020). See Box 1 for more information on the difference between the terms colonisation, contamination, local infection, spreading infection, systemic infection, debridement, disinfectant, antibiotics and antiseptics.

The IWII Wound Infection Continuum

      The IWII Wound Infection Continuum (WIC) is a well-recognised educational tool that provides a framework to conceptualise the impact that microorganisms have on the host, the wound and on wound healing (IWII, 2022).

The IWII-WIC consists of five distinct stages:

■ Contamination

■ Colonisation

■ Local infection (covert and overt stages)

■ Spreading infection

■ Systemic infection.

See Figure 1 (Page 6) for more information on each stage and its associated signs and symptoms.

 

Diagnosis of wound infection using microbiology

      Identification of wound infection is often the result of both clinical judgement and microbiological testing (Haalboom et al, 2019). However, subjectivity is a major challenge in the assessment of clinical signs and symptoms of wound infection, as they can manifest differently depending on the individual patient’s wound type and underlying comorbidities. It has been revealed that most patients receive initial antibiotic treatment based on clinical assessment and without the diagnostic confirmation of a microbiological test (World Health Organization [WHO], 2019). Therefore, there is a growing need for more rapid and reliable laboratory testing, which may also prove to be an important cornerstone of antimicrobial stewardship (AMS; Bogers et al, 2019).

      Although accurate diagnosis of wound infection should involve clinical microbiology and immunological testing, inappropriate/inadequate microbiological testing is a widely recognised problem (Bogers et al, 2019). There was a consensus from the expert panel that there is a global decline in the utilisation and correct use of clinical microbiological tests and diagnostic tools, which can have a negative effect on patient outcomes (WHO, 2016). Additionally, in some countries, barriers and constraints may impede the uptake of microbiological diagnostics, including availability of experts, costs, and issues with reimbursement and regulations. Not all healthcare facilities have access to a microbiology laboratory (WHO, 2019), and research have shown that the potential of microbiology testing may not be fully utilised due to prolonged turnaround times (Skodvin et al, 2019), lack of adequate diagnostic capabilities and distrust in results from the laboratory (Rolfe et al, 2021). Despite these challenges, effective and improved microbiological testing has the potential to positively influence patient outcomes and reduce the inappropriate use of antibiotics (Skodvin et al, 2019). However, clinicians need to bear in mind that a positive swab result is not necessarily an indication for administration of antibiotics.

Wound swabs versus tissue biopsies

      It is evident that more research and clarity is needed on whether wound swabs are sufficient to diagnose infection, or if tissue biopsies are needed. Wound swabs are unable to reveal the true microbiology of biofilms within the wound, which is generally the source of infection. It is also important to note that biofilm community is a structure that constantly varies in form, due to external and internal processes (Laverty et al, 2014), and this can cause challenges when taking swabs/biopsies. Although tissue biopsy has historically been considered the gold standard for wound culture, they are invasive, painful and expensive, and often require specialist training to carry out (Atkin et al, 2019; Høiby et al, 2015). It was revealed during the discussion with the expert panel that wound swabs are often taken, instead of tissue biopsies, due to cost and time constraints. The need for joined-up working and effective communication, between tissue viability teams and microbiologists/infection prevention teams, was emphasised.

      While there are studies claiming that biopsies yield the most accurate and reliable culture results (Brock et al, 2022), some studies show that non-invasive wound swabbing techniques can provide similar results to tissue biopsies (Esposito et al, 2017; Haalboom et al, 2018; 2019). Furthermore, the few available investigations that compare different yielding techniques do not sufficiently describe the transport and specimen pre-processing procedures. Currently, there is no evidence to suggest that either technique is better at diagnosing infection. As well as being non-invasive, wound swabs are relatively easy to perform and pose a lower burden on the patient – e.g. they may reduce fear and pain (Haalboom et al, 2019). However, when the presence of resistant bacteria or a systemic infection is suspected, tissue biopsies may be required.

Taking a whole-person approach to wound infection

      It has been shown that clinical signs and symptoms of wound infection are often missing in patients with arterial, or venous, insufficiency and diabetes neuropathy (Glaudemans et al, 2015; Leaper et al, 2015; Lipsky et al, 2016). Therefore, clinicians should take a whole-person approach and consider the patient’s disease status to decide which treatment option is most appropriate. In addition, any underlying disease/comorbidity needs to be controlled; for example, glycaemic control is necessary if the patient has diabetes. Moreover, evidence exists to suggest that socioeconomic status plays an important role in the development of wound healing complications (Sharma, 2018). Therefore, the impact of socioeconomic status, as well as individual patient comorbidities, needs to be considered when managing wound infection.

Biomarkers and other indicators of wound infection

      Clinicians usually rely on assessing clinical signs and symptoms to identify wound infection in practice (e.g. pain, erythema, oedema, heat and pus). However, these signs are not always indicative of infection (Haalboom et al, 2019). Although there are specific markers to diagnose infection, such as biomarkers, the use of these markers depends on the type of microbe present. No single marker currently exists to detect whether a wound is infected or not. Some biomarkers have been described as indicators of both bone and soft tissue infection, including erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) and procalcitonin (PCT). However, there is a difference between bone infection and soft tissue infection; they are treated differently and their reactions to intervention differ. Research has shown that enzymatic biomarkers related to wound infection may be useful for the early detection of wound infection (Mota et al, 2021). Other indicators that have been studied as potential biomarkers to help identify infection include bacteria, proteins and metabolites.

      Local temperature of wounds is often considered a predictor of infection (Tegl et al, 2015; Power et al, 2017). Zhang et al (2021) found differences in temperature among wounds infected with different pathogens. Another study by Power et al (2017) found that temperature measurements are highest in acute, non-healing or worsening wounds, and that as wounds progress towards healing, temperature reduces. However, there are few available methods to monitor infection and healing progression in wounds using temperature as an indicator. Moreover, it may be challenging to use high temperature as an indicator of infection in some conditions such as peripheral arterial disease, which can present with cold legs.

      The pH of a wound may also be a possible early indicator of infection, so wound pH monitoring can be a useful tool for determining the presence or absence of infection (Kordestani et al, 2023). As well as temperature and pH, other microenvironmental parameters and local indicators that could help predict infection include uric acid, lactic acid, glucose and exudate composition (Zhang et al, 2021). Although these factors are relevant to research, monitoring and measuring these indicators in practice can be challenging for clinicians.

Antiseptics for wound infection

      A culture of overprescribing antibiotics exists, especially for patients with chronic wounds. It is widely acknowledged that clinicians can find it challenging to distinguish when to use antibiotics prophylactically and when to use them to treat infection. However, there is a consensus that an infected wound should be treated antiseptically and application of antibiotics for locally colonised wound infections needs to be avoided (Kramer et al, 2018), due to the rising emergence of multidrug resistant bacteria and spread of AMR. It is important to bear in mind that antiseptics should never be the sole treatment to prevent or treat infection; they are an adjunct in a similar way to antibiotics. Other treatment modalities such as debridement are just as important and may be necessary depending on the patient’s wound – e.g. sharp or mechanical debridement [Box 2].

Experiences and practices around the world

      In many parts of the world, antiseptic agents are non-indicated in chronic wound care (BarrigahBenissan et al, 2022). In some countries, tap water or saline are the only recommended substances for the purpose of wound cleansing, and antisepsis is considered a controversial cleansing method. Although saline is the most widely used product for chronic wound cleansing in clinical practice, methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa can grow and survive in saline (Dong et al, 2020), and studies have shown the benefits of using antiseptic agents (Kramer et al, 2018; Schultz et al, 2021).

Experiences and practices around the world

      It was agreed by the expert panel that variations exist in practice between hospitals, as clinicians often have their own criteria to diagnose wound infection. In addition, some clinicians use antiseptics prophylactically while others use them solely as adjuncts. The risk of wound infection is influenced by characteristics of the individual (host), their wound and the environment, as well as the influence of caregivers (IWII, 2022); therefore, consideration needs to be given to all these factors.

Addressing the challenges of antisepsis

      There are various challenges that can be presented when using antiseptics for the prevention and treatment of wound infection, including issues with tolerability, inactivation by organic matter and the spread of AMR/cross-resistance (Punjataewakupt et al, 2019; Barreto et al, 2020). It was shared by the expert panel that in the United States (US), use of antiseptics and antimicrobials is based on five key considerations: activity, tolerability, safety, availability and cost. Clinicians need to consider efficacy; however, a view was raised that in Spain, many clinicians are unaware of the mode of action of the antibiotics, antiseptics and antimicrobials they prescribe, which is best for individual clinical scenarios and what their benefits of use are. Therefore, guidance is needed on when the most appropriate time to apply antiseptics is – e.g. when the wound is at risk of infection or when the wound is already infected.

     Availability can play a significant role in decisions concerning treatment of wound infection, as some clinicians treat patients with antibiotics without taking a wound swab first (WHO, 2019). Use of antiseptics can largely be driven by availability, what is on patients’ insurance plans and what is available in clinics/facilities. Additionally, first-line treatment is not always delivered by someone with sufficient training in wound care.

Differences in prescribing

      A view was raised by the expert panel that in the United Kingdom (UK), tissue viability teams generally manage wounds at first point of contact, and that tissue viability nurses are allowed to prescribe antiseptics in addition to doctors. When patients are transferred into the community and may have to pay prescription costs for certain antibiotics or antimicrobials, patients may refuse or use them inappropriately. Unlike in the UK, prescribing is restricted to doctors in some countries such as Germany – although it was suggested that many nurses have greater knowledge about caring for chronic wounds than doctors.

      There are also reimbursement considerations, especially across many countries in Europe, and in low and middle-income countries. In Germany and Austria, all antibiotics are reimbursed; however, antiseptics are not. As a result, German doctors tend to use antibiotics more than antiseptics to prevent infection from spreading, because otherwise they may find themselves in a position where they have to persuade patients to buy antimicrobials and antiseptics themselves. In addition, these patients often ask for antibiotics instead as they don’t have to pay for them. It was also discussed that in Spain, there can be issues with litigation, which may cause clinicians to feel pressure when using antiseptics prophylactically. There was a consensus from the expert panel that although the guidance discourages clinicians from using antibiotics on chronic wounds, when they are not needed, it was agreed that there needs to be more emphasis on the evidence that shows antimicrobials and antiseptics as being more effective for treating local wound infection than antibiotics. It needs to be clear that antibiotics are an exception, if not obsolete, in the treatment of chronic wounds, as the evidence shows that antiseptics can be more effective and are associated with little to no resistance.

Prevention is better than cure

      It is widely acknowledged that there needs to be a greater emphasis on prevention of infection, rather than treatment. In Austria, healthcare providers are only allowed to spend a specific amount for the treatment of existing illnesses. As a result, there is a lack of spending on prevention. A similar view was raised that in Brazil, budgets do not tend to cover spending on prevention; therefore, there are cost implications of using antiseptics in clinical practice. The expert panel agreed that globally, there is a need to change mindsets to move away from a reactive healthcare model to a proactive approach. This involves focusing less on treatment in isolation and increasing investment in preventative measures.

More evidence is needed

      There was a consensus from the expert panel that although the theoretical foundation for using antiseptics is strong, indirect evidence dominates the literature. There are difficulties in obtaining concrete evidence for the use of antiseptics to prevent infection, as comparable patients are needed, and this is challenging in the field of chronic wounds. Most research on antiseptics is in vitro and/or using animal models (Schwarzer et al, 2020). Alongside a lack of standardised methodology, there is also ongoing debate about the transferability of this research to clinical practice (IWII, 2022).  Although there is a lack of clinical evidence, judicious use of topical antiseptics has a role to play in preventing and managing wound infection (Schultz et al, 2017).

      Due to the growing emergence of multidrug resistant bacteria, alarming spread of AMR, development of new-generation antiseptic agents and improved formulation of existing antiseptics with fewer side effects, wound antisepsis is increasingly being considered as a vital asset for the prevention, treatment and management of wound infection (Barrigah-Benissan et al, 2022). There is a culture of overprescribing and misusing antibiotics in wound care – especially for chronic wounds – and according to the literature and expert opinion, antiseptics are more effective and most do not pose a risk for the development of bacterial resistance or cross-resistance (Hessam et al, 2016; Kramer et al, 2018; Dissemond et al, 2020). However, there are a limited number of studies that investigate the efficacy of antiseptic agents in the healing of chronic wounds (BarrigahBenissan et al, 2022).

Antiseptics versus antibiotics

      IWII (2022) has defined an antiseptic as a ‘topical agent with broad-spectrum activity that inhibits multiplication of, or sometimes kills, microorganisms’. Antiseptics are generally applied to skin, mucous membranes and surface wounds, as well as other living tissues, with the aim of inhibiting microbial growth without necessarily killing microbes (Babalska et al, 2021). Due to the emergence of new technologies, such as the introduction of oxidative cleansers, antiseptics can act beyond bacterial killing and without cytotoxicity (IWII, 2022). For example, some cleansers contain oxidative agents (e.g. hypochlorous acid [HOCl]), and these cleansers may play a role in removing microbes as well as softening and removing slough and necrotic tissue via oxidative processes, depending on concentration (Olszowski et al, 2003; Pattison et al, 2003).

      While antiseptics are unspecific/multitarget – which means they possess a broad spectrum of antimicrobial activity with a disruptive or biocidal effect on bacteria, fungi, parasites and viruses – antibiotics kill bacteria (biocidal effect) or inhibit their growth (static effect) only (Babalska et al, 2021; IWI, 2022; Malanovic et al, 2022). In addition, microorganisms can develop resistance to antibiotics, although resistance is not usually observed in antiseptic agents and various classes of cleansers (Kramer et al, 2018). However, research has shown that bacteria have developed resistance against silver and triclosan (Pareek et al, 2021). Moreover, while both antiseptics and antibiotics can be applied topically, only antibiotics can be administered systemically. To help reduce risk of further antibiotic resistance, antiseptics can help maintain efficacy and effectiveness of antibiotics, by preserving them for clinical scenarios that require appropriate systemic treatment (Roberts et al, 2017).

Differing modes of action

      Antiseptics vary in terms of characteristics, features, efficacy and intention for use, and it has been suggested that differences in antimicrobial spectrum of activity between antiseptics is the result of varying mechanisms of action (Alves et al, 2020). Antiseptics are broadly classified as pharmacological drugs or medical devices, depending on their primary mode of action (Kramer et al, 2018). Pharmacological antiseptics act pharmacologically, metabolically and/or immunologically; for example, these antiseptics may bind to adhesion proteins, or their biochemical or immunological destruction can inhibit attachment of bacteria. On the other hand, some antiseptics that are classed as medical devices act primarily through physical interactions (e.g. rinsing, absorption and moisture regulation). It is important to bear in mind that in some countries, including the US and Canada, antiseptics that act pharmacologically are sometimes classed as medical devices Through interactions with various cellular and extracellular mechanisms involved with wound healing, antiseptics can play a key part in not only inhibiting a wide range of disease causing microorganisms, but also in facilitating wound healing (Rothenberger et al, 2016).

      All antiseptics can be used either prophylactically or therapeutically, depending on the tissue compatibility with human cells. Prophylactic antiseptics are applied once or a few times over a short period of time. This form tends to be strong and fast-acting. In contrast, therapeutic antiseptics are often referred to as slow-acting; they are used continuously and often for longer periods of time.

Using antiseptics agents against biofilm

     A meta-analysis conducted by Malone et al (2017) found that biofilm is prevalent in up to 100% of all chronic wounds. Biofilms in chronic wounds can be highly tolerant to antibiotics and antiseptics (Alves et al, 2021), so debridement and dressing changes are key to remove most bacteria, biofilms, virulence factors, necrotic tissue and slough. However, some research suggests that debridement is insufficient on its own to reduce biofilm, so it is not recommended for use in isolation (Schultz et al, 2017). It has been suggested that following debridement, a ‘window of opportunity’ may exist that causes biofilm to become more susceptible than normal to topical antiseptics (Omar et al, 2017; Schultz et al, 2017; Alves et al, 2021). Therefore, antiseptics could help complement the debridement process by helping to delay biofilm reformation, and reduce infection risk and need for antibiotics. In particular, evidence shows that octenidine (OCT) and polyhexamethylene biguanide (PHMB) are effective at eroding the biofilm matrix and reducing microbial load (Rembe et al, 2020; Stuermer et al, 2021). Wound cleansing solutions containing PHMB and betaine surfactants can also be used as antiseptics, and it is suggested that their use can support wound bed preparation (WBP) and the removal of bacteria, debris and biofilm (Bellingeri et al, 2016). Box 3 provides an overview of the numerous indications for antiseptics in the prevention and treatment of wound infection.

Properties of an ideal antiseptic product

      One of the most essential properties of an ideal antiseptic agent is its ability to promote wound healing (Bigliardi et al, 2017). As well as promoting wound healing and reducing the microbial burden of a wound, an ideal antiseptic agent should exhibit good local tolerability (Bigliardi et al, 2017; Barreto et al, 2020). In order to kill a broad range of disease-causing microorganisms, antimicrobial activity of an antiseptic needs to be unspecific or multitarget (Malanovic et al, 2022). A list of the most important properties of an ideal antiseptic agent are listed in Box 4.

Use of antiseptics in practice

      Topical antiseptics can come in various preparations, including liquids, gels, pastes or impregnated dressings, although their effects tend to differ depending on type and concentration of the preparation (IWII, 2022). Examples of antiseptics used in the care of chronic wounds are halogenated compounds (e.g. iodophor agents, such as povidone iodine [PVP-I] and cadexomer iodine, and chlorine-containing agents, such as hypochlorite and HOCl), biguanides (e.g. polyhexanide, also known as PHMB, and chlorhexidine) and OCT (Kramer et al, 2018; Babalska et al, 2021). Alternative antiseptic therapies include silver. Honey can also be used, which mainly acts by dehydrating bacterial biofilm and, therefore, it may affect locally infected wounds. It is vital to bear in mind that the same type of antiseptic can differ in terms of regulatory class (medicinal products/medical devices), concentration, formulation and purpose, which may sometimes be overlooked by clinicians in practice.

      Through discussions with the expert panel, it was found that, other than traditional PVP-I, the antiseptic agents most commonly used in practice worldwide are biguanides, including PHMB, OCT and chlorinated agents, such as HOCl and Dakin's solution. It was shared that in Central Europe, OCT is predominantly used, while in North America and Australia, PHMB is the most available agent. In England, both chlorhexidine and OCT are widely used in practice. In the UK, chlorhexidine is often used for pre-operative skin antisepsis, but not during wound dressing changes. In the US, chlorhexidine is also used as a skin cleanser but it is not yet available as an antiseptic.

Octenidine

      OCT is a commonly used antiseptic, in the form of a gel or liquid, that is widely used for a large range of clinical applications for both acute and chronic wounds. OCT has a high safety profile; therefore, it is often the agent of choice in neonates. OCT possesses an antimicrobial spectrum that covers a wide range of multidrug resistant Gram-positive bacteria (e.g. Staphylococcus aureus), Gram-negative bacteria (e.g. Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosaAcinetobacter baumannii) and yeast/fungi (e.g. Candida auris and other Candida species; Alvarez Marin et al, 2017; Nikolić et al, 2019; Ponnachan et al, 2019; Malanovic et al, 2020; Spettel et al, 2022). Some research shows that antiseptic properties can change under the influence of substances such as exudate, mucins, albumin or blood (Pitten et al, 2003; Kapalschinski et al, 2017). However, compared to other antiseptic agents, OCT has been shown to be effective within a short contact time at low concentrations, and in the presence of substances, including blood and mucin (Pitten et al, 2003; Assadian, 2016; Alvarez-Marin et al, 2017; Conceição et al, 2019). OCT possesses both anti-inflammatory and immunomodulatory properties to positively influence various aspects of wound healing (Seiser et al, 2021), and alcoholic preparations of OCT are shown to have a sustained/remnant effect (Lutz et al, 2016). Furthermore, application of an OCT-containing wound gel has also been shown to improve scar quality, result in significantly fewer wound healing disorders, reduce frequency of hypertrophic scars and keloids, decrease transepidermal water loss and improve skin elasticity, in comparison to conventional wound care (Matiasek et al, 2018a).

Polyhexamethylene biguanide

      PHMB is an antiseptic that is available in the form of solutions, gels, non-adherence bacterial barriers and bio-cellulose dressings (To et al, 2016). It possesses a high therapeutic index and broad-spectrum antimicrobial activity that kills Gram-positive and Gram-negative bacteria (including Staphylococcus epidermidis and Escherichia coli), fungi, parasites and certain viruses (Worsley et al, 2019; Rippon et al, 2023). PHMB has not been shown to cause development of resistance, is safe (non-cytotoxic) and does not cause damage to newly growing tissue (Rippon et al, 2023). There is evidence to show that topical PHMB may promote healing of chronic stalled wounds, reduce bacterial burden, eliminate MRSA and alleviate wound-related pain (To et al, 2016). Moreover, PHMB has a sustained/remnant effect and may result in fewer dressing changes, which has both time and cost benefits (Worsley et al, 2019). However, research has shown that higher concentrations of PHMB require a comparatively long exposure time of 15minutes in order to reach full bactericidal efficacy (Radischat et al, 2020).

Povidone iodine

      PVP-I is used in various forms, including liquids, ointments and powder, and is the go-to antiseptic for acute wounds, including gunshot wounds, stab wounds and bites (Sopata et al, 2020), as well as lacerations, bruises and deep wounds (Gmur and Karpinski, 2020). Its antimicrobial activity is broad, and PVP-I has been shown to kill a range of Gram-negative and Gram-positive bacterial strains, and both enveloped and non-enveloped viruses (Bigliardi et al, 2017; Eggers et al, 2018; Lepelletier et al, 2020). Additionally, PVP-I is noted for its ability to penetrate biofilm, lack of resistance, anti-inflammatory properties, good tolerability and absence of negative effects on wound healing (Bigliardi et al, 2017). Although it has been described to have a low cytotoxicity (Bigliardi et al, 2017), in vitro experiments have shown that PVP-I can be cytotoxic (Day et al, 2017; Ortega-Llamas et al, 2022). Research has also shown that exposure of the body to large amounts of iodine may result in both hyperthyroidism and hypothyroidism (Burchés-Feliciano et al, 2015).

Hypochlorous acid

      HOCl is an oxidising agent with potent antimicrobial activity, and it is able to remove slough and necrotic tissue. A wide variety of chloride-containing solutions are associated with high efficacy against microorganisms (Severing et al, 2019). HOCl is also capable of inflicting damage to cellular components of microorganisms, depending on dose and concentration (Harriott et al, 2019). HOCl appears to possess biocidal and a broad spectrum of activity against both Gram-positive and Gram-negative bacteria (including Staphylococcus aureus and Pseudomonas aeruginosa), viruses, sores and fungi (Sakarya et al, 2014; Kiamco et al, 2019; Nair et al, 2019). As HOCl has both anti inflammatory and immunomodulatory properties, and positively influences various aspects of wound healing (Del Rosso and Bhatia, 2018; Kramer et al, 2018; Nair er al, 2023), it is implicated in both acute and chronic wound infections (Centers for Disease Control and Prevention [CDC], 2021). There is some in vitro evidence that for some antiseptics, such as HOCl, an exposure time of 3–10 minutes is sufficient to penetrate and affect biofilms (Day et al, 2017; Harriott et al, 2019; Robson, 2020). However, as is often the case with in vitro data, it is possible that these clinical observations may not directly translate to practice, under all conditions, since problems associated with biofilm in wounds have remained persistent despite the use of agents shown to be effective in in vitro situations. Nonetheless, HOCl meets the requirements for a topical antiseptic, as it is fastacting, non-toxic for humans at concentrations of use, easy to apply, cost-effective, non-irritating and non-sensitising (CDC, 2021; Wounds International, 2023). There are also numerous different formulations available, with different concentrations and various additives. The lack of cytotoxicity of HOCl as an antiseptic is explained by evidence that discusses the clearance pathways (Winterbourn and Brennan, 1997; Kearns and Dawson, 2000; Li et al, 2004). Furthermore, there is a substantial body of published clinical and health economic evidence that shows the benefit of using HOCl as an oxidative antiseptic cleanser (Wang et al, 2007; Nair et al, 2019; 2023).

Chlorhexidine

       Although primarily used for wound irrigation and cleansing (Norman et al, 2016), chlorhexidine is an antiseptic agent that is active against both Gram-positive and Gram-negative bacteria, fungi end enveloped viruses (Bednarek et al, 2020; Wei et al, 2021). For the purpose of pre-operative skin antisepsis and not wound treatment, chlorhexidine is widely used in clean surgeries (Wei et al, 2021), and is bacteriostatic at low concentrations and bactericidal at higher concentrations (Bednarek et al, 2020). There is evidence to suggest that chlorhexidine, for the purpose of pre-operative skin antisepsis may also protect against superficial SSI, bloodstream infection, nosocomial infections and pneumonia (Wei et al, 2021). However, recent evidence suggests that chlorhexidine gluconate is associated with levels of cytotoxicity (Cheong et al, 2022) and the rare, but serious, risk of anaphylactic reactions (Food and Drug Administration, 2022). Moreover, a recent study by Lescat et al (2021) showed that there was cross-resistance to chlorhexidine.

Biocompatibility or therapeutic index

      Considering an antiseptic’s biocompatibility index (BI), also known as therapeutic index, can help with selecting the most appropriate agent. It is generally referred to as a concept that measures the antibacterial activity of an antiseptic in practice compared to its cytotoxicity and, therefore, allows for comparison of different substances. A BI value of greater than 1 indicates that the antiseptic possesses a broad spectrum of activity against microorganisms and a low level of cytotoxicity against fibroblasts and keratinocytes – e.g. OCT and polyhexanide, which have a BI score of 1.7–2.1 and 1.4–1.5, respectively (Müller and Kramer, 2008; Table 1). In addition, considering the BI of an antiseptic can help with selecting a product based on both antimicrobial performance and cytotoxicity level. However, it is important to note that there is currently a lack of data on BI for HOCI.

Considerations for product selection in practice

      Use of an antiseptic or antimicrobial compound in isolation, and without anything else, is not considered best practice. An antiseptic should be used as an adjunct and should form part of a spectrum of treatment. Beyond antimicrobial action/performance, there is a need to consider and not lose sight of other benefits of antiseptics – e.g. oxidative debridement (associated with the presence of oxidative agents such as HOCl), matrix metalloproteinase (MMP) modulation, extracellular matrix degradation (ECM) and anti-inflammatory capabilities. For example, some antiseptics consist of oxidative substances that promote debridement such as HOCl. There was a consensus from the expert panel that sometimes clinicians do not have sufficient understanding of the different modes or chemistries of action, and why they are using a particular antiseptic or its indication. All antiseptics have slightly different modes of action, so they affect cellular components of disease-causing microorganisms, as well as any surrounding viable or non-viable tissues, differently. Some antiseptics can have a positive effect on the proliferation of fibroblasts or help control odour, so clinicians need to be aware of the modes of action of different antiseptics beyond their bacterial-killing properties. Additionally, some antiseptics may react with each other; for example, an oxidising agent such as HOCl may react with another oxidisable antiseptic agent. Clinicians also need to avoid mixing and matching products where considered inappropriate to do so.

      Nomenclature can sometimes be confusing; for example, hypochlorite and hypochlorous sound similar but are different – although they both have potent antimicrobial activity, they possess different levels of cytotoxicity, with hypochlorite being more cytotoxic and possessing a lower therapeutic index than HOCl (Hidalgo et al, 2002; Barsoumian et al, 2013; Ortega-Peña et al, 2017; Mangum et al, 2018). It is also important to keep in mind that there is a difference between efficiency and duration of developing efficiency; for example, HOCl and OCT are both fast-acting in their efficacy, but HOCl has no residual effect while OCT has a long-lasting residual effect. Fast-acting and fast-degrading antiseptics are often designed to be used frequently; for example, due to its high therapeutic index, HOCl-based cleansers can be used frequently, and with negative pressure wound therapy (NPWT) with instillation (Kim et al, 2018; Alberto et al, 2020). Depending upon its concentration, an antiseptic may have a toxic effect on human cells – e.g. hypochlorite. However, development of resistance to topical antiseptics is uncommon.

      Wound cleansing is a key component of WBP and is defined as the ‘active removal of surface contaminants, loose debris, non-attached non-viable tissue, microorganisms and/or remnants of previous dressings from the wound surface and its surrounding skin’ (Alavi and Maibach, 2020; Haesler et al, 2022; IWII, 2022; Haesler and Carville, 2023). Chronic wounds with devitalised tissue or suspected biofilm often require vigorous cleansing to dislodge loose devitalised tissue, microorganisms and debris from the wound bed (EPUAP/NPIAP/PPPIA, 2019). Therefore, the process of wound cleansing may differ depending on the wound, and clinicians should refer to the standard protocol of care for their individual organisations.

      Clinicians also need to be mindful of terminology; for example, ‘cleaning’ and ‘cleansing’ are often used interchangeably, but the latter is more commonly used in the context of wounds [Box 5]. Further clarification on terms that are commonly used in reference to wound cleansing is provided in Figure 2.

 

Wound bed preparation

      Wound care of chronic wounds should be conducted alongside WBP. The purpose of WBP is to help create a moist environment that optimises conditions for debridement and wound healing, by producing a well-vascularised stable wound bed to reduce bacterial load, decrease exudate level and increase granulation tissue formation (Wounds UK, 2021; Barrigah-Benissan et al, 2022). WBP is a framework for the assessment, diagnosis and treatment of wounds that can be implemented in combination with wound hygiene (Sibbald et al, 2011; Murphy et al, 2021; Shamsian, 2021). The dynamic and rapidly evolving concept of WBP was initially recognised by Schultz et al (2003), with Atkin et al (2019) developing the original TIME concept to TIMERS, comprising the six components that underpin WBP (Tissue, Inflammation/Infection, Moisture balance, Edge of wound/Epithelisation, Repair and regeneration, Social factors). The WBP model is reliant on effective, accurate and timely assessment to help clinicians identify patients with chronic wounds quickly, rather than failing to address problems and causing wounds to worsen for prolonged periods without treatment.

Tools for assessment

      Additional tools that can be used in clinical practice to improve local wound assessment are the Triangle of Wound Assessment and the MOIST (Moisture balance, Oxygen balance, Infection control, Support strategies and Tissue management) concept. The Triangle of Wound Assessment is a holistic framework that extends the current concepts of WBP and TIMERS beyond the wound edge (Wounds International, 2015). It is designed to assess and manage several wound areas, including the wound bed, wound edge and periwound skin, and is a useful tool to guide clinicians when evaluating a wound, setting goals and selecting the most appropriate treatment (Gil, 2020). Moreover, MOIST is a wound healing concept that builds on the existing TIME concept and takes into consideration several novel therapeutic options that have become available since the TIME concept was first introduced (Dissemond et al, 2022). MOIST aims to improve the local treatment of wounds and address factors that can adversely affect desired clinical outcomes (Gray et al, 2013). Both the Triangle of Wound Assessment and MOIST can be applied as part of a holistic wound assessment.

Selection of an appropriate wound cleansing solution

      Selection of a wound cleansing solution should reflect the goals of treatment as identified through an assessment of the patient and their wound. Choice should ultimately be influenced by the wound type, comorbidities and patient preferences. Although the ideal wound cleansing solution has not been established conclusively, important considerations are listed in Box 6.

Use of antiseptics during wound cleansing

      Historically, physiological saline, Ringer’s solution and tap water have been the mainstays of wound cleansing solutions. However, antiseptics are increasingly being explored for the cleansing of wounds and removal of biofilm (Sakarya et al, 2014), as well as removal of slough via oxidative mechanisms. A variety of topical antiseptics are commonly used in practice to cleanse and irrigate wounds, including chlorhexidine, OCT, hypochlorite, PHMB, PVP-I and HOCl (Snyder et al, 2017). Where wounds are cleansed with soap or an antimicrobial scrub, this should be performed carefully to avoid causing further trauma to the wound (Alves et al, 2021). Cleansing of the wound needs to be performed at every dressing change. If considered appropriate, debridement (e.g. mechanical [sharp or surgical], enzymatical or biosurgical [maggot therapy]) can help disrupt any remaining necrotic tissue and biofilm, and facilitate wound healing (Sun et al, 2016; Sibbald et al, 2021; De Francesco et al, 2022).

      There is a consensus that antiseptics and antimicrobials should only be used once a wound has been cleaned and debrided to remove barriers, including slough, necrotic tissue, biofilm and debris. However, more evidence is needed, as some experts believe that pre-treatment with antiseptics, such as those containing oxidising agents, can help loosen tissues and make debridement and detachment of tissues easier. Conversely, if a wound is exuding heavily, the performance of an antiseptic may be diluted; therefore, debridement and de-sloughing can be useful before an antiseptic is employed. In addition, further research should help address disparities in practice concerning the temperature at which antiseptics are used, with some clinicians warming/cooling them and others using antiseptics at room temperature.

Contact time

      There was a consensus from the expert panel that contact time (i.e. how long the wound is exposed to an antimicrobial) often depends on how much time the clinician has with the patient. In vitro studies and investigations using animal models dominate the literature (Schwarzer et al, 2020), but neither accurately reflect the use of antiseptics in real-world settings; for example, contact time in laboratory research is often 24 hours or longer while in clinic, antiseptics may only remain in contact with the wound for 10 to 15 minutes – e.g. during wound cleansing (Johani et al, 2018). If unsure, clinicians should always refer to a product’s Instructions for Use (IFU).

      Use of antiseptics needs to be tailored to the specific needs of the patient and their wound. As part of the decision-making process to determine whether an antiseptic agent is required, and what type, clinicians need to determine the wound’s aetiology and underlying cause of infection. The wound also needs to be managed according to healing phase and type (Kramer et al, 2018). Selection of an antiseptic agent depends on the target of its action and presence of interfering substances (Babalska et al, 2021). Clinicians need to possess comprehensive knowledge on a product before using it. Moreover, appropriate choice of antiseptics is critical, as some agents may cause skin irritation and colouring of disinfected areas (Matiasek et al, 2018b). Guidance on using antiseptics for wounds in practice is listed in Box 7.

Considering different wound aetiologies

      It is important to consider underlying pathophysiology when selecting an antiseptic agent. Some antiseptics may be better than others depending on the type of wound – e.g. pressure/venous/ diabetic ulcers. A study found that topical HOCl can accelerate healing times in venous leg ulcers (Bongiovanni, 2014), and there is low level evidence for the adjunct use of HOCl to resolve infection and improve healing in venous leg ulcers (Armstrong et al, 2015). However, more research is needed, and the effects of topical antiseptics on pressure ulcers is also unclear. It is suggested that healing may be promoted in ulcers if the number of microorganisms is reduced with the help of antimicrobial agents (Norman et al, 2016). Moreover, guidelines from EPUAP/NPIAP/PPPIA (2019) currently recommend the use of HOCl-based cleansers on pressure ulcers.

The two-week challenge

      There is ongoing debate about what the most appropriate duration of antimicrobial treatment is, with longer duration being associated with a heightened risk of inducing AMR. A two-week challenge is often recommended, in which healthcare professionals should use a topical antiseptic for at least two weeks before evaluating its efficacy in managing wound infection. After two weeks, the healthcare professional should reevaluate and either (Ayello et al, 2012; IWII, 2022):

1. Discontinue if signs and symptoms of infection have resolved

2. Continue with the antimicrobial if the wound is still progressing but there are still signs and symptoms of infection (treatment may be required for up to four weeks to attain results)

3. Consider an alternative antimicrobial if there is no improvement and refer to a wound care specialist

4. Reassess the underlying disease.

Figure 3 presents a pathway that has been created to guide the use of antimicrobial treatment for patients with wounds, with or without infection risk (Wounds UK, 2021).

      AMR is a global public health emergency that is estimated to contribute to over 5 million deaths worldwide each year (WHO, 2022). Inappropriate use and overuse of antibiotics has led to an increase in AMR, so there is an urgent need to improve the quality of antibiotic prescribing worldwide. AMS refers to the ‘organisational or healthcare system-wide approach to promoting and monitoring judicious use of antimicrobials to preserve their future effectiveness’ (National Institute for Health and Care Excellence, 2023). Ultimately, an AMS-focused approach recognises the importance of safeguarding the effectiveness of antibiotics to improve patient outcomes and reduce the spread of infections caused by multidrug resistant microorganisms. Numerous global initiatives have been created to measure the effects of these programmes in tackling AMR [Box 8], and key AMS strategies that have been identified include (Lipsky et al, 2016; Roberts et al, 2017; Stryja et al, 2020):

■ Increasing efforts towards effective infection control methods, including hand hygiene/ decontamination practices, using PPE as per local protocol, correct removal of PPE, good waste management, comprehensive documentation and management of the patient’s environment

■ Creating a consistent knowledge base and educational opportunities for clinicians on the effective use of antimicrobials, and to reduce variation in practice – thus reducing diagnostic uncertainty, clinical ignorance, ritualistic behaviour, clinical fear and patient demands

■ Prescribing the appropriate antimicrobial treatment when therapy is indicated, and minimising the unnecessary use of antimicrobials, overly broad-spectrum treatment regimens and the use of antibiotics for non-infected wounds

■ Prescribing the appropriate antimicrobial duration, at an optimal dose, administered through the most appropriate route for the indicated condition and patient status (the ‘Five Rights’; Box 9)

■ Using an agent that has the lowest risk of adverse effects.

Barriers to the implementation of antimicrobial stewardship (AMS) strategies

      Studies have highlighted several key barriers to the implementation of AMS strategies (Rolfe et al, 2021; Limato et al, 2022; Wu et al, 2022). Importantly, improving the adoption, implementation and sustainability of AMS programmes requires a systemic change in behaviour through increased public awareness and education (Wounds UK, 2020). Major barriers to the implementation of AMS strategies include (Limato et al, 2022; WHO, 2022):

■ Clinician knowledge deficits regarding optimal use of antibiotics

■ Ineffective resourcing and limited infrastructure for AMS programmes

■ Lack of communication and interprofessional relationships between healthcare providers

■ Cost-prohibitive bacterial culture testing and thresholds of national health insurance coverage

■ Limited access to antimicrobials, as well as concerns around cost

■ Resistance to changing current practices regarding antimicrobial prescribing

■ Limited access to reliable diagnostic or microbiological testing.

Guidance for AMS best practice

      There needs to be an environment that fosters behavioural change with a focus on a back-to basics approach to infection prevention, such as hand hygiene. The AWaRe (Access, Watch, Reserve) antibiotic book is a resource that was developed by WHO and contains guidelines for the management of common infections (WHO, 2022). It also helps with selecting the most appropriate intervention for each clinical setting. Most government organisations have published plans to tackle AMR, and these can be accessed online, so clinicians should always check and refer to their own country’s guidelines, as well as local protocols where available.

      There is strong and growing evidence that antiseptics can be useful agents for reducing AMR, but they are under-used, particularly in the fields of wound care and surgical site management (Roberts et al, 2017). It is believed that using antiseptics, where considered appropriate, will help reduce the use of antibiotics. However, this does not imply that clinicians should prescribe antiseptics every time without indication. Antiseptics need to be used judiciously and clinicians should refer to a consultant, microbiologist or appropriate expert if unsure at any point. For the optimal management of wound infection, working within a multidisciplinary team (MDT) of experts is essential – e.g. clinicians, surgeons, infectious disease experts, microbiologists, pharmacologists and geriatricians (Falcone et al, 2021). An MDT approach helps coordinate services as a team, to work together towards specific goals to optimise care and outcomes for the patient.

Clinician and patient/public education

      Each member of the MDT is responsible for reducing the impact of AMR. Ongoing education is vital to optimise care for patients, and the clinician’s responsibility is to educate themselves and the patient, so that members of the public are made aware of the importance of AMS programmes. Where patients are assessed as having the capacity and willingness to self-care, they should be supported to reduce their modifiable infection risk. Combating AMR requires a multi-modal approach led by education and better understanding of the infection continuum. Figure 4 illustrates the multimodal approach to AMS practices underpinned by education. Early identification of infection will lead to faster and more effective treatment; therefore, creating opportunities for training and education to increase clinicians’ confidence in recognising and identifying the signs of infection is essential (Wounds UK, 2020).

 References

1. Alavi A, Maibach HI, eds (2020) Local Wound Care for Dermatologists. Springer Cham: 25-34

2. Alberto EC, Cardenas L, Cipolle M et al (2020) Level 1 Trauma Center Experience Utilizing Negative Pressure Wound Therapy with Instillation: Hypochlorous Acid versus Normal Saline Solution in Complex or Infected Wounds. Journal of Medical Science and Clinical Research 8(6): 414-20

3. Alvarez-Marin R, Aires-de-Sousa M, Nordmann P et al (2017) Antimicrobial activity of octenidine against multidrug-resistant Gram-negative pathogens. Eur J Clin Microbiol Infect Dis 36(12): 2379-83

4. Alves PJ, Barreto RT, Barrois BM et al (2021) Update on the role of antiseptics in the management of chronic wounds with critical col onis ation and/or biofilm. Int Wound J 18(3): 342-58

5. Armstrong DG, Bohn G, Glat P et al (2015) Expert Recommendations for the Use of Hypochlorous Solution: Science and Clinical Application. Ostomy Wound Manage 61(5): S2-S19

6. Assadian O (2016) Octenidine dihydrochloride: chemical characteristics and antimicrobial properties. J Wound Care 25(3 Suppl): S3-6

7. Atkin L Bucko Z, Conde Montero E et al (2019) Implementing TIMERS: the race against hard-to-heal wounds. J Wound Care 28(3): S1-S49

8. Ayello EA, Carville K, Fletcher J et al (2012) Appropriate use of silver dressings in wounds. An expert working group consensus. Wounds International

9. Ayello EA et al (2016) Wound Debridement in Wound Care Essentials: Practice Principles. In Baranoski S and Ayello EA. (Eds)

10. Babalska Zt, Korbecka -Paczkowska M, Karpinski TM (2021) Wound Antiseptics and European Guidelines for Antiseptic Application in Wound Treatment. Pharmaceuticals (Basel) 14(12): 1253

11. Barreto R, Barrois B, Lambert J et al (2020) Addressing the challenges in antisepsis: focus on povidone iodine. Int J Antimicrob Agents 56(3): 106064

12. Barrigah-Benissan K, Ory J, Sotto A et al (2022) Antiseptic Agents for Chronic Wounds: A Systematic Review. Antibiotics (Basel) 11(3): 350

13. Barsoumian A, Sanchez CI, Mende K et al (2013) In vitro toxicity and activity of Dakin's solution, mafenide acetate, and amphotericin B on filamentous fungi and human cells. J Orthop Trauma 27(8): 428-36

14. Bednarek RS, Nassereddin A, Ramsey ML (2020) Skin Antiseptics. Available at: https://www.ncbi.nlm.nih. gov/books/NBK507853/ (accessed 13.09.2023)

15. Bellingeri A, Falciani F, Traspedini P et al (2016) Effect of a wound cleansing solution on wound bed preparation and inflammation in chronic wounds: a single-blind RCT.J Wound Care 25(3): 160-8

16.Bigliardi PL, Alsagoff SAL, EI-Kafrawi HY et al (2017) Povidone iodine in wound healing: A review of current concepts and practices. Int J Surg 44: 260-68

17. Bogers SJ, van Daalen FV, Kuil SD et al (2019) Barriers and facilitators and the need for a dlinical guideline for microbiological diagnostic testing in the hospital: a qualitative and quantitative study. Eur J Clin Microbiol Infect Dis 38(5): 913-20

18. Bongiovanni CM (2014) Effects of hypochlorous acid solutions on venous leg ulcers (VLU): experience With 1249 VLUs in 897 patients. J Am Coll Clin Wound Spec 6(3): 32-7

19. Bowers S, Franco E (2020) Chronic wounds: Evaluation
and management. Am Fam Physician 101: 159-66

20. Brock AK, Chamoun-Emanuelli AM, Howard EA et al (2022) Wound swabs versus biopsies to detect methicillin re sistant Sta phylococcus aureus in experimental equine wounds. Vet Surg 51(8): 1196-205

21. Burches-Feliciano MJ, Argente-Pla M, Garcia-Malpartida K et al (2015) Hyperthyroidism induced by topical iodine. Endocrinol Nutr 62(9): 465-6

22. Centers for Disease Control and Prevention (2021) Expert Committee on Selection and Use of Essential Medicines. Available at: https://cdn.who.int/media/ docs/default- source/essential-medicines/2021-eml-expert-committee/expert-reviews/a18_ hypochlorous- acid_ _rev2.pdf? sfvrsn=cc8d0fb3_ _11 (accessed 03.10.2023)

23. Cheong JZA, Liu A, Rust CJ et al (2022) Robbing Peter to Pay Paul: Chlorhexidine gluconate demonstrates short-term efficacy and long -term cytotoxicity. Wound Rep Reg 30(5): 573-84

24. Conceicao T, de Lencastre H, Aires-de-Sousa M (2019) Bactericidal activity of octenidine against Staphylococcus aureus harbouring genes encoding multidrug resistance efflux pumps. J Glob Antimicrob Resist 16: 239-41

25. Day A, Alkhalil A, Carney BC et al (2017) Disruption of Biofilms and Neutralization of Bacteria Using Hypochlorous Acid Solution: An In Vivo and In Vitro Evaluation. Adv Skin Wound Care 30(12): 543-51

26. De Francesco F, De Francesco M, Riccio M (2022) Hyaluronic Acid/Collagenase Ointment in the Treatment of Chronic Hard-to-Heal Wounds: An Observational and Retrospective Study. J Clin Med 11: 537

27. Del Rosso JQ, Bhatia N (2018) Status report on topical hypochlorous acid: dinical relevance of specific formulations, potential modes of action, and study outcomes. J Clin Aesthet Dematol 11): 36-9

28. Dissemond J, Gerber V, Lobmann R et al (2020) Therapeutic index for local infections score (TILI): a new diagnostic tool. J Wound Care 29(12): 720-6

29. Dissemond J, Malone M, Ryan H et al (2022) Implementation of the M.O.1.S.T. concept for the local treatment of chronic wounds into clinical practice. Wounds International 13(4): 34-43

30. Dong D, Thomas N, Ramezanpour M et al (2020) Inhibition of Staphylococcus aureus and Pseudomonas aeruginosa biofilms by quatsomes in low concentrations. Exp Biol Med (Maywood) 245(1): 34-41

31. Eggers M, Koburger-Janssen T, Eickmann M, Zorn J (2018) In vitro bactericidal and virucidal efficacy of povidone-iodine gargle/mouthwash against respiratory and oral tract pathogens. Infect Dis Ther 7:
249-59

32. EPUAP/NPIAPPPIA (2019) Prevention and Treatment of Pressure Ulcersy Injuries: Clinical Practice Guideline. In HaeslerE. (Ed)

33. Eriksson E, Liu PY, Schultz GS et al (2022) Chronic wounds: Treatment consensus. Wound Rep Reg 30(2): 156-71

34. Esposito S, De Simone G, Gioia R et al (2017) Deep tissue biopsy vs. superficial swab culture, including microbial loading determination, in the microbiological assessment of Skin and Soft Tissue Infections (SSTIs). J Chemother 29: 154-8

35. Falcone M, De Angelis B, Pea F et al (2021) Challenges in the management of chronic wound infections. J Glob Antimicrob Resist 26: 140-7

36. Food and Drug Administration (2022) FDA Drug Safety Podcast: FDA warns about rare but serious alergic reactions with the skin antiseptic chlorhexidine gluconate. Available at: https://www.fda.gov/drugs/ fda -drug-safety-podcasts/fda-drug- safety-podcast- fda-warns-about-rare-serious- alergic-reactions-skin- antiseptic (accessed 22.09.2023)

37. Gil SB (2020) Implementing the Triangle of Wound Assessment framework to transform the care pathway for diabetic foot ulcers. J Wound Care 29(6): 363-9

38. Glaudemans AW, Uckay , Lipsky BA et al (2015) Challenges in diagnosing infection in the diabetic foot. Diabet MedJ Br Diabet Assoc 32: 748e59

39. Gmur M, Karpinski T (2020) Povidone-iodine in wound healing and prevention of wound infections. European Joumal of Biological Research 10(3): 232-9

40. Gray MJ, Wholey W-Y, Jakob U (2013) Bacterial responses to reactive chlorine species Annu Rev Microbiol 67: 141-60

41. Haalboom M, Blokhuis-Arkes MHE, Beuk RJ et al (2018) Wound swab and wound biopsy yield similar culture results: Culture results of swab versus biopsy. Wound Repair and Regeneration 26(2): 192-9

42. Haalboom M, Blokhuis-Arkes MHE, Beuk RJ et al (2019) Culture results from wound biopsy versus wound swab: does it matter for the assessment of wound infection? Clin Microbiol Infect 25(5): 629.e7-629.e12

43. Haesler E, Carville K (2023) Australian Standards for Wound Prevention and Management. Australian Health Research Alliance, Wounds Australia and WA Health Translation Network. Available at: https://woundsaustralia.org/int/woundsaus/uploads/ Shop/Merchandise/ 2023%20wAustralian%20 Standards%20for%20Wound%20Prevention%20 and%20Management%204th%20(1).pdf (accessed 13.09.2023)

44. Haesler E, Swanson T, Ousey K et al (2022) Establishing a consensus on wound infection definitions. J Wound Care 31(Sup12): S48-S59

45. Harriott MM, Bhindi N, Kassis S et al (2019) Comparative antimicrobial activity of commercial wound care solutions on bacterial and fungal biofilms. Ann Plast Surg 83: 404-10

46. Hessam S, Sand M, Georgas D et al (2016) Microbial profile and antimicrobial susceptibility of bacteria found in inflammatory hidradenitis suppurativa lesions. Skin Phammacol Physiol 29: 161-7

47. Hidalgo E, Bartolome R, Dominguez C (2002) Cytotoxicity mechanisms of sodium hypochlorite in cultured human dermal fibroblasts and its bactericidal effectiveness. Chem Biol Interact 139(3): 265-82

48. Hoiby N, Bjarnsholt T, Moser C et al (2015) ESCMID guideline for the diagnosis and treatment of biofilm infections 2014. Clin Microbiol Infect 21(Suppl 1): S1-S25

49. International Wound Infection Institute (2022) Wound Infection in Clinical Practice. Wounds International .

50. Johani K, Malone M, Jensen SO et al (2018) Evaluation of short exposure times of antimicrobial wound solutions against microbial biofilms: from in vitro to in vivo. J Antimicrob Chemother 73(2): 494-502

51. Kadam S, Shai S, Shahane A, Kaushik KS (2019) Recent advances in non-conventional antimicrobial approaches for chronic wound biofilms: have we found the 'Chink in the armor'? Biomedicine 7(2): 3

52. Kapalschinski N, Seipp HM, Kiuckelhaus M et al (2017) Albumin reduces the antibacterial efficacy of wound antiseptics against Staphylococcus aureus. J Wound Care 26(4): 184-7

53. Kearns S, Dawson R Jr (2000) Cytoprotective effect of taurine against hypochlorous acid toxicity to PC12 cells. Adv Exp Med Biol 483: 563-70

54. Kiamco MM, Zmuda HM, Mohamed A et al (2019) Hypochlorous-Acid-Generating Electrochemical Scaffold for Treatment of Wound Biofilms. Sci Rep 9(1): 2683

55. Kim PJ, Applewhite A, Dardano AN et al (2018) Use of a Novel Foam Dressing With Negative Pressure Wound Therapy and Instillation: Recommendations and Clinical Experience. Wounds 30(3 suppl): S1-S17

56. Kordestani SS, Mohammadi FS, Noordadi M et al (2023) Wound Infection Detection Using a Rapid Biomarker. Adv Skin Wound Care 36(1): 35-40

57. Kramer A (2020) Case for wound cleansing. J Wound Care
29(Sup10a): S3-S4

58. Kramer A, Dissemond J, Kim S et al (2018) Consensus on Wound Antisepsis: Update 2018. Skin Phamacol Physiol 31(1): 28-58

59.Laverty G, Gorman SP, Gilmore BF (2014) Biofilms and implant-associated infections. In: Cooper IB, Barnes L. eds, Biomaterials and Medical Device - Associated Infection. 1st edn. Woodhead

60.Leaper D, Assadian O, Edmiston CE (2015) Approach to chronic wound infections. Br J Dermatol 173: 351e8

61. Lepelletier D, Maillard JY, Pozzetto B, Simon A (2020) Povidone lodine: Properties, Mechanisms of Action, and Role in Infection Control and Staphylococcus aureus Decoloniza tion. Antimicrob Agents Chemother 64(9): e00682-20

62. Lescat M, Magnan M, Kenmoe S et al (2021) Co-Lateral Effect of Octenidine, Chlorhexidine and Colistin Selective Pressures on Four Enterobacterial Species: A Comparative Genomic Analysis. Antibiotics (Basel) 11(1): 50

63. LiJX, Pang YZ, Tang CS, Li ZQ (2004) Protective efect of taurine on hypochlorous acid toxicity to nudear nucleoside triphosphatase in isolated nuclei from rat liver. World J Gastroenterol 10(5): 694-8

64. Limato R, Broom A, Nelwan EJ, Hamers RL (2022) A qualitative study of barriers to antimicrobial stewardship in Indonesian hospitals: governance, competing interests, cost, and structural vulnerablity. Antimicrob Resist Infect Contro/11(1): 85

65. Lipsky BA, Dryden M, Gottrup F et al (2016) Antimicrobial stewardship in wound care: a Position Paper from the British Society for antimicrobial Chemotherapy and European wound management Association. J Antimicrob Chemother 71: 3026e35

66. Lutz JT, Diener IV, Freiberg K et al (2016) Efficacy of two antiseptic regimens on skin colonization of insertion sites for two different catheter types: a randomized, clinical trial. Infection 44(6): 707-12

67. Mangum LC, Franklin NA, Garcia GR et al (2018) Rapid degradation and non-selectivity of Dakin's solution prevents effectiveness in contaminated musculoskeletal wound models. Injury 49(10): 1763-73

68. Malanovic N, Buttress JA, Vejzovic D et al (2022) Disruption of the Cytoplasmic Membrane Structure and Barrier Function Underlies the Potent Antiseptic Activity of Octenidine in Gram-Positive Bacteria. App/ Environ Microbiol 88(10): e0018022

69. Malanovic N, On A, Pabst G et al (2020) Octenidine: Novel insights into the detailed killing mechanism of Gram-negative bacteria at a cellular and molecular level. Int J Antimicrob Agents 56(5): 106146

70. Malone M et al (2017) The prevalence of biofilms in chronic wounds: a systematic review and meta-analysis of published data. Journal of Wound Care 26:20-5

71.Matiasek J et al (2018b) An intra-individual surgical wound comparison shows that octenidine-based hydrogel wound dressing ameliorates scar appearance following abdominoplasty. Intermational Wound Joumal 15: 914-20

72. Matiasek J, Kienzl P, Otti GR et al (2018a) Aseptic surgical preparation for upper eyelid blepharoplasty via full-ace octenidine antiseptic without antibiotic medication shows effective prophylaxis against post-surgical wound infection. Int WoundJ15(1): 84-9

73. Mota FAR, Pereira SAP, Araujo ARTS et al (2021) Biomarkers in the diagnosis of wounds infection: An analytical perspective. TrAC Trends in Analytical Chemistry 143(17): 116405

74. Miller G, Kramer A (2008) Biocompatibility index of antiseptic agents by parallel assessment of antimicrobial activity and cellular cytotoxicity.J Antimiarob Chemother 61(6): 1281-7

75. Murphy C, Atkin L, Hurlow J et al (2021) Wound hygiene survey: awareness, implementation, barriers and outcomes. J Wound Care 30(7): 582-90

76. Nair HKR, Choudhury S, Ramachandram K et al (2019) Investigation and review on the efficacy of super- oxidized solution (HYDROCYN aqua@) against biofilm. Wounds International 10<(4): 62-6

77. National Institute for Health and Care Excellence (2023) Antimicrobial stewardship. Available at: https:// bnf.nice.org. uk/medicines-guidance/antimicrobial- stewardship/ (accessed 11.09. 2023)

78. Nikoli N, Kienzl P, Tajpara P et al (2019) The Antiseptic Octenidine Inhibits Langerhans Cell Activation and Modulates Cytokine Expression upon Superficial Wounding with Tape Stripping. J Immuno/ Res 2019(9): 1-11

79. Norman G, Dumville JC, Moore ZE et al (2016) Antibiotics and antiseptics for pressure ulcers. Cochrane Data base Syst Rev 4(4): CD011586

80. Olszowski S, Mak P, Ols zowska E, Marcinkiewicz J (2003) Collagen type II modification by hypochlorite. Acta Biochim Pol 50(2): 471-9

81. Omar A, Wright JB, Schultz G et al (2017) Microbial biofilms and chronic wounds. Microorganisms 5(1):9

82. Ortega-L lamas L, Quinones-Vico MI, Garcia-Valdivia M et al (2022) Cytotoxicity and Wound Closure Evaluation in Skin Cell Lines after Treatment with Common Antiseptics for Clinical Use. Cells 11(9): 1395

83. Ortega-Pena S, Hidalgo-Gonzalez C, Robson MC, Krotzsch E (2017) In vitro microbicidal, anti-biofilm and cytotoxic effects of different commercial antiseptics. Int Wound J 14(3): 470-9

84. Ousey K, Blackburn J (2020) Understanding antimicrobial resistance and antimicrobial stewardship in wound management. Wounds UK 16(2): 36-9

85. Pareek V, Devineau S, Sivasankaran SK et al (2021) Silver Nanoparticles Induce a Triclosan-Like Antibacterial Action Mechanism in Multi-Drug Resistant Klebsiella pneumoniae. Front Microbiol 12: 638640

86. Pattison DI, Hawkins CL, Davies MJ (2003) Hypochlorous acid-mediated oxidation of lipid components and antioxidants present in low-density lipoproteins: absolute rate constants, product analysis, and computational modeling. Chem Res Toxicol 16(4): 439-49

87. Patton D, Avsar P, Sayeh A et al (2023) A meta-review of the impact of compression therapy on venous leg ulcer healing. Int Wound J 20(2): 430-47

88. Pitten FA, Werner HP, Kramer AA (2003) Standardized Test to Assess the Impact of Different Organic Challenges on the Antimicrobial Activity of Antiseptics. J Hosp. Infect 55: 108-15

89. Ponnachan P et al (2019) Antifungal activity of octenidine dihydrochloride and ultraviolet-C light against multidrug- resistant Candida auris. Joumal of Hospital Infection 102: 120-4

90. Power G, Moore Z, O'Connor T (2017) Measurement of pH, exudate composition and temperature in wound healing: a systematic review. J Wound Care 26: 381-97

91. Punjataewakupt A, Napavichayanun S, Aramwit P (2019) The downside of antimicrobial agents for wound healing. Eur J Clin Microbiol Infect Dis 38(1): 39-54

92. Radischat N, Augustin M, Herberger K et al (2020) Influence of human wound exudate on the bactericidal efficacy of antiseptic agents in quantitative suspension tests on the basis of European Standards (DIN EN 13727). Int Wound J17(3): 781-9

93. Rembe JD, Huelsboemer L, Plattfaut let al (2020) Antimicrobial Hypochlorous Wound lrigation Solutions Demonstrate Lower Anti-biofilm Efficacy Against Bacterial Biofilm in a Complex in-vitro Human
Plasma Biofilm Model (hpBIOM) Than Common Wound Antimicrobials. Front Microbiol 11: 564513

94. Rippon MG, Rogers AA, Ousey K (2023) Polyhexamethylene biguanide and its antimicrobial role in wound healing: a narrative review. J Wound Care 32(1): 5-20

95. Roberts CD, Leaper DJ, Assadian O (2017) The Role of Topical Antiseptic Agents Within Antimicrobial Stewardship Strategies for Prevention and Treatment of Surgical Site and Chronic Open Wound Infection. Adv Wound Care (New Rochelle) 6(2): 63-71

96. Robson MC (2020) Treating chronic wounds with hypochlorous acid disrupts biofilm. Wound Prevention and Management 66(5): 9-10

97. Rolfe R Jr, Kwobah C, Muro F et al (2021) Barriers to implementing antimicrobial stewardship programs in three low- and middle- income country tertiary care settings: findings from a multi-site qualitative study. Antimicrob Resist Infect Control 10(1): 60

98. Rothenberger J, Krauss S, Tschumi C et al (2016) The effect of Polyhexanide, Octenidine Dihydrochloride, and tea tree oil as topical antiseptic agents on in vivo microcirculation of the human skin: a noninvasive quantitative analysis. Wounds 28(10): 341-46

99. Rutter L (2018) Identifying and managing wound infection in the community Br J Community Nurs 23(Sup3): S6-S14

100. Sakarya S, Gunay N, Karakulak M et al (2014) Hypochlorous acid: an ideal wound care agent with powerful microbicidal, antibiofilm, and wound healing potency. Wounds 26(12): 342-50

101. Schaper NC, van Netten JI, ApelqvistJ et al (2020) IWGDF Editorial Board. Practical guidelines on the prevention and management of diabetic foot diseases (IWGDF 2019 update). Diabetes Metab Res 36: e3266

102. Schultz G, Bjarmsholt T, James GA et al (2017) Global Wound Biofilm Expert Panel. Consensus guidelines for the identification and treatment of biofilms in chronic nonhealing wounds. Wound Repair Regen 25(5): 744-57

103. Schultz GS, Sibbald RG, Falanga V et al (2003) Wound bed preparation: a systematic approach to wound management. Wound Repair Regen11: 1-28

104. Schwarzer S, James GA, Goeres D et al (2020) The efficacy of topical agents used in wounds for managing chronic biofilm infections: A systematic review. J Infect 80(3): 261-70

105. Seiser S, Janker L, Zila N et al (2021) Octenidine-based hydrogel shows anti-nflammatory and protease- inhibitory capacities in wounded human skin. Sci Rep 11(1): 32

106. Severing AL, Rembe JD, Koester V, Stuermer EK (2019) Safety and efficacy profiles of different commercial sodium hypochorite/hypochlorous acid solutions (NaCIO/HCIO): antimicrobial efficacy, cytotoxic impact and physicochemical parameters in vitro. J Antimicrob Chemother 74: 365-72 .

107. Shamsian N (2021) Wound bed preparation: an overview. Br. J Community Nurs 1;26(Sup9): S6-S11

108. Sharma S (2018) Association of postoperative wound infection with malnutition and low socio-economic status. Joumal of Medical Science and Clinical Research 6(3): 785-8

109. Sibbald RG, lliott JA, Persaud-Jaimangal R et al (2021) Wound Bed Preparation 2021. Adv Skin Wound Care 34: 183-95

110. Sibbald RG, Goodman L, Woo KY et al (2011) Special considerations in wound bed preparation 2011: an update. Adv Skin Wound Care 24(9): 415-36

111. Skodvin B, Wathne JS, Lindemann PC et al (2019) Use of microbiology tests in the era of increasing AMR rates- a multicentre hospital cohort study. Antimicrob Resist Infect Control 8: 28

112. Snyder RJ, Bohn G, Hanft J et al (2017) Wound biofilm: current perspectives and strategies on biofilm disruption and treatments. Wounds 29: S1-17

113. Sopata M, Jawien A, Mrozikiewicz- RakowskaB et al (2020) Guidelines for local management of uninfected wounds, wounds at risk of infection and infected wounds- An overview of the available antimicrobial substances used in the treatment of wounds. Recommendations of the Polish Wound Treatment Society. Leczenie Ran 17: 1-21

114. Spettel K, Bumberger D, Camp let al (2022) Efiacy of octenidine against emerging echinocandin-, azole- and multidrug-resistant C andida albicans and Candida glabrata. Joumal of Global Antimicrobial Resistance 29: 23-8

115. Stryja J, Sandy-Hodgetts K, Collier Met al (2020) Surgical site infection: preventing and managing surgical site infection across health care sectors. J Wound Care 29: 2 (Suppl 2b): S1-69

116. Stuermer EK, Besser M, Brill F et al (2021) Comparative analysis of biofilm models to determine the efficacy of antimicrobials. Int J Hyg Environ Health 234: 113744 Sun X, ChenJ, Zhang J et al (2016) Maggot debridement therapy promotes diabetic foot wound healing by up- regulating endothelial cell activity. J Diabetes Complicat 30: 318-22

117. Tegl G, Schiffer D, Sigl E, Heinzle A, Guebitz GM (2015) Biomarkers for infection: enzymes, microbes, and metabolites. App/ Microbiol Biotechnol 99: 4595-614

118. To E, Dyck R, Gerber S et al (2016) The Effectiveness of Topical Polyhexamethylene Biguanide (PHMB) Agents for the Treatment of Chronic Wounds: A Systematic Review. Surg Technol Int 29: 45-51

119. Villarmet J, Bourron O, Gaudric J et al (2016) Lower- extremity arterial revascularization: Is there any evidence for diabetic foot ulcer-healing? Diabetes Metab 42: 4-15

120. Wang L, Bassiri M, Najfi R et al (2007) Hypochlorous acid as a potential wound care agent: part I. Stabilized hypochlorous acid: a component of the inorganic armamentarium of innate immunity. J Bums Wounds 6:e5

121. WeiJ, He L Weng F, Huang F, Teng P (2021) Effectiveness of chlorhexidine in preventing infections among patients undergoing cardiac surgeries: a meta -analysis and systematic review. Antimicrob Resist Infect Control 10(1): 140

122. Wolcott RD, Hanson JD, Rees E et al (2016) Analysis of the chronic wound microbiota of 2,963 patients by 16S rDNA pyrosequencing. Wound Repair Regen 24(1): 163-74

123. World Health Organization (2016) Diagnostic stewardship: a guide to implementation in antimicrobial resistance surveillance sites. Available at: https://apps. who.int/iris/bitstream/handle/ 10665/ 251553/WHO- DGO-AMR-2016.3-eng pdf (accessed 11.09.2023)

124. World Health Organization (2019) Antimicrobial stewardship programmes in health-care facilities in low- and middle-income countries: A WHO practical toolkit. Available at: https://apps.who.int/iris/
bitstream/handle/10665/329404/ 9789241515481- eng.pdf (accessed 11.09.2023)

125. World Health Organization (2022) The WHO AWaRe (Access, Watch, Reserve) antibiotic book. Available at: https://www.who.int/publications/i/ item/9789240062382 (accessed 11.09. 2023)

126. Worsley A, Vassileva K, Tsui Jet al (2019) Polyhexamethylene Biguanide:Polyurethane Blend Nanofibrous Membranes for Wound Infection Control. Polymers (Basel) 11(5): 915

127. Wounds International (2023) Hydrocyn Aqua@ Made : Easy. Wounds Intemational

128. Wounds UK (2020) Best Practice Statement: Antimicrobial stewardship strategies for wound management. Wounds UK

129. Wounds UK (2021) Wound bed preparation made easy.Wounds UK

130. Winterbourn CC, Brennan SO (1997) Characterization of the oxidation products of the reaction between reduced glutathione and hypochlorous acid. Biochem J 326:87-92

131. Wu S, Tannous E, Haldane V et al (2022) Barriers and facilitators of implementing interventions to improve appropriate antibiotic use in low- and middle- income countries: a systematic review based on the Consolidated Framework for Implementation Research. Implement Sci17(1): 30

132. Zhang Y, Lin B, Huang R et al (2021) Flexible integrated sensing platform for monitoring wound temperature and predicting infection. Microb Biotechnol 14<4) 1566-79

133. Zhu X, Olsson MM, Bajpai R et al (2022) Health-elated quality of life and chronic wound characteristics among patients with chronic wounds treated in primary care:A cross-sectional study in Singapore. Int Wound J 19(5): 1121-32

This article is excerpted from the INTERNATIONAL CONSENSUS DOCUMENT by Wound World.

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