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      Less daily oral hygiene is more in the ICU: yes

      editorial
      1 , 2 , 3 , 4 , , 5 , 6
      Intensive Care Medicine
      Springer Berlin Heidelberg

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          Abstract

          Ventilator associated pneumonia (VAP) and halitosis can be considered to be the two scourges of the decade in the 2000s, one medical and one social of course. While these two problems may seem unrelated, both are conditions in which pressure to adopt oral therapies may result in more harm than good. VAP was certainly seen as the scourge of Critical Care Medicine and was identified as having ≥ 10% attributable mortality in early studies [1]. VAP prevention rapidly became the focus of Critical Care Quality Improvement Programs around the world [2] with healthcare organizations whose missions is “improving health and health care worldwide” jumping on the bandwagon and pushing the agenda forward with zeal [3]. They were supported in this odyssey by governmental and non-governmental organizations internationally, which described VAP as a treatable disease [4]. Oral care and ventilator care bundles came into vogue and all such guidelines contained the recommendation to prevent VAP using oral chlorhexidine solution. In sequence, chlorhexidine oral rinse became an accepted means to attenuate VAP and a social indicator of quality care [5]. The “social scourge” of halitosis was in fact a disease invented by pharmaceutical manufacturers to scare people into using their products—and it worked! Originally considered a surgical antiseptic, floor cleaner, and treatment for gonorrhea, listerine alcohol-based solution became the first over-the-counter mouthwash to “cure” bad breath [6]. The marketing transformation of a personal imperfection into an embarrassing medical condition changed personal oral hygiene practices worldwide. In organizing a desire to purchase the mouthwash, the manufacturer advertised bad breath as a widespread, serious, and treatable disease. In reality, alcohol-containing mouthwashes may contribute to dry mouth and make halitosis worse by reducing or eliminating saliva. Our mouths need saliva to control bacteria, minimize inflammation, and to stay fresh, meaning that the lack of saliva can cause bad breath and dental disease [7]. Nevertheless, the pursuit of the perfect smile and freshest breath is now a compulsion to millions around the world, so why should it not be so for the critically ill in critical care, right? In these enlightened days, at the beginning of the 2020s, we know better of course (or we would do if we weren’t trying to deal with a global pandemic). It turns out that the attributable mortality for VAP is probably closer to 1% and our previous studies were grossly confounded [8]. Further, and concerningly, it turns out that oral chlorhexidine may actually be causing more harm than good. Firstly, in most, but not all studies, oral chlorhexidine prevents VAP, but then again VAP is not the scourge it used to be. Secondly, meta-analysis of randomized evidence has suggested that oral chlorhexidine may be associated with increased mortality [9]. The reasons for this are unclear but they could be as simple as drug related toxicity. Further large, high-quality, randomised studies are underway to see whether this effect can be confirmed [10]. Thirdly, even if oral chlorhexidine doesn’t kill you while preventing VAP, it may be harmful in other important ways related to direct toxic effects on the oral mucosa [11]. So, that said, here is the problem that we face. We have falsely conflated good oral care with the application of oral chlorhexidine; well it is an antiseptic after all just like our favorite mouthwash, so chlorhexidine application meant a job well done! But applying an antiseptic to a healthy mouth may be very different from applying it to the mouth of a patient who is critically ill. All critically ill patients suffer from severe oral dysfunction due to a variety of contributory factors such as xerostomia (dry mouth from inadequate salivary flow), abnormal oropharyngeal colonization, tube-related pressure injury, etc. [12, 13]. Further, if you ask patients after they are treated in a critical care unit, severe oral symptoms are their main complaint, more than cognitive, psychiatric and physical disorders that get more attention). Studies suggest that oral chlorhexidine is applied far more frequently than an evidence-based oral care bundle and this evidence also suggests that nurses believe that they have completed good oral care for their patient by quickly swabbing the mouth with this antiseptic solution [14]. We encourage research to elucidate the potential toxic effects of oral chlorhexidine prophylactic rinse, including but not limited to mucosal lesions, acute pulmonary distress syndrome and increased mortality (Table 1). Table 1 Recommended research to investigate potential chlorhexidine-related adverse outcomes Research area Outcomes Suggested approach Mortality ICU mortality Randomized control trials Mucosal adverse events Oral mucosal lesions; dose response; patient predictors of oral lesions; sepsis; mortality Prospective observational studies; controlled trials; validated oral health indexes Pulmonary adverse events Acute respiratory distress syndrome (ARDS); ventilator-associated events (VAEs); duration of mechanical ventilation Retrospective and prospective observational studies Bacterial resistance Bacterial resistance; infection-related ventilator-associated complications (IVACs); sepsis Antimicrobial sensitivity testing Patient experience Behavioral pain scores; patient self-report of pain, dry mouth, bad taste Prospective observational studies; qualitative studies Good oral care actually involves a comprehensive set of interventions including oral hydration, lip moisturization, and careful toothbrushing to mechanically remove plaque, the sticky biofilm of bacteria that collects above and below the gum line; this does not, and should not include oral chlorhexidine [9]. Biofilm helps to protect bacteria from antiseptics rinses, increasing the likelihood of its survival. Eliminating interventions that may cause harm and focusing on those that promote oral health makes good sense. Further emphasizing the importance of comprehensive oral care is research demonstrating tooth loss among ICU survivors, placing them at risk of morbidity (e.g., malnutrition, depression) and reduced quality of life [15]. Good oral care, therefore, should attend to the prevention of debilitating oral disease—and not VAP alone. The appropriate application of a comprehensive oral care regimen is associated with better oral health outcomes in critically ill patients [12]. In conclusion, we support this motion (or at least support a modified version of the motion). Applying oral chlorhexidine is not the same as good oral care, in fact, it may be bad oral care. We need to stop conflating chlorhexidine application with good oral care. Good oral care (excluding oral chlorhexidine) is to be commended and recommended to relieve the severe symptoms suffered by critically ill patients and prevent dental disease. The state of the evidence base at this time suggest that we should place a moratorium on the use of oral chlorhexidine until high quality randomized trials have reported [10].

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          Most cited references13

          • Record: found
          • Abstract: found
          • Article: not found

          Attributable mortality of ventilator-associated pneumonia: a meta-analysis of individual patient data from randomised prevention studies.

          Estimating attributable mortality of ventilator-associated pneumonia has been hampered by confounding factors, small sample sizes, and the difficulty of doing relevant subgroup analyses. We estimated the attributable mortality using the individual original patient data of published randomised trials of ventilator-associated pneumonia prevention. We identified relevant studies through systematic review. We analysed individual patient data in a one-stage meta-analytical approach (in which we defined attributable mortality as the ratio between the relative risk reductions [RRR] of mortality and ventilator-associated pneumonia) and in competing risk analyses. Predefined subgroups included surgical, trauma, and medical patients, and patients with different categories of severity of illness scores. Individual patient data were available for 6284 patients from 24 trials. The overall attributable mortality was 13%, with higher mortality rates in surgical patients and patients with mid-range severity scores at admission (ie, acute physiology and chronic health evaluation score [APACHE] 20-29 and simplified acute physiology score [SAPS 2] 35-58). Attributable mortality was close to zero in trauma, medical patients, and patients with low or high severity of illness scores. Competing risk analyses could be done for 5162 patients from 19 studies, and the overall daily hazard for intensive care unit (ICU) mortality after ventilator-associated pneumonia was 1·13 (95% CI 0·98-1·31). The overall daily risk of discharge after ventilator-associated pneumonia was 0·74 (0·68-0·80), leading to an overall cumulative risk for dying in the ICU of 2·20 (1·91-2·54). Highest cumulative risks for dying from ventilator-associated pneumonia were noted for surgical patients (2·97, 95% CI 2·24-3·94) and patients with mid-range severity scores at admission (ie, cumulative risks of 2·49 [1·81-3·44] for patients with APACHE scores of 20-29 and 2·72 [1·95-3·78] for those with SAPS 2 scores of 35-58). The overall attributable mortality of ventilator-associated pneumonia is 13%, with higher rates for surgical patients and patients with a mid-range severity score at admission. Attributable mortality is mainly caused by prolonged exposure to the risk of dying due to increased length of ICU stay. None. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Recovery and outcomes after the acute respiratory distress syndrome (ARDS) in patients and their family caregivers.

            Outcomes after acute respiratory distress syndrome (ARDS) are similar to those of other survivors of critical illness and largely affect the nerve, muscle, and central nervous system but also include a constellation of varied physical devastations ranging from contractures and frozen joints to tooth loss and cosmesis. Compromised quality of life is related to a spectrum of impairment of physical, social, emotional, and neurocognitive function and to a much lesser extent discrete pulmonary disability. Intensive care unit-acquired weakness (ICUAW) is ubiquitous and includes contributions from both critical illness polyneuropathy and myopathy, and recovery from these lesions may be incomplete at 5 years after ICU discharge. Cognitive impairment in ARDS survivors ranges from 70 to 100 % at hospital discharge, 46 to 80 % at 1 year, and 20 % at 5 years, and mood disorders including depression and post-traumatic stress disorder (PTSD) are also sustained and prevalent. Robust multidisciplinary and longitudinal interventions that improve these outcomes are still uncertain and data in our literature are conflicting. Studies are needed in family members of ARDS survivors to better understand long-term outcomes of the post-ICU family syndrome and to evaluate how it affects patient recovery.
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              • Record: found
              • Abstract: found
              • Article: not found

              Attributable mortality of ventilator-associated pneumonia: a reappraisal using causal analysis.

              Measuring the attributable mortality of ventilator-associated pneumonia (VAP) is challenging and prone to different forms of bias. Studies addressing this issue have produced variable and controversial results. We estimate the attributable mortality of VAP in a large multicenter cohort using statistical methods from the field of causal inference. Patients (n = 4,479) from the longitudinal prospective (1997-2008) French multicenter Outcomerea database were included if they stayed in the intensive care unit (ICU) for at least 2 days and received mechanical ventilation (MV) within 48 hours after ICU admission. A competing risk survival analysis, treating ICU discharge as a competing risk for ICU mortality, was conducted using a marginal structural modeling approach to adjust for time-varying confounding by disease severity. Six hundred eighty-five (15.3%) patients acquired at least one episode of VAP. We estimated that 4.4% (95% confidence interval, 1.6-7.0%) of the deaths in the ICU on Day 30 and 5.9% (95% confidence interval, 2.5-9.1%) on Day 60 are attributable to VAP. With an observed ICU mortality of 23.3% on Day 30 and 25.6% on Day 60, this corresponds to an ICU mortality attributable to VAP of about 1% on Day 30 and 1.5% on Day 60. Our study on the attributable mortality of VAP is the first that simultaneously accounts for the time of acquiring VAP, informative loss to follow-up after ICU discharge, and the existence of complex feedback relations between VAP and the evolution of disease severity. In contrast to the majority of previous reports, we detected a relatively limited attributable ICU mortality of VAP.
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                Author and article information

                Contributors
                brian.cuthbertson@sunnybrook.ca
                Journal
                Intensive Care Med
                Intensive Care Med
                Intensive Care Medicine
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0342-4642
                1432-1238
                10 October 2020
                : 1-3
                Affiliations
                [1 ]GRID grid.413104.3, ISNI 0000 0000 9743 1587, Department of Critical Care Medicine, , Sunnybrook Health Sciences Center, ; 2075 Bayview Avenue, Toronto, Canada
                [2 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Inter-Departmental Division of Critical Care Medicine, , University of Toronto, ; Toronto, Canada
                [3 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Department of Anesthesiology and Pain Medicine, , University of Toronto, ; Toronto, Canada
                [4 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Institute of Health Policy, Management and Evaluation, , University of Toronto, ; Toronto, Canada
                [5 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Lawrence S. Bloomberg Faculty of Nursing, , University of Toronto, ; Toronto, Canada
                [6 ]GRID grid.413104.3, ISNI 0000 0000 9743 1587, Tory Trauma Program, , Sunnybrook Health Sciences Center, ; Toronto, Canada
                Author information
                http://orcid.org/0000-0003-4174-9424
                Article
                6261
                10.1007/s00134-020-06261-6
                7547300
                33037882
                8d9888b3-8bb6-48db-9faf-b110c4f2f055
                © Springer-Verlag GmbH Germany, part of Springer Nature 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 20 August 2020
                : 25 September 2020
                Categories
                Less is more in Intensive Care

                Emergency medicine & Trauma
                Emergency medicine & Trauma

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