Introduction
This third article for the 2014 Year in Review will report publications from intensive
care on severe infections (including endocarditis and peritonitis), septic shock,
healthcare and ventilator associated pneumonia, highly resistant bacteria, antimicrobial
therapy (including antibiotic stewardship, therapeutic drug monitoring and de-escalation),
invasive fungal infections, severe viral infections, Ebola virus disease and paediatrics.
Sepsis
Circulatory dysfunction is frequently present in patients admitted to the ICU. With
the literature on diagnoses, treatment and monitoring of shock updating frequently,
it is important to have up-to-date guidelines. An important process to facilitate
the establishment of national/local guidelines is the production of a consensus statement
of scientific societies. Therefore the European Society of Intensive Care Medicine
formed a taskforce to review literature and expert opinions on the diagnosis, treatment
and monitoring in circulatory shock. Their report was a long expected update on the
publication of the International Consensus Conference on hemodynamic monitoring in
shock in 2007 [1]. The Taskforce produced 44 statements using the GRADE system principles
[2] and included studies published up to October 1st 2014 [3]. Therefore this consensus
statement published in December 2014 issue of Intensive Care Medicine represents a
very up-to-date view on current evidence. The Taskforce recommends NOT using currently
recommended preload parameters as a sole target of fluid resuscitation or targeting
any ventricular filling pressure or volume. The Taskforce recommends to fluid resuscitate
patients using more than one single hemodynamic variable and to use dynamic instead
of static variables to predict fluid responsiveness whenever possible. This is in
sharp contrast with the recently published Guidelines on the treatment of sepsis and
septic shock from the Surviving Sepsis Campaign (SSC) [4]. In addition, guiding fluid
resuscitation by CVP might even prove to be harmful [5, 6]. Nevertheless the use of
the SSC guidelines has been reported to improve survival from severe sepsis and septic
shock [7]. Both the adherence to the resuscitation and the management bundles of the
guideline were associated with improved survival. Participation of an individual site
in the SSC resulted in a significant drop in hospital mortality every 3 months and
increases in site compliance with the resuscitation bundle significantly improved
ICU and hospital length of stay. In the context of the previous part the question
arises whether these important clinical effects of the SSC-guideline result from the
adequacy of the targets in the guideline or the effect of protocolized and standardized
care. Most likely it’s a combination of effects that warrants further optimization
of the SSC-guideline rather than discarding them [8].
The adequacy of (fluid) resuscitation in every kind of circulatory failure depends
on a good understanding of the physiology of the circulation. Three publications have
contributed to this important aspect. Two publications focused on the understanding
of venous return [9] and hypovolaemia [10]. These two topics are closely linked as
the therapy for hypovolaemia is increasing venous return. The use of CVP in this context
would be to assess whether the heart can efficiently handle the increase in venous
return rather than using in increase in CVP as an indicator of adequately increased
venous return [9]. In the most challenging circulatory failure (septic shock) where
all aspects of the three pillars of the circulation (the vasculature, the volume and
the heart) might be affected [9] the understanding the pathophysiology of cardiac
failure is important as is likely to affect your treatment [11].
Important to realize is that the circulation volume is not equal to the total blood
volume. This mistake is frequently made my junior doctors and nurses. In a compensated
state of hypovolemia, the total blood volume (the sum of stressed and unstressed volume)
is decreased while the stressed volume is maintained and therefore cardiac output
may be maintained as well. This results from an increased activity of the sympathetic
nervous system that translates in clinical practice into decreased peripheral perfusion.
An important marker of decreased peripheral perfusion is a prolonged capillary refill
time [12]. Many studies have now shown that abnormal peripheral perfusion is an important
warning sign in critically ill patients. Whether this is abnormal skin color [13],
abnormal tissue hemoglobin saturation [14] or increased capillary refill time [15,
16]. As abnormal peripheral tissue perfusion can be corrected by specific therapy
[17] the next logical step would be to incorporate the use of peripheral perfusion
parameters and specific treatment into diagnostic and therapeutic protocols to define
efficacy of the use of these parameters [18].
Although many techniques are available to assess the state of the circulation, echo
(cardiography) has gained importance over the last years. The Taskforce of the ESICM
recommends the use of echocardiography as the preferred modality in patients where
clinical examination fails to determine the type of shock [3]. In addition, echocardiography
is noninvasive technique to sequentially evaluate cardiac function in patients with
circulatory failure and thus preferred over the routine use of a pulmonary artery
catheter [3]. In mechanically ventilated critically ill patients the use of lung ultrasound
significantly changes clinical decisions and therapeutic management. In a study of
189 patients, therapy was changed directly in 47 % of the patients [19]. In patients
the combination of lung ultrasound and echocardiography has proven to be superior
to using lung ultrasound only [20]. Therefore thoracic echocardiography should be
an important competence of the current curriculum of a trainee in intensive care.
Sepsis and endocrinopathy
The role of the hypothalamic–pituitary–adrenal axis (HPA) in critically ill patients
remains a subject of interest as the discussion on supporting this axis by use of
hydrocortisone and vasopressin remains actual [21]. The HPA hormones seem to be related
to severity of disease in early sepsis and progression to septic shock [22]. Although
hydrocortisone has a vasopressor sparing effect, it doesn’t seem to affect vasopressin
levels nor mortality [21]. The role of both thus needs more clarification before recommendations
for combined treatment can be made [23]. Also the discussion on the use of vasopressin
as a hormone substitute or as a vasopressor needs clarification as the use as a vasopressor
is associated with serious adverse events not related to vasopressin blood levels
but more to the presence of a specific genotype [24].
The interaction between immune system and infectious organism in not fully understood.
In a recent What’s new article, Douglas et al. [25] emphasized the role of innate
response in sepsis. Indeed, Innate-like lymphocytes are a recently described subset
of the immune response with known antibacterial properties. Human trial in critically
ill patients provides the first evidence of the drop in MAIT cells during bacterial
sepsis, which compounds the already known immune defects. The persistent depletion
and potential for nosocomial infections is an interesting finding and likely to provide
fertile grounds for future studies.
Infection and antimicrobial therapy
While it is now well recognized that early appropriate antimicrobial therapy reduces
infection-related morbidity and mortality in the critically ill patients, the importance
of pharmacodynamic (PD) dosing to optimize drug exposure continues to evolve. Since
it is well recognized that beta-lactams efficacy is driven by the time the drug concentration
exceeds the MIC (T > MIC) of the target pathogen, many of these strategies focused
on altering infusion times. In the clinical setting, beta-lactam optimization strategies
often include the use of a prolonged infusion (i.e., same dose administered over 3–4 h)
for each dosing interval or as a continuous infusion where the total daily dose is
given at a constant rate over 24 h. Each of these strategies has been reported to
enhance the efficacy when compared to conventional regimens as reported by Bassetti
et al. [26] in his editorial. In their interesting and intriguing study, De Waele
et al. [27], using the DALI study (a prospective, multi-centre pharmacokinetic point-prevalence
study) shown that in 343 critically ill patients receiving 8 different β-lactam antibiotics,
antibiotic free drug concentrations remained below the MIC during 50 and 100 % of
the dosing interval in 66 (19.2 %) and 142 (41.4 %) patients, respectively. The use
of intermittent infusion was significantly associated with increased risk of non-attainment
for both targets; creatinine clearance was independently associated with not reaching
the 100 % free time above MIC (fT > MIC) target. The study demonstrated that when
simulating an empirical setting where a broad range of pathogens at the susceptibility
breakpoint is targeted, that target attainment using conventional β-lactam antibiotic
dosing was generally inadequate. Although several factors play a role, use of intermittent
infusion resulted in a three to four fold increase in the likelihood of not reaching
the desired PK/PD targets. In another study, De Waele et al. [28] prospectively analyzed
the effect of a dose adaption strategy using daily therapeutic drug monitoring (TDM)
on the target attainment for meropenem and piperacillin/tazobactam when pneumonia
was the primary infectious diagnosis. Forty-one patients were included in the study.
Eighty-five percent of patients in the TDM group needed dose adaptation, 5 required
an additional increase. At 72 h, target attainment rates for 100 % fT > 4MIC and 100 %
fT > MIC were higher in the TDM group: 58 vs. 16 % (p = 0.007) and 95 vs. 68 % (p = 0.045),
respectively. The study supports a strategy of dose adaptation based on daily therapeutic
drug monitoring that lead to an increase in PK/PD target attainment compared to conventional
dosing in critically ill patients with normal kidney function.
Aminoglycosides continue to be essential antibiotic in ICU. When aminoglycosides are
used in critically ill patients, it is crucial that their efficacy is maximized. Aminoglycosides
are concentration dependent antibiotics, and the peak concentration over MIC is the
relevant PK/PD parameter. Studies have shown that aminoglycosides have their maximal
effect at a C
max/MIC ratio of 8–10. This means that TDM for efficacy may be helpful to guide therapy.
Based on these considerations, as well as on the decreasing susceptibility of microorganisms,
actual PK-guided dosing based on individual plasma concentrations is preferable in
critically ill patients. Initial therapy (before any MIC is known) should use higher
doses (amikacin 25–30 mg/kg, gentamycin 7–9 mg/kg and tobramycin 7–9 mg/kg) to compensate
for the changes described, and the C
max of the previous dose should guide subsequent doses as reported by Dimopoulos [29]
in his editorial. Under this context, recent studies shed more light on the aminoglycoside
PK/PD properties in ICU patients. In a prospective study conducted by de Montmollin
et al. [30] in a general ICU, 33 % of patients that receives a loading dose of amikacin
of 25 mg/kg of total body weight (TBW), still had an amikacin C
max <60 mg/L. Positive 24-h fluid balance was identified as a predictive factor of
C
max <60 mg/L. Low BMI tended to be associated with amikacin underdosing, when TBW
was used, suggesting the need for higher doses in patients with a positive 24-h fluid
balance. Whether these regimens are associated with improved outcomes is unknown,
therefore other prospective randomized controlled studies are warranted to assess
the effects of higher loading doses of amikacin on C
max, infection control and survival, and its impact on renal and hearing functions.
Other compound such as tigecyclin has been extensively studied because of potential
activities on extensively drug-resistant bacterias. In 2010 and 2013, the US Food
and Drug Administration (FDA) reported an increased risk of mortality associated with
tigecycline use in comparison with other drugs in the treatment of serious infections.
The analysis used a pooled group of randomized clinical trials including hospital-acquired
pneumonia (HAP) and ventilator-associated pneumonia (VAP), complicated skin and soft
tissue infections (cSSTI), complicated intra-abdominal infections (cIAI), and diabetic
foot infections. On the basis of the pooled data analysis, the FDA recommended that
alternatives to tigecycline should be considered in patients with severe infections.
In their interesting article Montravers et al. [31] conclude that tigecyclin success
rates in patients in ICU with severe infections appear comparable to those reported
with other antibiotics; the overall success rate was 60 % at the end of treatment,
and 53 % 7 days later. Furthermore, they report a survival rate of 85 % at day 28.
Historically, clinical trials concerning management of critically ill and particularly
ICU-admitted patients with tigecyclin are limited. Despite the obscure vision provided
by an impressive number of meta-analyses, tigecyclin is expected to be used more often
in approved indications and in off-label combination regimens for the treatment of
MDR gram-negative infections in routine clinical practice. This is greatly supported
by the Montravers study mentioned above. The increased medical need represented by
the growing impact of multiresistant infections and the current lack of alternative
or new antibiotics suggests that tigecycline benefit–risk continues to be positive.
Antimicrobial de-escalation
Another way to save antimicrobials is to deescalate as often as possible. Many important
papers have been published in the journal on this field.
Antimicrobial de-escalation is a clinical approach to empirical antibiotic treatment
of serious infections that attempts to balance the need for appropriate initial therapy
with the need to limit unnecessary antimicrobial exposure in order to curtail the
emergence of resistance. Although the concept of antimicrobial de-escalation seems
to make intuitive sense, clinicians should ask themselves what the realistic expectations
of such a strategy are. Intensivists should expect that a de-escalation approach to
antimicrobial therapy in critically ill patients will optimize patient’s outcomes
as said by Dr Kollef [32] in his editorial. In his interesting and complete study,
Garnacho-Montero et al. [33] evaluated 628 patients with severe sepsis or septic shock
at ICU admission who were treated empirically with broad-spectrum antibiotics. Antibiotic
therapy was guided by written protocols advocating for de-escalation therapy once
the microbiological results became available (day of culture results), although this
decision was ultimately the responsibility of the physician in charge of the patient.
By multivariate analysis, factors independently associated with in-hospital mortality
were septic shock, SOFA score on the day of culture results, and inappropriate empirical
antimicrobial therapy, whereas de-escalation of antimicrobial therapy was found to
be a protective factor for hospital survival. Additionally, among patients receiving
appropriate therapy the only factor independently associated with mortality was SOFA
score on the day of culture results, whereas de-escalation therapy was again found
to be a protective factor.
In the setting of neutropenic patient with severe sepsis or septic shock, use of broad-spectrum
antibiotics is recommended. To date, the first study on the safety of de-escalation
in neutropenic patients has been published in this journal by Mokart et al. [34].
De-escalation of antimicrobial therapy consisted either to delete one of the empirical
antibiotic of a combined treatment, or, whenever possible, to use a betalactam antibiotic
with a narrower spectrum of activity. Cumulative incidence of de-escalation of the
empirical antimicrobial treatment among the 101 patients of the cohort, was 44 %,
(95 % confidence interval, CI 38–53 %), including 30 (68 %) patients with ongoing
neutropenia, while a microbiological documentation was available in 63 (63 %) patients.
De-escalation did not significantly modify the hazard of death within the first 30-day
[HR = 0.51 (95 % CI 0.20–1.33)], nor within the 1 year after ICU-discharge [HR = 1.06
(95 % CI 0.54–2.08)]. The results of the study are encouraging and impressive: for
the first time the authors has shown that, in ICU, de-escalation is frequently performed
in neutropenic cancer patients with severe sepsis and this approach appears not to
affect the outcomes.
Surprising and apparently not expected results for de-escalation therapy were shown
by Leone et al. [35] in their multicenter, non-blinded, randomized noninferiority
trial included patients with severe sepsis that were randomly assigned to de-escalation
or continuation of empirical antimicrobial treatment. The results shown the median
duration of ICU stay was 9 [interquartile range (IQR) 5–22] days in the de-escalation
group and 8 (IQR 4–15) days in the continuation group, respectively (p = 0.71). The
mean difference was 3.4 (95 % CI −1.7 to 8.5). A superinfection occurred in 16 (27 %)
patients in the de-escalation group and six (11 %) patients in the continuation group
(p = 0.03). The numbers of antibiotic days were 9 (28–30, 36–41) and 7.5 (27–30, 36–39)
in the de-escalation group and continuation group, respectively (p = 0.03). Mortality
was similar in both groups. The current study casts significant doubt whether the
reduction of the spectrum of the antibiotic can be considered safe as a routine measure.
The authors demonstrated that de-escalation, defined as narrowing the spectrum of
the antibiotic, was inferior to continuation of the initial antibiotic therapy with
length of stay as the primary outcome parameter. Furthermore, antibiotic use was higher
in the de-escalation group presumably driven by the number of superinfections in the
de-escalation group. A key element in the study of the potential role of de-escalation
is a uniform definition of de-escalation. De-escalation—defined as narrowing the spectrum
of an antibiotic treatment—should be cautiously applied, based on each particular
patient’s clinical status and considering the ICU environment as a whole.
Healthcare-associated pneumonia
Vallés et al. [42] prospectively compared the epidemiology, antibiotic therapy and
clinical outcomes between 449 patients with community acquired pneumonia (CAP), 133
health care acquired pneumonia (HCAP) and 144 immunocompromised patients (ICP) with
pneumonia admitted in 34 Spanish ICUs over a 1 year period. They found that HCAP patients
had more comorbidities and had a worse clinical status as compared to the two other
subgroups and that both HCAP and ICP more often needed mechanical ventilation and
more often underwent tracheostomy. The incidence of gram-negative pathogens, MRSA
and Pseudomonas aeruginosa was low overall, but higher in HCAP and ICP. Inappropriate
empirical antibiotic therapy was 6.5 % in CAP, 14.4 % in HCAP and 38.6 % in ICP while
mortality was the highest in ICP (38.6 %) and did not differ between CAP (18.4 %)
and HCAP (21.2 %). The authors concluded that empirical antibiotic regimens recommended
for CAP would be appropriate for 90 % of the patients with HCAP and that consequently
systematically covering multidrug-resistant pathogens in HCAP is not necessary.
Ventilatory-acquired pneumonia
Diagnosis of ventilator-associated pneumonia (VAP) is a problem that is not yet fully
solved. In fact, there have been no major advances since the last meta-analysis published
by the Cochrane Collaboration [43]. Real major advances will come from rapid PCR point-of-care
techniques, but these results are not yet available. In 2014, Bos et al. [44] published
an article in the What’s New in Intensive Care section on potential innovations that
could improve early recognition of VAP. Those authors suggested that new techniques
are promising in detecting airway colonization and pulmonary infection at the early
phase. The first technique would use colorimetric assays inside the endotracheal tubes
to detect the type of bacteria and the pattern of resistance. The second technique
is based on the detection of volatile compounds (hydrocarbons, alcohols, aldehydes,
ketones and, sulfide-containing molecules) released by bacteria that cause VAP. These
techniques are still in a very early clinical phase and need to be validated.
Postoperative nosocomial pneumonia is a threatening complication of major surgery
(cardiovascular, thoracic and abdominal), with very high morbidity and mortality.
All improvements that can help prevent postoperative pneumonia are welcome. Preoperative
oral care is a non-standard prophylactic measure. Bergan et al. [45] performed a prospective
study implementing several oral-hygiene measures, including a dentist visit, brushing
teeth and tongue and, oral rinse with chlorhexidine (0.12 %) twice a day until surgery.
With these measures, they were able to reduce pneumonia from an incidence rate of
32 cases to 1000 ventilator days in the 6 months period before the study to 10 cases
per 1000 days of mechanical ventilation during the 6 months following the study. Oral
chlorhexidine rinsing in the preoperative period (OR, 17) and on the day of surgery
significantly were significantly protective for post-operative pneumonia. Oral chlorhexidine
rinses and dental hygiene are cheap, easy and effective measures for preventing pneumonia
after cardiac surgery.
Colonization with resistant bacteria
Colonization is a better indicator for bacterial dynamics than infection, since colonization
only leads to infection in a small group but contributes significantly to the epidemiology
of these bacteria. Knowledge about the time until clearance of resistant bacteria
is of great importance for understanding nosocomial dynamics and for predicting effects
of interventions. In his study Haverkate et al. [46] studied all patients screened
on admission and twice weekly for resistant bacteria in 13 ICUs in 8 European countries
(MOSAR-ICU trial, 2008–2011). 125 unique patients had 141 episodes of colonization
and at least one readmission. Thirty-two patients were colonized with two or more
resistant bacteria. Median times until clearance were 4.8 months for all resistant
strains, 1.4 months for highly resistant enterobacteriaceae, less than 1 month for
MRSA, and 1.5 months for vancomycin resistant enterococci. For all antimicrobial-resistant
bacterial species, 50 % of the patients had lost colonization when readmitted two
or more months after the previous ICU admission. Although this study was performed
on a selection of hospital patients (i.e., patients admitted to ICUs), the results
are of critical importance since these patients are especially prone to colonization
and (subsequent) infection.
Bacteremia and MRSA
Bacteremia is one of the major causes of nosocomial infection in the intensive care
unit (ICU), ICU-acquired bloodstream infection (ICU-BSI) is associated with increased
morbidity and length of stay, resulting in excess costs and high mortality of critically
ill patients. Although there are variations due to heterogeneous information sources
and variety of local clinical practices, coagulase-negative staphylococci, Staphylococcus
aureus, and Enterobacteriaceae species are the pathogens most frequently responsible
for nosocomial bacteremia. Energy deficit in ICU patients is mainly caused by reduced
intake due to under-prescribed calories and frequent feeding interruptions. Cumulated
energy deficit build-up during the first days of ICU stay appears an independent factor
contributing to nosocomial infections. In their interesting study, Ekpe et al. [47]
investigated the impact of energy deficit on the microbiological results of the blood
cultures of prolonged acute mechanically ventilated patients who experienced a first
ICU-BSI episode. Daily energy balance was compared according to the microbiological
results of the blood cultures of 92 consecutive prolonged (>96 h) acute mechanically
ventilated patients who developed a first episode of ICU-BSI. Among the 92 ICU-BSI,
9 were due to methicillin-resistant Staphylococcus aureus (MRSA). The cumulated energy
deficit of patients with MRSA ICU-BSI was greater than those with ICUBSI caused by
other pathogens. ICU admission, risk factors for nosocomial infections, nutritional
status, and conditions potentially limiting feeding did not differ significantly between
the two groups. Patients with MRSA ICU-BSI had lower delivered energy and similar
energy expenditure, causing higher energy deficits. More severe energy deficit and
higher rate of MRSA blood cultures (p = 0.01 comparing quartiles) were observed. The
conclusions of the study were that early in-ICU energy deficit was associated with
MRSA ICU-BSI in prolonged acute mechanically ventilated patients. Results suggest
that limiting the early energy deficit could be a way to optimize MRSA ICU-BSI prevention.
Bacteremia is an important cause of mortality, prolonged stay and excess healthcare
costs even in paediatric intensive care units (PICU). An estimated 70 % of BSIs occurring
in PICU are thought to be related to the use of central venous catheters (CVCs). Adherence
to full sterile procedures may be compromised when CVCs are inserted as part of emergency
resuscitation and stabilisation, particularly outside the intensive care unit. Half
of emergency admissions to PICU in the UK occur after stabilisation at other hospitals.
In their study Harron et al. [48] made in UK determined whether bloodstream infection
(BSI) occurred more frequently in children admitted to PICU after inter-hospital transfer
compared to within hospital admissions. Multivariable regression showed no significant
difference in rates of PICU-acquired BSI by source of admission (incidence-rate ratio
for inter-hospital transfer versus within-hospital admission = 0.97, 95 % CI 0.87–1.07)
after adjusting for other risk-factors. Rates of inter-hospital transfers decreased
more rapidly between 2003 and 2012: 17.0 % (95 % CI 14.9–19.0 % per year) compared
with 12.4 % (95 % CI 9.9–14.9 % per year) for within hospital admissions. The median
time to first PICU-acquired BSI did not differ significantly between inter-hospital
transfers (7 days, IQR 4–13) and within-hospital admissions (8 days, IQR 4–15). The
authors concluded that inter-hospital transfer was no longer a significant risk factor
form PICU-acquired BSI. Given the large proportion of infection occurring in the second
week of admission, initiatives to further reduce PICU-acquired BSI should focus on
maintaining sterile procedures after admission.
Peritonitis
Faecal peritonitis (FP) is a common cause of secondary peritonitis caused by spillage
of faecal material from the large bowel into the peritoneum. The Genetics of Sepsis
and Septic Shock in Europe (GenOSept) project is investigating the influence of genetic
variation on the host response and outcomes in a large cohort of patients with sepsis
admitted to ICUs across Europe. Tridente et al. [49] reported in their study data
for 977 FP patients admitted to 102 centers across 16 countries. The most common causes
of FP were perforated diverticular disease (32.1 %) and surgical anastomotic breakdown
(31.1 %). The ICU mortality rate at 28 days was 19.1 %, increasing to 31.6 % at 6 months.
The cause of FP, pre-existing co-morbidities and time from estimated onset of symptoms
to surgery did not impact on survival. The strongest independent risk factors associated
with an increased rate of death at 6 months, included age, higher APACHE II score,
acute renal and cardiovascular dysfunction within one week of admission to ICU, hypothermia,
lower haematocrit and bradycardia on day 1 of ICU stay.
Infective endocarditis
Although recent literature is plenty of studies concerning all aspects of infective
endocarditis (IE), very few focus on severe IE requiring admission to the ICU. In
their “My paper 10 years later” Wolff et al. [50] affirmed that since the publication
of the paper in 2004 a lot of information has been accumulated on management of IE.
While 3 sets of blood cultures allow the identification of about 90 % of cases, culture
negative IE still remains a diagnostic challenge. Blood-polymerase chain reaction
in valve tissue may yield a microbiologic diagnosis. New imaging techniques such as
PET-CT scans have shown additive value in patient with intra-cardiac device or valvular
prosthesis. Systematic cerebral magnetic resonance imaging can lead to modification
of therapeutic plans. The decision to operate and the timing of cardiac surgery should
take into account the presence of congestive heart failure, neurological complications,
renal failure, and multiorgan dysfunction syndrome. The strongest independent predictor
of post-operative mortality was the pre-operative multiorgan failure score. Neurological
failure also represented a major determinant of mortality, regardless of the mechanism
of neurological complication.
Fungal infections and colonization
Fungal infections and in particular Candida species are responsible for between 9–12 %
of all bloodstream infections and are the fourth most common cause of nosocomial bloodstream
infections in most US population surveys and the sixth or seventh most common cause
in European surveys. Candida bloodstream infections occur at highest rates in the
ICU population, with this setting accounting for 33–55 % of all candidemias. In their
complete and useful review Leon et al. [36] described that a high proportion of ICU
patients become colonized with Candida species, but only 5–30 % develop invasive candidiasis.
Invasive candidiasis and candidaemia are difficult to predict and early diagnosis
remains a major challenge. In addition, microbiological documentation occurs often
late in the course of infection. Delays in initiating appropriate treatment have been
associated with increased mortality. In an attempt to decrease Candida-related mortality,
an increasing number of critically ill patients without documented candida infections
receive empirical systemic antifungal therapy, leading to concern for antifungal overuse.
Scores/predictive rules permit the stratification and selection of high risk patients
who may benefit from early antifungal therapy. However, they have a far better negative
predictive value than positive predictive value. New biomarkers [mannan, antimannan,
(1,3)-β-D-glucan and polymerase chain reaction] are being increasingly used to enable
earlier diagnosis and, ideally, to provide prognostic information and/or therapeutic
monitoring. Although reasonably sensitive and specific, these techniques remain largely
investigational, and their clinical usefulness has yet to be established.
In their elegant study, Lortholary et al. [37] reported the active hospital-based
surveillance program of incident episodes of candidemia in twenty-four tertiary care
hospitals in Paris area. Among 2507 adult cases included, 2571 Candida isolates were
collected and species were C. albicans (56 %), C. glabrata (18.6 %), C. parapsilosis
(11.5 %), C. tropicalis (9.3 %), C. krusei (2.9 %) and C. kefyr (1.8 %). Candidemia
occurred in ICU in 1206 patients (48.1 %). When comparing ICU vs. non-ICU patients,
the former had significantly more frequent surgery during the past 30 days, were more
often pre-exposed to fluconazole and treated with echinocandin, and were less frequently
infected with C. parapsilosis. A significant increased incidence in the overall population
and ICU was found. Echinocandins initial therapy increased over time in ICU (4.6 %
first year of study, to 48.5 % last year of study, p < 0.0001). ICU patients had a
higher day 30 death rate than non-ICU patients [odds ratio (OR) 2.12, 95 % CI 1.66–2.72,
p < 0.0001]. The day 30 and early (<day 8) death rates increased over time in ICU
(from 41.5 % the first to 56.9 % the last year of study (p = 0.001) and 28.7–38.8 %
(p = 0.0292), respectively). The authors concluded that the availability of new antifungals
and the publication of numerous guidelines did not prevent an increase of candidaemia
and death in ICU patients in Paris area. Apparently in contrast with the Paris study,
Colombo et al. [38] retrospectively analyzed 1392 episodes of candidaemia in adult
patients (647 in ICU) from 22 Brazilian hospitals. Comparing the characteristics of
candidaemia in ICU patients in 2 periods (2003–2007, period 1 and 2008–2012, period
2), and assessed predictors of 30-day mortality. They reported that 30-day mortality
rate decreased from 76.4 % in period 1–60.8 % in period 2 (p < 0.001). Predictors
of 30-day mortality by multivariate analysis were older age, period 1, receipt of
corticosteroids and higher APACHE II score, while treatment with an echinocandin were
associated with a higher probability of survival. The authors concluded that the incorporation
of echinocandins as primary therapy of candidemia seems to be associated with better
outcome. As in bacterial infections however, adequate treatment remains of paramount
importance in treating infections in critically ill patients. Also in patients with
candida blood stream infections, inadequate source control and antifungal treatment
have been associated with increased mortality [51]. Another important phenomenon in
the management of Candida infections is represented by the emergence of resistance
in Candida spp. Antifungal drug resistance was considered less problematic in Candida
spp. than in other pathogens, but recent increases in resistance to both echinocandins
and azoles have led to clinical failures. In their extensive review Maubon et al.
[39] reported that acquired fluconazole resistance is frequent in C. glabrata (from
4 to 16 %), which increasingly displays cross-resistance to voriconazole. So far,
multi-drug resistant phenotype against azole and echinocandins, has only been described
for C. glabrata and is a matter of serious concern. Fluconazole resistance remains
uncommon in C. albicans (<5 %), but is more prevalent in C. parapsilosis (4–10 %)
and C. tropicalis (4–9 %), however recent data shows that may reflect geographical
differences. Acquired resistance to echinocandins is increasingly reported for most
of the clinically important Candida spp. It remains uncommon in C. albicans (<1 %),
C. tropicalis (<5 %) and C. krusei (<7 %), but is now becoming frequent in C. glabrata
(8–15 %).
Candida spp. colonization of the airway is frequently reported in mechanically ventilated
critically ill patients, and its clinical significance is difficult to evaluate. Candida
has a low affinity for alveolar pneumocytes and histologically documented pneumonia
has been rarely reported. Hematogenous dissemination in the context of candidemia
may be responsible for multiple pulmonary abscesses and should be viewed as a distinct
entity. Hence the existence of true candidal pneumonia is doubtful and recovery of
Candida spp. from the respiratory tract should generally be considered as colonization
and does not justify antifungal therapy. In their double-blind, placebo-controlled,
multicenter pilot randomized trial, Martin et al. [40] tried to demonstrate a benefit
of antifungal therapy in critically ill patients with positive airway secretion specimens
for Candida spp. They recruited 60 patients into the randomized trial: 29 patients
specifically treated with antifungals. Markers of inflammation and all clinical outcomes
were comparable between placebo and antifungal treatment group at baseline and over
time. At baseline, plasma TNF-alpha levels were higher in the patients colonized with
Candida compared to the observational group (mean ± SD) (21.8 ± 23.1 vs. 12.4 ± 9.3 pg/ml
p = 0.02) and that these patients had lower innate immune function as evidenced by
reduced whole blood ex vivo LPS-induced TNF-alpha production capacity (854.8 ± 855.2
vs. 1559.4 ± 1290.6 pg/ml p = 0.01). This study does not provide evidence to support
a larger trial examining the efficacy of empiric antifungal treatment in patients
with Candida in the endotracheal secretions. Similar negative impact in duration of
mechanical ventilation has been obtained with inhaled amphotericin-B patients with
airway colonization with Candida sp. Ampho-B inhalation therapy was not associated
with increased decolonization and might even prolong duration of mechanical ventilation
possibly due to the toxicity of the drug on the lungs [52].
In addition, in a small randomized study on the efficacy of empiric treatment of suspected
ventilator associated pneumonia in patients with candida colonization of the respiratory
tract did not prove to be effective [40]. In this study persistent inflammation and
immunosuppression were associated with Candida colonization of the lung. What to do
with respiratory tract colonization in critically ill patients therefore remains an
important problem [53].
For the prevention of fungal infections, oral prophylaxis with nystatin has been recently
evaluated and shown to result in a reduction of Candida colonization [41].
The development of the Candida colonization index (CI) has been viewed as a major
conceptual advance in the characterization of supporting the progression from colonization
to infection in surgical patients [54]. In their “My paper twenty year later” Eggimann
et al. [55] affirmed that since the publication of the paper in 1994, many centers
have used the CI or a methodology derived from its original description to assess
the dynamics of Candida colonization in different sub-groups of critically ill patients
at risk of invasive candidiasis. Unfortunately, these data have not been validated
in large multicenter trials. Several studies have indirectly suggested the validity
and potential usefulness of the CI, but almost exclusively in surgical patients. Among
the pitfalls, it should be emphasized that it is work-intensive with a limited bedside
practicability. Furthermore, only limited data are available for nonsurgical patients,
and its cost effectiveness and usefulness for the management of critically ill patients
remain to be proven in large prospective clinical trials.
Koulenti et al. [56] analyzed data on epidemiology, clinical aspects and diagnostic
novelties in invasive pulmonary aspergillosis (IPA) in ICU patients. They concluded
that the identification of high-risk profiles for IPA of ICU patients without apparent
immunosuppression might help in achieving earlier IPA diagnosis as it would lead to
a higher level of suspicion and a lower threshold to perform thorough diagnostic work-out
for patients at high-risk. Epidemiological research with the aim to identify the high-risk
patient for IPA is going on (http://www.aspicu2.org).
In recent years, antineoplastic treatment regimens in hematological patients have
intensified. This has led to a significant increase in ICU admissions due to severe
infectious complications. Among these patients, pulmonary infiltrates with a fungal
etiology are among the most common findings associated with febrile episodes. The
increasing availability of high resolution and multislice CT has rendered the conventional
chest radiograph more or less obsolete for diagnosing lung infiltrates in febrile
neutropenic patients [57].
Viral pneumonia
In recent years, viral community-acquired pneumonia (CAP) has been reported as a frequent
microbial etiology in severe CAP. This is due in part to the new diagnostic techniques
that allow to detect old and new viruses. Middle East respiratory syndrome (MERS)
is one of these new viral diseases, which is caused by an RNA betacoronoravirus. Leung
and Gomersall [58] described in Intensive Care Medicine the epidemiology, pathogenesis,
clinical features, diagnosis, treatment, and implications for intensive care management.
The clinical features of this disease are indistinguishable from other viral diseases,
including viral pneumonitis. Diagnosis is made by means of epidemiological background
(Middle-East travel) plus the examination of blood, urine, stool, conjunctival swabs
and cerebrospinal fluid samples, in which the virus can be found using real-time reverse-transcription
PCR. Most patients admitted to the ICU require mechanical ventilation. Shock and renal
failure are also frequent. Unfortunately, there is no specific antiviral treatment.
Ebola infection
Ebola virus is one of the most virulent human pathogens. Since 1976, Ebola virus disease
(EVD) has caused more than 20 outbreaks in Africa, with case fatality rates of 30–90 %,
in the absence of any approved treatment or vaccination. It is transmitted by direct
contact through broken skin or mucous membranes with blood, urine, saliva, feces,
vomit, and other body fluids of symptomatic infected patients or convalescent persons,
or through contaminated needle sticks. The 2014 EVD outbreak in West Africa is a public
health emergency of international concern. Tattevin et al. [59] affirmed that every
physician active in emergency departments or ICU worldwide may turn out to be involved
in the care of patients suspected of EVD. Their take-home messages from this paper
were (1) suspect EVD in any patient who presents with fever within three weeks after
a stay in Guinea, Sierra Leone, Liberia, or Nigeria; (2) while implementing infection
control procedures to prevent any secondary cases (in case EVD is confirmed), ensure
that all plausible differential diagnoses are appropriately considered and managed.
Even Parkes-Ratanshi et al. [60] in their article urgently recommend that health facilities
consult national guidelines on EVD and develop local action plans. During this epidemic
this internet and social media such as Twitter are being effectively used to disseminate
information by the WHO, governments and the medical press. As the WHO are predicting
that that the end of the epidemic is far away and it may infect up to 100,000 people
before it is controlled; it is essential that the global medical community remains
informed and vigilant. The critical care teams working with patients who have been
evacuated to resource rich settings during the current epidemic must share their best
practices as soon as possible.
Regarding the organ dysfunction, Beeching et al. [61] in their article explained that
the pathogenesis of EVD shows both similarities with and differences from other causes
of viral haemorrhagic fever or bacterial sepsis. Systematic prospective observational
studies are essential to clarify the pathogenesis and pathophysiology of disease in
humans and to inform the development of evidence based clinical scoring systems and
management algorithms, as well as the evaluation of novel therapeutic agents. Improving
access to basic supportive care is essential. The role and possible benefit of more
aggressive critical care interventions continue to be debated.
Paediatrics
Deep trouble: unwanted effects of sedation and support
We have had a year of notable submissions including novel reviews of large datasets,
randomized controlled trials, and state-of-the-art “What’s new” articles. However,
arguably the most compelling piece of paediatric intensive care literature from 2014
in ICM was the simple but profound recollection of a month spent on a paediatric intensive
care unit: ‘Coma alarm dreams’ [62]. Written by a remarkable young man describing
his recovery from a gunshot wound to the head, this 500-word piece provides an uncomfortable
insight into our patient’s experiences. We may hardly notice monitor alarms; they
form the soundtrack of our working lives. But for our patients the experience may
be the complete opposite: dreams, nightmares and hallucinations.
Dr Emeriaud and colleagues [63] from Montreal, highlighted another problem during
paediatric critical illness that is easily overlooked. They performed repeated estimations
of maximal inspiratory diaphragmatic electrical activity (EAdimax) in 55 ventilated
children. This first systematic description of the natural history of this parameter
provides in number of insights; there were frequent periods of little or no detectable
diaphragmatic activity during mechanical ventilation; those values that were seen
during during full ventilation were much lower than pre-extubation or spontaneous
breathing; and patients intubated mainly because of a lung pathology exhibited higher
EAdi (p < 0.01) than did patients supported for other reasons. The authors add to
the emerging view that we may be oversedating and oversupporting many of our patients.
The possibility of using EAdi as a proxy endpoint for clinical trials or as a biomarker
for guiding mechanical ventilation is intriguing.
Ventilation/ARDS
“How to manage ventilation in pediatric acute respiratory distress syndrome” by Kneyber,
Jouvert and Rimensburger [64] returned to this theme of the limitations of our current
practice and the need to recognize the potential harm we might be causing. They present
a candid view of the many gaps in our knowledge: is our (new) Berlin definition sufficient
for selection of patients for randomized trials? Is it appropriate to infer guidance
from adult studies? Does ~6 mls/kg tidal volume really represent our best guess safe
and effective ventilation during both acute and recovery phase of lung injury? Can
we generate clinically meaningful guidance from the bedside tools such as transpulmonary
pressure (TPP) measurements and electrical impedance tomography (EIT)? Perhaps most
pressingly, many paediatric intensivists treasure the use of high frequency oscillation
in paediatric ARDS on very limited evidence. Surely we need clinical trial data in
the face of the results from the Oscillate and Oscar trials. We are again challenged
to provide data to systematise our sedation and weaning policies.
ECMO
Drs MacLaren, Brown and Thiagarajan [65] gave us a view of “What’s new in pediatric
ECMO” from four continents. Overall survival after ECMO is improving and therefore
other indications are starting to be considered (bridge to lung transplantation anyone?).
They highlighted specific area of concerns including the need for more information
about advantages of specific pumps or anticoagulant regimens. But above all there
is a clear need for long-term follow up. Recent reports of very high rates of late
death for cardiac ECMO make this point starkly: only 10 % of hypoplastic left heart
syndrome cases who received ECMO were alive 5 years later. The impact on the family
with high rates of post-traumatic stress, the importance of neurological complications,
and the value of neurodevelopment follow-up, as highlighted in the journal in 2013,
were noted [66–68].
Non-invasive ventilation
At the other end of the spectrum of severity of respiratory failure, we published
an important study from Kremlin-Bicetre Hospital in Paris, documenting the associations
of a change in practice from predominantly invasive ventilation to predominantly nasopharyngeal
CPAP support in infants with bronchiolitis [69]. The authors readily acknowledge that
they cannot account for potential confounders that might arise from other changes
in practice or case mix. That said, the numbers of cases observed (n = 525) and the
size of the effect: 81 % invasive ventilation falling to 12 % over 10 years with associated
significant reductions in length of stay and costs mean that we should not ignore
these data.
The increasing options and environments in which non-invasive ventilation may be useful
was highlighted by Dr Schlapbach and colleagues [70] from Brisbane Australia. High-Flow
Nasal Cannula was increasingly used in predominantly aeromedical transports over a
median distance of 205 km. The availability of HFNC was associated with a reduced
need for intubation when adjusted for PIM2 score, age, and the presence respiratory
disease. Changes in the case mix received in Brisbane do limit the interpretation
of these data but they form part of a steady trend towards increasing use of non-invasive
support in our speciality. This was reviewed by Argent and Biban [71] who asked: “What’s
new on NIV in the PICU: does everyone in respiratory failure require endotracheal
intubation”? In this piece they highlighted the very few published randomised studies
(5) and prospective cohort studies (10) which represent the best data on NIV in paediatric
critical illness currently available. One of the problems around generating evidence
is the variety of techniques, triggering mechanisms, patient interfaces as well as
options for patient selection and timing. These combine to make good research in this
area difficult. However this is no excuse for not attempting it. Argent and Biban
put it clearly: Non-invasive techniques have potential to “substantially improve the
safety of ventilator support for children, and improve access to ventilatory support
for both acute and chronic conditions. Given that respiratory problems are among the
most important cause of childhood deaths across the world, it behoves us to explore
the potential and collect the data.”
Paediatric airway
Research on the paediatric airway was a strong theme in this year’s ICM. Dr Wakeham
and colleagues [72] used the Virtual Paediatric Intensive Care database to document
the very wide variability in practice around tracheostomy use on 82 North American
paediatric intensive care units. Only 6.6 % of 13,323 admissions underwent tracheostomy
at a median length of stay of 14 days. Interquartile range was 7.4–25.7 days. Tracheostomy
rate amongst the larger contributors to the study varied from 0 to 13.4 %. The authors
right suggest that these differences are unlikely to be attributable to case mix differences
alone. This sets paediatric intensivists a serious challenge to remove unhelpful variability
on practice.
Dr Baranwal and colleagues [73] made a valuable contribution to another unknown in
paediatric airway management. They asked if 24-h dexamethasone pretreatment was superior
to 6-h pretreatment for prevention of postextubation airway obstruction in children?
They recruited 124 children between the ages of 3 months and 12 years in an elegant
randomized double-blind trial. The two groups were similar at baseline. The longer
(24 h) pre-treatment significantly reduced both the incidence (24 h pre-treatment
65 %, 43/66 vs. 6 h 83 %, 48/58; p = 0.02, relative risk 0.79, 95 % CI 0.63–0.97)
[74] and duration of post-extubation airway obstruction as assessed by a modified
croup score. The longer pre-treatment halved the re-intubation rate (0.53, 95 % CI
0.19–1.49): but the study was not powered to detect a difference in these relatively
rare events (only 14 re-intubations took place in the study). The implications of
these data are not clear since pre-treating for 24 h might mean delaying extubation
in some scenarios.
Outcome prediction
Prince et al. [75] from London examined the association of ‘weight-for-age’ and case
mix adjusted outcomes in 14,307 critically ill children. In addition to the size of
this dataset, a strength was the comparison to a healthy reference population in the
United Kingdom. Not surprisingly, critically ill children have lower weight-for-age
than do their healthly peers. This study confirmed the findings amongst adults and
in smaller paediatric studies that children with weight-for-age above the population
mean have significantly better case-mix adjusted survival. The similar ‘obesity paradox’
has been observed in adults with sepsis. Indeed the association of weight-for-age
and standardised mortality ratio follows a U-shaped distribution (as do many things
in intensive care). The accompanying editorial from Nadel and Argent points out how
much more information we need to understand the nutritional needs of our patient [76].
Zinter et al. [77] described outcomes for 10,365 paediatric cancer emergency admissions
out of 246,346 admissions to the US virtual PICU systems database. A diagnosis of
leukaemia of lymphoma ‘outside of first induction,’ still carries a ‘high-risk’ tariff
in the Paediatric Index of Mortality scoring system at ICU admission [78]. But things
may be changing. Overall survival for paediatric cancer continues to improve with
83 % 5 year survival but 38 % of paediatric cancer patients make at least one visit
to the ICU. This large series observed only a 6.8 % ICU mortality to cancer admissions
to PICU. This figure lower than many series quote for previously healthy children
with community-acquired sepsis or acute respiratory distress syndrome (ARDS) on PICU
The observed relative risk of PICU death with cancer is still highly significant at
2.9 (95 % CI 2.7–3.1), but the truth is that this reflects the overall improvement
in PICU outcomes more than cancer lagging behind. Acute myeloid leukaemia cases had
much worse outcome in multiple variant analysis. Strikingly a 50 % survival of ECMO
in both solid and haematological cancer patients was seen—though the post hematopoietic
stem cell transplant group did uniformly badly.
In summary, 2014 was characterized by two main themes: mining of large datasets to
reveal patterns in our care of which we were previously unaware, and observations
highlighting the many and varied gaps in our knowledge.