- Open Access
Cytomegalovirus infection in immunocompetent critically ill adults: literature review
© The Author(s) 2016
- Received: 27 May 2016
- Accepted: 17 October 2016
- Published: 3 November 2016
Cytomegalovirus (CMV) infection is increasingly recognized in critically ill immunocompetent patients. Some studies have demonstrated an association between CMV disease and increased mortality rates, prolonged intensive care unit and hospital length of stay, prolonged mechanical ventilation, and nosocomial infections. However, there is a considerable controversy whether such association represents a causal relationship between CMV disease and unfavorable outcomes or just a marker of the severity of the critical illness. Detection of CMV using polymerase chain reaction and CMV antigenemia is the standard diagnostic approach. CMV may have variety of clinical manifestations reflecting the involvement of different organ systems. Treatment of CMV in critical care is challenging due to diagnostic challenge and drug toxicity, and building predictive model for CMV disease in critical care setting would be promising to identify patients at risk and starting prophylactic therapy. Our objective was to broadly review the current literature on the prevalence and incidence, clinical manifestations, potential limitations of different diagnostic modalities, prognosis, and therapeutic options of CMV disease in critically ill patients.
- Critical illness
CMV disease is usually a disease acquired by adolescence and follows a benign course, while it might reactivate in patients with immune suppression and associated with high mortality and morbidity.
There is growing evidence that critically ill immunocompetent patients can develop CMV disease. Studies have described CMV infection in immunocompetent surgical, septic, burn, or trauma critically ill patients [1, 2]. Some studies have demonstrated an association between CMV disease and increased mortality rates, prolonged (ICU) and hospital length of stay, prolonged mechanical ventilation, and increased rate of nosocomial infections [2, 3]. However, there is a considerable controversy whether such association represents a causal relationship between CMV disease and unfavorable outcomes, or whether CMV disease only represents a marker for severe illness that carries poor clinical outcomes.
The objective of this review is to examine the up-to-date literature regarding CMV disease in critically ill patients. We will review the studies that assessed prevalence and incidence of CMV disease refuting the differences among them leading to different results, clinical manifestations, pathogenesis, potential limitations of different diagnostic modalities, association with outcomes, and treatment options of CMV disease in critically ill patients.
Primary CMV infection usually occurs during childhood and early adolescence and is usually asymptomatic or mild and self-limiting disease in immunocompetent patients. After the resolution of acute infection, CMV establishes latent phase mainly within leukocytes, namely mononuclear cells, and this stage is diagnosed with a positive anti-CMV IgG serology (seropositivity) and is characterized by maintenance of the viral genome in the absence of production of lytic infectious virions but with the ability of the viral genome to reactivate under certain conditions .
CMV literature focused on immunocompromized population like transplant and AIDS populations; therefore, CMV disease statuses and definitions were based on that literature which defined CMV infection as detection of CMV genetic or molecular material in the patients’ serum or body fluids, indicating active replication of the virus. CMV infection according to that literature can occur as a result of reactivation of latent CMV or reinfection with an exogenous strain. Recurrent infection in immunocompromized patients is the detection of CMV genetic or molecular material in a patient who had previous documented infection and who has not had virus detected for an interval of at least 4 weeks during active surveillance . Recurrent infection could be due to reactivation (if the detected strain is the same as the primary infecting strain) which is the most common mechanism of acquiring the disease in adulthood, especially in immunocompromized population (seropositivity of the donor or recipient has been recognized as the most likely mechanism of acquiring the disease after organ transplant; therefore, it is the recommended strategy for starting CMV prophylactic treatment across most guidelines) [5–7], or new infection (different strains) . Additionally, de novo primary infection may occur in adults but is rare. However, the distinction between the three scenarios, reactivation, new strain infection, and de novo primary infection, is difficult in practice, unless the patient is followed for a long time or the infecting source CMV genetic strains have been characterized.
CMV disease in critically ill adults will probably fall under one of these three mechanisms. Meta-analysis done by Osawa and Singh  has shown that CMV-seronegative critically ill patients rarely developed CMV infection across most studies, suggesting that reactivation is the most likely mechanism of CMV disease in this population. However, the other two mechanisms may be responsible for the infection in some cases.
CMV end-organ disease has been defined as evidence of virus replication associated with clinical manifestations due to viremia or the invasion of organs such as the lungs, bone marrow, and colon .
The scope of this article is to examine CMV disease literature in critically ill overtly immunocompetent patients.
In summary, CMV is usually acquired in childhood, and the most common mechanism of the disease in adulthood is reactivation of latent virus whether in immunocompromized or critically ill population, followed by rare incidence of recurrent new or de novo new infection.
CMV is the most common member of the herpes viruses to infect humans. Its double-stranded linear DNA duplex contains 165 genes that encode viral proteins that mimic and interact with human cellular proteins and are related to its virulence and latency.
CMV is maintained in a latent or low production state within monocytes mainly and dendritic cells (DC). They do not usually express viral genes in significant number due to the robust CD8+ cytotoxic T lymphocyte response and T memory cells. In immunocompetent individuals, asymptomatic viral shedding may be detectable in the saliva or urine; however, cell-mediated host immune responses prevent the development of overt CMV disease .
CMV genome is detected within early progenitor myeloid CD34+ cells, and monocytes and (DC) differentiation will be the only lineage that will pass the CMV genome. Viral expression is closely related to expression of immediate early (IE) genes within monocytes and (DC), but expression of infectious (lytic) virions only happens within (DC), a process regulated by major IE enhancer promoter (MIEP) which is normally under repressors closely related to other factors and cytokines within the cells .
CMV disease occurs as a result of immunosuppression associated with critical illness. A landmark study by Clari showed that CMV infection in critically ill patients was consistently associated with undetectable IFN-γ T cell responses within the first 2 days of admission to the ICU, and that viral load was inversely related to IFN-γ T cell responses . A study by Venet showed that septic patients display immune system paralysis, manifesting as reduced Th1 B cell function, increased IL-10 production (anti-inflammatory), and global lymphopenia affecting natural killer cells (NK) specifically quantitatively and most importantly qualitatively related to their interferon production, which is pivotal in attacking CMV-infected cells [10, 11]. CMV disease has also been linked to the cytokine storm associated with critical illness, specifically tumor necrosis factor alpha that activates nuclear factor κB, which enhances the replication of the dormant CMV DNA inside leukocytes, while enhancing the production of cytokines and other proteins . In animal models with bacterial sepsis, Toll-like receptor 4 signaling and secreted inflammatory cytokines all have been found to be potential triggers for reactivation of latent CMV in immunocompetent mice lungs .
Under such critical conditions observed during sepsis, burns, trauma, or major surgery, the CMV genes are expressed and viral replication is initiated [14, 15], invading cells in the lung, kidney, liver, bone marrow, and intestine , and exerts direct cytotoxic effects.
In addition, when CMV starts to replicate within leukocytes, it has inherent escape mechanisms from the host immune system, and the CMV unique short (US 2, 3, 6, 10, and 11) proteins down-regulate the surface expression levels of HLA-1 and HLA-2 on leukocytes that mark these cells to be attacked by CD8+ T lymphocytes .
Other CMV genes encode structural proteins, such as the matrix protein pp65, that is involved in down-regulation of HLA-1 leukocytes surface markers and used as a target of antigen detection immune assays .
In addition, virulence is also related to boosting immune response causing more tissue damage, and this is due to homology of some of CMV proteins to inflammatory cytokines as human tumor necrosis factor alpha receptor and CXC chemokine such as interleukin-8 .
Animal model studies suggested that the outcome after reactivation might be determined by the viral load of the original infection, which correlates with the number of CMV-specific T memory cells, i.e., immunological responses (higher IgG levels), CD-8 cytotoxic cells, and hence inflated immune response during reactivation, and this might be a promising marker to predict the outcome in patients with reactivation [13, 19].
In addition, the virus has an immunosuppressive effect via its modulatory effect on cytokine production, which may enhance the susceptibility to secondary bacterial and fungal infections. CMV also has a direct suppressive effect on the bone marrow.
Some CMV proteins are also related to antiviral mechanisms, including the viral DNA polymerase UL54 and UL97, which encodes a protein phosphotransferase enzyme that phosphorylates the antiviral drug ganciclovir, an essential activation step required for its inhibitory effect on CMV DNA replication [20–22].
In summary, CMV has a complicated genome that allows the virus to go into latent state and facilitate its evasion from immune response and homology to human chemokines, all of which is involved in its pathogenesis.
Risk factors for CMV disease in critical care setting and their strength of association
Strength of association
Strong association 
No evidence 
Inconsistent data 
Weak evidence 
Disease severity scores
Stress (catecholamines surge)
Weak association 
Blood transfusion, especially in the first 24 h of critical illness, has been shown to be an important risk factor for CMV disease , which has been linked to the timing and the amount of blood transfused, although the mechanisms involved are unclear. Contamination of transfused blood with CMV-infected leukocytes may be responsible for some cases, especially in cases where the blood bank does not perform leukocyte depletion pre-transfusion [32, 33], even though leukocyte-depleted blood is not completely clear of leukocytes; hence, its use does not completely eliminate the risk of CMV infection. In addition, the immunomodulatory effect of transfusion may also predispose patients to CMV reactivation.
In summary, mechanical ventilation and blood transfusion in the ICU have been associated with the development of CMV disease, but no association with severity scores was found.
Summary of studies assessing CMV disease in ICU patients
Year of publication
Method and specimen
Frequency of monitoring
Domart et al. 
Prospective, single center
Mediastinitis, post-cardiac surgery
Patients in whom viral cultures could be done within 10 days of surgical debridement
Serology for CMV IgG
Viral culture blood and urine. Positive cases: positive CMV culture
Within first 10 days of debridement then every 3 weeks
Docke et al. 
1—CMV culture in blood. 2—Immunocytological detection of CMV antigens in blood. 3—PCR amplification in blood. 4—TNF and interleukin six assays. Positive cases: any positive PCR or culture or antigen detection
Stephan et al. 
Prospective, single center
Blood and BAL
Papazian et al. 
Patients with ventilator-associated pneumonia
Autopsies and open lung biopsy
22.4 ± 8.8 days after admission to the intensive care unit
Kutza et al. 
Prospective, single center
Septic patients with positive CMV IgG serology
CMV IgG serology
CMV DNA PCR in blood
Serum cytokines: TNF alpha, IL-1b, and IL-6 measured by ELISAs. Positive cases: positive CMV antigenemia and/or CMV DNA PCR in blood
1—Blood samples were collected on day 1 of sepsis, then twice weekly during ICU stay, then once weekly after release from the ICU, until recovery or death
Cook et al. 
Prospective, case–control single center
Postoperative general SICU. Septic patients with no identifiable bacterial or fungal source. Positive BAL or blood or sputum CMV culture
CMV and HSV viral culture from BAL, blood or sputum. All cases included had positive CMV culture
CMV was cultured in diploid human foreskin fibroblast culture for 6 weeks
Plasma was evaluated by shell vial technique to IE antigen at 24 h. HSV cultures
Heininger et al. 
Prospective, single center
Patients with SAPS II >40 and positive serology
CMV DNA PCR and/or viral culture
Leukocytes, plasma, and lower respiratory tract secretions
Positive cases: positive PCR
Razonable et al. 
CMV and HHV-6 and HHV-7 DNA by PCR in blood
Positive cases: positive PCR
4th days after ICU admission
Cook et al. 
Patients staying for 5 days or more in SICU
Serology in blood
CMV and HSV cultures in blood and sputum
Positive cases: positive CMV culture
Once weekly until discharge from SICU
Jaber et al. 
Retrospective, matched case–control, single center
Medical, surgical, and transplant unit
Positive cases: positive CMV antigenemia
1—Clinical judgment. 2—The diagnosis of CMV antigenemia was defined by a positive CMV pp65 antigenemia assay result
von Muller et al. 
Prospective observational single center
Anesthesiological intensive care unit. Non-immunocompromized CMV IgG-seropositive patients with septic shock with ICU stay for at least 7 days
Blood. CMV reactive T helper 1 lymphocytes
Positive cases: positive CMV antigenemia
Twice during 1st week then weekly until discharge
Positive cases: positive antigenemia
Ziemann et al. 
Retrospective, single center
Patients treated for at least 14 days in ICU
CMV DNA PCR
Blood. Positive cases: at least two positive samples
Based on the decision of the treating team
Limaye et al. 
Mixed ICU, positive anti-CMV IgG
Positive cases: positive blood CMV PCR
Thrice weekly until death or discharge
CMV disease was significantly associated with death or continued hospitalization after 30 days
Chiche et al. 
Prospective, single center
Ventilated patients for at least 2 days
CMV serology and antigenemia. CMV culture on BAL if VAP suspected, antigenemia on the day of BAL. Other organ Virologic studies based on clinical suspicion. Positive cases: positive antigenemia or BAL CMV culture
Within 48 h of ICU admission and once weekly until discharge
Chilet et al. 
CMV-seropositive, ICU stay longer than 5 days
Tracheal aspirate and plasma
Plasma tumor necrosis factor alpha
Once a week
Smith et al. 
Prospective single center
Mechanically ventilated patients
Respiratory secretions CMV PCR
CMV IgG serology
PCR in blood
The overall mortality rate associated with active CMV infection was 1.93 times higher than that without CMV infection
Bordes et al. 
Severe burn unit
Burn surface area more than 15%
First sample on admission then one to twice weekly until discharge
After 7 days of admission if intensivists suspected CMV
Heininger et al. 
Prospective, observational, single center
Severe sepsis, positive anti-CMV IgG
Viral culture from tracheal secretions. Qualitative CMV DNA PCR from leukocytes, plasma, tracheal secretions
Quantitative CMV DNA PCR from positive plasma and tracheal secretions
HSV DNA PCR from tracheal secretions
Positive cases: positive PCR from any source
Once weekly until discharge from hospital or death
De Vlieger et al. 
Prospective, MICU and SICU, single center
(Van Den Berge study)
Admitted for at least 3 days in ICU
Mechanically ventilated in SICU
MICU regardless of mechanical ventilation
CMV IgG serology
Within first 2 days of admission
Chiche et al. 
Within 48 h of admission then once weekly until discharge
Coisel et al. 
Prospective single center
Mechanically ventilated suspected of having pneumonia
10% were previously immunocompromized
1—Serology (IgM and IgG) for cytomegalovirus (CMV) and herpes simplex (HSV) using (ELISA)
Blood PCR was not routinely done
2—CMV antigen detection in blood
3—CMV and HSV DNA PCR on BAL
Positive cases: positive CMV PCR in BAL or positive antigenemia or positive IgM
Within 12 h of pneumonia diagnosis
Clari et al. 
Prospective single center
Mechanically ventilated patients
CMV serology at baseline
CMV-specific interferon-γ-producing CD8, CD4 T lymphocytes
CMV PCR in blood and tracheal aspirate
2–8 samples per patient were analyzed for T lymphocytes subset and CMV PCR
Ishioka et al. 
CMV PP65 antigenemia
On admission, day 7 and day 14
Respiratory and geriatric ICU
Walton et al. 
MICU and SICU
Critically ill septic and non-septic patients versus healthy volunteers
Starting within 24–72 h of admission
Significant increase in 90 days mortality in CMV-positive patients compared to CMV-negative ones
Ong et al. 
Multicenter prospective cohort
Mixed ICU (tertiary care referral centers)
ARDS patients on mechanical ventilation for at least 4 days
CMV IgG if positive CMV PCR in blood
Weekly for maximum 30 days
Frantzeskaki et al. 
Prospective, observational two centers
Mixed ICU, mechanically ventilated, seropositive anti-CMV IgG
CMV DNA PCR
At admission, then weekly until day 28 or discharge from ICU or death
Ong et al. 
Multicenter prospective cohort
Mixed ICU (tertiary care referral centers)
ARDS patients on mechanical ventilation for at least 4 days
CMV IgG between days 5 and 14 of admission
If positive CMV DNA PCR in plasma
CMV DNA PCR on day 14 or ICU discharge date (whichever first) then weekly
Variation in diagnostic methods used including selecting different specimens, some used serum, while others used urine, saliva, or bronchoalveolar lavage samples, tests were performed at different points in the ICU stay and testing time and frequency was not standardized in all studies as some left it up to the judgment of the treating team. Recent studies showed that CMV disease typically occurs within the first 2 weeks of critical illness. A study performed by Kalil and Florescu  showed that the diagnosis rate of CMV infection increased significantly (from 1 to 21%) when patients who spent five or more days in the ICU were screened, pointing to a threshold in timing for the window to develop CMV in critical care setting. In a recent systematic review that included 13 studies (nine prospective and four retrospective), the incidence of CMV disease in critically ill patients, defined as the detection of antigenemia, DNAemia, or positive viral culture from blood samples with or without other clinical specimens, ranged from 0 to 36%. Notably, the reported incidence of the disease was much higher in studies that screened the patients weekly than those that screened only once within the first 4 days of admission to the ICU (6–33 vs. 0.8–1.2%), indicating that the disease happens frequently beyond the first 4 days post-admission. Among the studies using PCR detection (which is the most sensitive diagnostic test for CMV), the mean and median times of detection ranged from 4 to 12 days after ICU admission .
In summary, the incidence and demographics of CMV disease in the ICU were highly variable across studies, as a result of variation in study design and definition of the disease.
Identification of CMV disease in immunocompetent patients is complicated by its non-specific symptoms, multiorgan involvement, and the fact that its clinical manifestations converge with those of the critical illness. Heininger et al.  reported that serious organ involvement with CMV disease could occur in up to 10% of cases. A systematic review of studies reporting the clinical manifestations of severe CMV disease in immunocompetent ICU patients found that the gastrointestinal tract (hepatitis, gastroenteritis, duodenitis, enteritis, colitis, proctitis) is to be the most common, followed by central nervous system (encephalitis, myelitis, encephalomyelitis, meningitis, and meningioradiculopathy), and hematological system (hemolytic anemia, thrombocytopenia, disseminated intravascular coagulation, and pancytopenia) . Other organs, such as the lungs and eyes, were rarely involved. CMV myocarditis, a recognized entity in immunocompromized patients, was not documented.
Vascular manifestations have been reported such as portal or femoropopliteal vascular thrombosis and pulmonary embolism that is thought to be related to vascular endothelial cells damage .
CMV pneumonia is a well-known clinical manifestation of CMV disease in immunocompromized patients. However, lung involvement may be less recognizable in immunocompetent critically ill patients especially if they were intubated for other reasons, but few studies demonstrated that the prevalence of this disease in immunocompetent critically ill patients may be as high as 50% in patients with ventilator-associated pneumonia or ICU-acquired acute respiratory distress syndrome . However, CMV disease is not necessarily the pathologic cause of ICU-acquired pneumonia and discrimination between a causal or associative relationship is challenging because the diagnosis depends on quality of the respiratory sample, pathologist skills, and variation of the diagnostic test. As an example of this variation, Coisel et al.  studied patients mechanically ventilated who are seropositive for CMV and found significant increased mortality in CMV-positive group; in addition, the diagnostic yield of BAL CMV PCR was 73% in comparison with the detection of CMV antigenemia which was 46%. Heininger et al.  studied patients admitted with severe sepsis of whom 31% developed ICU-acquired pneumonia and have shown slightly different diagnostic yield of tracheal aspirate CMV PCR of 70 versus 62% using blood CMV PCR. In a previous study, the same authors included only CMV surgical seropositive patients and found equal diagnostic yield between BAL PCR and blood PCR. Chiche showed different results, as the diagnostic yield of BAL was 26% (using CMV shell vial culture) compared to 85% using CMV antigenemia . Papazian et al.  studied patients with ventilator-associated pneumonia and made histologic diagnosis of CMV pneumonia in 29% of the patients. The study found that BAL shell vial culture had a sensitivity/specificity of 53, 92% in comparison with histologic diagnosis. Ong et al.  studied immunocompetent patients with ARDS and found a CMV reactivation incidence of 27%, which was associated with significant increase in ICU mortality.
In general, CMV affects multiple organs at varying rates and severity. ICU-acquired pneumonia, especially VAP, appears to be a common CMV-associated disease that draw attention of ICU physicians and researchers.
Diagnostic methods of CMV, advantages, and disadvantages
Might be used for screening for latent CMV infection
Low sensitivity and specificity for active infection
CMV PCR assays
High sensitivity and specificity and considered gold standard, quick easy to perform, gives information of viral load, can be used for wide variety of samples
Better to be performed on whole blood, qualitative might be so sensitive and detect “innocent viral shedding” quantitative might be superior
CMV antigen assays
Quick and easy to perform, has comparable sensitivity and specificity to PCR
Might be inferior to PCR in case of leukopenia
Highly specific, can be performed on wide variety of samples
Time-consuming, low sensitivity
Highly specific, confirm CMV disease and pathogenicity and invasiveness
Invasive, low sensitivity, liable to sampling error, needs skilled pathologist and so operator dependent
Testing for CMV for the diagnosis of CMV disease should be based on predictors of CMV disease in addition to signs and other laboratory investigations directing toward viral origin of the current clinical status as indicators of liver and gastrointestinal involvement .
The most commonly used tests to measure CMV-specific IgM or IgG levels are the enzyme-linked immune assays and anticomplement immunofluorescence assays. The presence of IgM antibodies indicates an acute CMV infection and can last for 4–6 months . Because IgG seropositivity is long lasting, the measurement of IgG antibodies is not a reliable method to diagnose CMV infection. Critically ill patients may develop immune paralysis (anergy) that limits their ability to mount immune responses; therefore, it is important to note that negative serology does not exclude CMV infection. The main utility of serology testing at present is to screen for the potential of latent CMV reactivation .
Due to its high sensitivity and rapid turnaround time, PCR is considered the gold standard method of diagnosing CMV infection . Both qualitative and quantitative (viral load) PCR assays are available. However, quantitative tests are preferred as it quantifies viral load, which has prognostic importance . Whole blood testing is more sensitive than plasma testing because it enables the detection of cell-free and intracellular viruses .
CMV antigen assays
Antigen assays using immunofluorescent antibodies are quick and easy to perform and can be used to detect the CMV pp65 antigen in leukocytes . In one study that compared PCR to antigen detection to diagnose CMV infection in critically ill patients, the antigen detection method was unable to identify 5 of the 11 CMV-positive patients detected by PCR. In addition, the diagnostic time of the PCR method was ahead than that of the antigen detection method . However, meta-analyses performed by Osawa and Kalil revealed that the sensitivities and specificities of antigen detection methods are comparable to those of PCR detection methods [8, 44]. The only potential limitation of antigen assays is their low sensitivity in patients with leukopenia .
Culture-based assays are not clinically used due to their low sensitivity and delay in receiving the results . In a meta-analysis by Osawa and Singh , detection rate of CMV infection among studies using culture was 0–20% of CMV infections, whereas it was 0–32% using PCR and antigen assays. In a meta-analysis performed by Kalil and Florescu , the PCR/antigen detection methods achieved a CMV detection rate of 20%, whereas that the culture method was only 12%.
Histopathology is the most specific method for diagnosing CMV, especially by detecting organ-specific manifestations related to CMV. However, this method is invasive and has a limited sensitivity that depends on the sampling site and pathologist’s skills.
We suggest using CMV PCR or CMV antigen detection assays to diagnose CMV disease not earlier than 3 days and up to 2 weeks after the onset of critical illness, especially when the pretest probability of the disease is high [1, 8].
Studies addressing association of CMV disease and outcome in critically ill patients revealed inconsistent results.
A systematic review by Osawa and Singh  concluded that CMV disease in critically ill patients was associated with hepatic, respiratory, and renal dysfunctions; prolonged ICU stay, prolonged mechanical ventilation, increased incidence of bacterial and fungal infections, and increased mortality.
In a landmark prospective cohort study by Limaye et al.  of 120 CMV-seropositive critically ill patients, he found significant association between CMV disease and 30-day mortality and increased ICU length of stay. Notably high levels of viremia were associated with increased mortality and morbidity rates, as well as prolonged lengths of stay in the hospital, the latter of which increased with each log increase in the number of CMV copies (>1000 copies/ml up to 28 days of hospital length of stay). In addition, he observed higher rate of hospitalization beyond 30 days in CMV-infected patients indicating a long-term effect of CMV disease that persists beyond ICU discharge and even after clearance of the viremia. Of note, the study could not identify a relationship between the severity of critical illness (APACHE) and the risk of CMV disease, probably refuting the idea that CMV disease might be a marker of the underlying disease severity.
Regarding specific ICU population, a recent observational prospective study that included 86 CMV-seropositive septic patients found an association between CMV disease and longer ICU stay, prolonged mechanical ventilation, and impaired pulmonary gas exchange . Coisel examined critically ill patients with ventilator-associated pneumonia and found a significant increase in ICU and 60-day mortality (50% CMV group vs. 20% in control group), longer ICU stay, and less ventilator-free days in patient with CMV disease .
On the other hand, a prospective observational study of 80 mechanically ventilated patients that were seropositive for CMV found no association between CMV disease and 28-day mortality, ICU mortality, ICU length of stay, or duration of mechanical ventilation, although the SOFA score was significantly higher in CMV-infected group . Similar findings were also reported in a study that used CMV pp65 antigenemia as evidence of CMV disease .
These inconsistent findings are probably related to differences of studied populations, retrospective nature of several studies, differences in diagnostic tests, the unmeasured confounders; therefore, it is difficult to establish proved causality based on the existing studies, necessitating future studies with strict methodology in relation to blinding, studied population, testing timing, and method of testing preferably with tissue studies to clarify the causal relation between CMV disease and ICU mortality and morbidity.
In conclusion, although the current literature is inconsistent, there is strong evidence suggesting an association between CMV disease and higher morbidity and mortality in the ICU.
Treatment and prevention
The central controversy of CMV disease in critically ill patients is whether to treat or not and whether treatment makes a difference to the patient’s outcomes or not.
Treatment of CMV disease as any other disease should be based on a benefit/risk ratio, taking into consideration all other factors associated with the diagnostic process and treatment such as invasiveness of the diagnostic method, side effects of anti-CMV medications which might be serious especially in critical ill patients, and risk of emergence of CMV resistance to the medications . There is an agreement regarding treatment of established CMV disease and prophylactic treatment for certain populations of immunocompromized patients as is the case in organ transplant recipients, for whom the guidelines are well established [7, 44].
Similarly, the curative treatment of clinically confirmed CMV disease (detection of significant CMV viral load by PCR or antigen detection based on diagnostic method threshold, in addition to clinical condition attributed to CMV and ruling out other potential causes) in immunocompetent critically ill patients has been recommended, and support for such approach comes from studies like the one by Eddleston et al.  that examined the outcome of previously reported 34 cases of severe CMV disease in immunocompetent patients. It was found that multiorgan involvement was associated with poor outcome compared with isolated central nervous system involvement. Among patients with multiorgan involvement, 5 of 6 patients who received treatment of either ganciclovir or foscarnet recovered, while only 4 of 18 patients who did not receive either one of the above-mentioned drugs survived. The outcome noticed in this review pointed toward a potential benefit of antiviral treatment in this group of patients.
However, the benefit of preemptive treatment of subclinical detected viral replication with no proven direct organ pathology attributed to CMV, and the prophylactic treatment in immunocompetent patients deemed to be at risk of developing CMV disease is much less clear . It is plausible to assume that the best strategy to handle CMV disease in the ICU is to prevent reactivation in seropositive patients as these are at high risk of developing the disease. At present randomized clinical trials examining the safety and efficacy of preventative strategies in critically ill patients are still going on.
Anti-CMV medications and common associated side effects
Mechanism of action
Common side effects
Competitively inhibits the binding of deoxyguanosine triphosphate to DNA polymerase resulting in inhibition of viral DNA synthesis
Thrombocytopenia, leukopenia, increased creatinine, fever, vomiting, diarrhea
Converted to ganciclovir in the body, much higher bioavailability of ganciclovir compared to oral ganciclovir
Non-competitive inhibitor of many viral RNA and DNA polymerases
Electrolyte abnormalities, fever, vomiting, diarrhea, anemia, granulocytopenia, renal insufficiency, cardiotoxicity, central nervous system toxicity, hepatic toxicity
Suppresses CMV replication by selective inhibition of viral DNA synthesis
Fever, alopecia, rash, ocular, renal, and gastrointestinal toxicity, cough, dyspnea
The other challenge is the detection of CMV, the current used methods, namely CMV PCR and CMV antigenemia, are highly accurate regarding sensitivity and specificity, but the challenge is that detection of CMV is highly sensitive to the timing and frequency of testing which is related to the window of emergence of CMV infection within the first 2 weeks of critical illness but not earlier than 3 days [8, 44]; secondly, it is unclear whether some cases represent innocent viral DNA or antigen shedding not necessarily related to tissue invasiveness and thus does not require therapy, which stress against random screening for CMV .
Papazian recommended in his recent review that treatment for evident CMV replication (blood or BAL significant viral load or antigen titer) is not indicated unless it is associated with lung infiltrates and at least two factors (prolonged mechanical ventilation, absence of bacterial agent, leukopenia, hemophagocytosis, high liver enzymes, hyperbilirubinemia, fever, or diarrhea) which if found points for CMV being a pathogen invading multiple organs and not only a bystander or innocent viral shedding .
So far no definite criterion is available to guide which critically ill patients should be screened for CMV disease. According to available literature certain populations as septic, burns, trauma, ICU-acquired pneumonia especially mechanically ventilated patients have been found at high risk of developing CMV disease across multiple studies [26, 41, 47]. Many authors recommended in these populations especially in case of prolonged mechanical ventilation with evidence of pneumonia, unexplained liver derangement or fever or unexplained digestive tract pathology, to screen for CMV disease and in case of CMV detection using PCR or antigenemia detection methods; then, treatment should be taken as benefit/risk ratio [37, 41, 48] (Table 4).
Regarding preemptive treatment, immunological assessment of IFN-γ produced by CMV-specific CD8+ T cells and NK cell function as mentioned in virulence section might be a strong trigger to start preemptive treatment for detected CMV, because there is evidence that impaired CMV-specific CD8+ T cells IFN-γ production prior to CMV reactivation predicts poor outcome, which favors treatment. This has not been applied clinically so far but might be promising in the future for challenging cases .
CMV might acquire resistance to the limited number of medications that are currently available; hence, their prophylactic use should be confined to confirmed cases or preemptive treatment until clear risk assessment tools for prophylactic therapy are developed in high-risk groups in the ICU .
There are many uncertainties about CMV disease in the critically ill patients. First, while identification of the virus is common in critically ill patients, the actual rate of CMV as a disease in critically ill patients is unclear. Second, the importance of CMV detection in critically ill patients remains questionable, especially in the absence of histologic evidence of infection. On the other hand, the existing evidence is strong regarding the association between CMV detection and increased mortality and morbidity rates in ICU settings.
Still there are no high-quality data to guide the decision regarding when to treat detected CMV in ICU patients if there is no definite clinical confirmation of CMV disease (preemptive treatment), and there is no risk assessment tool to guide prophylactic therapy in ICU setting.
There is a need for well-conducted studies to develop risk assessment tool of CMV disease in critically ill patients, to estimate the real burden of CMV disease, and to examine the effect of prophylactic and preemptive treatment on morbidity and mortality. Potential answers to these questions will hopefully be answered by currently ongoing trials related to CMV in critical care. “Cytomegalovirus Control in Critical Care trial” (NCT01503918) is addressing the safety and success rate regarding preventing reactivation of latent cytomegalovirus infection in critically ill patients when treated with one of two different antiviral regimens: “Valaciclovir/Aciclovir or not.” “Study of Ganciclovir/Valganciclovir for Prevention of Cytomegalovirus Reactivation in Acute Injury of the Lung and Respiratory Failure” (NCT01335932) is addressing whether administration of ganciclovir in CMV-seropositive patients reduces serum IL-6 levels in immunocompetent adults with severe sepsis or trauma-associated respiratory failure based on the hypothesis that pulmonary and systemic CMV reactivation amplifies both lung and systemic inflammation mediated through specific cytokines. “Preemptive Treatment of Herpesviridae trial” (NCT02152358) is addressing whether preemptive treatment by ganciclovir (for positive CMV viremia) or aciclovir (for positive HSV oropharyngeal PCR) is able to increase the number of ventilator-free days at day 60 in ICU patients with prolonged mechanical ventilation having evident viral replication.
AA carried out the literature review of the studies addressing CMV prevalence and participated in drafting the manuscript. FA participated in reviewing the literature of clinical manifestations, risk factors and treatment and prevention sections and participated in drafting the manuscript. SS participated in reviewing literature addressing CMV diagnosis. YA and WA participated in drafting the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
The authors declare that they have not received any funding from any source.
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