key: cord-0006754-eevouvfq
authors: Lalueza, Antonio; Folgueira, Dolores; Muñoz-Gallego, Irene; Trujillo, Hernando; Laureiro, Jaime; Hernández-Jiménez, Pilar; Moral-Jiménez, Noelia; Castillo, Cristina; Ayuso, Blanca; Díaz-Pedroche, Carmen; Torres, Marta; Arrieta, Estibaliz; Arévalo-Cañas, Coral; Madrid, Olaya; Lumbreras, Carlos
title: Influence of viral load in the outcome of hospitalized patients with influenza virus infection
date: 2019-02-28
journal: Eur J Clin Microbiol Infect Dis
DOI: 10.1007/s10096-019-03514-1
sha: 12a2d60b1d2fbe08e499962d5c6c5bde0bdfbabf
doc_id: 6754
cord_uid: eevouvfq

The role of viral load in the outcome of patients requiring hospital admission due to influenza is not well established. We aim to assess if there is an association between the viral load and the outcome in hospitalized patients with a confirmed influenza virus infection. A retrospective observational study including all adult patients who were hospitalized in our center with a confirmed influenza virus infection from January to May 2016. Viral load was measured by real-time reverse-transcriptase–polymerase chain reaction (rRT-PCR) cycle threshold (Ct) value on upper respiratory tract samples. Its value was categorized into three groups (low Ct, ≤ 20; intermediate Ct, > 20–30; and high Ct, > 30). Two hundred thirty-nine patients were included. Influenza A/H1N1pdm09 was isolated in 207 cases (86.6%). The mean Ct value was 26.69 ± 5.81. The viral load was higher in the unvaccinated group when compared with the vaccinated patients (Ct 25.17 ± 5.55 vs. 27.58 ± 4.97, p = 0.004). Only 27 patients (11.29%) presented a high viral load. Patients with a high viral load more often showed abnormal findings on chest X-ray (p = 0.015) and lymphopenia (p = 0.097). By contrast, there were no differences between the three groups (according to viral load), in associated pneumonia, respiratory failure, need for mechanical ventilation, sepsis, or in-hospital mortality. Our findings suggest that in patients admitted to the hospital with confirmed influenza virus infection (mostly A/H1N1pdm09), a high viral load is associated with a higher presence of abnormal findings on chest X-ray but not with a significant worse prognosis. In these cases, standardized quantitative PCR could be useful.

We recently reported the potential role of severe hematological abnormalities as prognostic markers in hospitalized patients with influenza virus infection [1] . However, the role of viral load in the clinical outcome and/or in the appearance of some severe hematological abnormalities was not evaluated.

Previous studies have hypothesized that viral load of some respiratory viruses correlate with disease severity [2] , but this association is not clear in the case of influenza virus infection [3, 4] . On the contrary, other authors have found that high influenza viral load is associated with a longer duration of hospital stay in adults with viral acute respiratory illness [5] . On this basis, we decided to analyze the role of influenza viral load in the outcome of the patients included in the same cohort of our previous paper [1] .

The aim of the present study was to assess if there is an association between viral load measured by real-time reversetranscriptase-polymerase chain reaction (rRT-PCR) cycle threshold (Ct) value on upper respiratory tract samples and the outcome in patients who were admitted to the hospital with a confirmed influenza virus infection.

This is a retrospective observational study including all adult patients with a diagnosis of influenza virus infection hospitalized from January to May 2016 in a 1300-bed tertiary teaching hospital in Madrid, Spain. The study protocol was approved by the University Hospital B12 de Octubre^Review Board.

A case was defined by a positive result of a rRT-PCR assay performed at the local laboratory on respiratory samples (nasopharyngeal swabs (flocked swabs in UTM™ viral transport medium, Copan, Brescia, Italy)) from adult patients with respiratory symptoms suggestive of influenza. For the molecular diagnosis, RNA was extracted from 200 μl of the specimen using NucliSENS®easyMAG instrument (bioMérieux Diagnostics, Marcy l'Etoile, France) and eluted in 50 μl. Five microliters of the elution was used to perform each RT-PCR. The modular duplex rRT-PCR for influenza A/influenza B detection (Influenza A/B r-gene™, bioMérieux) was run in the LightCycler 480 instrument (Roche) [6] . This test has 45 cycles of amplification and a Ct > 40 is considered below the limit of detection of the technique according to the instructions of the manufacturer.

All samples testing positive for influenza A were sub-typed using a non-commercial rRT-PCR assay as previously described [7] to detect specific regions of subtypes H1 and H3 hemagglutinin from seasonal viruses. For the detection of influenza A (H1N1) pdm09 subtype, commercially available primers and probe (RealTime ready infA/H1N1 Detection set, Roche) [8] were used.

The real-time PCR cycle threshold (Ct) value represents the first PCR cycle in which the fluorescent signal for the target is greater than the minimal detection level [9, 10] .

Respiratory failure was defined as the need for mechanical ventilation, either non-invasive positive pressure ventilation or invasive mechanical ventilation, including those patients who had a clinical indication for ventilatory support but for some reason were finally not ventilated.

Sepsis, septic shock, and organ dysfunction were defined according to the terms proposed recently by the Third International Consensus Definitions for Sepsis and Septic Shock [11] , including the SOFA score and the qSOFA score. Acute respiratory distress syndrome (ARDS) was defined according to the American-European Consensus Conference on ARDS [12, 13] .

Poor outcome was defined as a composite endpoint in which at least one of the following criteria had to be fulfilled: (a) respiratory failure, (b) SOFA ≥ 2, or (c) death (related or not related to influenza infection).

Hematological abnormalities secondary to influenza virus infection were defined as cytopenias that were in the range of the HLH-04 updated criteria proposed by the Histiocyte Society [14] for the diagnosis of hematophagocytic syndrome (HPS) (hemoglobin ≤ 9 g/dl, platelets < 100,000/μl, neutrophils < 1000/μl). Since lymphopenia is not included in the HLH-04 criteria, we defined it as a total count less than 1000 lymphocytes/μl.

A descriptive analysis of patients was initially performed according to Ct value (viral load). Descriptive analysis was performed using means (± SD) or medians with interquartile ranges (IQR). Initially, the Ct value was categorized into three groups (low Ct, ≤ 20; intermediate Ct, > 20-30; and high Ct, > 30) and the Kruskal-Wallis test was used to explore differences across these groups. Later, we compared patients who had a high viral load (Ct ≤ 20) with those who did not have a high viral load (Ct > 20). Student's t test for independent samples was used to compare continuous variables. The Mann-Whitney U test was used to compare continuous variables with a non-normal distribution, and the Fisher exact test to compare proportions. Receiver operating characteristic (ROC) curve analysis was conducted to establish the best viral load that determined the presence of the composite endpoint or respiratory failure, and corresponding sensitivity and specificity were reported. The area under the ROC curve (AUC) with 95% confidence interval (CI) was also calculated. Statistical analysis was performed with IBM SPSS Statistics for Windows, Version 19.0 (Armonk, NY: IBM Corp and SAS/STAT 10.1; SAS Institute Inc., Cary, NC).

We included 239 hospitalized patients with confirmed influenza virus infection. The mean Ct value was 26.69 ± 5.81. Twenty-seven patients (11.29%) had a low Ct, 138 cases (57.74%) had an intermediate Ct, and 74 patients (30.96%) had a high Ct. Two hundred seven cases were positive for influenza A (86.6%), all of them by the H1N1pdm09 subtype, while the other 32 cases were positive for influenza B. First of all, we want to point out that most of the previous published information of the influence of viral load of H1N1pdm09 subtype on the prognosis of patients is prior to the introduction of this strain in the vaccine [4, [15] [16] [17] . In fact, only Spencer's work [18] includes patients after the modification of the vaccine, but focuses on factors associated with low Ct and not in the evolution or development of complications. Therefore, to the best of our knowledge, this is the first work that analyzes the influence of influenza A H1N1pdm09 viral load on the prognosis of patients after the inclusion of the strain in the vaccine.

Patient's demographic and clinical characteristics, as well as management of the infection, are shown in Table 1 . Ninety-six patients were previously vaccinated. Viral load was higher in the unvaccinated group when compared with that of the vaccinated patients (Ct 25.17 ± 5.55 vs. 27.58 ± 4.97, p = 0.004). Practically all of the patients were treated with oseltamivir (96.7%) in the early phase of the infection. As our work included a very homogeneous population, it is unlikely that the presence or absence of antiviral treatment has influenced the clinical course of the disease.

Very little is known about the potential influence of viral load of influenza virus on the development of cytopenias. In fact, the scarce existing information indicates that viral load of different respiratory viruses does not influence the white blood cell count in patients with an acute respiratory illness [5] .

Laboratory parameters of our study are presented in Table 2 . The mean Ct was 26.52 ± 6.45 in the group with 

As shown in Table 3 , we observed that pulmonary radiological findings are more frequently found in patients with higher viral loads as previously described by other authors [17, 19, 20] . Twenty-eight patients (11.7%) developed pneumonia in the course of admission (p = 0.45 between groups). Eight patients with pneumonia were vaccinated (28.5%) vs. 41.7% in the group without pneumonia (p = 0.29). Respiratory failure was present in 7.9% of patients. We observed a slightly higher percentage of this item in those with the higher viral load without reaching statistical significance. Results are expressed as mean ± standard deviation or median with interquartile range (IQR) or as absolute value (percentage). NA not available. ¶ Upper limit of LDH in the local laboratory is 225 mg/dl. *According to the HLH-04 criteria. a Across all Ct value groups. b Between high viral load group (Ct ≤ 20) and other groups combined. Bold font means significant differences between variables

Poor outcome was present in 21.4% of patients with no differences between groups according to the Ct value (p = 0.67). The mean Ct was 26.58 ± 6.06 in the group with poor outcome vs. 26.81 ± 5.81 in the good prognosis group (p = 0.82). We also analyzed the association between the viral load and the need for ICU admission, without finding significant differences between groups. To the extent of our knowledge, a high viral load has not been previously analyzed as a predisposing factor for septic shock, use of vasoactive drugs, or SOFA score ≥ 2. We did not find differences in these regards, although we observed a trend to a more frequent presence of each of these items in patients with higher viral loads, as well as with mortality and the composite endpoint. We analyzed with ROC curves if the viral load had any influence on the development of ventilatory failure or the composite endpoint, without finding statistically significant relationships (Fig. 1) . Overall inhospital mortality was 5.2% and influenza-related mortality was 4.6%, without differences between groups (p = 0.63).

As shown in Table 4 , there were no significant differences in the length of hospitalization according to viral load. Likewise, we did observe a slightly longer duration of admission in the subgroup of patients with pneumonia or ventilatory failure and higher viral loads. To the best of our knowledge, there is only one previous published study in patients with influenza infection that has analyzed the duration of hospitalization based on viral load [5] . However, this study was developed prior to the H1N1 influenza pandemic of 2009 and none of the patients were treated with neuraminidase inhibitors.

A limitation of our study is that all patients included were hospitalized, which obviously correspond to greater disease severity, and it is possible that the difference in viral load is less striking in this group than if we had compared it with patients who did not require hospital admission. However, previous reports have described that there is no difference between viral loads of admitted patients compared with those in the ambulatory setting [3] .

Another potential limitation of the study is that the commercially available diagnostic methods for the detection of influenza virus are qualitative techniques that do not allow the performance of a viral load in a strict sense. However, the Ct value is routinely used in virology laboratories as a semi-quantitative measure of the amount of virus present in samples as has been shown in previous studies [21] [22] [23] [24] . Our data would support the use of quantitative PCR for the management of hospitalized patients with influenza virus infection in order to discriminate the presence of abnormal findings on chest X-ray or lymphopenia. However, the currently available viral load assays present several technical problems, including the lack of an international standard, the lack of consensus on specimen types, and the influence of the timing of specimen collection in viral load results [25] . In our opinion, it would be useful to have a standardized quantitative PCR as a diagnostic tool to evaluate these hospitalized patients.

In conclusion, the findings of this study suggest that in hospitalized patients with influenza virus infection (mostly A/H1N1pdm09) receiving oseltamivir therapy, a high viral load is associated with some minor radiological changes but not with a significantly worse prognosis. 

Conflict of interest The authors declare that they have no conflicts of interest.

Ethical approval The study protocol was approved by the University Hospital B12 de Octubre^Review Board.

Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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