The authors have declared that no competing interests exist.
¶ Membership of the COVOCA Study Group is listed in the Acknowledgments.
During COVID-19 pandemic, the use of several drugs has represented the worldwide clinical practice. However, though the current increase of knowledge about the disease, there is still no effective treatment for the usage of drugs. Thus, we retrospectively assessed use and effects of therapeutic regimens in hospitalized patients on in-hospital mortality.
COVOCA is a retrospective observational cohort study on 18 COVID centres throughout Campania Region Hospitals. We included adult patients with confirmed SARS-CoV-2 infection, discharged/dead between March/June 2020.
618 patients were included, with an overall in-hospital cumulative mortality incidence of 23.1%. Most prescribed early treatments were antivirals (72%), antibiotics (65%) and hydroxychloroquine/anticoagulants (≈50%). Tocilizumab, indeed, was largely prescribed late during hospitalization. Multivariable models, with a cut-off at day 2 for early COVID-19 therapy administration, did not disclose any significant association of a single drug administration on the clinical outcome.
COVOCA represents the first multicenter database in Campania region. None drug class used during the pandemic significantly modified the outcome, regardless of therapy beginning, both overall and net of those already in non-invasive ventilation (NIV)/ orotracheal intubation (OTI) at hospitalization. Our cumulative incidence of mortality seems lower than other described during the same period, particularly in Northern Italy.
After the first outbreak of acute coronavirus-2 respiratory syndrome (SARS-CoV-2) reported in China in December of 2019 peak, named COVID-19 [
To date, no specific antiviral therapy has been identified yet. However, also in Italy the administration of monoclonal antibodies off-label has been recently approved, even though RCTs are few and still ongoing. The use of several drugs, usually in different associations, has represented the worldwide clinical practice and, more often, is still the first choice.
Antivirals (AVs), hydroxychloroquine (HyC), antibiotics (ATBs), Tocilizumab (mAbs), corticosteroids (CS) and low-molecular weight heparins (LMWH) have been the most frequently used drugs, usually accompanied by a supportive oxygen therapy.
During the course of pandemic, among all these drugs only corticosteroids, remdesivir and oxygen therapy seemed to determine a benefit in terms of both mortality and hospitalization rate reduction, though findings are still controversial [
The most recent evidence has shown how Hydroxychloroquine, largely used during the first months of pandemic, actually is not effective against COVID-19, especially in the mild to moderate stages [
The improved knowledge about COVID-19 physiopathology, which have shown similarities with pulmonary edema, have stressed the importance of a supportive oxygen therapy, currently considered essential, mostly in mild to moderate disease stages.
Up to now, whether a therapeutic regimen is better than another has been poorly investigated.
However, though the current increase of knowledge about the disease, there is still no effective treatment and information about a proper timeline for the usage of drugs.
On these bases, we aimed to retrospectively assess the frequency of use of drugs, both as a single class and in association with each other, and the effects of therapeutic regimens started in hospitalized patients, classified according to WHO COVID-19 severity scale [
Originally, we also evaluated whether an early or delayed use of these drugs could determine different outcomes. Finally, we also verified the potential efficacy of different regimens of oxygen therapy in cases of respiratory distress.
COVOCA (observational study on the COVID-19 population hOspitalized in CAmpania Region) is a retrospective observational cohort study, which involved 18 COVID centres throughout Hospitals of Campania Region, Italy. This cohort of COVID-19 patients has already been presented and described in a previous paper [
Briefly, we included all adult patients (≥ 18 years) with laboratory confirmed SARS-CoV-2 infection, who completed their hospitalization (discharged or dead) in the period between March 13, 2020 and June 30, 2020, of whom clinical records were available. All data were fully anonymized by the participating centres before being accessed. The study was approved by the local Ethics Committee (University of Campania Luigi Vanvitelli) and is in accordance with 1976 Declaration of Helsinki and its later amendments.
Microbiological diagnosis SARS-CoV-2 infection was defined by Real-Time Polymerase Chain Reaction of nasal-pharyngeal swab specimen. The outcome was in-hospital mortality, assessed either from data at discharge or death certificate.
Exposure variables were collected at hospital admission and have been extensively detailed in the first work regarding the cohort [
Data on drug therapies, either ongoing or introduced during hospitalization, were widely collected.
Specifically, ongoing therapies such as Antihyperglycemics, Antihypertensives, Diuretics, Anticoagulants (Subcutaneous or Oral), Antiplatelets (Aspirin, Double Antiplatelet or Other), defined as baseline therapy reflect patients’ comorbid conditions. Instead, during hospitalization, specific therapies were introduced to counteract COVID pathology and specifically, in our cohort, they were as follows: Hydroxychloroquine, Anticoagulants, Antibiotics, Monoclonal Antibodies, Antivirals, Cortisone, Immunosuppressive, Antiplatelets, Paracetamol, NSAIDs, Plasma recovered, Immunoglobulins, Antiarrhythmics, Vasoactive, Inotropes, Crystalloids, Electrolytes, Albumin.
Particularly for most reported treatment and of interest in COVID-19 literature, in parallel to the description of whether they were used, a time-lag variable was created to identify patients undergoing either to an early or late treatment. This was done to avoid survivorship bias, considering that patients who live longer are more likely to receive a certain treatment/combination. Specifically, the time-lags variable (early/late) was categorized using a cut-off time (day-2). Day-2 represents treatments performed within the first two days since admission, considering day-0 as the time of hospitalization. Under this pattern, treatments were classified as: No treatment, early treatment (if occurred until day 2) and late treatment (from day 3 onwards). Moreover, a variable Days symptoms (difference between date of the beginning of symptoms and date of admission) related to lag variables for the use of each drug has been calculated.
Categorical data were expressed as number and percentages, whilst continuous variables as mean ± standard deviation (SD). The presence of missing data has been reported. Kendall’s τb coefficient was used to measure the ordinal association between specific COVID-19 treatments, as they were represented through an ordinal categorical variable: No Treatment, Early Treatment and Late Treatment. Kendall’s τb coefficient has been interpreted according to the following criteria: very weak if lower than ± 0.10, weak if from ± 0.10 to ± 0.19, moderate if from ± 0.20 to ± 0.29, strong if higher than ± 0.30. Multivariable logistic regression models were performed to evaluate association between in-hospital mortality and specific COVID-19 treatments. Drug treatments were evaluated in the model individually using the time-lag cut-off and adjusted according to previous findings [
662 patients positive at Sars-Cov-2 swab specimen, which required hospitalization, were considered eligible for the study and, of these, 44 were excluded due to incomplete clinical records. 618 patients were finally included in the study, mainly males (61.3%), with a mean age of 65 years (SD 15.2) and a median duration of hospitalization of 20 days [IQR 13–29 days]. The median time elapsed between onset of symptoms and hospitalization was of 4.5 days [IQR 2–7]. At the time of hospitalization, 63.6% of patients did not show any symptom of ARDS, while moderate and severe symptoms were observed, respectively, in about the 13.1% and 7.4%.
In addition, as for the RSS, 330 patients (53.4%) received respiratory support, at the time of hospitalization, either with Venturi mask or nasal cannula. Only the 13% needed either NIV or OTI. 46 patients (7.4%) showed moderate to severe impaired consciousness according to Glasgow Coma Scales (GCS/15).
On admission, almost half of the study population was under anti-hypertensive therapy (298; 48.2%) and the 19.6% took diuretics. Likewise, about the 20% underwent to anti-hyperglycemic therapy (119; 19.3%). As for antithrombotic therapy, indeed, the 16.3% already took anticoagulants, mostly subcutaneous (10%), whilst about was under antiplatelet therapy (19%), mostly aspirin (13.4%).
All clinical characteristics at admission are reported in
65 (15.2) | |
379 (61.3)/239 (38.7) | |
448 (72.5) | |
46 (7.5) | |
124 (20.0) | |
211 (34.1) | |
330 (53.4) | |
48 (7.8) | |
29 (4.7) | |
35 (5.7) | |
53 (8.6) | |
|
119 (19.3)/473 (76.5) |
|
26 (4.2) |
|
298 (48.2)/292 (47.2) |
|
28 (4.5) |
|
121 (19.6)/460 (74.4) |
|
37 (6.0) |
|
62 (10.0) |
|
39 (6.3) |
|
455 (73.6) |
|
62 (10.0) |
|
83 (13.4) |
|
17 (2.8) |
|
17 (2.8) |
|
501 (81.1) |
Given the focus on the therapeutic regimens specific for COVID-19 treatment, we first classified patients according to the administration of anyone among the following classes of drugs: corticosteroids, hydroxychloroquine, monoclonal antibodies (Tocilizumab), antibiotics, anticoagulants and antiviral (lopinavir/ritonavir). Patients were differentiated based on either an early (within the first two days since admission) and late administration (from day 3 in after).
As reported in
Comparison of days with symptoms related to lag variables for each treatment in analysis. Box and whisker plots were used in each panel. Box describes median and interquartile range; whiskers were represented using Tukey method and points describe outliers. The median and Interquartile Range [IQR] for each lag and treatment were reported. Kruskal-Wallis (KW) test, rank-based nonparametric test, was used to determine if there were statistically significant differences between lag variables group in each treatment. When the KW test was significant, post hoc analysis was performed using the Dunn’s (D) test with Bonferroni correction for multiple comparisons. P-value is reported.
No | 189 (30.6%) |
early treatment | 349 (56.5%) |
late treatment | 80 (12.9%) |
No | 202 (32.7%) |
early treatment | 325 (52.6%) |
late treatment | 91 (14.7%) |
No | 153 (24.8%) |
early treatment | 402 (65.0%) |
late treatment | 63 (10.2%) |
No | 514 (83.2%) |
early treatment | 41 (6.6%) |
late treatment | 63 (10.2%) |
No | 107 (17.3%) |
early treatment | 445 (72.0%) |
late treatment | 66 (10.7%) |
No | 391 (63.3%) |
early treatment | 129 (20.9%) |
late treatment | 98 (15.8%) |
5 (0.8%) | |
No | 567 (91.7%) |
Aspirin | 38 (6.1%) |
Double Antiplatelet | 5 (0.8%) |
Other | 8 (1.3%) |
176 (28.5%) | |
14 (2.3%) | |
10 (1.6%) | |
9 (1.5%) | |
13 (2.1%) | |
14 (2.3%) | |
10 (1.6%) | |
99 (16.0%) | |
38 (6.1%) | |
33 (5.3%) | |
72 (11.7%) |
** the time-lags variable (early/late) was categorized using a cut-off time (day-2). In depth, treatments were classified as: No treatment, early treatment (if occurred until day 2) and late treatment (from day 3 onwards).
We further assessed whether there was a drug-drug correlation related to the administration timeline by the Kendall’s Tau correlation coefficient for ordinal data. We observed only a few strong correlations (τ ≥ ±0.30). Particularly, the 48.2% (n = 298) were administered both antibiotics and hydroxychloroquine on the day of admission, with a τ = 0.43. Strong positive correlations, though slightly lower, were observed also for what concerned early administration of both anticoagulants/antivirals and hydroxychloroquine (τ = 0.38 and τ = 0.32, respectively), as well as for the early combination of antibiotics and anticoagulants (τ = 0.36). All data are described in
During the observation period, 143 in-hospital mortality events were recorded, with a cumulative incidence of 23.1%.
We fitted different multivariable models to test for the association between in-hospital mortality and each COVID-19 specific therapy, stratified according to the time of administration. The models were adjusted according to previous findings [
We fitted multivariable models, establishing a cut-off for the COVID-19 early therapy administration at day-2, and each model was fitted on the whole population as well as on a subpopulation obtained by excluding those who were without any respiratory support on admission.
All models did not disclose any significant association of a single drug administration on the clinical outcome of our COVID-19 study cohort, both overall and net of those without any respiratory support at hospitalization. Only a trend was observed as for early treatment administration of antivirals in this latter subpopulation (OR 2.07; 95%CI 0.94–4.58; p = 0.072). However, the analyses confirmed the previous significant associations between a poorer prognosis and male sex, chronic liver disease and malignancies. Likewise, NIV/OTI respiratory supports confirmed the independent association with a higher in-hospital mortality both overall and in the selected subpopulation. As well, moderate-to-severe impaired consciousness at GCS/15, revealed similar findings. All data are reported in
Whole sample (n = 618) | Excluding patients without any respiratory support (n = 407) | |||||
---|---|---|---|---|---|---|
OR | 95% CI | p | OR | 95% CI | p | |
No (ref.) | ||||||
early treatment | 1.14 | 0.64–2.02 | 0.654 | 0.61 | 0.30–1.25 | 0.178 |
late treatment | 1.38 | 0.76–2.51 | 0.291 | 0.92 | 0.46–1.85 | 0.822 |
No (ref.) | ||||||
early treatment | 1.07 | 0.64–1.81 | 0.792 | 1.18 | 0.62–2.26 | 0.617 |
late treatment | 1.19 | 0.58–2.46 | 0.633 | 1.19 | 0.49–2.85 | 0.700 |
No (ref.) | ||||||
early treatment | 1.44 | 0.83–2.48 | 0.190 | 1.20 | 0.63–2.29 | 0.584 |
late treatment | 1.42 | 0.69–2.95 | 0.341 | 1.52 | 0.65–3.59 | 0.337 |
No (ref.) | ||||||
early treatment | 1.08 | 0.63–1.83 | 0.784 | 0.87 | 0.47–1.61 | 0.651 |
late treatment | 0.73 | 0.31–1.73 | 0.478 | 1.07 | 0.40–2.85 | 0.889 |
No (ref.) | ||||||
early treatment | 1.23 | 0.51–2.96 | 0.651 | 1.04 | 0.37–2.92 | 0.933 |
late treatment | 1.51 | 0.74–3.06 | 0.254 | 1.24 | 0.56–2.77 | 0.599 |
No (ref.) | ||||||
early treatment | 1.36 | 0.73–2.54 | 0.331 | 2.07 | 0.94–4.58 | 0.072 |
late treatment | 1.77 | 0.71–4.26 | 0.228 | 2.46 | 0.79–7.69 | 0.120 |
*adjusted by age, sex, GCS/15 (mild/moderate/severe), Respiratory Severity Scale, Chronic Liver Disease, Malignancies
** the time-lags variable (early/late) was categorized using a cut-off time (day-2). In depth, treatments were classified as: No treatment, early treatment (if occurred until day 2) and late treatment (from day 3 onwards).
In our multicenter observational study, we evaluated the association between drug therapy and Covid-19 in-hospital mortality during the pandemic in the Campania region. Originally, we classified patients according to early therapy administration, within the first two days of hospitalization, and late therapy. We observed that none of the drug classes analyzed modified the outcome, both overall and net of those without any respiratory support at hospitalization. Moreover, as already reported, male gender, chronic liver disease, malignancies and NIV/OTI respiratory supports showed an independent association with a higher in-hospital mortality [
Notably, during the first peak, Lombardy was the most affected Italian region. Reports from the “Istituto Superiore della Sanità” (Italian National Health Institute) confirm Lombardy as the region with the highest mortality between March and May 2020 with 16,233 deaths (47.7% of all Italian victims of that period). Particularly, in-hospital mortality accounted for the 28.1% [
A nationwide retrospective Italian study on data retrieved from 160 hospitals charts between March and April 2020 showed, out of 1,397 COVID-19 patients hospitalized in Lombardy, a 35.5% in-hospital mortality incidence [
Currently, to the best of our knowledge, there is no registry on hospitalized COVID-19 patients in Campania, thus COVOCA represents the first multicenter database in this region. Intriguingly, our study shows a mortality cumulative incidence of 23%, lower than in most of Northern Italy.
Certainly, the largest spread of the virus in Northern Italy was of upmost stress for the Lombard Health System, which may have strongly affected COVID-19 in-hospital mortality. Especially during the first pandemic phase, in absence of clinical RCTs and scientific Societies recommendations, the therapeutic choices were center-dependent.
A study conducted at Luigi Sacco Hospital, Milan, between February 21 and April, 30 2020, reported a very high risk of potential adverse events due to drug-drug interactions (DDIs) in COVID-19 patients. This result was consistent with INTERcheck®, a Computerized Prescription Support System (CPSS) developed by the Pharmacological Research Institute Mario Negri (IRCCS) of Milan (Italy) to improve the appropriateness of prescriptions. Currently, 88% of hospitalized Covid-19 patients had an increased risk of cardiotoxicity (QT prolongation, torsade de Pointes or life-threatening arrhythmias) due to in hospital treatment [
A retrospective study performed between March, 13 to April, 3 2020 at Niguarda Hospital, Milan has shown, according to the regional recommendations, a use of hydroxychloroquine, lopinavir/ritonavir and remdesivir as standard of care in 89.9%, 85.1% and 8.1% of COVID-19 patients, respectively [
In the COVOCA study, hydroxychloroquine and any antiviral drugs were used in 69.4% and 82.7% of patients, respectively. Moreover, 17.3% of COVID-19 patients did not receive any association of hydroxychloroquine with an antiviral drug, neither early nor late during hospitalization.
Therefore, our study cohort seems at lower risk of DDIs than the aforementioned populations from Northern Italy studies. The most brutal impact of the first pandemic peak in these regions has more likely led doctors to a more aggressive pharmacological attitude, with a consequent increase in serious adverse events due to dangerous drug associations.
Interestingly, most recent evidence has reported that in an early phase of disease, characterized by the beginning of the cytokines’ cascade, antimalarial drugs could be effective in its prevention, whilst monoclonal antibodies could better act in a more delayed phase, when the cascade is active [
Due to this evidence, we considered two in-hospital subpopulations, one for an early administration of drugs and a second with a late treatment. However, no significant difference emerged between the two subgroups. We could assume that lack of significance in the case of hydroxychloroquine is ascribable to a use in a more advanced phase of disease, likely due to the time between beginning of symptoms and hospitalization.
Likewise, corticosteroids, particularly dexamethasone, are recommended, especially if used after the first week of disease, when the inflammatory phase reaches the peak, and there is a need to initiate respiratory assistance [
The test for multiple comparisons showed that for all treatments the lag time is not significantly different between the Early and Late treatment groups. Intriguingly, for some drugs the lag time is significantly shorter in the no treatment group compared to both the Late and Early treatment groups. It can be hypothesized that patients in the no treatment group were hospitalized early and thus they did not require treatment, or all available drugs.
This study has several limitations. First, the observational design precludes the study from defining a certain cause-effect relationship. On the other hand, numerous RCTs over the last year have ruled out a protective role against COVID-19 mortality for different drug classes, thus confirming our real-life data. Second, due to the observational nature of the study, we cannot exclude the presence of confounding by indication, very common in this type of study. This bias could occur in relation to both beneficial and harmful outcomes and may lead to either an increase or decrease in the apparent risk of the outcome [
This retrospective observational study conducted on 18 COVID Centers is the first to report both management and in-hospital mortality in Campania region. According to our findings, no drug class used during the pandemic, significantly changed mortality risk, regardless of therapy beginning. The cumulative incidence of mortality in this setting seems lower than that described during the same period in other series, particularly in northern Italy. This difference could be due to the different association of drugs at a higher risk for DDIs. Further pharmacovigilance studies are needed to clarify this hypothesis.
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Dr. Raffaele Galiero, Dr. Pia Clara Pafundi and Dr. Vittorio Simeon were supported by the Programma VALERE, University of Campania “Luigi Vanvitelli”.
The Authors thank all the colleagues, nurses and workers who are facing COVID 19 disease.