This executive summary of a national living guideline aims to provide rapid evidence based recommendations on the role of drug interventions in the treatment of hospitalized patients with COVID-19.
The guideline makes use of a systematic assessment and decision process using an evidence to decision framework (GRADE) as recommended standard WHO (2021). Recommendations are consented by an interdisciplinary panel. Evidence analysis and interpretation is supported by the CEOsys project providing extensive literature searches and living (meta-) analyses. For this executive summary, selected key recommendations on drug therapy are presented including the quality of the evidence and rationale for the level of recommendation.
The guideline contains 11 key recommendations for COVID-19 drug therapy, eight of which are based on systematic review and/or meta-analysis, while three recommendations represent consensus expert opinion. Based on current evidence, the panel makes strong recommendations for corticosteroids (WHO scale 5–9) and prophylactic anticoagulation (all hospitalized patients with COVID-19) as standard of care. Intensified anticoagulation may be considered for patients with additional risk factors for venous thromboembolisms (VTE) and a low bleeding risk. The IL-6 antagonist tocilizumab may be added in case of high supplemental oxygen requirement and progressive disease (WHO scale 5–6). Treatment with nMABs may be considered for selected inpatients with an early SARS-CoV-2 infection that are not hospitalized for COVID-19. Convalescent plasma, azithromycin, ivermectin or vitamin D3 should not be used in COVID-19 routine care.
For COVID-19 drug therapy, there are several options that are sufficiently supported by evidence. The living guidance will be updated as new evidence emerges.
The ongoing COVID-19 pandemic causes an enormous pace and volume of research output of varying quality and reliability which is challenging for clinical decision making. To provide a clinical treatment guideline that includes a profound evaluation of rapidly changing evidence, the scientific medical societies conduct a living treatment guideline for hospitalized patients with COVID-19 moderated by the Association of the Scientific Medical Societies in Germany (AWMF) in collaboration with the COVID-19 Evidence Ecosystem Project (CEOsys). CEOsys is an association of 20 German university hospitals whose goal is to compile, summarize, and assess the quality of study results within a structured approach and meta-analysis. Evidence profiles of treatment strategies provided by CEOsys form the basis for a structured decision process using the GRADE (Grading of recommendations assessment, development and evaluation) Evidence to Decision Framework  with predefined outcomes in compliance with the WHO Handbook for Guideline Development . Here, we present key recommendations for the most pertinent drug interventions that derived from this national living treatment guideline (last updated 17.05.2021). A full length guideline and evidence report is available in German language . The following assessments are subject to constant evaluation and will be re-evaluated, revised or supplemented at short intervals.
Aims of the guideline
The AMWF S3 guideline aims to provide a comprehensive overview of evidence based recommendations on therapeutic strategies for hospitalized patients with COVID-19. The guideline addresses physicians involved in the inpatient care of patients with COVID-19 but is also intended to provide information for individuals and organizations directly or indirectly involved in this topic. This compendium highlights the key pharmacologic treatment recommendations of the guideline that are most important for clinical care.
Determination of guideline questions and relevant outcomes
The guideline group comprises actually 23 delegates from 15 participating scientific medical societies and organizations, as well as a patient representative (appendix 1).The guideline developed from an intensive care guideline based on an expert consensus in March 2020  to an interdisciplinary evidence and consensus based guideline for all in-patients with COVID-19 with definition of complementary clinically relevant questions and formal consensus conferences starting in October 2020 . A systematic evidence analysis was first integrated in February 2021 and now updated in Mai 2021. The following outcomes were defined as clinically relevant: 28-day mortality (up to); improvement/worsening of clinical status up to 28 days (including need for respiratory support, ventilator free days); weaning/liberation from mechanical ventilation, increase in WHO clinical progression scale (WHO scale) , adverse events (any grade), severe adverse events, need for dialysis (up to 28 days), neurological function/functional independence, duration of hospitalization, time to discharge, time to symptom resolution, viral clearance and specific outcomes for the assessment of prophylactic or intermediate anticoagulation (major bleeding or thrombotic events).
Systematic literature search and processing of available evidence
Clinical questions on treatment of COVID-19 were assessed by a structured literature search and analysis supported by CEOSys (appendix 1) using the Patient-Intervention-Comparison-Outcome (PICO) format. Detailed search strategies are displayed in the full length evidence report . Results of the weekly searches were screened in duplicate. Additionally, the guideline group performed literature searches on Medline database to ensure that recently published study results of relevance are included. Evidence for medical therapeutic strategies derived from (peer-reviewed) randomized clinical trials was extracted and bias assessed using Risk of bias 2.0. A meta-analysis was performed for all PICO questions where sufficient evidence and comparable outcomes were available. The quality of the evidence was assessed using the GRADE (Grading of recommendations assessment, development, and evaluation) methodology on predefined outcomes described earlier. The GRADE approach provides a standardized evaluation of the quality of the evidence which can finally be classified as high, moderate, low or very low . Comprehensive evidence profiles for the different therapeutic strategies were created inside MAGICapp (https://app.magicapp.org), a digital platform and evidence ecosystem committed to support rapid recommendations and living guidelines during the COVID-19 pandemic . Online manuscripts of clinical trials that were published as pre-prints were noticed but excluded from the systematic evaluation. Due to insufficient clinical data or COVID-19 specific data, key recommendations 2.4 (SARS-CoV-2 neutralizing monoclonal antibodies), 3.1, and 3.2 (anticoagulation) represent expert opinions based on available (partly observational or retrospective) evidence.
Preparation of recommendations
All members of the panel had access to the evidence profiles on the MAGICapp platform  in preparation for the consensus conferences. During two consensus conferences, evidence profiles were presented by a dedicated editor of the CEOsys group responsible for the respective evidence profile before results were discussed in plenary under neutral moderation. Based on the evidence profiles a structured evaluation of the respective treatment strategy was performed that included an appraisal of the following criteria by the guideline group: benefit and harm balance, quality of the evidence, patient preferences, resources, equity, acceptability, and feasibility. Based on the evidence profile and overall assessment, recommendations were written and graded according to the AWMF standards (↑↑ = Strong recommendation (should/should not), ↑ = Recommendation (ought/ought not), ↔ = Recommendation open (may be considered)) . For each recommendation one delegate per medical society and organization had to vote (agree, disagree, abstention). Guideline group members with conflicts of interest were excluded from the respective voting. A strong consensus (agreement > 95%) was achieved for 9 out of 11 key recommendations while a consensus (agreement > 75%) was achieved for two of them. For each recommendation, background information was summarized by working groups within the guideline group to describe available evidence and rationale for the chosen grading to make the decision process as transparent as possible. Contents were finally reviewed by all members of the guideline group and officially validated by the participating medical societies and organizations as well as the AWMF Task Force COVID-19 and experts from the Robert Koch Institute.
Selection of key recommendations
For this summary, key recommendations of the guideline were selected that represent the most pertinent drug interventions for hospitalized patients with COVID-19. Background information and rationales for the respective recommendation are presented in a summarized format. A full length version of the guideline (in German) and a comprehensive evidence report is available at: https://www.awmf.org/leitlinien/detail/ll/113-001LG.html .
1. Immunomodulatory therapy
1.1 Corticosteroids (meta-analysis)
Patients with severe (SpO 2 < 90%, respiratory rate > 30/min) or critical COVID-19 (ARDS, sepsis, ventilation, vasopressor administration) should be treated with dexamethasone ⇑⇑
[Quality of evidence: 28d mortality: moderate, adverse events: low; strong consensus].
Evidence: Six RCTs with a total 7595 randomized patients were included [9,10,11,12,13,14]. For the clinically most relevant endpoint, a reduction in mortality by day 28, the meta-analysis of five RCTs that reported on this outcome with a total of 7527 hospitalized COVID-19 patients (WHO scale 4–9) demonstrated an overall reduction in mortality by day 28 with an absolute risk reduction of 2.8% in hospitalized patients treated with corticosteroids (moderate quality evidence). There was an apparent trend towards a higher effect with increased disease severity. The clearest evidence existed for dexamethasone administered at a dose of 6 mg daily. In the largest RCT on dexamethasone, an absolute mortality reduction of 12% was demonstrated in patients that require invasive ventilation (WHO scale 7–9), and 3% for patients requiring oxygen supplementation but no respiratory support (WHO scale 5–6) . In contrast, dexamethasone showed no beneficial effects in hospitalized patients without any oxygen requirement (WHO scale 4). Actually, the meta-analysis showed a numerically higher 28-day mortality for this sub group when treated with dexamethasone (statistically significant subgroup difference) . The CODEX trial did not demonstrate a significant reduction in 28-day mortality for invasively ventilated patients (secondary endpoint analysis), but a beneficial effect on the number of ventilator-free days (primary endpoint) . The safety and tolerability of corticosteroids in hospitalized patients with COVID-19 was generally good in clinical trials (low quality evidence). The currently available data do not suggest an increased susceptibility for secondary (bacterial) infections due to corticosteroid regimens used in COVID-19 trials.
Rationale for the level of recommendation: Given the beneficial effects on mortality in patients requiring supplemental oxygen or invasive ventilation, a favorable safety profile and its wide availability, the guideline group strongly recommends the use of dexamethasone in these patient groups. The recommended dose is 6 mg dexamethasone p.o./i.v. daily for 10 days. In justified cases, another systemic glucocorticoid (e.g., hydrocortisone 50 mg i.v. every 8 h) can be used as an alternative.
1.2 Tocilizumab (meta-analysis)
Tocilizumab may be administered to patients with high-dose supplemental oxygen progressing to severe COVID-19 (WHO scale 5–6). Tocilizumab should not be used in patients with no or low supplemental oxygen requirement and in patients on invasive ventilation ⇔
[Quality of evidence: 28d mortality: moderate, adverse events: low; strong consensus].
Evidence: Nine RCTs with a total of 6481 patients were included to evaluate tocilizumab [15,16,17,18,19,20,21,22,23]. Most patients additionally received concomitant therapy with dexamethasone as current standard of care. The meta-analysis showed a statistically significant effect on the clinically relevant endpoints mortality (36 fewer cases per 1000, 95% CI 57–12 fewer) and progression to invasive (mechanical) ventilation (44 fewer cases per 1000, 95% CI 63–25 fewer; moderate quality of evidence). Overall, a clinically relevant benefit can be concluded for oxygenated patients with progressive disease (WHO scale 5–6), but not for patients on invasive ventilation (for more than 24 h). The RECOVERY trial with 2022 patients included in the tocilizumab arm (intention-to-treat population), had a major impact on the overall effect in the meta-analysis . In this trial, C-reactive protein (CRP) elevation > 75 mg/L was applied as an inclusion criterion reflecting a surrogate marker of systemic inflammation. Safety and tolerability of tocilizumab was favorable in the trials that provided detailed reporting of safety data, with no evidence of increased rates of (serious) adverse events. However, safety data from the RECOVERY trial seems to be incompletely reported (low quality of evidence).
Rationale for the level of recommendation: Based on the statistically significant but small net effect of tocilizumab, an open recommendation (may be used) was made for the use of this agent in combination with corticosteroids (SOC) for patients requiring oxygen supplementation and progressive disease. Patients should demonstrate evidence of a systemic inflammation (e.g., markedly elevated CRP) and increased oxygen demand. For patients already requiring invasive ventilation for a period longer than 24 h, the guideline group found no evidence for a clinical benefit of tocilizumab. Tocilizumab should generally not be used in patients with confirmed intolerance to tocilizumab or with active bacterial or fungal infection. Currently, no data are available on the safety of tocilizumab in pregnancy. Dosing of tocilizumab is based on body weight (> 90 kg: 800 mg; ≤ 90 kg: 600 mg; ≤ 65 kg: 400 mg; ≤ 40 kg: 8 mg/kgKG) as a single intravenous dose. Due to lack of comparative study data no recommendation for repeated administration can be made. Evaluating the clinical use of tocilizumab the guideline group took into account existing qualitative uncertainties of the evidence  and relatively high costs with undefined reimbursement regulations.
2. Antiviral therapy
2.1 Remdesivir (meta-analysis)
For hospitalized, non-ventilated patients with COVID-19 pneumonia and oxygen demand, no fundamental recommendation can be made neither for nor against therapy with remdesivir
[Quality of evidence: 28d mortality: moderate, adverse events: low; consensus].
Evidence: A total of four RCTs were included in the assessment [24,25,26,27]. In a randomized, double-blind trial of 1062 hospitalized patients (ACTT-1), a 10-day course of remdesivir reduced the time to recovery from a median of 15 to 10 days compared to placebo [risk ratio for recovery, 1.29; 95% CI, 1.12–1.49; P < 0.001]. There was a numerical reduction in all-cause mortality at day 29 (11.4% vs. 15.22%, hazard ratio, 0.73; 95% CI, 0.52–1.03) . Comparing the efficacy of a 5 vs. 10–day course of remdesivir, 10 days of remdesivir was not superior for patients with moderate to severe COVID-19 (WHO scale 5–6) and radiographic evidence of pulmonary infiltrates . A smaller RCT of 237 patients failed to demonstrate a beneficial effect of remdesivir on time to clinical improvement , and results of another trial remained inconclusive . In the WHO SOLIDARITY trial, 2750 patients received remdesivir. No benefit was found regarding clinical endpoints (mortality, initiation of ventilation, duration of hospitalization) . In the meta-analysis based on 7142 patients, no significant effect of remdesivir on 28-day mortality (moderate quality of evidence) or other predefined clinical endpoints was found (very low to moderate quality of evidence). Subgroup analyses were hampered by the heterogeneity of the trial protocols and outcome definitions, so that no clear conclusion can be made on possible effects upon specific patient populations. The safety and tolerability of remdesivir in clinical trials was good. Fewer severe adverse events (SAE) were reported in remdesivir treated groups compared to placebo (relative risk 0.75; CI 95% 0.63–0.90; low quality evidence).
Rationale for the level of recommendation: Due to persisting uncertainties regarding a potential benefit of remdesivir in hospitalized, non-ventilated patients, and relevant costs that must be considered, no recommendation was made. The World Health Organization (WHO) has issued a conditional recommendation against the use of remdesivir in hospitalized patients, due to insufficient evidence for improved survival and other clinical outcomes . The use of remdesivir in ventilated patients is not appropriate due to lack of any clinical benefit in this population. The guideline group considers a potential benefit for specific subgroups and/or on clinical endpoints that were not included in the meta-analysis, especially time to recovery (primary endpoint of the ACTT-1 study). In the light of its favorable safety profile and tolerability, no recommendation against the use of remdesivir was established within the structured guideline process. If treatment with remdesivir is considered by clinicians, the dose should be 200 mg i.v. on day 1, followed by 100 mg daily for 5 days. A prolonged therapy for up to 10 days may be considered if the effect is considered insufficient. Daily monitoring of liver and renal function parameters is recommended; remdesivir should not be administered in patients with a GFR < 30 ml/min. Regarding the optimal timing of antiviral therapy, there are theoretical considerations and indications that treatment initiation as early as possible in the course of the disease might be favorable .
2.2 Convalescent plasma (meta-analysis)
Convalescent plasma should not be used in hospitalized patients with COVID-19. No recommendation can be made upon specific subgroups based on current evidence ⇓⇓
[Quality of evidence: 28d mortality: moderate, adverse events: low; strong consensus].
Evidence: Four randomized controlled trials with a total of 931 patients [31,32,33,34] built up the evidence base for this recommendation. Based on the meta-analysis, no clinical benefit was identified regarding 28-day mortality and clinical status (moderate quality of evidence). Concurrently, there was a trend towards an increased occurrence of adverse events and serious adverse events in groups treated with convalescent plasma (very low to low quality of evidence). There is an inherent risk of transfusion-related reactions that must be taken into account when administering plasma preparations.
Rationale for the level of recommendation: In weighing the risks and benefits of convalescent plasma, the guideline group strongly recommends against its use in hospitalized patients with COVID-19. Besides the lack of evidence supporting a clinical benefit, the panel included additional considerations for the recommendation such as limited resources for logistics of donation, administration, processing, storage and distribution as well as financial aspects. Production of convalescent plasma requires sufficient donor availability. Considering these aspects, a widespread availability of this treatment seems unlikely.
2.3 SARS-CoV-2 neutralizing monoclonal antibodies (nMABs)
2.3.1 Bamlanivimab monotherapy (systematic analysis)
The SARS-COV-2 neutralizing monoclonal antibody (nMAB) bamlanivimab should not be used to treat patients hospitalized due to moderate to severe COVID-19 (WHO scale 4–6) ⇓
[Quality of evidence: 28d mortality: moderate, adverse events: low; strong consensus].
Evidence: One RCT of 314 hospitalized patients was available. A clinical benefit of bamlanivimab in patients hospitalized for moderate to severe COVID-19 (WHO scale 4–6) was not shown in the ACTIV3/TICO trial (low to moderate quality evidence; ). In the intervention group, there was a numerically higher incidence of hemodialysis (13/1000 vs. 0/1000), delirium (26/1000 vs. 7/1000), and grade 3–4 adverse events (227/1000 vs. 179/1000), so that potentially harmful effects cannot be completely excluded (low quality of evidence).
Rationale for the level of recommendation: Based on available evidence, the guideline group strongly recommends against bamlanivimab monotherapy in patients hospitalized for COVID-19. There is currently insufficient evidence on combinational therapy with multiple nMABs, so no recommendation can be formulated.
2.3.2 SARS-CoV-2 neutralizing monoclonal antibodies in nosocomial infection
In early SARS-CoV-2-infected hospitalized patients without respiratory COVID-19 symptoms (< 72 h after first positive NAAT and/or < 7 days since symptom onset), with at least one risk factor for a severe course of disease, SARS-CoV-2 specific monoclonal antibodies may be administered ⇔
[Expert opinion; consensus].
Evidence: Currently, there are insufficient data to evaluate the use of neutralizing SARS-CoV-2 monoclonal antibodies (nMABs) in hospitalized patients. Results from outpatient trials cannot be adequately extrapolated to (often nosocomial) infected inpatients not hospitalized for COVID-19. This recommendation, therefore, represents consented expert opinions considering available evidence on the efficacy and tolerability of nMABs in general as well as personal off-label use experience.
Rationale for the level of recommendation: Interim analyses of ongoing phase II trials indicate that early (≤ 7 days after symptom onset) administration of combination therapies with bamlanivimab and etesevimab, as well as casirivimab and imdevimab might be beneficial in outpatients with mild to moderate COVID-19 disease (WHO scale 1–3) and at least one risk factor for disease progression. Early administration of nMABs resulted in a significant reduction in viral load, and (numerical) reduction in hospitalization rate or subsequent physician contacts [36,37,38]. However, rates for hospitalization or physician contacts were generally low in the patient population included in published trial data. A conclusive assessment on clinical endpoints is currently not possible on this basis. Known risk factors for a severe course of COVID-19 include: Age > 65 years, obesity with body mass index (BMI) > 35, immunosuppression, chronic renal failure, chronic lung disease such as COPD, or trisomy 21. The guideline group emphasizes the risk for a progressive (nosocomial) SARS-CoV-2 infection in patients hospitalized for an indication other than COVID-19. An additional argument is the opportunity of very rapid nMAB administration early in the course of infection due to the hospitalized state. Ideally, nMABs should be given ≤ 72 h after the initial SARS-CoV-2 detection (by PCR or other Nucleic Acid Amplification Technology, NAAT) and (if appropriate) ≤ 7 days after symptom onset. When considering therapy with nMABs, the prevalence of circulating resistant variants must be taken into account. In the presence of an E484K mutation (B.1.351 or P1 variant), bamlanivimab (± etesevimab) cannot expected to be effective . As nMAB-monotherapy has been associated with the emergence of escape mutations, experts discuss the preferential use of combination drugs, especially in immunosuppressed patients.
3.1 Pharmacological thromboprophylaxis
Hospitalized patients with COVID-19 should receive prophylactic anticoagulation with standard dose low molecular weight heparin (LMWH) in the absence of contraindications. Alternatively, fondaparinux may be used  ⇑⇑
[Expert opinion; strong consensus].
Evidence: Thromboembolic events are common complications of moderate to severe COVID-19 predominantly affecting the venous system and to a lesser extend arterial vessels [41, 42]. There are no specific data or insights regarding pharmacological thromboprophylaxis in COVID-19. The recommendation is, therefore, based on the AWMF S3 guideline ‘Prophylaxis of Venous Thromboembolism’ that addresses the general hospitalized patient population . The benefit of prophylactic anticoagulation, preferably with LMWH, in hospitalized patients has been prospectively investigated in several randomized trials and demonstrated high efficacy in reducing the risk of venous thromboembolisms (VTE) without significantly increasing the risk of major bleeding [43,44,45].
Rationale for the level of recommendation: Based on a large body of evidence for the use of pharmacological thromboprophylaxis in hospitalized patients the guideline group strongly recommends its use for all hospitalized patients with COVID-19, preferentially with low-molecular-weight heparin (LMWH) at a dosage approved for the high-risk setting. Alternatively, e.g., in case of heparin intolerance, previous heparin-induced thrombocytopenia (HIT) or other specific contraindications, fondaparinux can be used.
3.2 Intensified anticoagulation
In hospitalized patients with COVID-19 and additional risk factors for venous thromboembolism (VTE), intensified anticoagulation* may be used if the bleeding risk is low. Additional risk factors for VTE include obesity (BMI > 35 kg/m2), previous VTE, known thrombophilia, intensive care treatment and highly increased D-dimers (> 2–3 mg/l)  ⇔
[Expert opinion; strong consensus].
*For example: intermediate, half-therapeutic dose of LMWH. No universal definition exists for intermediate dose of unfractionated heparin (UFH). A dose of 250 IU/kg over 24 h and/or a 1.5-fold prolongation of the baseline aPTT value can serve as guidance.
Evidence: Observational data suggest that prophylactic dose anticoagulation may not be sufficiently effective for VTE prophylaxis in patients with COVID-19, especially those that require ICU treatment [47, 48]. In a systematic meta-analysis of (mostly retrospective) observational studies, the rate of VTE was numerically lower when using intermediate-dose anticoagulation compared to prophylactic anticoagulation . In a prospective randomized trial of 600 intensive care patients, intermediate-dose NMH (enoxaparin 1 mg/kg daily) showed no advantage over prophylactic NMH (enoxaparin 40 mg daily) regarding the combined efficacy endpoint of venous or arterial thromboembolism, need for ECMO therapy, and 30-day mortality (event rate 45.7% vs. 44.1%; odds ratio 1.06; 95% CI 0.76–1.48; P = 0.70). While VTE rates were similar in both groups (3.3% vs. 3.5%), intermediate-dose anticoagulation led to a numerically higher rate of clinically relevant bleedings (6.2% vs. 3.1%.; OR 2.02; 95% CI 0.89–4.61; P = 0.08) . To date, no specific RCT on intermediate-dose anticoagulation in hospitalized patients with non-critical COVID-19 has been published but one is now under peer-review .
Rationale for the level of recommendation: Due to the risk of thromboembolic complications in patients with COVID-19, especially in case of severe disease requiring intensive care therapy, the panel suggests that intensified anticoagulation, e.g., with an intermediate, half-therapeutic dose of NMH, may be used in patients with additional risk factors for VTE and a low bleeding risk. Risk factors for bleeding include severe hepatic or renal impairment, thrombocytopenia, previous bleeding, antiplatelet therapy or recent surgery. Due to the potential harms of intensified anticoagulation and an unclear net benefit, routine use of intermediate-dose anticoagulation in patients with COVID-19 is not recommended.
Azithromycin should not be administered to hospitalized COVID-19 patients as antiviral therapy ⇓⇓
[Quality of evidence 28d mortality: high, adverse events: moderate; strong consensus].
Evidence: Based on in vitro antiviral effects, azithromycin has been evaluated as therapeutic agent for the treatment of COVID-19 in four randomized controlled trials including a total of 8759 patients [51,52,53,54]. Within the largest trial RECOVERY, more than 7700 hospitalized patients (94% did not require invasive ventilation), were randomized to receive azithromycin in addition to SOC therapy . The meta-analysis revealed no benefit of azithromycin with respect to patient-relevant outcomes such as mortality, clinical improvement, need for invasive ventilation, and length of hospitalization (moderate to high quality of evidence). Adverse events and secondary infections were slightly increased in groups treated with azithromycin compared to placebo (low to moderate quality of evidence) while severe adverse events and cardiac arrhythmias were not increased.
Rationale for the level of recommendation: A beneficial effect of azithromycin could not be proven but the guideline group cannot exclude potential harms of this treatment for patients with COVID-19 (without additional bacterial infection). A negative impact of increased macrolide on the spread of antibiotic-resistant bacteria has not been systematically investigated in the context of COVID-19 but seems possible. It is important to note that azithromycin was assessed for (antiviral) effects on COVID-19, but not for its (known) antibacterial activity. For cases of suspected or proven bacterial co-infection we refer to comprehensive and specific guidelines [3, 5, 55, 56].
Ivermectin should not be used to treat hospitalized patients with COVID-19 ⇓⇓
[Quality of evidence time to virus elimination: very low, length of hospital stay: very low; strong consensus].
Evidence: Numerous preprints are available online reporting solely on viral load reduction rather than clinically relevant endpoints or with significant methodological issues and a high risk of bias (exemplary [57,58,59]). At the time of consensus for this recommendation, February 2021, only one peer-reviewed publication of a randomized controlled trial with a total of 72 patients was available for consideration . In this trial, hospitalized patients without oxygen supplementation (WHO scale 4) were treated with ivermectin, ivermectin in combination with doxycycline, or with placebo. Based on the results the authors suggest a faster viral elimination in consecutive nasopharyngeal swabs of patients treated with ivermectin in monotherapy (low quality evidence). However, there was no apparent effect on clinical endpoints such as symptoms or duration of hospitalization and results do not support any conclusion regarding mortality or improvement of clinical status.
Rationale for the level of recommendation: Considering potential toxic effects of ivermectin as well as interactions with other drugs, the guideline group strongly recommends against its use in patients with COVID-19. Besides the absence of a proven benefit, the appraisal included basic pharmacokinetic considerations as tissue concentrations achievable with oral administration of ivermectin seems to be far below the half maximal inhibitory concentration in vitro .
4.3 Vitamin D3
Vitamin D 3 should not be used to treat hospitalized patients with COVID-19 ⇓⇓
[Quality of evidence: mortality very low; strong consensus].
Evidence: Due to the lack of randomized controlled trials (February 2021) only one study with a total of 76 patients could be included into the assessment . In this clinical trial, administration of vitamin D3 demonstrated no benefit on patient-relevant outcomes (very low quality of evidence). Decreases in serum vitamin D3 are frequently observed in severely ill patients requiring intensive care treatment and may correlate with disease severity . In analogy to other serious infections decreased serum vitamin D3 levels seem to be a relatively common phenomenon in COVID-19. This observation does not indicate a causal relationship and does not justify vitamin D3 supplementation in this setting. After completion of the primary evidence analysis, another study was published . In this randomized controlled trial, vitamin D3 was administered to 240 hospitalized patients with COVID-19. No benefit was found with respect to clinical endpoints (duration of hospitalization, mortality, admission to the intensive care unit, initiation of ventilation).
Rationale for the level of recommendation: Considering available evidence, the guideline group strongly recommends against the use of vitamin D3 to treat hospitalized patients with COVID-19. Besides the lack of evidence, the guideline group took into account the generally widespread availability of vitamin D3 and low costs, the intention to avoid wrong incentives for self-medication and potential adverse effects that can result from overdosing. Due to the lack of therapeutic consequences, routine determination of serum vitamin D3 in COVID-19 is also not recommended which is in line with guidelines released by the German Nutrition Society .
5. Combinations of drug therapies
Despite theoretical considerations that combinational therapy might improve efficacy of COVID-19 treatment regimens , only few data are available. From the final ACTT-1 publication, a post-hoc analysis of a subgroup treated with remdesivir and steroids suggested a potential additive effect . Further controlled trial data are lacking to date. The ACTT-2 study of 1033 patients showed that the combination of the Janus kinase inhibitor baricitinib with remdesivir was beneficial compared with remdesivir alone in terms of a 7 vs. 8-day median time to recovery and 30% higher probability of clinical recovery at day 15 . A statistically significant mortality benefit was not shown. To date, there are no published peer-reviewed data from randomized controlled trials on the use of baricitinib compared to corticosteroids.
Summary of key recommendations
Reliable evidence for clinical efficacy in hospitalized patients with moderate to severe COVID-19 is available for dexamethasone. The use of dexamethasone in patients requiring oxygen (WHO scale 5) and patients with severe/critical disease requiring ventilation (WHO 6–9) significantly reduces mortality (moderate quality of evidence). The interleukin-6 antagonist tocilizumab demonstrated a statistically significant but low absolute effect on mortality and progression to invasive ventilation in our meta-analysis for patients with moderate to severe COVID-19 (WHO 5–6, low to moderate quality of evidence). The guideline panel recommends to consider tocilizumab for patients with higher level of supplemental oxygen requirement and progressive disease but not for those with more than 24 h of mechanical ventilation. Evidence regarding antiviral treatment with remdesivir is conflicting and currently no fundamental recommendation is made. The use of remdesivir in patients with invasive ventilation or without oxygen supplementation in not reasonable based on current clinical evidence. If remdesivir is used in patients with oxygen supplementation, an early treatment and 5-day course of remdesivir seems the most rational approach. The use of pharmacological thromboprophylaxis is strongly recommended for all patients hospitalized with COVID-19 while an intensified anticoagulation may be considered in patients with additional risk factors for venous thromboembolisms (VTE) and a low bleeding risk (expert opinion). In the setting of SARS-CoV-2 infection and hospitalization due to other indications than COVID-19 and/or nosocomial SARS-CoV-2 infection, an early treatment (< 72 h after first positive PCR and/or < 7 days since symptom onset) with SARS-CoV-2 neutralizing monoclonal antibodies (nMABs) can be considered as it might reduce the risk of disease progression in patients with at least one risk factor for severe COVID-19 (expert opinion). Other agents cannot be recommended for use outside clinical trials and eligible clinical settings (Table 1).
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Open Access funding enabled and organized by Projekt DEAL. All delegates of the scientific medical societies were volunteers and the scientific medical societies received no sponsorship by third parties. The COVID-19 Evidence Ecosystem (CEOsys) project is funded under a scheme issued by the Network of University Medicine (Nationales Forschungsnetzwerk der Universitätsmedizin (NUM)) by the Federal Ministry of Education and Research of Germany (Bundesministerium für Bildung und Forschung (BMBF)) grant number 01KX2021.
Conflict of interest
C. D. Spinner received consultancy fees, speaker’s honoraria, and/or reimbursement of travel expenses from Gilead Sciences, Eli Lilly, Janssen-Cilag, MSD and received consultancy fees from Molecular Partners and Formycon in the context of COVID-19. He also received research support indirectly from Apeiron, Eli Lilly, Gilead Sciences, and Janssen-Cilag. Outside this context, he received consultancy fees, speaker’s honoraria, and reimbursement of travel expenses from AbbVie, Gilead Sciences, Janssen-Cilag, MSD, and ViiV Healthcare/GSK, as well as research support (indirectly to his employer) from Gilead Sciences, GSK, Jansen-Cilag, MSD, and ViiV Healthcare. T. Welte received consultancy fees from AstraZeneca, Basilea, Biotest, Bayer, Boehringer, GSK, Janssens, Novartis, Pfizer and Roche. He received lecture fees and travel cost support from AstraZeneca, Basilea, Biotest, Bayer, Boehringer, Berlin Chemie GSK, Infectopharm, MSD, Novartis, Pfizer, Roche and research support By DFG, BMBF, EU, WHO. S. Weber-Carstens is working in a scientific cooperation project with the company Dräger. F. Langer has received personal fees for lectures, advisory boards or consultancy and/or research support from Aspen, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, LEO Pharma, Pfizer, and Sanofi, outside the submitted work. M. Westhoff received lecture honoraria from Actelion, Boehringer, Novartis, Löwenstein, and research support from Bayer. M. Pfeifer received lecture fees from Astra-Zeneca, Boehringer, Chiesi, Glaxo-Smith-Kline, Novartis, and Roche. He received consulting fees from Boehringer, Chiesi, Novartis, and Roche, and travel support from Boehringer. K. F. Rabe has received consultancy fees from AstraZeneca, Boehringer, Sanofi Aventis, MSD, and Novartis. He received lecture fees and travel support from Roche, Chiesi Pharmaceuticals, Pfizer, TEVA Pharmaceuticals, Orion Cooperation, Berlin Chemie, Boehringer, AstraZeneca, MSD, Novartis, and Sanofi Aventis, research support from the German Federal Ministry of Education and Research. B. W. Böttiger received fees for lectures from the following companies: Forum für medizinische Fortbildung (FomF), Baxalta Deutschland GmbH, ZOLL Medical Deutschland GmbH, C.R. Bard GmbH, GS Elektromedizinische Geräte G. Stemple GmbH, Novartis Pharma GmbH, Philips GmbH Market DACH, Bioscience Valuation BSV GmbH. J. Weinmann-Menke received research support from GSK, DIAMED, Miltenyi Biotech, lecture fees from Astellas, Astra Zeneca, Norvartis, Bial, Roche, Chiesi, GSK, Boehringer-Ingelheim, Miltenyi, Bayer, Vifor, Fresenius. She received consultancy fees from Bayer, Bial, Boehringer-Ingelheim, Chiesi, Astra Zeneca and GSK. M. Nothacker is a guideline methodologist payed by the AWMF. G. Marx received consultancy fees and research support from Biotest, B.Braun, and Adrenomed, and lecture fees from B.Braun, Biotest, and Philips. He holds a patent for modulation of the TLR4 signaling pathway (European Patent 2855519). C. Karagiannidis has received consultancy fees from Bayer and Xenios. S. Kluge has received research support from Ambu, Daiichi Sankyo, ETView Ltd, Fisher & Paykel, Pfizer, and Xenios. He has received lecture honoraria from Astra, C.R. Bard, Baxter, Biotest, Cytosorbents, Daiichi Sankyo, Fresenius, Gilead, Mitsubishi Tanabe Pharma, MSD, Pfizer, Philips, ZOLL. He received consultancy fees from Bayer, Fresenius, Gilead, MSD and Pfizer. J. J. Malin, U. Janssens, G. Schälte, P. Gastmeier, M. Wepler, F. Hoffmann, A. Kersten, P. Berlit, M. Krawczyk, W. Nehls, F. Fichtner, S. Laudi, M. Stegemann and N. Skoetz report no potential conflicts of interest.
COVID-19 Evidence Ecosystem Project (CEOsys) Memebers are added in Appendix Section.
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Malin, J.J., Spinner, C.D., Janssens, U. et al. Key summary of German national treatment guidance for hospitalized COVID-19 patients Key pharmacologic recommendations from a national German living guideline using an Evidence to Decision Framework (last updated 17.05.2021). Infection (2021). https://doi.org/10.1007/s15010-021-01645-2
- Living guideline
- Living meta-analysis