Analgesics
Antiandrogens
Azvudine
Bromhexine
Budesonide
Colchicine
Conv. Plasma
Curcumin
Famotidine
Favipiravir
Fluvoxamine
Hydroxychlor..
Ivermectin
Lifestyle
Melatonin
Metformin
Minerals
Molnupiravir
Monoclonals
Naso/orophar..
Nigella Sativa
Nitazoxanide
Paxlovid
Quercetin
Remdesivir
Thermotherapy
Vitamins
More

Other
Feedback
Home
Top
Results
Abstract
All sotrovimab studies
Meta analysis
 
Feedback
Home
next
study
previous
study
c19early.org COVID-19 treatment researchSotrovimabSotrovimab (more..)
Melatonin Meta
Metformin Meta
Azvudine Meta
Bromhexine Meta Molnupiravir Meta
Budesonide Meta
Colchicine Meta
Conv. Plasma Meta Nigella Sativa Meta
Curcumin Meta Nitazoxanide Meta
Famotidine Meta Paxlovid Meta
Favipiravir Meta Quercetin Meta
Fluvoxamine Meta Remdesivir Meta
Hydroxychlor.. Meta Thermotherapy Meta
Ivermectin Meta

All Studies   Meta Analysis    Recent:   
0 0.5 1 1.5 2+ Severe case -20% Improvement Relative Risk Sotrovimab  Kneidinger et al.  EARLY TREATMENT Is early treatment with sotrovimab beneficial for COVID-19? Retrospective 218 patients in Germany (January - March 2022) No significant difference in severe cases c19early.org Kneidinger et al., Infection, September 2022 Favors sotrovimab Favors control

Outcome of lung transplant recipients infected with SARS-CoV-2/Omicron/B.1.1.529: a Nationwide German study

Kneidinger et al., Infection, doi:10.1007/s15010-022-01914-8
Sep 2022  
  Post
  Facebook
Share
  Source   PDF   All   Meta
Sotrovimab for COVID-19
38th treatment shown to reduce risk in May 2023
 
*, now known with p = 0.0017 from 22 studies, recognized in 37 countries. Efficacy is variant dependent.
Lower risk for hospitalization.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
4,000+ studies for 60+ treatments. c19early.org
Retrospective 218 COVID+ lung transplant patients in Germany, showing no significant difference in severe cases with early sotrovimab use.
Efficacy is variant dependent. In Vitro studies predict lower efficacy for BA.1 Liu, Sheward, VanBlargan, BA.4, BA.5 Haars, XBB.1.9.3, XBB.1.5.24, XBB.2.9, CH.1.1 Pochtovyi, and no efficacy for BA.2 Zhou, ХВВ.1.9.1, XBB.1.16, BQ.1.1.45, and CL.1 Pochtovyi. US EUA has been revoked.
Study covers remdesivir, casirivimab/imdevimab, sotrovimab, and molnupiravir.
risk of severe case, 20.2% higher, RR 1.20, p = 0.79, treatment 21 of 125 (16.8%), control 13 of 93 (14.0%).
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Kneidinger et al., 9 Sep 2022, retrospective, Germany, peer-reviewed, 11 authors, study period 1 January, 2022 - 20 March, 2022, lung transplant patients. Contact: nikolaus.kneidinger@med.uni-muenchen.de.
This PaperSotrovimabAll
Outcome of lung transplant recipients infected with SARS-CoV-2/Omicron/B.1.1.529: a Nationwide German study
Nikolaus Kneidinger, Matthias Hecker, Vasiliki Bessa, Ina Hettich, Alexandra Wald, Sabine Wege, Anna-Barbara Nolde, Maike Oldigs, Zulfiya Syunyaeva, Heinrike Wilkens, Jens Gottlieb
Infection, doi:10.1007/s15010-022-01914-8
Purpose Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) is currently the major threat for immunocompromised individuals. The course of COVID-19 in lung transplant recipients in the Omicron era remains unknown. The aim of the study was to assess outcome and associated factors in lung transplant recipients in a German-wide multicenter approach. Methods All affected individuals from January 1st to March 20th, 2022 from 8 German centers during the Omicron wave were collected. Baseline characteristics and antiviral measures were associated with outcome. Results Of 218 patients with PCR-proven SARS-CoV-2 infection 166 patients (76%) received any early (< 7 days) antiviral therapy median 2 (interquartile range 1-4) days after symptom onset. Most patients received sotrovimab (57%), followed by remdesivir (21%) and molnupiravir (21%). An early combination therapy was applied in 45 patients (21%). Thirty-four patients (16%) developed a severe or critical disease severity according to the WHO scale. In total, 14 patients (6.4%) died subsequently associated with COVID-19. Neither vaccination and antibody status, nor applied treatments were associated with outcome. Only age and glomerular filtration rate < 30 ml/min/1.73m 2 were independent risk factors for a severe or critical COVID-19. Conclusion COVID-19 due to Omicron remains an important threat for lung transplant recipients. In particular, elderly patients and patients with impaired kidney function are at risk for worse outcome. Prophylaxis and therapy in highly immunocompromised individuals need further improvement.
Author contributions NK and JG designed and directed the project. All authors contributed to the data collection. NK and JG performed the analysis and drafted the manuscript. All authors were involved in interpretation of results reviewed the manuscript. Funding Open Access funding enabled and organized by Projekt DEAL. Not applicable. Declarations Competing interests The authors declare no competing interests. Conflict of interest The authors have no competing interests as defined by Springer, or other interests that might be perceived to influence the results and/or discussion reported in this paper. Ethical approval The study was approved by the central institutional ethics committee (LMU Munich, Germany; project number 22-0078). Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the..
References
Aversa, Benvenuto, Anderson, COVID-19 in lung transplant recipients: a single center case series from New York City, Am J Transplant, doi:10.1111/ajt.16241
Bernal, Da Silva, Musungaie, Molnupiravir for oral treatment of covid-19 in nonhospitalized patients, N Engl J Med, doi:10.1056/NEJMoa2116044
Bouzid, Visseaux, Kassasseya, Comparison of patients infected with delta versus omicron COVID-19 variants presenting to paris emergency departments: a retrospective cohort study, Ann Intern Med, doi:10.7326/M22-0308
Coll, Fernández-Ruiz, Sánchez-Álvarez, COVID-19 in transplant recipients: the Spanish experience, Am J Transplant, doi:10.1111/ajt.16369
Fall, Eldesouki, Sachithanandham, variant delta with omicron: unprecedented spike in COVID-19 cases associated with fewer admissions and comparable upper respiratory viral loads, doi:10.1101/2022.01.26.22269927
Gleeson, Martin, Thomson, Kidney transplant recipients and omicron: outcomes, effect of vaccines and the efficacy and safety of novel treatments, medRxiv, doi:10.1101/2022.05.03.22274524
Gottlieb, Kolditz, Gade, Welte, Kneidinger, Benefit of monoclonal antibodies in early treatment of COVID-19 after lung transplantation-a retrospective analysis in two centers, Eur Respir J, doi:10.1183/13993003.00124-2022
Gottlieb, Vaca, Paredes, Early remdesivir to prevent progression to severe covid-19 in outpatients, N Engl J Med, doi:10.1056/NEJMoa2116846
Gupta, Gonzalez-Rojas, Juarez, Early treatment for covid-19 with SARS-CoV-2 neutralizing antibody sotrovimab, N Engl J Med, doi:10.1056/NEJMoa2107934
Gupta, Gonzalez-Rojas, Juarez, Effect of sotrovimab on hospitalization or death among high-risk patients with mild to moderate COVID-19: a randomized clinical trial, JAMA, doi:10.1001/jama.2022.2832
Hadi, Naqvi, Kupec, Sofka, Sarwari, Outcomes of COVID-19 in solid organ transplant recipients: a propensitymatched analysis of a large research network, Transplantation, doi:10.1097/TP.0000000000003670
Havlin, Skotnicova, Dvorackova, Impaired humoral response to third dose of BNT162b2 mRNA COVID-19 vaccine despite detectable spike protein-specific T cells in lung transplant recipients, Transplantation, doi:10.1097/TP.0000000000004021
Havlin, Svorcova, Dvorackova, Immunogenicity of BNT162b2 mRNA COVID-19 vaccine and SARS-CoV-2 infection in lung transplant recipients, J Heart Lung Transplant, doi:10.1016/j.healun.2021.05.004
Heldman, Kates, Safa, Changing trends in mortality among solid organ transplant recipients hospitalized for COVID-19 during the course of the pandemic, Am J Transplant, doi:10.1111/ajt.16840
Hoffmann, Krüger, Schulz, The Omicron variant is highly resistant against antibody-mediated neutralization: implications for control of the COVID-19 pandemic, Cell, doi:10.1016/j.cell.2021.12.032
Hui, Ho, Cheung, Omicron variant replication in human bronchus and lung ex vivo, Nature, doi:10.1038/s41586-022-04479-6
Iketani, Liu, Guo, Antibody evasion properties of SARS-CoV-2 Omicron sublineages, Nature, doi:10.1038/s41586-022-04594-4
Kamp, Hinrichs, Fuge, Ewen, Gottlieb, COVID-19 in lung transplant recipients-risk prediction and outcomes, PLoS One, doi:10.1371/journal.pone.0257807
Koczulla, Sczepanski, Koteczki, SARS-CoV-2 infection in two patients following recent lung transplantation, Am J Transplant, doi:10.1111/ajt.15998
Maslo, Friedland, Toubkin, Characteristics and outcomes of hospitalized patients in South Africa during the COVID-19 omicron wave compared with previous waves, JAMA, doi:10.1001/jama.2021.24868
Pulliam, Van Schalkwyk, Govender, Increased risk of SARS-CoV-2 reinfection associated with emergence of Omicron in South Africa, Science, doi:10.1126/science.abn4947
Ravanan, Mumford, Ushiro-Lumb, Two doses of SARS-CoV-2 vaccines reduce risk of death due to COVID-19 in solid organ transplant recipients: preliminary outcomes from a UK registry linkage analysis, Transplantation, doi:10.1097/TP.0000000000003908
Salerno, Jennings, Lange, Kovac, Shertel et al., Early clinical experience with nirmatrelvir/ritonavir for the treatment of COVID-19 in solid organ transplant recipients, Am J Transplant, doi:10.1111/ajt.17027
Takashita, Kinoshita, Yamayoshi, Efficacy of antiviral agents against the SARS-CoV-2 omicron subvariant BA.2, N Engl J Med, doi:10.1056/NEJMc2201933
Uraki, Kiso, Iida, Characterization and antiviral susceptibility of SARS-CoV-2 Omicron/BA, Nature, doi:10.1038/s41586-022-04856-1
Verleden, Glanville, Lease, Chronic lung allograft dysfunction: definition, diagnostic criteria, and approaches to treatment-a consensus report from the pulmonary council of the ISHLT, J Heart Lung Transplant, doi:10.1016/j.healun.2019.03.009
Wolter, Jassat, Walaza, Early assessment of the clinical severity of the SARS-CoV-2 omicron variant in South Africa: a data linkage study, Lancet, doi:10.1016/S0140-6736(22)00017-4
Wratil, Stern, Priller, Three exposures to the spike protein of SARS-CoV-2 by either infection or vaccination elicit superior neutralizing immunity to all variants of concern, Nat Med, doi:10.1038/s41591-022-01715-4
Wu, Mcgoogan, Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72 314 cases from the chinese center for disease control and prevention, JAMA, doi:10.1001/jama.2020.2648
Loading..
Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. FLCCC and WCH provide treatment protocols.
  or use drag and drop   
Submit