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1.
Clin Infect Dis ; 74(10): 1786-1794, 2022 05 30.
Article in English | MEDLINE | ID: mdl-34383032

ABSTRACT

BACKGROUND: Our objective is to describe the presentation and complications, including relapses, of coronavirus disease 2019 (COVID-19) in patients under anti-CD20 treatments. In addition, to describe viral clearance and determine the safety of reintroducing anti-CD20 treatment. METHODS: Retrospective cohort study of 422 patients under anti-CD20 treatment that was administered from 1 January 2019 to 31 December 2020. RESULTS: Fifty-seven patients were diagnosed with COVID-19 (13.5%). Twenty-five patients (43.9%) required hospital admission. Five patients died (8.8%), and 10 developed severe COVID-19 and acute respiratory distress syndrome. Mortality rate was higher among patients infected during the first 3 months following the last dose of anti-CD20 (14.7% vs 0%, P = .046). The median time of persistence of positive reverse transcription polymerase chain reaction (RT-PCR) was 22 days (IQR 13-40).Nine out of 52 survivors (17.3%) presented relapses. All of them received the last dose of anti-CD20 less than 6 months before the COVID-19 episode. Clinical presentation was fever (n = 8; 88.9%), dyspnea (n = 7; 77.8%), cough (n = 7; 77.8%), worsening of previous infiltrates (n = 5; 55.6%) and new pulmonary infiltrates (n = 8; 88.9%). An increase in lymphocytes with CD4/CD8 ratio inversion was observed in all cases. Among the 25 patients who resumed anti-CD20 drug, 4 (16.0%) presented relapses vs 5/28 among those who did not (17.9%), (P = .857). CONCLUSIONS: Patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during the 6 months after anti-CD20 administration had a worse outcome and a higher mortality rate. The duration of infectivity may be longer. Relapses of COVID-19 occurred in more than 15% and were associated with viral replication. Once the infection is resolved, it is safe to restart treatment with anti-CD20.


Subject(s)
Antineoplastic Agents , COVID-19 , Antibodies, Monoclonal/therapeutic use , Humans , Incidence , Recurrence , Retrospective Studies , SARS-CoV-2
2.
Mycoses ; 64(7): 742-747, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33768563

ABSTRACT

BACKGROUND: Recently, several scores to quantify compliance with the guidelines in candidaemia management (EQUAL, GEMICOMED, Valerio) have been developed. Evidence supporting the association of these scores to the prognosis is scarce. We aim to evaluate the performance of these candidaemia guideline adherence scores to predict candidaemia outcome. METHODS: We recorded retrospectively data from candidaemia episodes (January 2017-December 2018). We analysed adherence to guidelines for candidaemia management according to EQUAL, GEMICOMED and Valerio scores, and we correlated those to outcome. RESULTS: Fifty-four first episodes of candidaemia were retrieved. Five patients who died in the first 48 hours after blood cultures were not included. Thirty-day mortality in evaluable patients was 18.4%. Median adherence to guidelines according to EQUAL score was 17 (interquartile range [IQR]: 15-19), and according to GEMICOMED was 86% (IQR: 72.5%-100%). According to Valerio score, adequacy of antifungal prescription was 8.5/10 (SD: 1.9). A cut-off of ≥17 for EQUAL or compliance >70% for GEMICOMED was associated with inferior 30-day mortality (7.1% vs 33.3%, P = .028 and 7.9% vs 54.5%, P = .002, respectively). Infectious diseases (ID) evaluated cases obtained a better EQUAL score (>17; 82.1% vs 42.9%, P = .006), had inferior 30-day mortality (9.4% vs 35.3%, P = .049) and a better antifungal prescription adequacy (Valerio score 9.0 vs 7.5, P = .011). CONCLUSION: Adherence to guidelines for candidaemia management evaluated by means of EQUAL and GEMICOMED score was associated with a decreased 30-day mortality. Adequacy of antifungal prescription can be ameliorated. ID consultation improved guideline adherence and was associated with decreased 30-day mortality.


Subject(s)
Candidemia , Guideline Adherence , Aged , Antifungal Agents/therapeutic use , Candida/drug effects , Candida/pathogenicity , Candidemia/complications , Candidemia/drug therapy , Communicable Diseases/complications , Communicable Diseases/drug therapy , Female , Humans , Male , Middle Aged , Mortality , Prognosis , Quality of Health Care , Referral and Consultation , Retrospective Studies , Spain/epidemiology
6.
Rev. esp. quimioter ; 30(6): 458-463, dic. 2017. tab, graf
Article in Spanish | IBECS (Spain) | ID: ibc-169400

ABSTRACT

Introducción. La prevalencia de enterobacterias productoras de carbapenemasas (EPC) es creciente en España. El objetivo de este trabajo ha sido describir las características epidemiológicas, clínicas y microbiológicas de los casos de infección y/o colonización por EPC en dos centros sanitarios del noroeste de Madrid: un hospital comarcal de agudos (HCA) y un hospital de media estancia (HME). Material y métodos. Se recogieron durante los años 2013 y 2014 datos microbiológicos, epidemiológicos y clínicos de todos los pacientes colonizados o infectados por EPC. Desde la aparición del primer caso, en marzo de 2013, se detectaron un total de 197 nuevos casos. Resultados. Un 33,5% de los pacientes presentaron infección clínica y el 66,5% restante fueron colonizaciones. Klebsiella pneumoniae fue la especie predominante (87,8%) y OXA-48 la carbapenemasa más frecuente (91,9%), observándose diferencias entre ambos centros. El análisis de las cepas mostró una mayor diversidad genética en el HME con respecto al HMA. Conclusión. Al estudiar el patrón de transmisión se encontró un aumento de la incidencia en un corto periodo de tiempo y una rápida diseminación de las cepas entre ambos hospitales. Esto pone de manifiesto la necesidad de estandarizar medidas de cribado de posibles portadores y de instaurar programas de control de la infección en este tipo de hospitales (AU)


Introduction. In Spain, the overall prevalence of carbapenem-resistant Enterobacteriaceae (CRE) is increasing. We describe the epidemiological, clinical and microbiological characteristics features of patients with colonization or infection due to CRE in two hospitals in the north-west of Madrid during two years. One hospital was a community acute hospital and the second one was a non-acute rehabilitation hospital. Material and methods. A total of 197 CPE isolates were detected during 2013-2014. Microbiological, epidemiological and clinical data were collected, since the first isolate was found in March 2013. Results. A 33.5% of patients with CRE had symptomatic infection and the remaining 66.5% were colonizations. Klebsiella pneumoniae (87.8%) was the most prevalent species and OXA-48 the most frequent carbapenemase (91.9%). We found intra-interhospital spread and some differences in the epidemiology of CRE depending on the hospital, such as more genetic variability in the non-acute rehabilitation hospital. Conclusions. Studying the CRE transmission we founded an increased incidence in a short period of time and a rapid dissemination of strains between both hospitals. This highlights the need to standardize screening measures for potential carriers and infection control programs in our hospitals (AU)


Subject(s)
Humans , Carbapenems/pharmacokinetics , Drug Resistance, Microbial , Enterobacteriaceae/pathogenicity , Enterobacteriaceae Infections/epidemiology , Risk Factors , Carrier State , Hospitals, Community/statistics & numerical data , Cross Infection/epidemiology
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