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1.
QJM ; 114(7): 464-470, 2021 Nov 05.
Artigo em Inglês | MEDLINE | ID: mdl-34254132

RESUMO

BACKGROUND: Mucormycosis (MM) is a deadly opportunistic fungal infection and a large surge in COVID-19-associated mucormycosis (CAM) is occurring in India. AIM: Our aim was to delineate the clinico-epidemiological profile and identify risk factors of CAM patients presenting to the Emergency Department (ED). DESIGN: This was a retrospective, single-centre, observational study. METHODS: We included patients who presented with clinical features or diagnosed MM and who were previously treated for COVID-19 in last 3 months of presentation (recent COVID-19) or currently being treated for COVID-19 (active COVID-19). Information regarding clinical features of CAM, possible risk factors, examination findings, diagnostic workup including imaging and treatment details were collected. RESULTS: Seventy CAM patients (median age: 44.5 years, 60% males) with active (75.7%) or recent COVID-19 (24.3%) who presented to the ED in between 6 May 2021 and 1 June 2021, were included. A median duration of 20 days (interquartile range: 13.5-25) was present between the onset of COVID-19 symptoms and the onset of CAM symptoms. Ninety-three percent patients had at least one risk factor. Most common risk factors were diabetes mellitus (70%) and steroid use for COVID-19 disease (70%). After clinical, microbiological and radiological workup, final diagnosis of rhino-orbital CAM was made in most patients (68.6%). Systemic antifungals were started in the ED and urgent surgical debridement was planned. CONCLUSION: COVID-19 infection along with its medical management have increased patient susceptibility to MM.


Assuntos
COVID-19 , Mucormicose , Adulto , Serviço Hospitalar de Emergência , Feminino , Humanos , Masculino , Mucormicose/diagnóstico , Mucormicose/epidemiologia , Estudos Retrospectivos , SARS-CoV-2
3.
Natl Med J India ; 27(3): 138-40, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25668083

RESUMO

BACKGROUND: Patients with HIV/AIDS are at a high risk of being infected with toxin-producing strains of Clostridium difficile (C. difficile) because of frequent hospitalization, exposure to antibiotics and antibiotic prophylaxis for opportunistic infections. There are little data from India on the prevalence of C. difficile infection in such patients. METHODS: We assessed the occurrence of C. difficile infections in HIV-positive patients with diarrhoea by looking for the presence of its toxin as well as by culturing. Enzyme immunoassay (EIA, Premier toxins A and B; Meridian Diagnostic Inc.) was used to detect toxin from 237 fresh stool samples collected from HIV-positive patients with diarrhoea. Culture was done on cycloserine-cefoxitin-fructose agar and brain- heart infusion agar. RESULTS: C. difficile was found in 12 of 237 (5.1%, 95% CI 2.64%-8.68%) HIV-positive patients with diarrhoea (9 patients were positive by EIA and 3 by culture). The presence of C. difficile in patients who had received antiretroviral therapy (7/66 [10.6%]) was significantly higher (p < 0.016) compared with those who had not (5/171 [3%]). Of the 12 patients positive for C. difficile, 7 were on antiretroviral therapy for a mean (SD) of 34.4 months with mean CD4+ count of 186 (98.81) cells/cmm and 5 patients were anti-retroviral-naïve with mean CD4+ count of 181 (68.7) cells/cmm. All the 12 patients were on antibiotics for previous 2 months and 4 of 12 had been hospitalized in the previous 30 days. CONCLUSION: C. difficile infections occurred more frequently in patients who had received antiretroviral therapy. Our study population had a lower frequency of C. difficile infections compared to previous studies.


Assuntos
Clostridioides difficile/efeitos dos fármacos , Diarreia/epidemiologia , Enterocolite Pseudomembranosa/epidemiologia , Infecções por HIV/epidemiologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antirretrovirais/uso terapêutico , Clostridioides difficile/isolamento & purificação , Coinfecção/epidemiologia , Coinfecção/prevenção & controle , Estudos Transversais , Diarreia/tratamento farmacológico , Diarreia/microbiologia , Enterocolite Pseudomembranosa/tratamento farmacológico , Enterocolite Pseudomembranosa/prevenção & controle , Feminino , Infecções por HIV/tratamento farmacológico , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Fatores de Risco , Adulto Jovem
4.
Talanta ; 33(12): 1009-13, 1986 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18964245

RESUMO

Chromate and cyanide have been determined by their ability to displace iodate from sparingly soluble lead iodate. The released iodate is treated with acidified iodide to give iodine, which is determined either by titration with thiosulphate, or spectrophotometrically as its blue complex with starch. Chromium(III) has been determined as chromate after its oxidation with peroxydisulphate. Sulphate, iodide, bromide, chloride, fluoride, oxalate, tartrate, phosphate and thiocyanate do not interfere. Thiosulphate, sulphite, sulphide, hexacyanoferrate(II) and molybdate ions vitiate the results. Silver, mercury, barium and iron(III) should be masked. Mixtures of cyanide, thiocyanate and halides have been analysed by using complementary procedures that employ the iodates of lead and mercury, and bromine oxidimetry. It has been shown that cyanide or thiocyanate interferes in the determination of iodide by oxidation to iodic acid, because of formation of cyanogen bromide.

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