Paula Pecanha

Dr. Paula Pecanha

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Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 November 2021 in Mycoses
Verified
Journal Article
Open access
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TLTobias Lahmer
Tobias Lahmer
PPPaula Pecanha
Paula Pecanha
RSRoland M. Schmid
Roland M. Schmid
ACArnaldo Lopes Colombo
Arnaldo Lopes Colombo
Patients with acute and chronic liver impairment are susceptible to invasive fungal infections such as candidemia and invasive pulmonary aspergillosis as a result of cirrhosis‐associated immune dysfunction, humoral immunodeficiency, cell‐mediated dysfunction and systemic inflammation. Besides classical risk factors for invasive fungal infection, acute‐on‐chronic liver failure, corticosteroid use, gastrointestinal bleeding, and prophylactic use of antibiotics are all additional conditions which are related to the potential development of fungal infections. Therefore, high‐risk patients should be carefully followed by microbiological surveillance including cultures but also by imaging and fungal biomarkers for providing early diagnosis. Echinocandins are still the mainstay and first line antifungal therapy in cases of invasive candidiasis. Due to concerns of liver toxicity and in cases of renal impairment liposomal amphotericin B is a suitable alternative to voriconazole in patients with invasive pulmonary aspergillosis. Although, data of isavucoanzole and posaconazole use in those patients are also promising more specific studies in the subgroup of patients with liver impairment are needed. Especially, due to the late diagnosis and multiple organ dysfunction usually present in patients with liver impairment morbidity and mortality rates remain high. Based on the broad spectrum of diverse reports with varying content and quality and in some cases lack of evidence we performed a systematic review on this topic.

26 December 2018 in Journal of Fungi
Verified
Journal Article
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JJJoão Nobrega De Almeida Júnior
João Nobrega De Almeida Júnior
PPPaula Pecanha
Paula Pecanha
Arnaldo L. ColomboArnaldo L. Colombo
Arnaldo L. Colombo
Paracoccidioidomycosis (PCM) is an endemic mycosis found in Latin America that causes systemic disease mostly in immunocompetent hosts. A small percentage of PCM occurs in immunocompromised patients where low clinical suspicion of the infection, late diagnosis, and uncertainties about its management are factors that negatively impact their outcomes. We conducted a literature review searching reports on PCM associated to HIV, cancer, maligned hemopathies, solid organ transplantation, and immunotherapies, in order to check for peculiarities in terms of natural history and challenges in the clinical management of PCM in this population. HIV patients with PCM usually had low T CD4+ cell counts, pulmonary and lymph nodes involvement, and a poorer prognosis (≈50% mortality). Most of the patients with PCM and cancer had carcinoma of the respiratory tract. Among maligned hemopathies, PCM was more often related to lymphoma. In general, PCM prognosis in patients with malignant diseases was related to the cancer stage. PCM in transplant recipients was mostly associated with the late phase of kidney transplantation, with a high mortality rate (44%). Despite being uncommon, reactivation of latent PCM may take place in the setting of immunocompromised patients exhibiting clinical particularities and it carries higher mortality rates than normal hosts.

25 May 2021 in PLOS ONE
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Journal Article
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DADanilo Candido Almeida
Danilo Candido Almeida
MFMaria Do Carmo Pinho Franco
Maria Do Carmo Pinho Franco
DSDavi Rettori Pardo dos Santos
Davi Rettori Pardo dos Santos
MSMarina Colella Santos
Marina Colella Santos
IMIsabela Soucin Maltoni
Isabela Soucin Maltoni
MGMiguel Angelo Goes
Miguel Angelo Goes
Background: COVID-19 is a multisystemic disorder that frequently causes acute kidney injury (AKI). However, the precise clinical and biochemical variables associated with AKI progression in patients with severe COVID-19 remain unclear.Methods: We performed a retrospective study on 278 hospitalized patients who were admitted to the ward and intensive care unit (ICU) with COVID-19 between March 2020 and June 2020, at the University Hospital, São Paulo, Brazil. Patients aged ≥ 18 years with COVID-19 confirmed on RT-PCR were included. AKI was defined according to the Kidney Disease Improving Global Outcomes (KDIGO) criteria. We evaluated the incidence of AKI, several clinical variables, medicines used, and outcomes in two sub-groups: COVID-19 patients with AKI (Cov-AKI), and COVID-19 patients without AKI (non-AKI). Univariate and multivariate analyses were performed.Results: First, an elevated incidence of AKI (71.2%) was identified, distributed across different stages of the KDIGO criteria. We further observed higher levels of creatinine, C-reactive protein (CRP), leukocytes, neutrophils, monocytes, and neutrophil-to-lymphocyte ratio (NLR) in the Cov-AKI group than in the non-AKI group, at hospital admission. On univariate analysis, Cov-AKI was associated with older age (>62 years), hypertension, CRP, MCV, leucocytes, neutrophils, NLR, combined hydroxychloroquine and azithromycin treatment, use of mechanical ventilation, and vasoactive drugs. Multivariate analysis showed that hypertension and the use of vasoactive drugs were independently associated with a risk of higher AKI in COVID-19 patients. Finally, we preferentially found an altered erythrocyte and leukocyte cellular profile in the Cov-AKI group compared to the non-AKI group, at hospital discharge.Conclusions: In our study, the development of AKI in patients with severe COVID-19 was related to inflammatory blood markers and therapy with hydroxychloroquine/azithromycin, with vasopressor requirement and hypertension considered potential risk factors. Thus, attention to the protocol, hypertension, and some blood markers may help assist doctors with decision-making for the management of COVID-19 patients with AKI.

8 April 2015 in Clinical Rheumatology
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OBOn Behalf Of Biobadabrasil
On Behalf Of Biobadabrasil
BFBárbara P. Fafá
Bárbara P. Fafá
PLPaulo Louzada-Junior
Paulo Louzada-Junior
DTDavid C. Titton
David C. Titton
EZEliana Zandonade
Eliana Zandonade
VVValeria Valim
Valeria Valim

7 February 2023 in Journal of Fungi
Verified
Journal Article
Open access
PDF file
PPPaula Pecanha
Paula Pecanha
ATAndrés Tirado-Sánchez
Andrés Tirado-Sánchez
SGSarah Santos Gonçalves
Sarah Santos Gonçalves
ABAlexandro Bonifaz
Alexandro Bonifaz
Arnaldo L. ColomboArnaldo L. Colombo
Arnaldo L. Colombo
Coccidioidomycosis (CM) and paracoccidioidomycosis (PCM) are systemic mycoses that are highly endemic in Latin America and have recently been included on the World Health Organization (WHO) Fungal Priority Pathogens List. Coccidioides immitis and Coccidioides posadasii are recognized as etiological agents of CM, with peculiarities in their geographic distribution. The genus Paracoccidioides now includes Paracoccidioides lutzii and the Paracoccidioides brasiliensis complex, which encompasses four phylogenetic species. In both diseases, pulmonary signs and symptoms are the main reasons for patients to seek medical assistance, and they are frequently misdiagnosed as tuberculosis. In this paper, we present a critical view of the strategies for diagnosis and clinical management of CM and PCM. Over the past few decades, there has been an increase in the number of reports of endemic fungal infections in areas previously thought to be “non-endemic” due to climate change and increased travel, among other factors. Learning to recognize their main epidemiological aspects and clinical manifestations is crucial so that clinicians can include them in the differential diagnosis of lung disease and avoid late diagnosis.

30 January 2020 in Seminars in Respiratory and Critical Care Medicine
Verified
Journal Article
Closed access
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FQFlavio Queiroz-Telles
Flavio Queiroz-Telles
PPPaula Pecanha
Paula Pecanha
MJMarcos Rosa Júnior
Marcos Rosa Júnior
RBRodrigo de Melo Baptista
Rodrigo de Melo Baptista
PPPaulo Mendes Peçanha
Paulo Mendes Peçanha
Paracoccidioidomycosis (PCM) is one of the most relevant systemic endemic mycoses in Latin American countries, especially in South American countries, with endemic and hyperendemic areas. The real burden of PCM may be underestimated because of a lack of compulsory case notification. Recent phylogenetic data revealed that Paracoccidioides brasiliensis comprises several cryptic species including P. brasiliensis and P. lutzii. However, the genetic biodiversity of Paracoccidioides does not affect the clinical manifestations or therapeutic response to therapy. Lung involvement is a common finding, especially in patients experiencing the chronic form of the disease, and, because of its similarities with tuberculosis, clinicians must be alert to the possibility of PCM in patients with chronic respiratory manifestations and epidemiological risk factors for this fungal disease.