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Dive into the research topics where Candice Estellat is active.

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Featured researches published by Candice Estellat.


Clinical Infectious Diseases | 2004

Determinants of Immune Reconstitution Inflammatory Syndrome in HIV Type 1-Infected Patients with Tuberculosis after Initiation of Antiretroviral Therapy

Guillaume Breton; Xavier Duval; Candice Estellat; Xavier Poaletti; Daniel Bonnet; David Mvondo Mvondo; Pascale Longuet; Catherine Leport; Jean-Louis Vildé

Immune reconstitution inflammatory syndrome (IRIS) occurred in 16 of 37 antiretroviral-naive patients who were treated subsequently for tuberculosis and human immunodeficiency virus (HIV) type 1 infection. IRIS was related to increases in the CD4 cell percentage and in the ratio of CD4 cells to CD8 cells after 1 month of antiretroviral therapy and to dissemination of tuberculosis. These results have implications for the diagnosis of IRIS and the understanding of its pathogenesis.


Clinical Infectious Diseases | 2015

High Rate of Acquisition but Short Duration of Carriage of Multidrug-Resistant Enterobacteriaceae After Travel to the Tropics

E. Ruppé; Laurence Armand-Lefevre; Candice Estellat; Paul-Henri Consigny; Assiya El Mniai; Yacine Boussadia; Catherine Goujon; Pascal Ralaimazava; Pauline Campa; Pierre-Marie Girard; Benjamin Wyplosz; Daniel Vittecoq; Olivier Bouchaud; Guillaume Le Loup; Gilles Pialoux; Marion Perrier; Ingrid Wieder; Nabila Moussa; Marina Esposito-Farèse; Isabelle Hoffmann; Bruno Coignard; Jean-Christophe Lucet; Antoine Andremont; Sophie Matheron

BACKGROUNDnMultidrug-resistant Enterobacteriaceae (MRE) are widespread in the community, especially in tropical regions. Travelers are at risk of acquiring MRE in these regions, but the precise extent of the problem is not known.nnnMETHODSnFrom February 2012 to April 2013, travelers attending 6 international vaccination centers in the Paris area prior to traveling to tropical regions were asked to provide a fecal sample before and after their trip. Those found to have acquired MRE were asked to send fecal samples 1, 2, 3, 6, and 12 months after their return, or until MRE was no longer detected. The fecal relative abundance of MRE among all Enterobacteriaceae was determined in each carrier.nnnRESULTSnAmong 824 participating travelers, 574 provided fecal samples before and after travel and were not MRE carriers before departure. Of these, 292 (50.9%) acquired an average of 1.8 MRE. Three travelers (0.5%) acquired carbapenemase-producing Enterobacteriaceae. The acquisition rate was higher in Asia (142/196 [72.4%]) than in sub-Saharan Africa (93/195 [47.7%]) or Latin America (57/183 [31.1%]). MRE acquisition was associated with the type of travel, diarrhea, and exposure to β-lactams during the travel. Three months after return, 4.7% of the travelers carried MRE. Carriage lasted longer in travelers returning from Asia and in travelers with a high relative abundance of MRE at return.nnnCONCLUSIONSnMRE acquisition is very frequent among travelers to tropical regions. Travel to these regions should be considered a risk factor of MRE carriage during the first 3 months after return, but not beyond.nnnCLINICAL TRIALS REGISTRATIONnNCT01526187.


Eurosurveillance | 2014

Acquisition of carbapenemase-producing Enterobacteriaceae by healthy travellers to India, France, February 2012 to March 2013.

Ruppé E; Laurence Armand-Lefevre; Candice Estellat; El-Mniai A; Boussadia Y; Paul-Henri Consigny; Girard Pm; Vittecoq D; Olivier Bouchaud; Gilles Pialoux; Marina Esposito-Farèse; Bruno Coignard; Lucet Jc; Antoine Andremont; Matheron S

Healthy travellers to countries where carbapenemases-producing Enterobacteriaceae (CPE) are endemic might be at risk for their acquisition, even without contact with the local healthcare system. Here, we report the acquisition of CPE (two OXA-181, one New Delhi metallo-beta-lactamase 1 (NDM-1)) in three healthy travellers returning from India. The duration of CPE intestinal carriage was less than one month. The results indicate that healthy travellers recently returning from India might be considered as at risk for CPE carriage.


Heart | 2015

Haemodynamic and anatomic progression of aortic stenosis

Virginia Nguyen; C. Cimadevilla; Candice Estellat; Isabelle Codogno; Virginie Huart; Joelle Benessiano; Xavier Duval; Philippe Pibarot; Marie Annick Clavel; Maurice Enriquez-Sarano; David Messika-Zeitoun

Background Aortic valve stenosis (AS) is a progressive disease, but the impact of baseline AS haemodynamic or anatomic severity on AS progression remains unclear. Methods In 149 patients (104 mild AS, 36 moderate AS and 9 severe AS) enrolled in 2 ongoing prospective cohorts (COFRASA/GENERAC), we evaluated AS haemodynamic severity at baseline and yearly, thereafter, using echocardiography (mean pressure gradient (MPG)) and AS anatomic severity using CT (degree of aortic valve calcification (AVC)). Results After a mean follow-up of 2.9±1.0u2005years, mean MGP increased from 22±11 to 30±16u2005mmu2005Hg (+3±3u2005mmu2005Hg/year), and mean AVC from 1108±891 to 1640±1251u2005AU (arbitrary units) (+188±176u2005AU/year). Progression of AS was strongly related to baseline haemodynamic severity (+2±3u2005mmu2005Hg/year in mild AS, +4±3u2005mmu2005Hg/year in moderate AS and +5±5u2005mmu2005Hg/year in severe AS (p=0.01)), and baseline haemodynamic severity was an independent predictor of haemodynamic progression (p=0.0003). Annualised haemodynamic and anatomic progression rates were significantly correlated (r=0.55, p<0.0001), but AVC progression rate was also significantly associated with baseline haemodynamic severity (+141±133u2005AU/year in mild AS, +279±189u2005AU/year in moderate AS and +361±293u2005AU/year in severe AS, p<0.0001), and both baseline MPG and baseline AVC were independent determinants of AVC progression (p<0.0001). Conclusions AS progressed faster with increasing haemodynamic or anatomic severity. Our results suggest that a medical strategy aimed at preventing AVC progression may be useful in all subsets of patients with AS including those with severe AS and support the recommended closer follow-up of patients with AS as AS severity increases. Clinical trial registration COFRASA (clinicalTrial.gov number NCT 00338676) and GENERAC (clinicalTrial.gov number NCT00647088).


European Journal of Radiology | 2015

Interstitial lung disease in anti-synthetase syndrome: Initial and follow-up CT findings

Marie-Pierre Debray; R. Borie; Marie-Pierre Revel; Jean-Marc Naccache; Antoine Khalil; Cécile Toper; D. Israel-Biet; Candice Estellat; Pierre-Yves Brillet

PURPOSEnTo describe the initial and follow-up CT features of interstitial lung disease associated with anti-synthetase syndrome (AS-ILD).nnnMATERIALS AND METHODSnTwo independent thoracic radiologists retrospectively analysed thin-section CT images obtained at diagnosis of AS-ILD in 33 patients (17 positive for anti-Jo1, 13 for anti-PL12, and three for anti-PL7 antibodies). They evaluated the pattern, distribution and extent of the CT abnormalities. They also evaluated the change in findings during follow-up (median 27 months; range 13-167 months) in 26 patients.nnnRESULTSnAt diagnosis, ground-glass opacities (100%), reticulations (87%) and traction bronchiectasis (76%) were the most common CT findings. Consolidations were present in 45% of patients. A non-specific interstitial pneumonia (NSIP), organizing pneumonia (OP) or mixed NSIP-OP CT pattern were observed in 15 out of 33 (45%), seven out of 33 (21%) and eight out of 33 (24%) patients, respectively, whereas the CT pattern was indeterminate in three patients. During follow-up, consolidations decreased or disappeared in 11 out of 12 patients (92%), among which seven within the first 6 months, but honeycombing progressed or appeared in ten out of 26 patients (38%) and overall disease extent increased in nine out of 26 patients (35%).nnnCONCLUSIONnCT features at diagnosis of AS-ILD mainly suggest NSIP and OP, isolated or in combination. Consolidations decrease or disappear in most cases but the disease may progress to fibrosis in more than one third of patients.


PLOS ONE | 2014

Timing of intermittent seminal HIV-1 RNA shedding in patients with undetectable plasma viral load under combination antiretroviral therapy.

Xavier Ferraretto; Candice Estellat; Florence Damond; Pascale Longuet; Sylvie Epelboin; Pauline Demailly; Chadi Yazbeck; Marie-Astrid Llabador; Blandine Pasquet; Yazdan Yazdanpanah; Sophie Matheron; Catherine Patrat

It was demonstrated that combination antiretroviral therapy (cART) reduces the HIV-1 viral load (VL) in the blood and the seminal compartment. Some studies have reported that the seminal HIV-1 VL is undetectable in individuals with an undetectable blood plasma viral load (bpVL) under cART. However, some recent studies have demonstrated that seminal HIV-1 RNA may still be detected, and potentially infectious, even in the case of an undetectable bpVL. The aim of this retrospective study was to determine the detection rate of a seminal VL and whether shedding could be intermittent over a very short time. From January 2006 to December 2011, 88 HIV-1 infected men, enrolled in an Assisted Reproduction program, provided 306 semen samples, corresponding to 177 frozen sperm samples (two samples delivered at a one-hour interval (nu200a=u200a129) or one sample (nu200a=u200a48)). All enrolled men were under cART, with an undetectable bpVL for more than 6 months. HIV-1 RNA was quantified in seminal plasma using a Roche COBAS Ampliprep COBAS TaqMan HIV-1 test. Seminal HIV-1 RNA was detected in 23 samples (7.5%) from 17 patients (19.3%). This detection rate was stable over years. With regards to the freezing of two samples delivered at a one-hour interval, the proportion of discordance between the first and second samples was 9.3% (12/129). Our results confirm the intermittent shedding of HIV-1 in semen. While this finding has been shown by studies examining longer time intervals, to our knowledge, this has never been demonstrated over such a short time interval.


BMC Pregnancy and Childbirth | 2017

Association between maternal social deprivation and prenatal care utilization: the PreCARE cohort study

Clémentine Gonthier; Candice Estellat; Catherine Deneux-Tharaux; Béatrice Blondel; Toni Alfaiate; Thomas Schmitz; Jean-François Oury; Laurent Mandelbrot; Dominique Luton; Philippe Ravaud; Elie Azria

BackgroundMaternal social deprivation is associated with an increased risk of adverse maternal and perinatal outcomes. Inadequate prenatal care utilization (PCU) is likely to be an important intermediate factor. The health care system in France provides essential health services to all pregnant women irrespective of their socioeconomic status. Our aim was to assess the association between maternal social deprivation and PCU.MethodsThe analysis was performed in the database of the multicenter prospective PreCARE cohort study. The population source consisted in all parturient women registered for delivery in 4 university hospital maternity units, Paris, France, from October 2010 to November 2011 (Nu2009=u200910,419). This analysis selected women with singleton pregnancies that ended after 22xa0weeks of gestation (Nu2009=u20099770). The associations between maternal deprivation (four variables first considered separately and then combined as a social deprivation index: social isolation, poor or insecure housing conditions, no work-related household income, and absence of standard health insurance) and inadequate PCU were tested through multivariate logistic regressions also adjusted for immigration characteristics and education level.ResultsAttendance at prenatal care was poor for 23.3% of the study population. Crude relative risks and confidence intervals for inadequate PCU were 1.6 [1.5–1.8], 2.3 [2.1–2.6], and 3.1 [2.8–3.4], for women with a deprivation index of 1, 2, and 3, respectively, compared to women with deprivation index of 0. Each of the four deprivation variables was significantly associated with an increased risk of inadequate PCU. Because of the interaction observed between inadequate PCU and mother’s country of birth, we stratified for the latter before the multivariate analysis. After adjustment for the potential confounders, this social gradient remained for women born in France and North Africa. The prevalence of inadequate PCU among women born in sub-Saharan Africa was 34.7%; the social gradient in this group was attenuated and no longer significant. Other factors independently associated with inadequate PCU were maternal age, recent immigration, and unplanned or unwanted pregnancy.ConclusionSocial deprivation is independently associated with an increased risk of inadequate PCU. Recognition of risk factors is an important step in identifying barriers to PCU and developing measures to overcome them.


Heart | 2016

Determinants and prognostic value of Galectin-3 in patients with aortic valve stenosis

Dimitri Arangalage; Virginia Nguyen; Tiphaine Robert; Maria Melissopoulou; Tiffany Mathieu; Candice Estellat; Isabelle Codogno; Virginie Huart; Xavier Duval; Claire Cimadevilla; Alec Vahanian; Monique Dehoux; David Messika-Zeitoun

Objective Myocardial fibrosis has been proposed as an outcome predictor in asymptomatic patients with severe aortic stenosis (AS) that may lead to consider prophylactic surgery. It can be detected using MRI but its widespread use is limited and development of substitute biomarkers is highly desirable. We analysed the determinants and prognostic value of galectin-3, one promising biomarker linked to myocardial fibrosis. Methods Patients with at least mild degenerative AS enrolled between 2006 and 2013 in two ongoing studies, COFRASA/GENERAC (COhorte Française de Rétrécissement Aortique du Sujet Agé/GENEtique du Rétrécissement Aortique), aiming at assessing the determinants of AS occurrence and progression, constituted our population. Results We prospectively enrolled 583 patients. The mean galectin-3 value was 14.3±5.6u2005ng/mL. There was no association between galectin-3 and functional status (p=0.55) or AS severity (p=0.58). Independent determinants of galectin-3 were age (p=0.0008), female gender (p=0.04), hypertension (p=0.002), diabetes (p=0.02), reduced left ventricular ejection fraction (p=0.01), diastolic dysfunction (E/e′, p=0.02) and creatinine clearance (p<0.0001). Among 330 asymptomatic patients at baseline, galectin-3 was neither predictive of outcome in univariate analysis (p=0.73), nor after adjustment for age, gender, rhythm, creatinine clearance and AS severity (p=0.66). Conclusions In a prospective cohort of patients with a wide range of AS severity, galectin-3 was not associated with AS severity or functional status. Main determinants of galectin-3 were age, hypertension and renal function. Galectin-3 did not provide prognostic information on the occurrence of AS-related events. Our results do not support the use of galectin-3 in the decision-making process of asymptomatic patients with AS. Trial registration number COFRASA NCT00338676 and GENERAC CT00647088


British Journal of Obstetrics and Gynaecology | 2018

Association between inadequate antenatal care utilisation and severe perinatal and maternal morbidity: an analysis in the PreCARE cohort

Morgane Linard; Béatrice Blondel; Candice Estellat; Catherine Deneux-Tharaux; Dominique Luton; Jean-François Oury; Thomas Schmitz; Laurent Mandelbrot; Elie Azria

Because the effectiveness of antenatal care in reducing pregnancy complications is still discussed despite widespread recommendations of its use, we sought to assess the association between utilisation of recommended antenatal care and severe maternal (SMM) and perinatal morbidity (SPM).


Drug and Alcohol Dependence | 2016

Impact of a computer-assisted Screening, Brief Intervention and Referral to Treatment on reducing alcohol consumption among patients with hazardous drinking disorder in hospital emergency departments. The randomized BREVALCO trial

David Duroy; Isabelle Boutron; Gabriel Baron; Philippe Ravaud; Candice Estellat; Michel Lejoyeux

OBJECTIVEnTo assess the impact of a computer-assisted Screening, Brief Intervention, and Referral to Treatment (SBIRT) on daily consumption of alcohol by patients with hazardous drinking disorder detected after systematic screening during their admission to an emergency department (ED).nnnDESIGNnTwo-arm, parallel group, multicentre, randomized controlled trial with a centralised computer-generated randomization procedure.nnnSETTINGnFour EDs in university hospitals located in the Paris area in France.nnnPARTICIPANTSnPatients admitted in the ED for any reason, with hazardous drinking disorder detected after systematic screening (i.e., Alcohol Use Disorder Identification Test score ≥5 for women and 8 for men OR self-reported alcohol consumption by week ≥7 drinks for women and 14 for men).nnnINTERVENTIONSnThe experimental intervention was computer-assisted SBIRT and the comparator was a placebo-controlled intervention (i.e., a computer-assisted education program on nutrition). Interventions were administered in the ED and followed by phone reinforcements at 1 and 3 months.nnnMAIN OUTCOME MEASUREnThe primary outcome was the mean number of alcohol drinks per day in the previous week, at 12 months. Results From May 2005 to February 2011, 286 patients were randomized to the computer-assisted SBIRT and 286 to the comparator intervention. The two groups did not differ in the primary outcome, with an adjusted mean difference of 0.12 (95% confidence interval, -0.88 to 1.11).nnnCONCLUSIONSnThere was no additional benefit of the computer-assisted alcohol SBIRT as compared with the computer-assisted education program on nutrition among patients with hazardous drinking disorder detected by systematic screening during their admission to an ED.

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Elie Azria

Paris Descartes University

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Bruno Coignard

Institut de veille sanitaire

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Béatrice Blondel

Paris Descartes University

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Isabelle Colombet

Paris Descartes University

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Morgane Linard

Paris Descartes University

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