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  1. Article: Neurologic Outcomes and Quality of Life in Children After Extracorporeal Membrane Oxygenation.

    Michel, Alizée / Vedrenne-Cloquet, Meryl / Kossorotoff, Manoëlle / Thy, Michaël / Levy, Raphaël / Pouletty, Marie / De Marcellus, Charles / Grimaud, Marion / Moulin, Florence / Hully, Marie / Simonnet, Hina / Desguerre, Isabelle / Renolleau, Sylvain / Oualha, Mehdi / Chareyre, Judith

    Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies

    2023  Volume 25, Issue 3, Page(s) e158–e167

    Abstract: Rationale: Use of life support with extracorporeal membrane oxygenation (ECMO) is associated with brain injury. However, the consequences of these injuries on subsequent neurologic development and health-related quality of life (HRQoL) are poorly ... ...

    Abstract Rationale: Use of life support with extracorporeal membrane oxygenation (ECMO) is associated with brain injury. However, the consequences of these injuries on subsequent neurologic development and health-related quality of life (HRQoL) are poorly described in children.
    Objectives: The aim of this preliminary study was to describe short- and long-term neurologic outcomes in survivors of ECMO, as well as their HRQoL.
    Design: Retrospective identified cohort with contemporary evaluations.
    Setting: Necker Children's Hospital academic PICU.
    Patients: Forty survivors who underwent ECMO (October 2014 to January 2020) were included in follow-up assessments in May 2021.
    Interventions: None.
    Measurement and main results: We first reviewed the outcomes of ECMO at the time of PICU discharge, which included a summary of neurology, radiology, and Pediatric Overall/Cerebral Performance Category (POPC/PCPC) scores. Then, in May 2021, we interviewed parents and patients to assess HRQoL (Pediatric Quality of Life Inventory [PedsQL]) and POPC/PCPC for children 3 years old or older, and Denver II test (DTII) for younger children. An evaluation of DTII in the youngest patients 1 year after ECMO decannulation was also added. Median age at ECMO was 1.4 years (interquartile range [IQR], 0.4-6 yr). Thirty-five children (88%) underwent a venoarterial ECMO. At PICU discharge, 15 of 40 patients (38%) had neurologic impairment. Assessment of HRQoL was carried out at median of 1.6 years (IQR, 0.7-3.3 yr) after PICU discharge. PedsQL scores were over 70 of 100 for all patients (healthy peers mean results: 80/100), and scores were like those published in patients suffering with chronic diseases. In May 2021, seven of 15 patients had a normal DTII, and 36 of 40 patients had a POPC/PCPC score less than or equal to 3.
    Conclusions: None of our patients presented severe disability at long term, and HRQoL evaluation was reassuring. Considering the risk of neurologic impairment after ECMO support, a systematic follow-up of these high-risk survivor patients would be advisable.
    MeSH term(s) Child ; Humans ; Infant ; Child, Preschool ; Quality of Life ; Extracorporeal Membrane Oxygenation/adverse effects ; Retrospective Studies ; Health Status ; Nervous System Diseases/epidemiology ; Nervous System Diseases/etiology
    Language English
    Publishing date 2023-12-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2052349-X
    ISSN 1947-3893 ; 1529-7535
    ISSN (online) 1947-3893
    ISSN 1529-7535
    DOI 10.1097/PCC.0000000000003419
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Respiratory complications in pediatric epidermal necrolysis: A retrospective study of 22 cases.

    Schmartz, Sophie / Welfringer-Morin, Anne / Le Bourgeois, Muriel / Delacourt, Christophe / Berteloot, Laureline / Rabia, Smail Hadj / Bellon, Nathalia / Moulin, Florence / Pouletty, Marie / Garcelon, Nicolas / Bodemer, Christine / Drummond, David

    Journal of the American Academy of Dermatology

    2023  Volume 89, Issue 4, Page(s) 857–859

    MeSH term(s) Humans ; Child ; Retrospective Studies ; Stevens-Johnson Syndrome/complications ; Stevens-Johnson Syndrome/diagnosis
    Language English
    Publishing date 2023-06-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 603641-7
    ISSN 1097-6787 ; 0190-9622
    ISSN (online) 1097-6787
    ISSN 0190-9622
    DOI 10.1016/j.jaad.2023.05.092
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Visiting Policies and Parental Presence During PICU Admission: A Survey in French Units.

    Bergerat, Manon / De Saint Blanquat, Laure / Milesi, Christophe / Grimaud, Marion / Le Bourgeois, Fleur / Renolleau, Sylvain / Pouletty, Marie / Oualha, Mehdi / Leteurtre, Stéphane / Recher, Morgan / Béranger, Agathe

    Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies

    2023  Volume 24, Issue 10, Page(s) e498–e504

    Abstract: Objectives: To describe the policies about parent visiting and involvement in care during admission to French PICUs.: Design: A structured questionnaire was emailed to the chief of each of 35 French PICUs. Data about visiting policies, involvement in ...

    Abstract Objectives: To describe the policies about parent visiting and involvement in care during admission to French PICUs.
    Design: A structured questionnaire was emailed to the chief of each of 35 French PICUs. Data about visiting policies, involvement in care, evolution of policies, and general characteristics were collected from April 2021 to May 2021. A descriptive analysis was conducted.
    Setting: Thirty-five PICUs in France.
    Patients: None.
    Interventions: None.
    Measurements and main results: Twenty-nine of 35 (83%) PICUs replied. Twenty-four-hour access for parents was reported for all PICUs responding. Other allowed visitors were grandparents (21/29, 72%) and siblings (19/29, 66%) with professional support. Simultaneous visits were restricted to two visitors in 83% (24/29) of PICUs. Family presence was always permitted during medical rounds for 20 of 29 (69%) PICUs. Most of the units rarely or never allowed parental presence during the most invasive procedures, such as central venous catheter placement (18/29, 62%) and intubation (22/29, 76%).
    Conclusions: Unrestricted access to the PICU, for both parents, was available in all responding French units. There were, however, restrictions on the number of visitors and the presence of other family members at the bedside. Moreover, permission for parental presence during care procedures was heterogenous, and mainly restricted. National guidelines and educational programs are needed to support family wishes and promote acceptance by healthcare providers in French PICUs.
    MeSH term(s) Humans ; Child ; Surveys and Questionnaires ; Parents ; Policy ; France ; Intensive Care Units, Pediatric
    Language English
    Publishing date 2023-05-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2052349-X
    ISSN 1947-3893 ; 1529-7535
    ISSN (online) 1947-3893
    ISSN 1529-7535
    DOI 10.1097/PCC.0000000000003284
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Response to: 'Exaggerated neutrophil extracellular trap formation in Kawasaki disease: a key phenomenon behind the outbreak in western countries?' by Yamashita

    Pouletty, Marie / Dingulu, Glory / Ouldali, Naim / Corseri, Olivier / Ducrocq, Camille / Meinzer, Ulrich / Faye, Albert / Galeotti, Caroline / Melki, Isabelle

    Annals of the rheumatic diseases

    2020  

    Keywords covid19
    Language English
    Publishing date 2020-08-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/annrheumdis-2020-218644
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Voiding cystography: an unusual route of induced hypothyroidism by iodine overdose in two newborns with chronic kidney disease.

    Cohen, Laure / Pouletty, Marie / Frerot, Alice / Tanase, Anca / Ali, Liza / Baudouin, Véronique

    Pediatric nephrology (Berlin, Germany)

    2019  Volume 34, Issue 7, Page(s) 1295–1297

    Abstract: Background: Iatrogenic induced hypothyroidism had been described in newborns and more particularly in preterm infants after cutaneous or intravenous exposure to iodine. CASE-DIAGNOSIS : We reported a new risk of iodine intoxication with the cases of two ...

    Abstract Background: Iatrogenic induced hypothyroidism had been described in newborns and more particularly in preterm infants after cutaneous or intravenous exposure to iodine. CASE-DIAGNOSIS : We reported a new risk of iodine intoxication with the cases of two newborns who developed hypothyroidism after intra vesical iodine injection during a cystography, which was performed to confirm antenatal diagnosis of posterior urethral valves (PUV). The newborns both developed transient hypothyroidism due to an iodine overdose.
    Conclusions: These two observations suggest that voiding cystourethrography (VCUG) should be carefully considered in newborns with severe uropathy, particularly in the case of renal insufficiency. If indicated, thyroid function should be monitored in the following weeks, and in case of hypothyroidism treatment should be started.
    MeSH term(s) Contrast Media/adverse effects ; Cystography ; Humans ; Hypothyroidism/chemically induced ; Infant, Newborn ; Iodine/adverse effects ; Iopamidol/adverse effects ; Iopamidol/analogs & derivatives ; Iothalamic Acid/adverse effects ; Iothalamic Acid/analogs & derivatives ; Kidney Failure, Chronic/complications ; Male
    Chemical Substances Contrast Media ; Iothalamic Acid (16CHD79MIX) ; iomeprol (17E17JBP8L) ; Iodine (9679TC07X4) ; ioxitalamic acid (967RDI7Z6K) ; Iopamidol (JR13W81H44)
    Language English
    Publishing date 2019-04-01
    Publishing country Germany
    Document type Case Reports ; Journal Article
    ZDB-ID 631932-4
    ISSN 1432-198X ; 0931-041X
    ISSN (online) 1432-198X
    ISSN 0931-041X
    DOI 10.1007/s00467-019-04247-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Response to: 'Correspondence on 'Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort' by Ventura

    Chommeloux, Juliette / Pouletty, Marie / Ouldali, Naim / Kerneis, Mathieu / Mathian, Alexis / Mestiri, Raphaele / Rohmer, Julien / Hekimian, Guillaume / Melki, Isabelle

    Annals of the rheumatic diseases

    2020  Volume 81, Issue 12, Page(s) e240

    MeSH term(s) Child ; Humans ; COVID-19 ; SARS-CoV-2 ; Kava ; Mucocutaneous Lymph Node Syndrome/diagnosis
    Language English
    Publishing date 2020-11-20
    Publishing country England
    Document type Multicenter Study ; Journal Article ; Comment
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/annrheumdis-2020-218984
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Response to: 'Correspondence on 'Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID19): a multicentre cohort'' by Mastrolia

    Borocco, Charlotte / Pouletty, Marie / Galeotti, Caroline / Meinzer, Ulrich / Faye, Albert / Koné-Paut, Isabelle / Ouldali, Naim / Melki, Isabelle

    Annals of the rheumatic diseases

    2020  Volume 81, Issue 11, Page(s) e219

    MeSH term(s) COVID-19/complications ; Child ; Humans ; Kava ; Mucocutaneous Lymph Node Syndrome/diagnosis ; SARS-CoV-2 ; Systemic Inflammatory Response Syndrome
    Keywords covid19
    Language English
    Publishing date 2020-10-06
    Publishing country England
    Document type Multicenter Study ; Letter ; Comment
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/annrheumdis-2020-218814
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Response to: 'Correspondence on 'Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort' by Pouletty

    Ouldali, Naim / Pouletty, Marie / Lokmer, Johanna / Benzouid, Cherine / Beyler, Constance / Deho, Anna / Meinzer, Ulrich / Faye, Albert / Melki, Isabelle

    Annals of the rheumatic diseases

    2020  

    Keywords covid19
    Language English
    Publishing date 2020-08-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 7090-7
    ISSN 1468-2060 ; 0003-4967
    ISSN (online) 1468-2060
    ISSN 0003-4967
    DOI 10.1136/annrheumdis-2020-218614
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Juvenile neuropsychiatric systemic lupus erythematosus: A specific clinical phenotype and proposal of a probability score.

    Labouret, Mathilde / Trebossen, Vincent / Ntorkou, Alexandra / Bartoli, Sophie / Aubart, Mélodie / Auvin, Stéphane / Bader-Meunier, Brigitte / Baudouin, Véronique / Corseri, Olivier / Dingulu, Glory / Ducrocq, Camille / Dumaine, Cécile / Elmaleh, Monique / Fabien, Nicole / Faye, Albert / Hau, Isabelle / Hentgen, Véronique / Kwon, Théresa / Meinzer, Ulrich /
    Ouldali, Naim / Parmentier, Cyrielle / Pouletty, Marie / Renaldo, Florence / Savioz, Isabelle / Benoist, Jean-François / Le Roux, Enora / Ellul, Pierre / Melki, Isabelle

    Lupus

    2024  Volume 33, Issue 4, Page(s) 328–339

    Abstract: Objective: Juvenile systemic lupus erythematosus (j-SLE) is a rare chronic auto-immune disease involving several organs. Neuropsychiatric (NP) SLE (NPSLE) is frequent in j-SLE and associated with increased morbidity/mortality. Although NPSLE ... ...

    Abstract Objective: Juvenile systemic lupus erythematosus (j-SLE) is a rare chronic auto-immune disease involving several organs. Neuropsychiatric (NP) SLE (NPSLE) is frequent in j-SLE and associated with increased morbidity/mortality. Although NPSLE classification criteria exist, attributing NP features to j-SLE remains a major challenge. The study objective is to thoroughly describe j-NPSLE patients and assist in their diagnosis.
    Methods: This is a 4-year retrospective monocentric study of j-SLE patients. NP events were attributed to j-SLE using standardised diagnostic criteria and multidisciplinary paediatric clinical expertise. Clinical features, brain magnetic resonance imaging (MRI)s and samples analysis including cerebrospinal fluid were assessed. A risk of j-NPSLE score was developed based on multivariable logistic regression analysis.
    Results: Of 39 patients included, 44% were identified as having j-NPSLE. J-NPSLE diagnosis was established at the onset of j-SLE in 59% of patients. In addition to frequent kidney involvement (76%) and chilblains (65%), all j-NPSLE patients displayed psychiatric features: cognitive symptoms (82%), hallucinations (76%), depressed mood (35%), acute confused state (18%) and catatonia (12%). Neurological involvement was often mild and nonspecific, with headache (53%) in about half of the patients. The main features reported on brain MRI were nonspecific T2/FLAIR white matter hyperintensities (65%), and cerebral atrophy (88%). Upon immunosuppressive treatment, clinical improvement of NP features was observed in all j-NPSLE patients. The score developed to attribute j-NPSLE probability, guide further investigations and appropriate treatments is based on hallucinations, memory, sleep and renal involvement (Sensitivity: 0.95 Specificity: 0.85). Cerebrospinal fluid (CSF) neopterin assessment increases the score sensitivity and specificity.
    Conclusion: Physicians should carefully and systematically assess the presence of NP features at diagnosis and early stages of j-SLE. For j-NPSLE patients with predominant psychiatric features, a multidisciplinary collaboration, including psychiatrists, is essential for the diagnosis, management and follow-up.
    MeSH term(s) Humans ; Child ; Lupus Vasculitis, Central Nervous System/pathology ; Lupus Erythematosus, Systemic/complications ; Lupus Erythematosus, Systemic/diagnosis ; Lupus Erythematosus, Systemic/pathology ; Retrospective Studies ; Brain/diagnostic imaging ; Brain/pathology ; Magnetic Resonance Imaging/methods ; Hallucinations/complications ; Hallucinations/pathology
    Language English
    Publishing date 2024-02-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 1154407-7
    ISSN 1477-0962 ; 0961-2033
    ISSN (online) 1477-0962
    ISSN 0961-2033
    DOI 10.1177/09612033241229022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Response to: 'Exaggerated neutrophil extracellular trap formation in Kawasaki disease: a key phenomenon behind the outbreak in western countries?' by Yamashita et al

    Pouletty, Marie / Dingulu, Glory / Ouldali, Naim / Corseri, Olivier / Ducrocq, Camille / Meinzer, Ulrich / Faye, Albert / Galeotti, Caroline / Melki, Isabelle

    Ann. rheum. dis

    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #726101
    Database COVID19

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