J. Prat

ORCID: 0000-0002-8974-0827
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About
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Research Areas
  • Congenital Diaphragmatic Hernia Studies
  • Congenital Anomalies and Fetal Surgery
  • Tracheal and airway disorders
  • Esophageal and GI Pathology
  • Neonatal Respiratory Health Research
  • Intestinal Malrotation and Obstruction Disorders
  • Urological Disorders and Treatments
  • Sympathectomy and Hyperhidrosis Treatments
  • Congenital gastrointestinal and neural anomalies
  • Allergic Rhinitis and Sensitization
  • Hernia repair and management
  • Tumors and Oncological Cases
  • Cardiac, Anesthesia and Surgical Outcomes
  • Asthma and respiratory diseases
  • COVID-19 and healthcare impacts
  • Drug-Induced Adverse Reactions
  • Viral gastroenteritis research and epidemiology
  • Antibiotics Pharmacokinetics and Efficacy
  • Antibiotic Use and Resistance
  • Hip and Femur Fractures
  • Urologic and reproductive health conditions
  • Digestive system and related health
  • Dysphagia Assessment and Management
  • Infant Nutrition and Health
  • Inflammatory mediators and NSAID effects

Hospital Sant Joan de Déu Barcelona
2012-2025

Universitat de Barcelona
2003-2024

Centre for Biomedical Network Research on Rare Diseases
2024

Bellvitge University Hospital
2003

Hospital Clínic de Barcelona
1993

Naomi Wright Andrew Leather Niyi Ade‐Ajayi Nick Sevdalis Justine Davies and 95 more Dan Poenaru Emmanuel A. Ameh Adesoji Ademuyiwa Kokila Lakhoo Emily R. Smith Abdel Douiri Maria Elstad Marcus Sim Cristiana Riboni Bruno Martínez-Leo Melika Akhbari Stephen Tabiri Ashrarur Rahman Mitul Dayang Anita Abdul Aziz Camila Girardi Fachin Alliance Niyukuri Muhammad Arshad Fowzia Ibrahim Natalie Moitt Mohamed Fahmy Doheim Hannah R. Thompson Harmony Ubhi Isabelle Williams Sophia Hashim Godfrey Sama Philipo Laura Herrera Aayenah Yunus Dominique Vervoort Samuel Parker Yousra-Imane Benaskeur Osaid Alser Nana Adofo-Ansong Ahmad Alhamid Hosni Salem Mahmoud Saleh Safa Elrais Sadi A. Abukhalaf Patricia Shinondo Ibrahim Nour Emrah Aydın Agota Vaitkienė Kelly Naranjo Andile Dube Sodumisa Ngwenya Mina A Yacoub Henang Kwasau Gabriella Hyman S M.elghazaly Ibrahim Al‐Slaibi Intisar Hisham Helena Franco Hana Arbab Lubna Samad Aqil Soomro Muhammad Amjad Chaudhry Safina Karim Muhammad Adnan Khattak Shireen Anne Nah Doris Mae Dimatatac Candy S. C. Choo Niveshni Maistry Ashrarur Rahman Mitul Samiul Hasan Sabbir Karim Hina Yousuf Taimur Qureshi Ibrahim Nour Raed Al-Taher Osama Abdul Kareem Sarhan Luis García‐Aparicio J. Prat Eva Blázquez-Gómez Xavier Tarrado Martí Iriondo P Bragagnini Rodríguez Segundo Rite Gracia Lars Hagander Emma Svensson Sheila Agyeiwaa Owusu Alhassan Abdul‐Mumin Dominic Bagbio Vijay Anand Ismavel Ann Miriam T Shajin Marlene Anaya Domínguez Monica Ivanov Andreea Mădălina Șerban Miliard Derbew Mahmoud Elfiky Maricarmen Olivos Perez Marcia Abrunhosa Matias Alexis Arnaud Ahmed Negida Sebastian King Mohamad Rafi Fazli

BackgroundCongenital anomalies are the fifth leading cause of mortality in children younger than 5 years globally. Many gastrointestinal congenital fatal without timely access to neonatal surgical care, but few studies have been done on these conditions low-income and middle-income countries (LMICs). We compared outcomes seven most common low-income, middle-income, high-income globally, identified factors associated with mortality.MethodsWe did a multicentre, international prospective cohort...

10.1016/s0140-6736(21)00767-4 article EN cc-by The Lancet 2021-07-01

Although the mechanism of aspirin-induced asthma and rhinitis is unknown, it has been suggested that adverse nasal bronchial reactions are caused by an increased production lipoxygenase products. In examining this hypothesis we have measured release peptide leukotrienes (PeptLTs), 15-HETE, prostaglandins in fluids obtained lavages after instillation acetylsalycilic acid (ASA) placebo (saline). Ten ASA-sensitive asthmatics, 10 ASA-insensitive seven healthy subjects were challenged a...

10.1164/ajrccm/145.1.65 article EN American Review of Respiratory Disease 1992-01-01
Cunera M. C. de Beaufort Dalia Aminoff Ivo de Blaauw Célia Cretolle Jens Dingemann and 95 more Natalie Durkin Wout Feitz JoAnne Fruithof Caterina Grano Carmen Mesas Burgos Nicole Schwarzer Graham Slater Tutku Soyer Cristiano Violani René Wijnen Paolo De Coppi Ramon R. Gorter Olivier Abbo Rossella Angotti Sanja Sindjic Antunovic Stefan Anzelewicz Christoph Arneitz Marion Arnold Zaki Assi Emrah Aydın Quentin Ballouhey Patricia Barila Sonia Basson Manuel Besendörfer Antonio Di Cesare Anne Dariel Inga Dekerytė Ivona Djordjević Vincenzo Domenichelli Lise Duranteau Çiǧdem Ulukaya Durakbaşa Anne‐Karoline Ebert Verena Ellerkamp Francesco Fascetti Leon Margit Fisch Araceli García Vázquez Christoph Gielok Gülnur Göllü Frank-Martin Haecker Gundela Holmdahl Sabine Irtan Ceri Jones M. Hassan Kakar Ali Keshtgar Kolja Kvist F. Laconi Marie Laurance Eduardo López Candel Johanna Ludwiczek Barbara Ludwikowski Francesco Macchini Mark Malota Lucas Matthyssens Benjamin Martin L Martínez Paola Midrio Marc Miserez Giovanni Mosiello Francisco Murcia Pascual Bernardo Nunez Roger Olén Can İhsan Öztorun Ayşe Parlak Alessio Pini Prato Anna Poupalou Marcos Prada Arias J. Prat Carlos Gil Luis Felipe Avila Ramirez Bertram Reingruber Giovanna Riccipetitoni Silke Riechardt Toni Risteski W Rogula Udo Rolle Carmelo Romeo Frank‐Mattias Schäfer G. Scirè Rony Sfeir Georg Singer Pim Sloots Michael Stanton Pernilla Stenström Maria Stockinger M. Surhan Janne Suominen Julia Syed Isabelle Talon Halil Tanrıverdi Osman Uzunlu Laura Valfrè Marieke J. Witvliet Elisa Zambaiti Cinzia Zanatta Augusto Zani

Transition of care (TOC; from childhood into adulthood) patients with anorectal malformations (ARM) and Hirschsprung disease (HD) ensures continuation for these patients. The aim this international study was to assess the current status TOC adult (AC) programs ARM HD.A survey developed by members EUPSA, ERN eUROGEN, ERNICA, including patient representatives (ePAGs), comprising four domains: general information, questions about transition adulthood, disease-specific regarding AC programs....

10.1016/j.jpedsurg.2023.06.008 article EN cc-by Journal of Pediatric Surgery 2023-06-15

Objective: Congenital high airway obstruction syndrome (CHAOS) normally has a dire prognosis due to laryngeal atresia and association with other anomalies. However, rare cases an isolated tracheal membrane have been described. We assessed systematically the larynx vocal cords in fetuses CHAOS, goal of identifying such attempting fetoscopic deobstruction. Methods: Between 2008 2012, 7 CHAOS were referred our institution. The ultrasonographic aspect trachea was assessed. report ultrasound...

10.1159/000350697 article EN Fetal Diagnosis and Therapy 2013-01-01

<title>Abstract</title> Purpose: Frenotomy is the procedure of choice for treating ankyloglossia. The literature reports that readhesion frenulum occurs in 2.6-13% cases. There no published evidence to support performing tongue exercises prevent this readhesion. We routinely recommend parents perform them. aimed determine recurrence rate ankyloglossia necessitating a refrenotomy and benefits massage prevention Methods: Prospective, observational study neonates who underwent frenotomy between...

10.21203/rs.3.rs-6226251/v1 preprint EN cc-by Research Square (Research Square) 2025-04-01

This is the first report of fetoscopy to successfully treat a case bilobar bronchial atresia presenting in form massive right lung tumor causing severe thoracic compression with mediastinal shift, pulmonary hypoplasia and eventually fetal hydrops. The presence an echolucent tubular structure hilum was identified as intrapulmonary continuation interrupted main bronchus, led diagnosis atresia. After extensive discussion counseling, fetoscopic operation designed indicated. procedure consisted...

10.1159/000339681 article EN Fetal Diagnosis and Therapy 2012-07-19

&lt;i&gt;Objective:&lt;/i&gt; To analyze the impact of in utero tracheal occlusion (TO) on lung tissue blood perfusion, as measured by fractional moving volume (FMBV) and conventional spectral Doppler, a rabbit model congenital diaphragmatic hernia (CDH). &lt;i&gt;Methods:&lt;/i&gt; In 50 fetal rabbits, left CDH was surgically created at 23 days gestational age (GA). At 28 GA, surviving fetuses were randomly assigned to undergo either TO (CDH+TO group) or sham operation (CDH group). Twenty...

10.1159/000254485 article EN Fetal Diagnosis and Therapy 2009-01-01

• An embryonal rhabdomyosarcoma that initially was seen as a polyp in the external auditory canal underwent uncontrollable direct extension along facial nerve through internal meatus, with encasement of base brain and entire spinal cord despite radical surgery, supervoltage irradiation, multidrug chemotherapy. This degree massive neuraxial spread without systemic metastases appears to be unique. (<i>Arch Otolaryngol</i>103:301-303, 1977)

10.1001/archotol.1977.00780220095014 article EN Archives of Otolaryngology - Head and Neck Surgery 1977-05-01

We report our experience in the postnatal management of congenital diaphragmatic hernia (CDH) after fetal endoluminal balloon tracheal occlusion (FETO).Out 19 CDH fetuses diagnosed since December 2005, 13 had a lung-to-head ratio (LHR) < 1.1 (0.86 +/- 0.11) and underwent FETO at mean gestational age (GA) 27.9 weeks. The was removed 3 cases through puncture EXIT (ex utero intrapartum treatment); there were trans-utero punctures, fetoscopies balloons deflated spontaneously. One patient died...

10.1055/s-2007-989275 article EN European Journal of Pediatric Surgery 2007-12-01

An abnormal platelet release of oxygen-free radicals has been described in acetylsalicylic acid (aspirin)-induced asthma, a finding which might suggest the existence an intrinsic, specific abnormality arachidonic metabolism these patients. The objective this study was to evaluate asthmatic patients with or without intolerance aspirin.Thirty subjects distributed into three groups were studied: group 1, 10 healthy subjects; 2, aspirin tolerance; and 3, aspirin-intolerant asthmatics. Platelets...

10.1136/thx.50.5.490 article EN Thorax 1995-05-01

For evaluation of two methods nasal cell identification, morphology and immunocytologic analysis, lavage was performed in 16 healthy subjects 29 patients suffering from rhinitis. Nasal smears were stained with May‐Grünwald‐Giemsa (MGG), cells identified according to their structure as epithelial cells, neutrophils, lymphocytes, eosinophils, metachromatic (basophils mast cells). Immunocytologic analysis monoclonal antibodies by the immunoalkaline phosphatase method. The following used: CK1,...

10.1111/j.1398-9995.1993.tb00753.x article EN Allergy 1993-11-01

Nutritional complications have an impact in both short- and long-term morbidity of patients with congenital diaphragmatic hernia (CDH). We aimed to compare time full enteral tube feeding depending on route -gastric (GT) or transpyloric (TPT)- newborns left CDH (L-CDH).Retrospective cohort study L-CDH admitted a referral tertiary care NICU between January 2007 December 2014. Lethal chromosomal abnormalities death before initiation nutrition were exclusion criteria.37 fed through GT, 46 by...

10.1016/j.jpedsurg.2023.06.018 article EN cc-by-nc-nd Journal of Pediatric Surgery 2023-07-05

The effectiveness of antimicrobial stewardship programs (ASP) in reducing use (AU) children has been proved. Many interventions have described suitable for different institution sizes, priorities, and patients, with surgical wards being one the areas that may benefit most. We aimed to describe results on AU length stay (LOS) a pre-post study during three years before (2014–2016) after (2017–2019) implementation an ASP based postprescription review feedback adolescents admitted...

10.3390/antibiotics10010005 article EN cc-by Antibiotics 2020-12-23
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