Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Felicia Berroa is active.

Publication


Featured researches published by Felicia Berroa.


Clinical & Experimental Allergy | 2014

The usefulness of plasma histamine and different tryptase cut‐off points in the diagnosis of peranaesthetic hypersensitivity reactions

Felicia Berroa; Alberto Lafuente; Gracia Javaloyes; Marta Ferrer; Rafael Moncada; Goikoetxea Mj; C. M. Urbain; Sanz Ml; Gabriel Gastaminza

Anaesthetic hypersensitivity reactions can be IgE‐ or not IgE‐mediated and are a challenge to find the causal agent. Histamine and tryptase determination are classically considered useful in the diagnosis of these reactions. The aim of our study was to assess the diagnostic usefulness of plasma histamine and different cut‐off points of serum tryptase.


Allergy | 2013

Early skin testing is effective for diagnosis of hypersensitivity reactions occurring during anesthesia.

Alberto Lafuente; Gracia Javaloyes; Felicia Berroa; Goikoetxea Mj; Rafael Moncada; J. M. Núñez-Córdoba; Paula Cabrera-Freitag; C. D'Amelio; Sanz Ml; Gabriel Gastaminza

Allergic skin tests have to be performed 4–6 weeks after an allergic anesthetic reaction. Patients with allergic reactions during anesthesia were prospectively included (n = 44). Skin tests were performed in two stages: (i) Stage 1 (S1), 0–4 days after the reaction; and (ii) Stage 2 (S2), 4–8 weeks after. Five (11.5%) surgical procedures were suspended due to the reaction. Positive skin tests were obtained in 25/44 patients (57%). Allergic diagnosis was carried out at S1 in 15/25 (60%) and at S2 in 10/25 (40%). Three patients resulted positive only in S1. Overall agreement among S1 and S2 skin tests was 70.45%. The kappa statistic was 0.41 (P‐value = 0.002). Odds ratio of obtaining a false negative in S1 (compared with S2) was 3.33. Early allergological study is useful, could minimize false negatives, but should be considered as a complement to late skin tests.


Anesthesia & Analgesia | 2015

The incidence of perioperative hypersensitivity reactions: a single-center, prospective, cohort study.

Felicia Berroa; Alberto Lafuente; Gracia Javaloyes; Paula Cabrera-Freitag; Juan M. de la Borbolla; Rafael Moncada; Goikoetxea Mj; Sanz Ml; Marta Ferrer; Gabriel Gastaminza

BACKGROUND:The incidence of perioperative hypersensitivity reactions, which can be life-threatening, ranges from 1 in 20,000 to 1 in 1361. These reactions are usually classified as IgE or non-IgE mediated. The aim of this study was to determine the incidence of allergic reactions during general anesthesia in our hospital, to establish the incidence of the allergic reactions for each drug used, to assess the frequency of IgE-mediated reactions in even mild reactions, and to compare the degree of agreement between anesthesiologist suspicion and allergy diagnosis. METHODS:We included patients diagnosed with a clinical hypersensitivity reaction during a procedure under general anesthesia over a 30-month period (February 2008 to August 2010). Plasma histamine and serum tryptase concentrations were determined in these patients. We performed skin tests to diagnose the causative agent. Data from the hospital electronic prescribing system were collected to determine the ratio of reactions for each drug. RESULTS:During the study period, 16,946 anesthetic procedures were performed (53% involved males; mean age, 51.6 years). Forty-four perianesthetic reactions were recorded, and the ratio of reactions was 1 in 385 operations (95% confidence interval, 1/529–1/287). Twenty-five reactions (25/44; 57%) occurred during the induction of anesthesia. Twenty-one reactions (21/44; 48%) were mild, involving only skin, and 23 of 44 (52%) were anaphylactic reactions. Four of 10 patients who had only a rash experienced IgE-mediated reactions. Five surgeries (11%) were suspended because of the severity of the reactions. Fifteen reactions (15/30; 50%) were IgE mediated, and, in 2 of 30 (7%), a non-IgE agent was found (cold urticaria and nonsteroidal anti-inflammatory drug intolerance). The ratio of reactions for each drug was as follows: protamine, 1 in 468; cisatracurium, 1 in 1388; amoxicillin-clavulanate, 1 in 1968; atracurium, 1 in 2039; and dipyrone, 1 in 3159. CONCLUSIONS:Perioperative reactions are more common than previously reported. Mild hypersensitivity perioperative reactions—involving only skin—should be considered in evaluating patients because a substantial number of these reactions are IgE mediated.


International Archives of Allergy and Immunology | 2014

Pomegranate (Punica granatum L.) Expresses Several nsLTP Isoforms Characterized by Different Immunoglobulin E-Binding Properties

Michela Bolla; Sara Zenoni; Stephan Scheurer; Stefan Vieths; Maria del Mar San Miguel Moncin; M. Olivieri; Andrea Antico; Marta Ferrer; Felicia Berroa; Ernesto Enrique; Linda Avesani; Francesco Marsano; Gianni Zoccatelli

Background: Pomegranate allergy is associated with sensitization to non-specific lipid transfer proteins (nsLTPs). Our aim was to identify and characterize the non-specific nsLTPs expressed in pomegranate at the molecular level and to study their allergenic properties in terms of immunoglobulin E (IgE)-binding and cross-reactivity with peach nsLTP (Pru p 3). Methods: A non-equilibrium two-dimensional (2-D) electrophoretic approach based on acid-urea PAGE and sodium dodecyl sulfate PAGE was set up to separate pomegranate nsLTPs. Their immunoreactivity was tested by immunoblotting carried out with anti-Pru p 3 polyclonal antibodies and sera from pomegranate-allergic patients. For final identification, pomegranate nsLTPs were purified by chromatography and subjected to trypsin digestion and mass spectrometry (MS) analysis. For this purpose, the sequences obtained by cDNA cloning of three pomegranate nsLTPs were integrated in the database that was subsequently searched for MS data interpretation. Results: Four nsLTPs were identified by 2-D immunoblotting. The detected proteins showed different IgE-binding capacity and partial cross-reactivity with Pru p 3. cDNA cloning and MS analyses led to the identification of three nsLTP isoforms with 66-68% amino acid sequence identity named Pun g 1.0101, Pun g 1.0201 and Pun g 1.0301. Conclusions: By 2-D electrophoresis, we could separate different nsLTP isoforms possessing different IgE-binding properties, which might reflect peculiar allergenic potencies. The contribution of Pru p 3 to prime sensitization is not central as in other plant nsLTPs.


International Archives of Allergy and Immunology | 2016

Lipid Transfer Protein Syndrome in a Non-Mediterranean Area.

Julián Azofra; Felicia Berroa; Gabriel Gastaminza; Noemí Saiz; Pedro M. Gamboa; Catalina Vela; Blanca E. García; Susana Lizarza; Miguel Angel Echenagusia; Alejandro Joral; María Ascensión Aranzabal; María D. Quiñones; Jáuregui I; Juan F. Madera; Jose Antonio Navarro; Maria Teresa Lizaso; Amalia Bernad; Goikoetxea Mj


Journal of Investigational Allergology and Clinical Immunology | 2015

Do Skin Prick Test and In Vitro Techniques Diagnose Sensitization to Peach Lipid Transfer Protein and Profilin Equally Well in Allergy to Plant Food and Pollen

Goikoetxea Mj; Felicia Berroa; Paula Cabrera-Freitag; Marta Ferrer; Núñez-Córdoba Jm; Sanz Ml; Gabriel Gastaminza


Annals of Allergy Asthma & Immunology | 2013

In vivo and in vitro techniques in the diagnosis of lipid transfer protein sensitization.

Felicia Berroa; Gabriel Gastaminza; Noemí Saiz; Julián Azofra; Pedro M. Gamboa; Catalina Vela; Blanca E. García; Susana Lizarza; Miguel Angel Echenagusia; Alejandro Joral; María Ascensión Aranzabal; María D. Quiñones; Jáuregui I; Juan F. Madera; Jose Antonio Navarro; Maria Teresa Lizaso; Goikoetxea Mj


The Journal of Allergy and Clinical Immunology | 2011

Diagnostic Reliability Of The Component-based Allergen-microarray In Grass, Cypress And Olive Pollens Allergy

Paula Cabrera-Freitag; Sanz Ml; Goikoetxea Mj; Gracia Javaloyes; Felicia Berroa; Marta Ferrer


Enfermedades Infecciosas Y Microbiologia Clinica | 2017

Chronic hand infection

Isabel Bernad; Felicia Berroa; Maria Pilar Gil


Enfermedades Infecciosas Y Microbiologia Clinica | 2017

Infección crónica en la mano

Isabel Bernad; Felicia Berroa; Maria Pilar Gil

Collaboration


Dive into the Felicia Berroa's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Sanz Ml

University of Navarra

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge