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1.
J Oncol Pharm Pract ; 30(4): 777-779, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38486509

RÉSUMÉ

INTRODUCTION: In prostate cancer, androgens are key in the growth of both normal prostate and cancer cells. Abiraterone acetate inhibits CYP17, an important target in prostate cancer given its central role in the production of adrenal and tumor-derived androgens. Although abiraterone is generally well tolerated, common adverse effects such as hypertension, hypokalemia, and hepatotoxicity have been reported. CLINICAL CASE: We present the case of an 83-year-old Mexican man with high-volume EC IV prostate cancer resistant to castration, orchiectomy, and bone, liver, and lung metastases. First-line treatment with the CHAARTED scheme was indicated, by patient decision refuse chemotherapy treatment. On the fourth day of starting treatment, he developed pruritic erythematous macular skin lesions and urticaria on the posterior chest that resolved spontaneously. A generalized erythematous and pruritic maculopapular rash appeared 12 days after starting abiraterone, for which she was referred to allergies. MANAGEMENT AND RESULTS: An oral provocation test was performed for two days, presenting localized macular lesions eight hours after the administration of abiraterone. An oral desensitization protocol was carried out for ten days in which no hypersensitivity reactions were observed, thus achieving the successful administration of abiraterone.


Sujet(s)
Androstènes , Désensibilisation immunologique , Hypersensibilité médicamenteuse , Tumeurs de la prostate , Humains , Mâle , Sujet âgé de 80 ans ou plus , Tumeurs de la prostate/traitement médicamenteux , Désensibilisation immunologique/méthodes , Hypersensibilité médicamenteuse/étiologie , Androstènes/usage thérapeutique , Androstènes/effets indésirables , Androstènes/administration et posologie , Antinéoplasiques/effets indésirables , Antinéoplasiques/administration et posologie , Antinéoplasiques/usage thérapeutique , Tumeurs prostatiques résistantes à la castration/traitement médicamenteux
2.
J Asthma ; 60(5): 981-990, 2023 05.
Article de Anglais | MEDLINE | ID: mdl-36066123

RÉSUMÉ

OBJECTIVE: While advances in asthma care have been made in Latin America, there is still a large unmet need in patients with uncontrolled asthma. This post hoc analysis of the QUEST study assessed safety and efficacy of dupilumab in the subgroup of patients enrolled in Latin American countries with a type 2 inflammatory asthma phenotype (blood eosinophils ≥ 150cells/µL or FeNO ≥25ppb). METHODS: LIBERTY ASTHMA QUEST (NCT02414854) was a phase 3, multinational, randomized, double-blind, placebo-controlled study in patients with uncontrolled, moderate-to-severe asthma. Eligible patients ≥ 12 years of age were randomized in a 2:2:1:1 ratio to receive 52 weeks of add-on subcutaneous dupilumab 200 or 300 mg every 2 weeks or matched-volume placebos. Pre-specified co-primary efficacy endpoints were the annualized rate of severe exacerbations during the treatment period and the change from baseline in pre-bronchodilator FEV1 at treatment week 12. Asthma control, changes in asthma biomarker levels, and dupilumab safety were also evaluated. RESULTS: 530 (27.9% of the overall QUEST population; dupilumab: 353, placebo: 177) Latin-American patients were recruited; 420 (79.2%) had a type 2 inflammatory asthma phenotype. Dupilumab vs placebo reduced the annualized rate of severe exacerbations by 52.7% (P < 0.001) and increased pre-bronchodilator FEV1 at week 12 by 0.15 L (P < 0.001), in the type 2 population. Safety was consistent with the known dupilumab safety profile. CONCLUSIONS: Consistent with the results in the overall population, dupilumab reduced the risk of severe asthma exacerbations and improved lung function in Latin American patients with uncontrolled, moderate-to-severe asthma and a type 2 phenotype.


Sujet(s)
Antiasthmatiques , Asthme , Humains , Asthme/traitement médicamenteux , Amérique latine , Bronchodilatateurs/usage thérapeutique , Anticorps monoclonaux , Méthode en double aveugle , Résultat thérapeutique , Antiasthmatiques/effets indésirables
3.
J Oncol Pharm Pract ; 28(6): 1441-1445, 2022 Sep.
Article de Anglais | MEDLINE | ID: mdl-35119322

RÉSUMÉ

INTRODUCTION: High-grade serous primary peritoneal cancer is highly sensitive to platinum-based chemotherapy with response rates above 80%. Incidence of immediate hypersensitivity reactions to carboplatin is estimated to be between 15% and 20%, usually seen after a mean of 6-8 infusions, with patients developing moderate to severe reactions. CASE REPORT: A 62-year-old female patient with stage IIIC primary high-grade serous carcinoma of the peritoneum was diagnosed and chemotherapy with carboplatin and Paclitaxel was indicated by the oncology service and patient shows response. At 6 months the patient returns, a new PET/CT reports progression of the disease. Carboplatin/paclitaxel cycles are restarted and in the eight cycle of carboplatin within 40 min of administration, she presented severe anaphylaxis with skin, pulmonary, cardiac and atypical symptoms. Infusion is suspended and intramuscular epinephrine with hydrocortisone and chlorphenamine are administered resolving symptoms. MANAGEMENT AND OUTCOME: Intradermal skin test with carboplatin at the concentration of 10 mg / ml (dilution 1: 100) was positive. Due to the symptoms presented and to continue the safe reintroduction to carboplatin, a 4 bag 16-step drug desensitization protocol was carried out at a total dose of 620 mg with no hypersensitivity reactions. DISCUSSION: Prolonged carboplatin use is associated with an increased incidence of carboplatin-related hypersensitivity reactions. And in patients that present hypersensitivity reactions, a safe and effective carboplatin desensitization protocol can be carried out to reach the administration of a full dose. Desensitization protocol induces tolerance to a drug temporarily and is dependent on continuous exposure.


Sujet(s)
Antinéoplasiques , Hypersensibilité médicamenteuse , Tumeurs de l'ovaire , Tumeurs du péritoine , Antinéoplasiques/effets indésirables , Carboplatine/effets indésirables , Désensibilisation immunologique/méthodes , Hypersensibilité médicamenteuse/traitement médicamenteux , Hypersensibilité médicamenteuse/étiologie , Femelle , Humains , Adulte d'âge moyen , Tumeurs de l'ovaire/complications , Paclitaxel , Tumeurs du péritoine/traitement médicamenteux , Tomographie par émission de positons couplée à la tomodensitométrie
4.
J Oncol Pharm Pract ; 28(5): 1264-1268, 2022 Jul.
Article de Anglais | MEDLINE | ID: mdl-35060420

RÉSUMÉ

INTRODUCTION: Brentuximab vedotin (BV) is a monoclonal antibody that targets CD30 antigen. It is indicated for the treatment of CD30 + lymphomas and classical Hodgkin lymphoma (HL), including advanced (stage III-IV) untreated disease, relapsed/refractory disease, and consolidation after autologous hematopoietic stem cell transplantation. In clinical trials the incidence of a hypersensitivity reaction is 1.2%. CASES REPORT: We present 3 cases of patients with refractory HL and anaphylaxis to the administration of BV ( Table 1). Symptoms are analyzed using a grading system described by Brown (2004) and a desensitization protocol was performed with a total dose of 100 mg of BV in 4 solution bags with an initial concentration of 1:1000 of total dose for cases of severe anaphylaxis, and desensitization of 3 solution bags with baseline concentration of 1: 100 for cases of moderate anaphylaxis. MANAGEMENT & OUTCOME: Intradermal skin tests were positive. Before desensitization, premedication with methylprednisolone and chlorphenamine was administered, as well as fluid therapy with 0.9% physiological solution at 100 cc/hour at induction stage, 250 cc/hour at maintenance stage, and increased to 500 cc/hour in case of hypersensitivity reaction. DISCUSSION: Drug desensitization in 12 or 16 steps allows tolerable administration of brentuximab vedotin after moderate to severe anaphylaxis. The favorable response to treatment of these patients may indicate that desensitization is a viable strategy for patients with relapsed or refractory HL.


Sujet(s)
Anaphylaxie , Maladie de Hodgkin , Immunoconjugués , Humains , Brentuximab védotine/usage thérapeutique , Maladie de Hodgkin/traitement médicamenteux , Anaphylaxie/induit chimiquement , Anaphylaxie/traitement médicamenteux , Immunoconjugués/effets indésirables , Récidive tumorale locale/traitement médicamenteux
5.
World Allergy Organ J ; 14(2): 100515, 2021 Feb.
Article de Anglais | MEDLINE | ID: mdl-33552380

RÉSUMÉ

BACKGROUND: The COVID-19 outbreak brought an unprecedented challenge to the world. Knowledge in the field has been increasing exponentially and the main allergy societies have produced guidance documents for better management of allergic patients during this period. However, few publications so far have provided real-life data from the allergy community concerning allergy practice during the COVID-19 outbreak. Therefore, we proposed an international survey on the management of allergic patients during the current pandemic. METHODS: We performed an online survey undertaken to reach out the worldwide allergy community by e-mail and social media. The web-based questionnaire contained 24 questions covering demographic data from the participants, clinical practice during this period, and questions related to the new international classification and coding tools addressed for COVID-19. It was circulated for 8 weeks and had anonymous and volunteer context. RESULTS: Data are presented for 635 participants from 78 countries of all continents. Allergists with long-term professional experience were the main audience. As expected, we received many responses as "I have no data" or "I don't know" to the questions of the survey. However, most with more experience on managing allergic patients during the pandemic agreed that patients suffering from allergic or hypersensitivity conditions have no increased risk of contracting COVID-19 or developing SARS CoV-2. Also, participants mentioned that none of the allergy treatments (inhaled corticosteroids, allergen immunotherapy, biological agents) increased the risk of contracting COVID-19 infection including severe presentations. CONCLUSION: The data presented are a starting point in the process of getting feedback on all the recommendations provided by the allergy societies; it could also be the basis of new strategies to support health professionals while new COVID-19 specific treatments and vaccines are being explored. The information here presented intends to be helpful to the community but represents a course of action in a highly specific situation due to the state of emergency, and it should be helpful to health systems.

6.
J Oncol Pharm Pract ; 27(2): 490-493, 2021 Mar.
Article de Anglais | MEDLINE | ID: mdl-32635810

RÉSUMÉ

INTRODUCTION: Platinum compounds are frequently used for the treatment of colorectal cancer as initial chemotherapy. Oxaliplatin is a third-generation platinum used for the treatment of stage III colorectal cancer and is associated with hypersensitivity reactions. The incidence of hypersensitivity reaction is approximately 12%, with 1-2% of patients developing moderate to severe reactions. CASE REPORT: A 54-year-old male patient with stage III B colon cancer was diagnosed and chemotherapy with oxaliplatin was indicated by the oncology service. Within 20 min of the first cycle of oxaliplatin, he developed dyspnea, laryngeal spam, foreign body sensation in the throat, nausea, and diarrhea; therefore, the infusion of oxaliplatin was suspended, and intramuscular epinephrine was administered and intravenous hydrocortisone along with chlorpheniramine with adequate resolution of symptoms.Management and outcome: Intradermal skin test performed at the concentration of 5 mg/ml (dilution 1:100) was positive. Due to the symptoms presented we decided to perform desensitization to oxaliplatin (total dose: 250 mg) with three bags-12 steps protocol with an initial concentration dose of 1/100 of the total dose in a course of 5.56 h with no hypersensitivity reactions. DISCUSSION: Approximately 50% of patients who are exposed to oxaliplatin may have hypersensitivity despite premedication. Desensitization protocol induces tolerance to a drug temporarily and is dependent on continuous exposure.


Sujet(s)
Antinéoplasiques/effets indésirables , Tumeurs colorectales/traitement médicamenteux , Tumeurs colorectales/anatomopathologie , Désensibilisation immunologique/méthodes , Hypersensibilité médicamenteuse/thérapie , Oxaliplatine/effets indésirables , Anti-inflammatoires/usage thérapeutique , Antinéoplasiques/usage thérapeutique , Chlorphénamine/usage thérapeutique , Épinéphrine/usage thérapeutique , Antihistaminiques des récepteurs H1/usage thérapeutique , Humains , Hydrocortisone/usage thérapeutique , Tolérance immunitaire , Mâle , Adulte d'âge moyen , Métastase tumorale/traitement médicamenteux , Oxaliplatine/usage thérapeutique
7.
Rev. bras. hematol. hemoter ; Rev. bras. hematol. hemoter;39(3): 202-209, July-Sept. 2017. tab, graf
Article de Anglais | LILACS | ID: biblio-898927

RÉSUMÉ

Abstract Background l-Asparaginase is essential in the treatment of childhood acute lymphoblastic leukemia. If immunoglobulin G anti-l-asparaginase antibodies develop, they can lead to faster plasma clearance and reduced efficiency as well as to hypersensitivity reactions, in which immunoglobulin E can also participate. This study investigated the presence of immunoglobulin G and immunoglobulin E anti-l-asparaginase antibodies and their clinical associations. Methods Under 16-year-old patients at diagnosis of B-cell acute lymphoblastic leukemia confirmed by flow cytometry and treated with a uniform l-asparaginase and chemotherapy protocol were studied. Immunoglobulin G anti-l-asparaginase antibodies were measured using an enzyme-linked immunosorbent assay. Intradermal and prick skin testing was performed to establish the presence of specific immunoglobulin E anti-l-asparaginase antibodies in vivo. Statistical analysis was used to investigate associations of these antibodies with relevant clinical events and outcomes. Results Fifty-one children were studied with 42 (82.35%) having anti-l-asparaginase antibodies. In this group immunoglobulin G antibodies alone were documented in 10 (23.8%) compared to immunoglobulin E alone in 18 (42.8%) patients. Immunoglobulin G together with immunoglobulin E were simultaneously present in 14 patients. Children who produced exclusively immunoglobulin G or no antibodies had a lower event-free survival (p-value = 0.024). Eighteen children (35.3%) relapsed with five of nine of this group who had negative skin tests suffering additional relapses (range: 2-4), compared to none of the nine children who relapsed who had positive skin tests (p-value < 0.001). Conclusion Children with acute lymphoblastic leukemia and isolated immunoglobulin G anti-l-asparaginase antibodies had a higher relapse rate, whereas no additional relapses developed in children with immunoglobulin E anti-l-asparaginase antibodies after the first relapse.


Sujet(s)
Asparaginase , Immunoglobuline E , Immunoglobuline G , Escherichia coli , Leucémie-lymphome lymphoblastique à précurseurs B et T , Anticorps neutralisants , Hypersensibilité
8.
Rev Bras Hematol Hemoter ; 39(3): 202-209, 2017.
Article de Anglais | MEDLINE | ID: mdl-28830598

RÉSUMÉ

BACKGROUND: l-Asparaginase is essential in the treatment of childhood acute lymphoblastic leukemia. If immunoglobulin G anti-l-asparaginase antibodies develop, they can lead to faster plasma clearance and reduced efficiency as well as to hypersensitivity reactions, in which immunoglobulin E can also participate. This study investigated the presence of immunoglobulin G and immunoglobulin E anti-l-asparaginase antibodies and their clinical associations. METHODS: Under 16-year-old patients at diagnosis of B-cell acute lymphoblastic leukemia confirmed by flow cytometry and treated with a uniform l-asparaginase and chemotherapy protocol were studied. Immunoglobulin G anti-l-asparaginase antibodies were measured using an enzyme-linked immunosorbent assay. Intradermal and prick skin testing was performed to establish the presence of specific immunoglobulin E anti-l-asparaginase antibodies in vivo. Statistical analysis was used to investigate associations of these antibodies with relevant clinical events and outcomes. RESULTS: Fifty-one children were studied with 42 (82.35%) having anti-l-asparaginase antibodies. In this group immunoglobulin G antibodies alone were documented in 10 (23.8%) compared to immunoglobulin E alone in 18 (42.8%) patients. Immunoglobulin G together with immunoglobulin E were simultaneously present in 14 patients. Children who produced exclusively immunoglobulin G or no antibodies had a lower event-free survival (p-value=0.024). Eighteen children (35.3%) relapsed with five of nine of this group who had negative skin tests suffering additional relapses (range: 2-4), compared to none of the nine children who relapsed who had positive skin tests (p-value<0.001). CONCLUSION: Children with acute lymphoblastic leukemia and isolated immunoglobulin G anti-l-asparaginase antibodies had a higher relapse rate, whereas no additional relapses developed in children with immunoglobulin E anti-l-asparaginase antibodies after the first relapse.

9.
World Allergy Organ J ; 6(1): 19, 2013 Nov 04.
Article de Anglais | MEDLINE | ID: mdl-24180521

RÉSUMÉ

BACKGROUND: In 2011 the Latin America Asthma Insight and Management (LA AIM) survey explored the realities of living with asthma. We investigated perception, knowledge, and attitudes related to asthma among Latin American asthma patients. METHODS: Asthma patients aged ≥12 years from four Latin American countries (Argentina, Brazil, Mexico, Venezuela) and the Commonwealth of Puerto Rico responded to questions during face-to-face interviews. A sample size of 2,169 patients (approximately 400 patients/location) provided an accurate representation of asthma patients' opinions. Questions probed respondents' views on topics such as levels of asthma control, frequency and duration of exacerbations, and current and recent use of asthma medications. RESULTS: A total of 2,169 adults or parents of children with asthma participated in the LA AIM survey. At least 20% of respondents experienced symptoms every day or night or most days or nights. Although 60% reported their disease as well or completely controlled, only 8% met guideline criteria for well-controlled asthma. 47% of respondents reported episodes when their asthma symptoms were more frequent or severe than normal, and 44% reported seeking acute care for asthma in the past year. Asthma patients in Latin America overestimated their degree of asthma control. CONCLUSIONS: The LA AIM survey demonstrated the discrepancy between patient perception of asthma control and guideline-mandated criteria. Additional education is required to teach patients that, by more closely following asthma management strategies outlined by current guidelines more patients can achieve adequate asthma control.

10.
Rev Alerg Mex ; 60(4): 184-92, 2013.
Article de Espagnol | MEDLINE | ID: mdl-24912911

RÉSUMÉ

Allergic rhinitis and asthma represent global problems of public health affecting all age groups; asthma and allergic rhinitis frequently coexist in the same patients. In Latin American prevalence of allergic rhinitis, although variable, is very high. Allergic rhinitis and its Impact on Asthma (ARIA) started during a workshop of the World Health Organization performed in 1999 and was published in 2001. ARIA proposed a new classification of allergic rhinitis in intermittent or persistent and mild or moderate-severe. This approach of classification reflects more nearly the impact of allergic rhinitis in patients. In its review of 2010 ARIA developed guidelines for diagnosis and treatment of allergic rhinitis and of clinical practices for management of comorbidities of allergic rhinitis and asthma based on GRADE (Grading of Recommendations, Development and Evaluation). ARIA has been spread and implemented in more than 50 countries. In Latin American an intense activity has been developed to spread these recommendations in almost all the countries of the region and it is important to record the obtained goals in the diffusion and implementation of ARIA, as well as to identify the unsatisfied needs from the clinical, research and implementation points of view. Final objective is to reinforce the priority that allergy and asthma should have, especially in children, in the programs of public health, as they have been prioritized in European Union in 2011.


La rinitis alérgica y el asma representan problemas globales de salud pública que afectan a todos los grupos etarios; el asma y la rinitis alérgica frecuentemente coexisten en los mismos pacientes. En América Latina la prevalencia de rinitis alérgica, aunque variable, es muy elevada. La iniciativa Rinitis Alérgica y su Impacto en Asma (globalmente conocida como ARIA, de su nombre en inglés Allergic Rhinitis and its Impact on Asthma) comenzó durante un taller de la Organización Mundial de la Salud (OMS) realizado en 1999 que se publicó en el año 2001. ARIA propuso una nueva clasificación de rinitis alérgica en intermitente o persistente y leve o moderada-severa. Este esquema de clasificación refleja más estrechamente el impacto de la rinitis alérgica en los pacientes. En su revisión de 2010, la guía ARIA desarrolló pautas para el diagnóstico y tratamiento de la rinitis alérgica y de prácticas clínicas para el manejo de las comorbilidades de la rinitis alérgica y el asma basadas en GRADE (Gradación de Recomendaciones, Desarrollo y Evaluación). ARIA se ha diseminado e implantado en más de 50 países. En América Latina se ha desarrollado una intensa actividad para diseminar estas recomendaciones en casi todos los países de la región y es importante llevar un registro de los logros obtenidos en la difusión e implantación de ARIA, además de identificar las necesidades insatisfechas desde el punto de vista clínico, de la investigación y de la implantación. El objetivo final es reforzar la prioridad que deben tener la alergia y el asma ­especialmente en niños­ en los programas de Salud Pública, tal como los priorizó la Unión Europea en 2011.


Sujet(s)
Allergie et immunologie/organisation et administration , Asthme/épidémiologie , Besoins et demandes de services de santé/tendances , Rhinite spasmodique apériodique/épidémiologie , Sociétés médicales/organisation et administration , Allergie et immunologie/tendances , Asthme/classification , Asthme/prévention et contrôle , Asthme/thérapie , Congrès comme sujet , Expertise , Prévision , Gouvernement , Politique de santé , Humains , Amérique latine/épidémiologie , Phénotype , Guides de bonnes pratiques cliniques comme sujet , Secteur privé , Essais contrôlés randomisés comme sujet , Rhinite allergique , Rhinite spasmodique apériodique/classification , Rhinite spasmodique apériodique/prévention et contrôle , Rhinite spasmodique apériodique/thérapie , Sociétés médicales/tendances , Organisation mondiale de la santé
11.
Rev Alerg Mex ; 57(1): 11-7, 2010.
Article de Espagnol | MEDLINE | ID: mdl-20857624

RÉSUMÉ

BACKGROUND: Allergic rhinitis can be caused by allergens such as house dust mites, pollen, fungi, and animals. A less common cause is allergy to Ficus benjamina. OBJECTIVES: To determine the prevalence of sensitization to Ficus benjamina on patients with moderate-severe allergic rhinitis, and to describe the epidemiologic factors associated to Ficus benjamina sensitization. PATIENTS AND METHOD: It is an observational, transversal, prospective study; patients with persistent moderate-severe allergic rhinitis diagnosis were included; skin tests to the most frequent aeroallergens and to Ficus benjamina were applied to these patients, as well as a questionnaire in order to investigate the degree of exposure to Ficus benjamina. RESULTS: 89 patients with persistent moderate-severe allergic rhinitis were included. 59% had a Ficus benjamina plant at home or at work, 97% were located outdoors. Nine patients (10.1%) were sensitized to Ficus benjamina. A statistically significant association was found between sensitization to Ficus benjamina and to Felix domesticus, Canis familiaris, and Periplaneta. CONCLUSIONS: Prevalence of sensitization to Ficus benjamina was similar to that reported in the literature, and it is associated to three or more indoor allergens. Patients with allergic rhinitis should avoid contact with Ficus benjamina because of the risk of acquiring sensitization.


Sujet(s)
Allergènes/effets indésirables , Allergènes/immunologie , Ficus , Rhinite/immunologie , Adolescent , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Études transversales , Femelle , Humains , Mâle , Adulte d'âge moyen , Prévalence , Études prospectives , Rhinite/épidémiologie , Indice de gravité de la maladie , Jeune adulte
12.
Allergy Asthma Proc ; 31(4): e53-e62, 2010.
Article de Anglais | MEDLINE | ID: mdl-20819316

RÉSUMÉ

The epidemiology of allergic diseases has not been studied extensively in Mexico. The present study, based on the International Study of Asthma and Allergies in Childhood Phase IIIB survey, reports the prevalence of allergic rhinitis and the associated risk factors in the pediatric population in four cities in northern Mexico. Children (6-7 years old) and adolescents (13-14 years old) in public elementary and secondary schools were surveyed in 2002 and 2003. The subjects were chosen randomly from Ciudad Victoria, Mexicali, Monterrey, and Tijuana. The following categories were analyzed: occurrence of rhinitis symptoms (currently or in the last 12 months), rhinoconjunctivitis symptoms, a previous diagnosis of allergic rhinitis, and relevant environmental factors. Factors associated with rhinitis that were identified previously with the chi-squared test were analyzed using logistic regression. The number of valid questionnaires was 10,892 for schoolchildren and 12,299 for adolescents. In 6- to 7-year-old children, the following frequencies were determined: rhinitis (ever), 27.9%; current rhinitis, 24.2%; rhinoconjunctivitis, 9.2%; and diagnosis of allergic rhinitis, 5.5%. The corresponding frequencies in 13- to 14-year-old children were 33.3, 34.1, 18.4, and 3.8%. In both 6- to 7-year-old and 13- to 14-year-old children, all rhinitis items were associated with asthma symptoms, dermatitis symptoms, paracetamol consumption, and maternal smoking (odds ratio, >1; p < 0.05). The main risk factors associated with allergic rhinitis symptoms in children and adolescents from cities in northern Mexico were other allergic conditions, paracetamol consumption, and passive smoking.


Sujet(s)
Asthme/épidémiologie , Eczéma de contact allergique/épidémiologie , Rhinite spasmodique apériodique/épidémiologie , Rhinite allergique saisonnière/épidémiologie , Acétaminophène/effets indésirables , Adolescent , Enfant , Femelle , Humains , Mâle , Mexique , Prévalence , Rhinite spasmodique apériodique/physiopathologie , Rhinite allergique saisonnière/physiopathologie , Facteurs de risque , Enquêtes et questionnaires , Pollution par la fumée de tabac
13.
Allergy Asthma Proc ; 31(4): 341-8, 2010.
Article de Anglais | MEDLINE | ID: mdl-20819326

RÉSUMÉ

There are few reports of pollen count and identification in Mexico; therefore, it is important to generate more information on the subject. This study was designed to describe the prevalence of pollen in the city of Monterrey, Mexico, during the year 2004. Atmospheric pollen was collected with a Hirst air sampler, with an airflow of 10 L/minute during 2004. Pollen was identified with light microscopy; the average monthly pollen count as well as total was calculated from January 2004 to January 2005. The months with the highest concentration of pollen were February and March (289 and 142 grains/m(3) per day, respectively), and July and November had the lowest concentration (20 and 11 grains/m(3) per day, respectively). Most of the pollen recollected corresponded to tree pollen (72%). Fraxinus spp had the highest concentration during the year (19 grains/m(3) per day; 27.5% of the total concentration of pollen). Tree pollen predominated from January through March; with Fraxinus spp, Morus spp, Celtis spp, Cupressus spp, and Pinus spp as the most important. Weed pollen predominated in May, June, and December and the most frequently identified, were Amaranthaceae/Chenopodiaceae, Ambrosia spp, and Parietaria spp. The highest concentration of grass pollen was reported during the months of May, June, September, October, and December with Gramineae/Poaceae predominating. Tree pollen was the most abundant during the year, with the ash tree having the highest concentration. Weed and grass pollen were perennial with peaks during the year.


Sujet(s)
Air/analyse , Allergènes/immunologie , Pollen/immunologie , Rhinite allergique saisonnière/épidémiologie , Rhinite allergique saisonnière/immunologie , Surveillance de l'environnement , Surveillance épidémiologique , Humains , Mexique , Poaceae , Pollen/cytologie , Rhinite allergique saisonnière/diagnostic , Rhinite allergique saisonnière/prévention et contrôle , Saisons , Arbres
14.
Rev Alerg Mex ; 57(3): 79-84, 2010.
Article de Espagnol | MEDLINE | ID: mdl-21255516

RÉSUMÉ

BACKGROUND: Allergic reactions to insect bites are a global problem, the true incidence and prevalence of morbidity from adverse reactions to mosquito bites are unknown. OBJECTIVE: To describe the adverse reactions to mosquito bites in school-age children of Monterrey, Nuevo Leon. MATERIAL AND METHODS: A cross-sectional descriptive study was made via a randomized application of questionnaires to children from public elementary schools in the metropolitan area of Monterrey, Nuevo Leon. RESULTS: A total of 11 public schools randomly selected were included in the study. One thousand questionnaires were submitted, of which 506 fulfilled the inclusion criteria; 55% were females. Seventy-six percent referred adverse reactions to mosquito bites, itching (75%) and rash (72%) being the most frequent ones, in the last 12 months. CONCLUSIONS: Adverse reactions to mosquito bites occur frequently. Early detection is important to establish a prompt treatment.


Sujet(s)
Hypersensibilité , Morsures et piqûres d'insectes , Études transversales , Culicidae , Humains , Hypersensibilité/épidémiologie , Mexique/épidémiologie
15.
Rev Alerg Mex ; 53(5): 189-93, 2006.
Article de Espagnol | MEDLINE | ID: mdl-17357566

RÉSUMÉ

Hereditary angioedema is an uncommon disorder mainly caused by defects of the gene for C1 inhibitor. These patients present recurrent edema episodes in the different regions of the body, including larynx edema in some cases. Low plasma levels of C1 inhibitor confirm the diagnosis. It is important to establish an early diagnosis and prompt treatment to this disorder due to its potential of fatal consequences and multiple alterations in the quality of life that have been associated with. The indicated treatment is substitutive therapy of C1 inhibitor concentrate. We present the case of a patient a 27 year-old female with a history of seven years of evolution, with daily periorbital, upper and lower extremities and labial edema episodes who was classified as C1 inhibitor deficiency type II. She began treatment with attenuated androgens in progressive increased doses with poor response, appearing torpid evolution without a favorable response. This case corresponds to a very atypical presentation of C1 inhibitor deficiency with daily symptoms, unlike the typical intermittent course of the classic disease.


Sujet(s)
Angioedème/génétique , C1 Inhibiteur/génétique , Douleur abdominale/étiologie , Adulte , Angioedème/complications , Angioedème/diagnostic , Angioedème/immunologie , Antiallergiques/usage thérapeutique , Maladie chronique , C1 Inhibiteur/analyse , Complément C4/déficit , Danazol/effets indésirables , Danazol/usage thérapeutique , Résistance aux substances , Paupières/anatomopathologie , Dermatoses faciales/génétique , Dermatoses faciales/immunologie , Femelle , Gastrite/complications , Infections à Helicobacter/complications , Helicobacter pylori , Humains , Phénotype , Virilisme/induit chimiquement
16.
Rev Alerg Mex ; 52(2): 72-6, 2005.
Article de Espagnol | MEDLINE | ID: mdl-16158779

RÉSUMÉ

BACKGROUND: Exercise-induced asthma is a transitory bronchospasm, which occurs after 6 to 8 minutes of continuous exercise. Diagnosis is done by a suggestive clinical history and by 15 to 20% post-challenge fall in FEV1. It happens in about 6 to 13% of general population, 90% of asthmatic individuals and 40% of individuals with allergic rhinitis. OBJECTIVE: To know the frequency of asthma induced by exercise in a group of asthmatic children and teenagers who went to a summer camp. MATERIAL AND METHODS: A cross-sectional, descriptive and observational study, which included 33 patients suffering from intermittent mild asthma, was based on espirometric measurements made before and after 8 minutes of continuous exercise (running). None of them had previous diagnosis of exercise-induced asthma. FEV1 greater than or equal to 15% was considered exercise-induced asthma. The test was performed at a room temperature of 73F and humidity of 40%. All patients were asymptomatic before the study and were given short-acting inhaled beta2-agonists as rescue medication, which was not administered during the 12 previous hours to the test. Data analysis was made by means of descriptive statistic. RESULTS: Thirty-three children aged 8-16 years with diagnosis of asthma were studied, with an average age of 12.5 years; 42.4% were female and 57.5% male. Of the 33 patients, 6 had (18.2%) a 15% fall in FEV1 after exercise; 50% of these patients showed exercise-induced mild asthma, 33% moderate and 17% severe. At the end of the test, in six patients (100%) FEV1 increased by 15%, five minutes after the administration of a beta2-agonist. CONCLUSIONS: Exercise-induced asthma is frequent among asthmatic pediatric patients, occurring in 18.8% of this study. Likelihood of having exercise-induced asthma must be deliberately investigated in all asthmatic patients, in order to establish an opportune diagnosis of this condition and provide recommendations of preventing therapy.


Sujet(s)
Asthme à l'effort/épidémiologie , Camping , Adolescent , Agonistes des récepteurs béta-2 adrénergiques , Agonistes bêta-adrénergiques/usage thérapeutique , Antiasthmatiques/usage thérapeutique , Asthme/traitement médicamenteux , Asthme/épidémiologie , Asthme à l'effort/diagnostic , Asthme à l'effort/traitement médicamenteux , Asthme à l'effort/prévention et contrôle , Enfant , Études transversales , Épreuve d'effort , Femelle , Volume expiratoire maximal par seconde , Humains , Mâle , Course à pied
17.
Rev Alerg Mex ; 52(2): 83-9, 2005.
Article de Espagnol | MEDLINE | ID: mdl-16158781

RÉSUMÉ

BACKGROUND: The Global Initiative for Asthma (GINA) is a collaborative effort to disseminate updated guidelines about the diagnosis and management of patients that suffer from asthma. Implementation of these guidelines by the primary care practitioners reduces the morbidity of these patients. OBJECTIVE: To evaluate the efficacy of a training course of asthma on the knowledge of the primary care physicians. PATIENTS AND METHODS: Sixty physicians were evaluated before and after a lecture-based educational intervention on asthma. The overall score and per-topic subscores were compared. Likewise, differences among physicians from distinct specialties were assessed. The correlation between perceived and actual usefulness was calculated. RESULTS: The mean score before the training course was of 65.76 (SD = 11.95) points, and after the course of 84.87 (SD = 9.27) points; p < 0.0001. The mean improvement percentage was of 34.48% for the overall score, 41.47% for general knowledge, 47.57% for diagnosis and 28.4% for treatment. Improvement had no relation with physician's specialty. The correlation between perceived and actual usefulness was of -0.005 (p > 0.05) for the absolute score change and 0.025 (p>0.05) for the percentage change. CONCLUSIONS: A short lecture-based training course of asthma increases the knowledge of bronchial asthma and GINA guidelines among primary health care physicians. Differences among physicians of distinct specialties were not significant.


Sujet(s)
Allergie et immunologie/enseignement et éducation , Asthme , Programme d'études/normes , Formation médicale continue comme sujet , Médecins de famille/enseignement et éducation , Soins de santé primaires , Adulte , Évaluation des acquis scolaires , Médecine de famille , Humains , Médecine , Pédiatrie , Médecins de famille/psychologie , Guides de bonnes pratiques cliniques comme sujet , Spécialisation , Enquêtes et questionnaires
18.
Rev Alerg Mex ; 51(2): 45-8, 2004.
Article de Espagnol | MEDLINE | ID: mdl-15237908

RÉSUMÉ

BACKGROUND: Atopic dermatitis is a chronic inflamatory disease of the skin which mainly affects children. It is characterized by itch and cutaneous hyperactivity with typical lesions that depend on the affected age group and the disease stage. It is frequently associated to rhinitis and asthma. OBJECTIVE: To identify the clinical characteristics of atopic dermatitis in patients treated at the Regional Center of Allergy and Clinical Immunology of Monterrey, NL, Mexico. MATERIAL AND METHODS: A retrospective and descriptive study was done by the review of clinical files of patients with atopic dermatitis diagnosis from January 1997 to May 2002. The statistical analysis was done by central tendency measures. RESULTS: We reviewed 119 clinical files, 53 (44.5%) were male and 66 (55.5%) female. The most frequent clinical manifestations were pruritus and eczematous lesions, both in 117 patients (98.3%). Fifty-five percent of the patients initiated symptoms before 6 years of age. Eighty eight patients (74%) had family and/or personal history of atopia. Other associated manifestations were allergic rhinitis in 38 patients (31.9%), asthma and rhinitis in 25 patients (21%) and only asthma in 2 patients (1.7%). In 44 patients, food skin tests were done with a positive result in 25 patients, the most frequent was to egg (68%) and in 64 patients these were positive to aeroallergens being the most frequent Dermatophagoides p teronyssinus (85.1%). CONCLUSIONS: The pruritus and eczematous lesions were the most constant manifestations in this group of patients where family and/ or personal history of atopia was frequent.


Sujet(s)
Eczéma atopique/diagnostic , Adolescent , Enfant , Enfant d'âge préscolaire , Études transversales , Femelle , Établissements de santé , Humains , Nourrisson , Mâle , Mexique , Études rétrospectives
19.
Rev Alerg Mex ; 49(4): 112-5, 2002.
Article de Espagnol | MEDLINE | ID: mdl-12374043

RÉSUMÉ

BACKGROUND: The correct control of asthmatic children and teenagers substantially improves their quality of life. The use of the peak flowmeter permits to monitor the pulmonary function and to control this disease. OBJECTIVE: To gather information about the use of the peak flowmeter in asthmatic children and teenagers. MATERIAL AND METHODS: It was a descriptive and observational study done in 81 asthmatic children and teenagers who attended a summer camp. They answered a questionnaire in order to know their knowledge about the peak flowmeter's use. RESULTS: The age of the studied group ranked from five to 18 years (54.3% between five to 10 years). Out of the 81 children and teenagers, 64 knew about the peak flow. In spite of the knowledge, only 38 (46.9%) had used it in at least one occasion and 20 (24.7%) in an ambulatory manner (16 used it when they feel bad, and four, every day). Only nine of these 20 children knew the correct way to use it, to interpret the results and what the normal peak flow was. All of these children and teenagers were under medical control. Allergists were attending 66.7%. Independently of the specialty of their doctors, the average of the children that didn't use the peak flowmeter in their control of asthma was always over than 50%. CONCLUSIONS: In spite that all these children and teenagers were on medical care, the knowledge of the peak flowmeter usage was not enough to take advantage.


Sujet(s)
Asthme/psychologie , Débit expiratoire de pointe , Rhéologie , Adolescent , Asthme/physiopathologie , Enfant , Enfant d'âge préscolaire , Connaissances, attitudes et pratiques en santé , Humains , Éducation du patient comme sujet , Enquêtes et questionnaires
20.
Rev Alerg Mex ; 49(3): 95-8, 2002.
Article de Espagnol | MEDLINE | ID: mdl-12190005

RÉSUMÉ

The aspiration of foreign bodies into the airway is a common problem in childhood, mainly in children younger than 10-years old. Foreign bodies located in the tracheobronchial tree can cause episodic cough, dyspnea and wheezing, and generate a misdiagnosed of asthma if physicians do not consider the possibility of a bronchial foreign body as a differential diagnosis of this disease. In these cases, chest X-ray films are very important because those can show the most of foreign bodies or indirect radiographic signs of a bronchial foreign body. Nowadays, bronchoscopy is the method of choice for removal foreign bodies from the tracheobronchial tree. If there are not complications, most of patients may recover and become non-symptomatic in a short-term after the foreign body extraction. We show the case of a nine years old boy who suffered the aspiration of a tack, which stayed in a bronchi during several years, and was misdiagnosed as asthmatic.


Sujet(s)
Asthme/diagnostic , Bronches , Erreurs de diagnostic , Corps étrangers/diagnostic , Salbutamol/usage thérapeutique , Antiasthmatiques/usage thérapeutique , Antibactériens/usage thérapeutique , Bronchoscopie , Enfant , Toux/étiologie , Diagnostic différentiel , Dyspnée/étiologie , Expectorants/usage thérapeutique , Fièvre/étiologie , Corps étrangers/complications , Corps étrangers/imagerie diagnostique , Corps étrangers/thérapie , Humains , Mâle , Atélectasie pulmonaire/étiologie , Radiographie , Bruits respiratoires/étiologie , Sinusite/complications
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