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unspecified allergy vaccine (Staloral)

✓ Approved

Stallergenes · 治疗药物

什么是 unspecified allergy vaccine?

unspecified allergy vaccine 是一种治疗药物,由Stallergenes研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Oral (PO)、Subcutaneous Injection、Sublingual (SL)/Oral Transmucosal。

药物档案

商品名Staloral
公司Stallergenes
给药途径Injectable (Others), Oral (PO), Subcutaneous Injection, Sublingual (SL)/Oral Transmucosal
状态Approved

治疗适应症

unspecified allergy vaccine 针对 2 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Respiratory, thoracic and mediastinal disordersAsthma✓ Approved
Respiratory, thoracic and mediastinal disordersRhinitis allergic✓ Approved

相关研究文献

PubMedGynecologic oncology2026-06-13

Raising the bar on surgical site infection bundles: Preoperative penicillin allergy testing in gynecologic oncology patients with a reported penicillin allergy - A quality improvement study.

Desravines Nerlyne N, Tschudy Megan M MM, Hazimeh Dana D, Brown Kristin K et al.

Practice guidelines advise cefazolin for surgical prophylaxis to reduce surgical site infection (SSI) in clean-contaminated procedures but recommend alternative antibiotics for patients with reported penicillin (PCN) allergy despite increased odds of SSI with alternative antibiotics. We aimed to increase use of cefazolin for SSI prophylaxis from 42% in a 3-year period (preintervention) to 80% by 34 months postintervention by implementing preoperative penicillin allergy testing (PAT) in patients with a reported PCN allergy. This was a prospective quality improvement (QI) initiative from 03/2021 to 12/2023. An EMR-embedded best practice advisory (BPA) alert prompted preoperative PAT for patients with reported PCN allergies. Our primary outcome measure was use of cefazolin for SSI prophylaxis at surgery, when indicated. We deployed iterative process modifications based on successive plan-do-study-act (PDSA) cycles using the Model for Improvement. Process and outcome data were analyzed using run charts. We identified 119 patients who initially reported a penicillin allergy during our study period. The use of cefazolin at the time of surgery significantly increased from 42% (3-year pre-intervention period) to 77.3% (2-year postintervention period), p ≤0.01. Postintervention, the median cefazolin use was 66% of cases by 34 months. 29.4% of patients completed PAT compared to none in the 12 months preceding our intervention. Following the intervention, our SSI rate was 0% (0 of 119) compared to 2.8% pre-intervention (5 of 176). Preoperative PAT is a feasible strategy for increasing the best practice use of cefazolin for SSI prophylaxis in those reporting PCN allergy. PAT as routine preoperative care may promote antimicrobial stewardship and decrease SSI risk.

PMID 42284712
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PubMedCurrent opinion in allergy and clinical immunology2026-06-13

Drug-induced anaphylaxis in pregnant women: a call for correct labeling antibiotic allergies.

Bassani Cintia C, Demoly Pascal P, Tanno Luciana Kase LK

Drug-induced anaphylaxis during pregnancy, although uncommon, represent potentially serious clinical situation with significant maternal-fetal impact and relevant therapeutic implications. This topic is particularly timely given the need for guidance of health professionals dealing with this challenge and correct labelling patients with drug allergy/hypersensitivity. Recent studies report a high prevalence of self-reported β-lactam allergy during pregnancy, with poor correlation with true allergy, underscoring the value of structured, safe, and effective diagnostic evaluation for appropriate delabeling. These findings highlight the need for a systematic approach to drug-induced anaphylaxis in pregnancy, including accurate diagnosis and protocol-based management. Incorporating allergological evaluation into prenatal care can reduce unnecessary risks, optimize maternal and fetal outcomes, and promote rational medication use. Important knowledge gaps remain, emphasizing the need for prospective studies with standardized methodologies and expanded immunological assessment.

PMID 42286949
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PubMedAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology2026-06-13

Practice Trends in Allergy and Immunology in the United States from 2015 to 2023.

Witt Bryan B, Cheung Robin R, Jaffery Syed S, Rukasin Christine Rf CR

PMID 42285296
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PubMedJournal of affective disorders2026-06-13

Sustainable eating for a healthy mind: Association between the EAT-Lancet diet and depression subtypes in a Swiss cohort.

Martins Laís Bhering LB, Ranjbar Setareh S, Strippoli Marie-Pierre F MF, Lasserre Aurelie M AM et al.

Higher adherence to healthy dietary patterns appears to play a role in the prevention of Major Depressive Disorder (MDD). However, the association between the EAT-Lancet diet, developed to promote both human health and environmental sustainability, and MDD remains largely unexplored. To explore the association between adherence to the EAT-Lancet diet and MDD subtypes and assess how dietary patterns among individuals with and without MDD align with EAT-Lancet recommendations. We conducted a cross-sectional analysis of 3558 adults from the CoLaus|PsyCoLaus cohort. Adherence to the EAT-Lancet diet was scored based on intake of 12 food components and categorized into tertiles (low, medium, high). Psychiatric information was obtained using the Diagnostic Interview for Genetic Studies. MDD subtypes (melancholic, atypical, and unspecified) were diagnosed according to DSM-IV specifiers. Multinomial logistic regression models assessed associations between diet adherence and MDD subtypes. High EAT-Lancet adherence was associated with a lower relative risk of atypical MDD (RRR: 0.68, 95% CI: 0.55-0.84). No clear associations were observed for melancholic or unspecified MDD. Across all groups, intake of unsaturated oils, legumes, and whole grains was insufficient, while red meat, potatoes, and added sugars exceeded recommendations. The association of a sustainable and healthy diet with MDD differs across clinical subtypes, suggesting that diet may play distinct roles in the pathophysiology of each. Improving specific dietary components may support mental health and sustainability goals.

PMID 42285530
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PubMedCurrent opinion in allergy and clinical immunology2026-06-13

Beta-lactam de-labelling as a core antimicrobial stewardship strategy in the era of the antimicrobial resistance pandemic: a narrative review.

Bhattacharya Sudip S, Kundu Soumi S

Antimicrobial resistance (AMR) is increasingly recognised as a global public health emergency that threatens the foundations of modern medicine. While much attention has focused on antimicrobial overuse, under-emphasised drivers such as inaccurate drug allergy labels continue to undermine antibiotic stewardship efforts. Beta-lactam allergy (BLA) labels, particularly penicillin allergy labels, are among the most prevalent and most consequential of these inaccuracies. Mounting evidence demonstrates that the vast majority of individuals labelled as beta-lactam allergic are not truly allergic, yet these labels persist across healthcare systems and generations, driving the use of broader-spectrum, less effective, more toxic and resistance-promoting antibiotics. In this timely review, we argue that beta-lactam de-labelling should no longer be viewed as a niche allergy intervention but as a core antimicrobial stewardship strategy and an ethical obligation in the era of the AMR pandemic. Drawing on emerging inpatient and outpatient evidence, including recent paediatric inpatient de-labelling studies, we examine clinical, behavioural, system-level and ethical barriers to de-labelling and propose a reframing of beta-lactam de-labelling as a public health intervention essential for preserving antibiotic effectiveness. We conclude by outlining policy-relevant recommendations for embedding de-labelling into routine care pathways, particularly in low and middle-income countries (LMICs), where the consequences of AMR are likely to be most severe.

PMID 42286950
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PubMedCurrent opinion in allergy and clinical immunology2026-06-13

Updates on drug-induced anaphylaxis in children.

Pereira Tiago T, Marques Maria Luís ML, Gomes Eva E

Data on pediatric drug-induced anaphylaxis (DIA) are scarce, as drugs are less common triggers of anaphylaxis in children; however, drugs are associated with more severe reactions and unusual presentations. This review summarizes evidence on pediatric DIA, covering epidemiology, clinical manifestations, triggers, and management focusing on pediatric specificities. Available data shows that drugs are responsible for up to one-third of childhood anaphylaxis. Approximately half of DIA cases occur in healthcare facilities and triggers vary according to settings. In addition to beta-lactams and NSAIDs, other medications raise concerns in specific populations. Age-dependent and trigger-dependent differences regarding symptoms have been reported. Undertreatment remains a major problem. The importance of DIA in children increases with age. Boys appear more frequently affected. Diagnosis is clinical but challenging especially in younger age groups and in perioperative settings. Elevated tryptase supports diagnosis but lacks sensitivity. Antibiotics and NSAIDs are major culprits, but in hospitalized patients, anesthetics and chemotherapeutic drugs are also relevant. Vaccines, biologicals, and immunotherapy extracts may be important in pediatric allergy practice. Immediate treatment is adrenaline, largely underused in children, even in hospital settings. All patients with DIA should undergo allergy evaluation to prevent recurrences and overlabeling of drug allergy.

PMID 42286953
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