131 Venom specific G (VSG) and G4 (VSG4) levels in patients (PTS) with positive skin tests (SKT) and a history of anaphylaxis (ANP) prior to immunotherapy (VIT)

1988 ◽  
Vol 81 (1) ◽  
pp. 201
Author(s):  
RJM Engler ◽  
H Kaloka ◽  
E Squire ◽  
L Smith ◽  
RS Summers
Keyword(s):  
1979 ◽  
Vol 1 (5) ◽  
pp. 132-158

A (massive) multicenter study of 3,000 patients has demonstrated that skin tests to penicillin G and penicilloyl-polylysine (PPL-now commercially available) predict and confirm penicillin allergy. Of patients with a history of penicillin reaction, 19% were positive to either, compared to 7% of controls. A history of anaphylaxis led to 46% positive. Of those with a history of urticaria 17% were positive, and those with maculopapular eruptions did not differ from controls (7% positive). Challenge with penicillin led to a reaction in 6% with a positive history (compared to 2% with a negative) and 67% with a combined positive history and positive skin test (to either).


2020 ◽  
Vol 46 (1) ◽  
Author(s):  
A. Piccorossi ◽  
G. Liccioli ◽  
S. Barni ◽  
L. Sarti ◽  
M. Giovannini ◽  
...  

Abstract Background and objective Drug Hypersensitivity Reactions (DHRs) are considered adverse effects of medications that resemble allergy symptoms. The reported positive clinical history of pediatric drug reactions is about 10%, however, after allergy investigations, only a small percent is confirmed as hypersensitivity. The aim of this study was to analyze the clinical history, allergy work-up results and sensitization profile of children and adolescents referred to our Allergy Unit for suspected DHRs. Methods The study evaluated data related to a group of children with a positive history of drug reactions during a two-year period. The allergy work-up consisted of in vivo and in vitro tests, in accordance with the recommendations of the ENDA/EAACI guidelines. Results Data from a group of 637 patients [348 M (54.6%); 289 F (45.4%)] were retrospectively analyzed. Beta lactams (BLs) were the most common drugs involved in the reported clinical history, followed by non-steroidal anti-inflammatory drugs (NSAIDs). Severe cutaneous adverse reactions (SCARs) were most frequently observed during BL treatment. The confirmation of BL hypersensitivity was higher for immediate reactions (IRs) [9.4%; 5.1% through positive skin tests (STs) and 5.5% through drug provocation test (DPT)] compared to non-immediate reactions (non-IRs) (8.1%; 2.2% through STs and 6.2% through DPT). A higher number of positive results was obtained for BLs and macrolides when the tests were performed within 12 months after the index reaction (p < 0.05). During DPTs with amoxicillin-clavulanic acid, four hypersensitivity reactions (including one anaphylaxis) occurred despite negative STs. Conclusion Our data demonstrated that only 9.1% of patients resulted in being positive to allergy tests which is in line with the data in literature. An allergy work-up is mandatory for excluding suspected hypersensitivity.


PEDIATRICS ◽  
1973 ◽  
Vol 52 (2) ◽  
pp. 309-309
Author(s):  
Renee K. Bergner

In its statement, "Anaphylaxis," The American Academy of Pediatrics Committee on Drugs states in part: "If there is a possibility of sensitivity to . . . penicillin, skin testing for immediate hypersensitivity to the agent should be performed prior to its therapeutic administration."1 The Penicillin Study Group of the American Academy of Allergy reported in 1971 that only 17 (30.4%) of 56 patients with a history of immediate (including anaphylactic) reactions to penicillin exhibited positive skin tests to penicillin G.2


1996 ◽  
Vol 3 (1) ◽  
pp. 53-57 ◽  
Author(s):  
Kitaw Demissie ◽  
Pierre Ernst ◽  
Margaret R Becklake

BACKGROUND:Variation in the prevalence of allergic disorders among socioeconomic groups could be due either to differences in the type of allergens encountered or to actual differences in susceptibility to sensitization to any particular antigen.OBJECTIVE:To examine the relationship of skin test positivity to inhaled aeroallergens and socioeconomic status (SES).METHODS:A total of 989 Montreal elementary school children were studied. A short questionnaire was completed by parents, and the children performed spirometry before and after a free-running exercise challenge. A subsample of 309 children underwent allergy skin prick tests to common inhaled aeroallergens. SES was established using parental occupation.RESULTS:Higher social class was associated with an increased likelihood of having positive skin tests to cat and trees, while there was a trend towards an inverse relationship between SES and skin test sensitivity to cockroach and moulds. Reported history of asthma, hay fever or eczema were unrelated to SES.CONCLUSIONS:The results of this study suggest differences in levels of exposure to different allergens by social class. From the public health point of view, community-based allergen avoidance measures need to be adapted to social class.


PEDIATRICS ◽  
1971 ◽  
Vol 48 (6) ◽  
pp. 930-938
Author(s):  
William C. Deamer

The most effective treatment of allergy is discovery and removal of the allergen. Injection therapy, while useful in some forms of inhalant allergy such as hay fever, is a less effective measure. Respiratory tract allergy is frequently mistaken for respiratory tract infection. A history of repeated episodes of bronchitis or pneumonia should suggest the possibility of asthma. Similarly, a history of repeated "colds" should suggest allergic rhinitis. Increased sneezing and itching and rubbing of the nose are frequent minor symptoms of allergic rhinitis. Coughing at night and coughing on exertion are common minor symptoms of asthma. Since allergic rhinitis and asthma often occur together and share the same etiology, all four of these minor symptoms may serve as a guide in identifying and treating asthma. Positive skin tests for allergy may be found in as much as 50% of "normal" individuals, many of whom may have no recognized clinical allergy. Positive skin tests therefore do not constitute evidence of clinical symptoms. Nonspecific trigger factors such as nervous tension, respiratory tract infections, fatigue, climate, exercise, and smoke or strong odors may precipitate an attack of asthma. Frequently overlooked are the more important specific factors such as pollens, house dust, animal danders, and foods. An important variable factor in asthma is the state of the patient's sympathetic-parasympathetic nervous system balance. At times this may act to augment synergistically the action of the chemical mediators of the allergic reaction, thus involving non-immunological as well as immunological factors. Food allergy or intolerance is a frequently unrecognized cause of asthma and allergic rhinitis. It is also a frequent cause of the tension-fatigue syndrome–a common but little known entity.


2014 ◽  
Vol 5 (2) ◽  
pp. ar.2014.5.0080 ◽  
Author(s):  
Samantha R. Gendelman ◽  
Lily C. Pien ◽  
Ravi C. Gutta ◽  
Susan R. Abouhassan

The Center for Disease Control guidelines recommend desensitization to metronidazole in patients with trichomoniasis and hypersensitivity to metronidazole. There is only one published oral metronidazole desensitization protocol. The purpose of this study was to design a new, more gradual oral desensitization protocol to decrease systemic reactions that may occur when using the previously published protocol. We present two patients with presumed IgE-mediated allergy to metronidazole who underwent oral desensitization using our modified protocol. Case 1 was a 65-year-old woman with trichomoniasis who presented for metronidazole desensitization with a history of intraoperative anaphylaxis and positive skin tests to metronidazole. The patient tolerated six doses of the modified desensitization but developed systemic symptoms of nasal congestion and diffuse pruritus after the 25- and 100-mg doses. Both reactions were treated with intravenous (i.v.) antihistamines. Because of gastrointestinal irritation, the desensitization was completed at a dose of 250 mg orally every 6 hours. Case 2 was a 42-year-old woman with trichomoniasis and a history of hives immediately after administration of i.v. metronidazole who presented for desensitization. The patient had negative skin-prick and intradermal testing to metronidazole. She developed lip tingling and pruritus on her arms 15 minutes after the 10-mg dose. Fexofenadine at 180 mg was given orally and symptoms resolved. She tolerated the rest of the protocol without reaction and received a total dose of 2 g of metronidazole. Our oral metronidazole desensitization for presumed IgE-mediated reactions offers a second option for physicians wishing to use a more gradual escalation in dose.


2021 ◽  
Vol 12 (2) ◽  
pp. 106-112
Author(s):  
Beata Sadowska ◽  
Marlena Sztormowska ◽  
Marika Gawinowska ◽  
Marta Chelminska

Background: Sodium metabisulfite is a recognized, but rare, trigger of urticaria, wherein the IgE mechanism has been sporadically proven. The aim of this study was to identify the potential reaction to sodium metabisulfite (MBS) based on a placebo-controlled oral challenge in patients with urticaria and suspected hypersensitivity to food additives. Materials and Methods: A total of 110 adult patients (76 females and 34 males with a mean age of 46 years) were included in the study between 2017 and 2019. All subjects underwent MBS skin prick tests (SPT) and patch tests (PT). Patients with a positive skin test or suspected MBS hypersensitivity were qualified for a placebo-controlled oral challenge (OC). Results: Skin testing was positive in 24 patients: SPT in 20% (n = 22), PT in 5% (n = 6). Out of 64 oral challenges, 13 positive results were obtained. Patients with a positive challenge typed sulfite foods twice as often as a culprit compared to those with a negative OC. Conclusions: In patients with urticaria, both the IgE and non-IgE mechanism of MBS hypersensitivity has been demonstrated. Skin tests with a detailed medical history of potentially guilty foods may be helpful in determining sulfite hypersensitivity.


2003 ◽  
Vol 9 (4) ◽  
pp. 675-688
Author(s):  
W. Al Kubaisy ◽  
A. Al Dulayme ◽  
H. D. Selman

In a prospective cohort study in Iraq, schoolchildren with a positive tuberculin skin test during the nationwide survey in 2000 were followed up in 2002 to determine prevalence of latent tuberculosis [TB] infection and risk factors among household contacts. Of 205 children, 191 remained skin-test positive in 2002. Based on X-ray and clinical examination, 9 children [4.4%] were active TB cases. Among 834 household contacts, there were 144 new TB cases, giving a cumulative incidence of 17.3%. Risk factors for TB among household contacts were: age > / = 15 years; technical/professional job; smoking; low body mass index; diabetes mellitus; steroid therapy; and closeness of contact with the index cases. Based on past history of TB in index children and their contacts, 77.2% of new TB cases were attributable to household contacts


Author(s):  
Florian Stehlin ◽  
Rima Mahdi-Aljedani ◽  
Loris Canton ◽  
Véronique Monzambani-Banderet ◽  
Alix Miauton ◽  
...  

Background: The newly developed mRNA-based COVID-19 vaccines can provoke anaphylaxis, possibly induced by polyethylene glycol (PEG) contained in the vaccine. The management of persons with a history of PEG allergy, or with an allergic-like reaction after the first dose remains to be defined.  Methods: We studied two cohorts of individuals: one pre-vaccination, the second post-vaccination. Skin testing was performed with COVID-19 mRNA vaccines. Upon negative skin test, a two-step (10%-90%) vaccination protocol was performed. Positive skin tests were confirmed with basophil activation tests (BAT). Vaccine-sensitized patients were offered a five-step induction protocol. Results: We identified 187 patients with high-risk profiles for developing anaphylaxis. In parallel, among 385’926 doses of vaccine, 87 allergic-like reactions were reported to our division for further investigations: 18/87 (21%) were consistent with anaphylaxis, 78/87 (90%) were female, and 47/87 (54%) received the BNT162b2 mRNA vaccine. Vaccine skin tests were negative in 96% and 76% in the pre- and post-vaccination cohorts, respectively. A two-step vaccination was tolerated in 232/236 (98%) of individuals with negative tests. Four individuals experienced acute asthma exacerbation during the two-step challenge. Vaccine-positive skin tests were consistently confirmed by BAT; CD63 and CD203c expression was selectively inhibited with ibrutinib, suggesting an IgE-dependent mechanism. Finally, 13 sensitized patients were successfully vaccinated with a five-step vaccination protocol. Conclusion: A two-step 10%-90%-vaccination protocol can be safely administered upon negative skin testing. Yet, it should be delayed in individuals with poorly controlled asthma. Importantly, mRNA vaccine sensitized individuals may receive a five-step vaccination protocol.


PEDIATRICS ◽  
1978 ◽  
Vol 61 (4) ◽  
pp. 550-555
Author(s):  
Koichi Baba ◽  
Hyakuji Yabuuchi ◽  
Hidekazu Okuni ◽  
Michiaki Takahashi

In December 1975, a patient with varicella was admitted to a ward for children less than 2 years of age. Among 76 children without a history of varicella, 33 children more than 1 year of age were immediately vaccinated with a small viral dose of 80 plaque-forming units per person. Forty-three children less than 1 year of age were left unvaccinated. Among the vaccinated children, only eight exhibited mild varicella, while typical varicella developed in all 43 unvaccinated children during the next ten weeks. In July 1976, another patient with varicella was admitted to a ward with 49 children 3 to 5 years old. The children were immediately given the skin reaction test with mactivated varicella antigen. Seventeen of the 20 children with negative reactions were vaccinated, while the index patient and two children with fever were not vaccinated. Only one of the 17 vaccinated children showed mild varicella symptoms within two weeks after vaccination, while typical varicella developed in two unvaccinated children during the four weeks after appearance of the index case. Varicella developed in none of the 29 children who had positive skin tests. In the sequential skin test of seven vaccinated children, a positive skin reaction was observed as early as five days after vaccination, which preceded the appearance of neutralization antibody by seven to nine days.


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