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  1. Article ; Online: Salmon roe (ikura)-induced anaphylaxis in a child.

    Minhas, Jasmit / Saryan, John A / Balekian, Diana S

    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology

    2017  Volume 118, Issue 3, Page(s) 365–366

    Language English
    Publishing date 2017-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1228189-x
    ISSN 1534-4436 ; 0003-4738 ; 1081-1206
    ISSN (online) 1534-4436
    ISSN 0003-4738 ; 1081-1206
    DOI 10.1016/j.anai.2016.11.020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Hypertriglyceridemia-induced Acute Pancreatitis.

    Minhas, Jasmit / Thakkar, Dhaval / Dargin, James

    The Journal of emergency medicine

    2017  Volume 52, Issue 3, Page(s) e89–e90

    MeSH term(s) Abdominal Pain/etiology ; Adult ; Humans ; Hypertriglyceridemia/complications ; Hypertriglyceridemia/drug therapy ; Male ; Nausea/etiology ; Obesity ; Pancreatitis/etiology ; Tomography, X-Ray Computed/methods
    Language English
    Publishing date 2017-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605559-x
    ISSN 0736-4679
    ISSN 0736-4679
    DOI 10.1016/j.jemermed.2016.10.018
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Independent lung ventilation in the management of ARDS and bronchopleural fistula.

    Minhas, Jasmit S / Halligan, Kyle / Dargin, James M

    Heart & lung : the journal of critical care

    2016  Volume 45, Issue 3, Page(s) 258–260

    Abstract: Independent lung ventilation is a decades-old, but infrequently used technique for physiological separation in critically-ill patients with asymmetric lung disease. Here we present a case report of bilateral necrotizing pneumonia complicated by acute ... ...

    Abstract Independent lung ventilation is a decades-old, but infrequently used technique for physiological separation in critically-ill patients with asymmetric lung disease. Here we present a case report of bilateral necrotizing pneumonia complicated by acute respiratory distress syndrome and bronchopleural fistula, which was successfully managed with independent lung ventilation. The use of independent lung ventilation allowed for adequate oxygenation with use of high positive end expiratory pressure in the "good lung" while simultaneously allowing for closure of the bronchopulmonary fistula in the contralateral lung by maintaining relatively low airway pressures.
    MeSH term(s) Aged ; Bronchial Fistula/complications ; Bronchial Fistula/therapy ; Critical Illness ; Female ; Humans ; Respiration, Artificial/methods ; Respiratory Distress Syndrome, Adult/complications ; Respiratory Distress Syndrome, Adult/therapy
    Language English
    Publishing date 2016-05
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 193129-5
    ISSN 1527-3288 ; 0147-9563
    ISSN (online) 1527-3288
    ISSN 0147-9563
    DOI 10.1016/j.hrtlng.2016.02.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Immune-mediated reactions to vancomycin: A systematic case review and analysis.

    Minhas, Jasmit S / Wickner, Paige G / Long, Aidan A / Banerji, Aleena / Blumenthal, Kimberly G

    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology

    2016  Volume 116, Issue 6, Page(s) 544–553

    Abstract: Background: Vancomycin is a broad-spectrum antibiotic whose use may be limited by adverse drug reactions (ADRs). Although vancomycin toxic effects are known, there are limited data on vancomycin hypersensitivity reactions (HSRs).: Objective: To ... ...

    Abstract Background: Vancomycin is a broad-spectrum antibiotic whose use may be limited by adverse drug reactions (ADRs). Although vancomycin toxic effects are known, there are limited data on vancomycin hypersensitivity reactions (HSRs).
    Objective: To understand the most commonly reported vancomycin HSRs through systematic case review.
    Methods: We performed a literature search for English-language case reports and series from 1982 through 2015 (last search July 31, 2015) on Ovid MEDLINE and PubMed. The search included the subject heading vancomycin with the subheading adverse effects and separate text searches for vancomycin with a list of specified HSRs. References of identified articles were reviewed to find additional articles. Clinical data were collected and summarized.
    Results: Of 201 identified articles, 84 were screened and 57 fully assessed; these 57 articles contained 71 vancomycin HSR cases that were included in analysis. Vancomycin HSRs were immediate (anaphylaxis, n = 7) and nonimmediate (n = 64). Nonimmediate HSRs included linear IgA bullous dermatosis (LABD, n = 34), drug rash eosinophilia and systemic symptoms (DRESS) syndrome (n = 16), acute interstitial nephritis (AIN, n = 8), and Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN, n = 6). Median times of vancomycin therapy before HSR onset was 7 days (interquartile range [IQR], 4-10 days) for LABD, 9 days (IQR, 9-22 days) for SJS/TEN, 21 days (IQR, 17-28 days) for DRESS syndrome, and 26 days (IQR, 7-29 days) for AIN. Overall, 11 patients (16%) died, and 4 (6%) had deaths attributed to the HSR.
    Conclusion: Vancomycin causes a variety of HSRs; the most commonly identified were nonimmediate HSRs, with LABD being most frequent. We observed a high frequency of HSR mortality. Further data are needed to understand the frequency and severity of vancomycin HSRs.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Anaphylaxis/chemically induced ; Anti-Bacterial Agents/adverse effects ; Drug Hypersensitivity/etiology ; Female ; Humans ; Immunoglobulin E/immunology ; Male ; Middle Aged ; Nephritis, Interstitial/chemically induced ; Skin Diseases, Vesiculobullous/chemically induced ; Stevens-Johnson Syndrome/etiology ; Vancomycin/adverse effects ; Young Adult
    Chemical Substances Anti-Bacterial Agents ; Immunoglobulin E (37341-29-0) ; Vancomycin (6Q205EH1VU)
    Language English
    Publishing date 2016-05-04
    Publishing country United States
    Document type Journal Article ; Systematic Review
    ZDB-ID 1228189-x
    ISSN 1534-4436 ; 0003-4738 ; 1081-1206
    ISSN (online) 1534-4436
    ISSN 0003-4738 ; 1081-1206
    DOI 10.1016/j.anai.2016.03.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Gastrointestinal Manifestations in X-linked Agammaglobulinemia.

    Barmettler, Sara / Otani, Iris M / Minhas, Jasmit / Abraham, Roshini S / Chang, Yenhui / Dorsey, Morna J / Ballas, Zuhair K / Bonilla, Francisco A / Ochs, Hans D / Walter, Jolan E

    Journal of clinical immunology

    2017  Volume 37, Issue 3, Page(s) 287–294

    Abstract: Purpose: X-linked agammaglobulinemia is a primary humoral immunodeficiency characterized by hypogammaglobulinemia and increased susceptibility to infection. Although there is increased awareness of autoimmune and inflammatory complications in X-linked ... ...

    Abstract Purpose: X-linked agammaglobulinemia is a primary humoral immunodeficiency characterized by hypogammaglobulinemia and increased susceptibility to infection. Although there is increased awareness of autoimmune and inflammatory complications in X-linked agammaglobulinemia (XLA), the spectrum of gastrointestinal manifestations has not previously been fully explored.
    Methods: We present a case report of a family with two affected patients with XLA. Given the gastrointestinal involvement of the grandfather in this family, we performed a retrospective descriptive analysis of XLA patients with reported diagnoses of GI manifestations and inflammatory bowel disease (IBD) or enteritis registered at the United States Immunodeficiency Network, a national registry of primary immunodeficiencies.
    Results: In this cohort of patients with XLA, we found that up to 35% had concurrent gastrointestinal manifestations, and 10% had reported diagnoses of IBD or enteritis. The most commonly reported mutations were missense, which have been associated with a less severe XLA phenotype in the literature. The severity of symptoms were wide ranging, and management strategies were diverse and mainly experimental.
    Conclusions: Patients with XLA may require close monitoring with particular attention for GI manifestations including IBD and infectious enteritis. Further studies are needed to improve diagnosis and management of GI conditions in XLA patients.
    MeSH term(s) Agammaglobulinemia/complications ; Agammaglobulinemia/diagnosis ; Agammaglobulinemia/therapy ; Aged, 80 and over ; Biomarkers ; Gastrointestinal Diseases/diagnosis ; Gastrointestinal Diseases/etiology ; Gastrointestinal Tract/pathology ; Genetic Association Studies ; Genetic Diseases, X-Linked/complications ; Genetic Diseases, X-Linked/diagnosis ; Genetic Diseases, X-Linked/therapy ; Humans ; Immunoglobulin Isotypes/blood ; Immunophenotyping ; Infant ; Lymphocyte Subsets/immunology ; Lymphocyte Subsets/metabolism ; Male ; Mutation ; Pedigree ; Phenotype
    Chemical Substances Biomarkers ; Immunoglobulin Isotypes
    Language English
    Publishing date 2017-02-24
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 779361-3
    ISSN 1573-2592 ; 0271-9142
    ISSN (online) 1573-2592
    ISSN 0271-9142
    DOI 10.1007/s10875-017-0374-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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