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1.
Allergy Rhinol (Providence) ; 11: 2152656720927703, 2020.
Article in English | MEDLINE | ID: mdl-32489715

ABSTRACT

INTRODUCTION: Atopic dermatitis (AD, eczema) is familial chronic inflammatory skin disease of complex etiology and increasing prevalence. Dupilumab is an IL-4 receptor subunit alpha (IL-4Rα) antagonist that is the first Food and Drug Administration-approved biological therapy for moderate-to-severe adult AD inadequately controlled with topical therapies. Adverse effects reported in the literature include injection site reactions, conjunctivitis, headache, and nasopharyngitis. OBJECTIVE: We report the first cases of hyperhidrosis and bromhidrosis as side effects from dupilumab (Dupixent®) for the treatment of AD. CASE REPORTS: Case 1 is a 20-year-old woman with controlled allergic rhinitis and severe AD reported axillary hyperhidrosis with bromhidrosis, comparable to sweat from high-intensity exercise, with no relief from several different over-the-counter antiperspirants. Case 2 is a 61-year-old woman with history of chronic asthma, allergic contact dermatitis, allergic rhinitis, and AD noticed markedly increased sweating with bromhidrosis that was reminiscent of her menopausal symptomology, about 3 months after initiating dupilimab. DISCUSSION: Traditional immunosuppressive agents and corticosteroids have limited efficacy, numerous side effects, and increased risk of infection. The safety profile and efficacy of the newly approved IL-4Rα antagonist dupilumab may be favorable to oral immunosuppressants, but its use remains limited to severe recalcitrant cases, due to financial implications and lack of long-term safety data and comparative head-to-head trials. CONCLUSION: We report improved outcomes with dupilumab, in addition to unpublished cases of bromhidrosis and hyperhidrosis in 2 patients with AD. This report of additional complications may inspire further clinical research and assist clinicians in considering the option of dupilumab for uncontrolled AD, despite aggressive traditional treatment.

2.
J Am Osteopath Assoc ; 120(3): 144-152, 2020 Mar 01.
Article in English | MEDLINE | ID: mdl-32091558

ABSTRACT

CONTEXT: Inefficiencies in care coordination-specifically, the lack of an effective method of communication among multiple health care professionals-often leads to an unnecessary increase in length of hospital stay. OBJECTIVE: To determine whether daily integrated care conferences (ICCs) would significantly reduce the length of stay for patients with chronic obstructive pulmonary disease (COPD) exacerbation. METHOD: Patients with COPD exacerbation were selected for the study using electronic medical records from 2 osteopathic community hospitals located in northeastern Ohio. One hospital used daily ICCs and the other hospital did not use daily ICCs. The average length of stay for patients at each hospital was retrospectively investigated. RESULTS: A total of 1683 patients with COPD exacerbation were selected. The mean (SD) length of stay in the hospital with daily ICCs was 3.37 (2.89) days compared with 5.55 (3.99) days in the hospital without daily ICCs (P<.0001). At the hospital with daily ICCs, patients aged 40 to 69 years had a 67% shorter hospital stay and patients aged 70 to 99 years or older had a 36% shorter length of stay compared with patients at the hospital without daily ICCs. CONCLUSION: Daily integrated care conferences significantly reduced the length of stay for patients with COPD exacerbation at an osteopathic community-based hospital. Implementing daily ICCs may make current health care services and coordinated care more efficient, resulting in decreased costs and length of stay for patients with COPD exacerbation.


Subject(s)
Delivery of Health Care, Integrated/methods , Length of Stay/statistics & numerical data , Pulmonary Disease, Chronic Obstructive/therapy , Teaching Rounds/methods , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Ohio , Retrospective Studies
3.
Allergy Rhinol (Providence) ; 10: 2152656719890315, 2019.
Article in English | MEDLINE | ID: mdl-31819808

ABSTRACT

INTRODUCTION: Allergic rhinitis (AR) is a widely prevalent immunoglobulin E-mediated inflammatory nasal condition resulting from reexposure to an allergen in a sensitized individual. The genetic associations behind AR and other allergic conditions have been studied. However, familial success with AR therapies, specifically allergen desensitization through subcutaneous immunotherapy (SCIT), has never been reported in the literature. Pharmocogenetics has been gradually applied to link heritable genetic variants with drug responses, such as intergenic region variants APOBEC3B and APOBEC3C and ß2-adrenergic receptor and glycoprotein ADAM33 polymorphisms as predictive biomarkers for biologic treatment response in asthma. We provide the first reported survey of familial success with SCIT. METHODS: We administered a month-long, institutional review board-approved (20190493) questionnaire to 200 adult patients receiving SCIT in a suburban allergy/immunology practice. The anonymous survey inquired about demographics, target allergens for their SCIT, current symptom improvement on SCIT, and family history of allergies and SCIT management. RESULTS: Twenty-six percent (52 of 200, 26%) SCIT patients reported familial success with the same allergy treatment modality. AR diagnosis and symptom improvement from SCIT was similar among previous/same (18 of 52, 38%; 26 of 52, 54%) and subsequent (10 of 52, 21%; 19 of 52, 40%) generations of family members. A combination of seasonal and perennial allergies was most prevalent (81%) among this population. CONCLUSION: In a subpopulation of SCIT patients, there appears to be a familial success rate with this allergen desensitization treatment. This is the first reported pharmocogenetic evidence of assessing hereditary influence on effective AR therapy. Understanding pharmacogenetic associations involved with SCIT may improve allergists' recommendations for this treatment option.

4.
J Immunol Methods ; 459: 29-34, 2018 08.
Article in English | MEDLINE | ID: mdl-29802879

ABSTRACT

Murine models are readily used to investigate mechanisms potentially involved in anaphylaxis. Determining successful sensitization with current methods remain potentially lethal, invasive, expensive and/or cumbersome. Here we describe the use of thermography to read intradermal testing to detect peanut allergic sensitization in the murine model and as a first time sensitive tool for anaphylaxis stratification. The relative wheal size in the thermal image can be used to stratify anaphylaxis severity risk groups prior to a challenge. This screening method is nonlethal, inexpensive, minimally invasive and can be carried out expeditiously.


Subject(s)
Anaphylaxis/diagnosis , Arachis/immunology , Peanut Hypersensitivity/diagnosis , Thermography/methods , Urticaria/diagnosis , Allergens , Animals , Disease Models, Animal , Female , Histamine/administration & dosage , Intradermal Tests/methods , Mice , Severity of Illness Index , Urticaria/chemically induced , Urticaria/immunology
5.
J Matern Fetal Neonatal Med ; 31(16): 2223-2225, 2018 Aug.
Article in English | MEDLINE | ID: mdl-28562129

ABSTRACT

Penicillin desensitization is indicated in pregnant patients with severe allergies to penicillin with syphilis. The immediate effects of intramuscular epinephrine on the fetus during desensitization remain unreported. We describe a pregnant patient with secondary syphilis and penicillin allergy who developed anaphylaxis during penicillin desensitization. Anaphylaxis resolved after administration of intramuscular epinephrine. Throughout the procedure, continuous electronic fetal monitoring showed a stable fetus without a decrease in variability, tachycardia, decelerations, or signs of fetal distress. This case showed that intramuscular epinephrine is effective in treatment of anaphylaxis in a pregnant patient with little to no immediate effects on the fetus.


Subject(s)
Anaphylaxis/drug therapy , Desensitization, Immunologic/methods , Epinephrine/administration & dosage , Fetus/drug effects , Penicillins , Pregnancy Complications, Infectious/drug therapy , Syphilis/drug therapy , Anaphylaxis/immunology , Desensitization, Immunologic/adverse effects , Drug Hypersensitivity/drug therapy , Epinephrine/adverse effects , Female , Heart Rate, Fetal/drug effects , Humans , Injections, Intramuscular , Penicillins/administration & dosage , Penicillins/adverse effects , Penicillins/immunology , Pregnancy , Pregnancy Trimester, Second , Young Adult
6.
Ann Allergy Asthma Immunol ; 120(1): 109-110, 2018 01.
Article in English | MEDLINE | ID: mdl-29273124
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