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3.
J Allergy Clin Immunol Glob ; 2(2): 100076, 2023 May.
Artículo en Inglés | MEDLINE | ID: mdl-37780792

RESUMEN

Background: mAbs (biologics) are indicated in patients with poorly controlled moderate-to-severe asthma. The process of prior authorization and administration of a biologic requires exceptional commitment from clinical teams. Objective: Our aim was to evaluate the process of approval and administration of biologics for asthma and determine the most common reasons associated with denials of biologics and delays in administration. Methods: We examined the records of patients with asthma who were prescribed biologics from January 2018 to January 2020 at 2 centers, Montefiore Medical Center (Bronx, NY) and Scripps Clinics (San Diego, Calif). Demographics, insurance information, and details on the approval process were collected. Results: After querying of electronic health records, the records of 352 and 70 patients with moderate-to-severe asthma were included from Montefiore and Scripps, respectively. Most patients at Montefiore (58.2%) were insured under Managed Care Medicaid (MC Medicaid), whereas most patients at Scripps (61.4%) had commercial insurance. The median times from prescription to administration of a biologic were similar: 34 days (interquartile range [IQR] = 18-63 days) and 34 days (IQR = 22.5-56.0 days) (P = .97) for Montefiore and Scripps, respectively. However, the median approval time for Montefiore was 6 days (IQR = 1-20 days) and that for Scripps was 22 days (IQR = 10-36 days) (P < .001). Approval times for prescriptions requiring appeals were significantly longer than for prescriptions approved after the initial submission: 23 days versus 2.5 days and 40.5 days versus 15.5 days (for Montefiore and Scripps, respectively [P < .001 for both]). Conclusions: Lengthy appeals contribute to delays between prescribing and administering a biologic. Site-specific practices and insurance coverage influence approval timing of the biologics for asthma.

4.
Pol Arch Intern Med ; 133(9)2023 09 29.
Artículo en Inglés | MEDLINE | ID: mdl-37548592

RESUMEN

Nonsteroidal anti­inflammatory drug-exacerbated respiratory disease (N­ERD) is a unique and often clinically severe disease affecting a subgroup of adults with asthma, chronic rhinosinusitis with nasal polyposis, and respiratory reactions with exposure to all cyclooxygenase 1-inhibiting nonsteroidal anti­inflammatory drugs. N­ERD has a high disease burden and is estimated to affect 7% of adults with asthma and 30% of patients who have both asthma and nasal polyps. The disease is underdiagnosed and underrecognized by physicians on a routine basis, which leads to a delay in appropriate management. The goal of this review is to focus on the disease recognition, diagnosis, and different modes of up­to­date therapies, including medical management, surgical intervention, aspirin desensitization, and biologic therapy.


Asunto(s)
Asma , Pólipos Nasales , Trastornos Respiratorios , Adulto , Humanos , Aspirina/uso terapéutico , Antiinflamatorios no Esteroideos/efectos adversos , Trastornos Respiratorios/tratamiento farmacológico , Pólipos Nasales/terapia , Pólipos Nasales/tratamiento farmacológico , Asma/tratamiento farmacológico , Enfermedad Crónica
5.
Clin Case Rep ; 8(12): 2661-2663, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-33363800

RESUMEN

Posterior reversible encephalopathy syndrome (PRES) is a reversible disease process in which cerebral edema is secondary to a trigger causes neurological symptoms. Our case presents an unusual MRI location and CSF analysis in a patient with PRES.

6.
Clin Case Rep ; 8(10): 1962-1964, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-33088529

RESUMEN

It has long been believed that the patients with thyrotoxic hypokalemic periodic paralysis (THPP) may harbor genetic mutations commonly found in familial hypokalemic periodic paralysis. Despite extensive testing, such a mutation has escaped detection until now.

7.
Clin Case Rep ; 8(8): 1376-1378, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32884757

RESUMEN

Recurrent GBS is a rare neurological condition in which patients develop similar symptoms of motor weakness after different preceding infections and suffer shorter intervals in between subsequent episodes of GBS. However, the majority of RGBS patients undergo full recovery.

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