scholarly journals De-labeling severe asthma diagnosis: the challenge of DIPNECH

2022 ◽  
pp. 00485-2021
Author(s):  
Caroline Hurabielle ◽  
Camille Taillé ◽  
Grégoire Prévot ◽  
Maud Russier ◽  
Alain Didier ◽  
...  
Author(s):  
Iwona Dziewa ◽  
Timothy Craig ◽  
Taha Al-Shaikhly

Worldwide, asthma-related healthcare cost remains a major burden. Individuals with severe asthma account for 50% of that cost. Although they are expensive, biologics such as anti-IL5 and anti-IgE agents promise cost-effectiveness when judiciously used to decrease asthma-related hospitalization and the debilitating side effects of systemic corticosteroids. Before considering biologics to treat patients with asthma, current guidelines recommend confirmation of asthma and control of comorbid diseases. Diagnostic confirmation of asthma can be challenging among individuals with severe asthma. In this quality assessment study, we determined the frequency of objective asthma confirmation and addressing of comorbidities prior to starting biologics at a group practice of allergists and immunologists. We surveyed our specialty providers to understand habit(s) leading to the observed results. We identified 40 adult patients who started on biologic modifiers for asthma over the past 5 years. Only 58% of these patients had a proper diagnosis of asthma. Providers underutilized several diagnostic methods that may prove useful in confirming asthma diagnosis in this patient population. The factors contributing to poor asthma control were rarely addressed. A sense of urgency to initiate biologics was the primary reason for the observed results. Further interventions are needed to improve asthma diagnosis and management prior to the initiation of biologic therapeutics.


2014 ◽  
Vol 21 (1) ◽  
pp. e1-e3 ◽  
Author(s):  
Natasha Satkunam ◽  
Zaeem A Siddiqi ◽  
Dilini Vethanayagam

Severe asthma constitutes a subgroup of approximately 10% of all asthma cases. Approximately one-half of these individuals have a refractory form of the disease in which atopy and T-helper cell 2-skewed immunological response may not be as closely linked to the disease as in other phenotypes of asthma. This suggests that not all asthma is explained by a T-helper cell 2-skewed immunological response, and that other immunological mechanisms may be important in this category of nonatopic asthma. The authors present a case involving a 55-year-old Caucasian man with nonatopic, adult-onset asthma, nonsteroidal anti-inflammatory drug sensitivity and idiopathic urticaria. This individual presented two years following his initial asthma diagnosis with diplopia and mild ptosis, and was subsequently diagnosed with seropositive myasthenia gravis.


2014 ◽  
Vol 45 (1) ◽  
pp. 87-97 ◽  
Author(s):  
Nadzeya V. Marozkina ◽  
Xin-Qun Wang ◽  
Vitali Stsiapura ◽  
Anne Fitzpatrick ◽  
Silvia Carraro ◽  
...  

S-Nitrosoglutathione is an endogenous airway smooth muscle relaxant. Increased airway S-nitrosoglutathione breakdown occurs in some asthma patients. We asked whether patients with increased airway catabolism of this molecule had clinical features that distinguished them from other asthma patients.We measured S-nitrosoglutathione reductase expression and activity in bronchoscopy samples taken from 66 subjects in the Severe Asthma Research Program. We also analysed phenotype and genotype data taken from the program as a whole.Airway S-nitrosoglutathione reductase activity was increased in asthma patients (p=0.032). However, only a subpopulation was affected and this subpopulation was not defined by a “severe asthma” diagnosis. Subjects with increased activity were younger, had higher IgE and an earlier onset of symptoms. Consistent with a link between S-nitrosoglutathione biochemistry and atopy: 1) interleukin 13 increased S-nitrosoglutathione reductase expression and 2) subjects with an S-nitrosoglutathione reductase single nucleotide polymorphism previously associated with asthma had higher IgE than those without this single nucleotide polymorphism. Expression was higher in airway epithelium than in smooth muscle and was increased in regions of the asthmatic lung with decreased airflow.An early-onset, allergic phenotype characterises the asthma population with increased S-nitrosoglutathione reductase activity.


Thorax ◽  
2015 ◽  
Vol 70 (Suppl 3) ◽  
pp. A8.2-A8
Author(s):  
A von Bülow ◽  
V Backer ◽  
U Bodtger ◽  
NU Soes Petersen ◽  
T Skjold ◽  
...  

2010 ◽  
Vol 44 (4) ◽  
pp. 2
Author(s):  
HEIDI SPLETE
Keyword(s):  

2007 ◽  
Vol 37 (5) ◽  
pp. 36
Author(s):  
MICHELE G. SULLIVAN

Pneumologie ◽  
2017 ◽  
Vol 71 (S 01) ◽  
pp. S1-S125
Author(s):  
I Pouliquen ◽  
D Austin ◽  
N Gunsoy ◽  
SW Yancey

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