Translate

Κυριακή 17 Νοεμβρίου 2019

Deranged Pulmonary Function Tests in Allergic Rhinitis in North Indian Patients,


Seema Monga, Junaid Malik, Arun Parkash Sharma, Sabeena Jan, Nighat Nabi, Sudhir BahadurFirst Published November 15, 2019 Research Article
https://doi.org/10.1177/1179550619888856
Article information
 Open Access Creative Commons Attribution, Non Commercial 4.0 License
Abstract
Introduction:
Significant associations between allergic rhinitis and bronchial asthma have been established and as a result of bronchial hyper-responsiveness, patients can have deranged pulmonary function tests. We aim to compare previous such studies with the result of our study done in India wherein we identify among allergic rhinitis patients who despite not having overt asthmatic symptoms, have pulmonary function derangements, quite possibly at a subclinical disease level.

Materials and Methods:
We studied 74 patients of allergic rhinitis and after meticulous clinical work up, they underwent blood tests including hemogram, absolute eosinophil count, and total serum IgE followed by pulmonary function tests.

Results:
Out of 74 patients 60 (81%) had intermittent allergic rhinitis whereas only 14 (19%) had persistent allergic rhinitis. Pulmonary function tests showed reversible obstruction, ie, >10% improvement in FEV1 with inhaled bronchodilators (as seen in asthma) in 18 (24.3%), mild obstruction in 14, and moderate obstruction in 4 cases.

Conclusion:
The study emphasizes the importance of pulmonary symptoms and the performance of pulmonary function tests in cases of allergic rhinitis patients to rule out latent asthma.

Keywords Allergic rhinitis, asthma, forced expiratory volume, bronchodilator agents
Introduction
Allergic rhinitis (AR), a common inflammatory condition affecting upper airways mainly the nose and often eyes, is characterized by symptoms such as sneezing, rhinorrhea, pruritus, and congestion which usually occur on exposure to allergens such as pollen, mites, dust, and other stimuli. Allergic rhinitis patients often have comorbidities, asthma being one of the most common. At least as many as 80% of asthma patients have symptoms of AR and up to 40% of patients with AR have associated asthma.1,2 Current pathophysiological studies suggest both conditions as manifestations of chronic inflammatory syndrome of the common airway or ‘united airway disease’.3,4 Both of these disorders affect between 25% and 50% of the population and mar the health and quality of life of individuals and societies leading to social and financial burdens at a global level.

The frequent co-occurrence of both these conditions and their proven close relationship in various studies led World health Organization (WHO) and the ARIA (Allergic Rhinitis and its Impact on Asthma) initiative to issue documents in 2001 and in 2008, which provide a comprehensive overview of the etiopathogenesis, diagnosis, and treatment of AR. The update proposes that management as one condition one airway-one disease, may alleviate the other coexisting disorders.5 Patients having persistent AR should be checked for asthma. This also is one of the key goals in the Finish Allergy Programme 2008-2018, to reduce the load of allergic rhinitis and asthma in the community.6 Although few studies have been done in India to see the prevalence of asthma in patients of AR, results of our study compare previous studies and help further analyse, assess, and model to propose standards of evaluation, norms, and guidelines for AR patients.

We also aim to recognize elements which help better identify cases with AR who, despite having absent overt asthmatic symptoms, may have pulmonary function alterations, possibly at a subclinical disease level.

Materials and Methods
This is a prospective study done in the department of Otorhinolaryngology, Head and Neck Surgery, of a tertiary care hospital during a period of 2 years from January 2013 to December 2015. A total of 74 patients with features of AR who presented to our outpatient department were enrolled in the study. After obtaining written informed consent, the patients were given a structured questionnaire requesting demographic details (age, gender, and residence), data on smoking, personal history, family history, history of atopy, and clinical features of AR (frequency and severity). They were further classified into intermittent AR, and persistent AR as per WHO-ARIA initiative. Recruited patients subsequently underwent hemogram with erythrocyte sedimentation rate (ESR), total serum IgE testing, absolute eosinophil count (AEC), chest X-ray, and pulmonary function tests. Presence of asthma was indicated by reversible airway obstruction with administration of a bronchodilator agent as shown by ⩾10% increase in FVC (forced vital capacity) or FEV1 (forced expiratory volume in 1 second).

All cases were put on medical treatment as per ARIA guidelines and then examined for symptom relief on follow up.

Results
Out of 74 patients diagnosed with AR, 41 were males and 33 females (1.24:1 male-to-female ratio). Age ranged from 8 years to 51 years with maximum patients in 21-30 age group. History of smoking was present in 19 (25.6%) of patients out of which 7 (9.4%) were active and 12 (16.2%) passive smokers whereas 55 (74.4%) were nonsmokers. In total, 11 (14.8%) had positive family history of ‘united airway’ disease (asthma or AR) whereas 63 (85.2%) had no such family history. Maximum patients 44 (59.4%) belonged to lower socioeconomic group. Absolute eosinophil count was raised in 28 (37.8%) of patients whereas it was normal in the rest. Total serum IgE was raised in 55 (74.3%) of patients. Table 1 shows the clinical profile of the study group.

Table
Table 1. Clinical profile of patients with allergic rhinitis.

Table 1. Clinical profile of patients with allergic rhinitis.


View larger version
Watering nose and sneezing were the most common symptoms seen in 65 cases (87%) followed by nasal blockage in 58 (78.3%) cases. They were classified into intermittent AR and persistent AR as per WHO initiative ARIA. Out of 74 patients 60 (81%) had intermittent AR wheras only 14 (19%) had persistent AR. Mild AR symptoms were present in 35 (47.2%) and moderate-severe symptoms of AR were seen in 39 (52.8%) patients. Pulmonary function test (PFT) showed reversible obstruction, ie, >10% improvement in FEV1 with inhaled bronchodilators in 18 (24.3%), mild obstruction in 14 and moderate obstruction in 4 cases – Table 2. Comorbid latent asthma was more commonly detected in persistent AR group (35.7%) as compared with intermittent AR cases (21.6%) – Table 3.

Table
Table 2. Status of pulmonary function in patients with allergic rhinitis.

Table 2. Status of pulmonary function in patients with allergic rhinitis.


View larger version
Table
Table 3. Break up of allergic rhinitis cases and presence of associated latent asthma.

Table 3. Break up of allergic rhinitis cases and presence of associated latent asthma.


View larger version
Discussion
The percentage of males (53.8%) was seen marginally higher than females (46.1%) in our study. This is similar to a study done by Patel et al7 wherein out of 70 AR patients 52.8% were males and 47.1% females. Many of our AR cases were within agegroup of 21-30 years and the mean age of patients in our study was 33.12 years although one patient (1.3%) was elderly. This inference that elder patients had lesser risk of asthma, AR, and their association is in accordance with various studies8 although many authors have validated the opposite pattern as well.9,10

In our study, watering nose and sneezing were the most common presenting symptoms in 65 (87.8%) patients. This is similar to the study done by Patel et al7 in which most common symptom was rhinorrhea (100%) followed by sneezing present in 95.7% patients and nasal blockage in 22.8% patients. Only 25.6% of AR patients in our study were smokers (9.4% active and 16.2% passive). This is also in agreement with study done by Bugiani et al11 who also found lower prevalence of AR in smokers. Bugiani gave a possible explanation that AR patients either do not start smoking or they stop sooner.

The association between allergic diseases and socioeconomic status is contentious. Most of our patients belonged to lower socio-economic class 44 (59.4%) and this is in accordance with studies which have suggested AR and asthma to be more frequent in families with low socioeconomic status, whereas sensitization to aerial allergens appears to be more common in persons with higher socioeconomic status during childhood.12 However, this might also be linked to other uncontrolled variances in life style and environmental exposures among the groups, and demands for further studies.

The basic investigations required in the evaluation of a patient with suspected AR include complete blood picture with peripheral eosinophil percentage, AEC, total IgE levels, nasal smear examination for eosinophils. A normal eosinophil count is less than 350 cells/µL of blood. The relationship between eosinophilia and allergic conditions has been well established in various studies.13 In our study, AEC was raised only in 37.6% of patients of AR which is similar to studies done by Venkateswarlu and Murali Mohan14 and Sonawane et al.15 IgE facilitated allergic sensitization is the cause of allergic diseases and raised total IgE. Despite wellknown limitations it is frequently included diagnostic criterion for allergic diseases. In 1985, Bousquet et al in a study reported the mean total serum IgE levels was 38 ± 43 KU/L-180 KU/L in normal people and 94 ± 93 KU/L in allergic individuals. Moreover asthmatics had higher mean IgE levels than those suffering from AR.16 In our study, serum IgE was raised in 74.3% of patients.

Routinely carrying out skin prick tests or radio-allergosorbent test (RAST), enzyme linked immunesorbent assay (ELISA) tests to evaluate the atopic skin status of all these cases is not feasible in most of the outpatient clinics of developing countries. Similar to other authors we too made an attempt to determine the patients who could be given treatment related to allergic symptoms based on the findings acquired from correlation of specific symptoms with the blood markers (total IgE levels and peripheral eosinophils).17

Allergic Rhinitis and its Impact on Asthma (ARIA) classification has been endorsed by numerous studies. In total, 81% of our patients had intermittent AR, whereas only 19% had persistent AR, and mild AR was present in 35 (47.2%) and moderate-severe symptoms of AR were seen in 39 (52.8%) patients. This is similar to study done by Bachert et al18 who found that 59% of his subjects had intermittent, 41% persistent rhinitis, 25% mild, and 75% moderate-severe AR whereas in a study done by Navarro et al19 46% were intermittent, 54% persistent, 43% mild, and 57% moderate-severe AR.

There is evidence showing that patients with AR may have an increased prevalence of bronchial hyper-responsiveness and alterations in the functional testing of breathing.20 In a study done by Jeffery et al21 on 107 patients of AR deranged pulmonary function tests were observed in 39.1% of cases and 26.1% of patients were diagnosed with asthma. Our study showed 18 (24.3%) of AR patients had PFT similar to asthma. Pulmonary function test showed mild obstruction in 14 (18.9%) whereas moderate obstruction in 4 (5.4%). This is in accordance with studies done by Simons4 and Patel et al7 wherein associated asthma was present in 15.3% patients. These results point to the presence of substantial variations in the prevalence of the different types of AR as per characteristics of study population and in context to health care.

Conclusion
The study highlights the significance of PFT in AR for recognizing the upper and lower airway disease as a continuum of single disease process and thus importance be given to history of chest symptoms in AR patients to check for latent asthma.

Funding:
The author(s) received no financial support for the research, authorship, and/or publication of this article.

Declaration of conflicting interests:
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Author Contributions
SM: Protocol design

JM: Data collection and analysis, manuscript review

APS Technical assistance

SJ and NN: Study execution and Data collection

SB: Manuscript editing and Final approval.

Protection of human subjects and animals in research
Protection of human and animal subjects: The authors declare that no experiments were performed on humans or animals for this investigation.

Right to privacy and informed consent: The authors declare that no patient data appears in this article and all the patients included in the study have received sufficient information and have given their informed consent in writing to participate in the study.

ORCID iD
Junaid Malik  https://orcid.org/0000-0002-9888-761X

References
1. Guerra, S, Sherrill, DL, Martinez, FD, Barbee, RA. Rhinitis as an independent risk factor for adult-onset asthma. J Allergy Clin Immunol. 2002;109:419-425.
Google Scholar | Crossref | ISI
2. Wright, AL, Holberg, CJ, Martinez, FD, Halonen, M, Morgan, W, Taussig, LM. Epidemiology of physician-diagnosed allergic rhinitis in childhood. Pediatrics. 1994;94:895-901.
Google Scholar | ISI
3. Grossman, J. One airway, one disease. Chest. 1997;111:11S-16S.
Google Scholar | Crossref
4. Simons, FER . Allergic rhinobronchitis: the asthma–allergic rhinitis link. J Allergy Clin Immunol. 1999;104:534-540.
Google Scholar | Crossref | ISI
5. Bousquet, J, Khaltaev, N, Cruz, AA, et al. Allergic Rhinitis and Its Impact on Asthma (ARIA) 2008 update. Allergy. 2008;63:8-160.
Google Scholar | Crossref | ISI
6. Haahtela, T, von Hertzen, L, Mäkelä, M. Allergy programme working group Finnish allergy programme 2008—2018: time to act and change the course. Allergy. 2008;63:634-645.
Google Scholar | Crossref
7. Patel, AK, Nagpal, TP. Comparison of blood absolute eosinophil count and nasal smear eosinophils with symptoms and severity of clinical score in patients of allergic rhinitis. Indian J Allergy Asthma Immunol. 2014;28:74-77.
Google Scholar | Crossref
8. Corren, J. The impact of allergic rhinitis on bronchial asthma. J Allergy Clin Immunol. 1998;101:S352-S356.
Google Scholar | Crossref | ISI
9. De Marco, R, Locatelli, F, Cerveri, I, Bugiani, M, Marinoni, A, Giammanco, G. Incidence and remission of asthma: a retrospective study on the natural history of asthma in Italy. J Allergy Clin Immunol. 2002;110:228-235.
Google Scholar | Crossref | ISI
10. Settipane, RJ, Hagy, GW, Settipane, GA. Long-term risk factors for developing asthma and allergic rhinitis: a 23-year follow-up study of college students. Allergy Proc. 1994;15:21-25.
Google Scholar | Crossref
11. Bugiani, M, Carosso, A, Migliore, E, et al. Allergic rhinitis and asthma comorbidity in a survey of young adults in Italy. Allergy. 2005;60:165-170.
Google Scholar | Crossref | ISI
12. Almqvist, C, Pershagen, G, Wickman, M. Low socioeconomic status as a risk factor for asthma, rhinitis and sensitization at 4 years in a birth cohort. Clin Exp Allergy. 2005;35:612-618.
Google Scholar | Crossref | ISI
13. Kumar, N, Bylappa, K, Ramesh, AC, Reddy, S. A study of eosinophil count in nasal and blood smear in allergic respiratory diseases in a rural setup. Internet J Med Update. 2012;7:40-46.
Google Scholar
14. Venkateswarlu, V, Murali Mohan, KV. A comparative study of nasal smear eosinophilia vs absolute eosinophilic count in patients with allergic rhinitis. MRIMS J Health Sci. 2015;3:36-38.
Google Scholar
15. Sonawane, R, Ahire, N, Patil, S, Korde, A. Blood smear in allergic respiratory diseases. MVP J Med Sci. 2016;3:44-51.
Google Scholar | Crossref
16. Bousquet, J, Coulomb, Y, Arrendal, H, Robinet-Levy, M, Michel, FB. Total serum IgE concentrations in adolescents and adults using the Phadebas IgE PRIST technique. Allergy. 1982;37:397-406.
Google Scholar | Crossref
17. Jagdeeshwar, K, Venumadhav, V, Chowdary, S, Sudharani, V, Kumar, V. A study on serum IgE levels, peripheral eosinophils and individual symptoms in patients with non infective rhinitis and asthma and related conditions. Int J Pharm Pharmaceut Sci. 2012;4:88-92.
Google Scholar
18. Bachert, C, van Cauwenberge, P, Olbrecht, J, van Schoor, J. Prevalence, classification and perception of allergic and non-allergic rhinitis in Belgium. Allergy. 2006;61:693-698.
Google Scholar | Crossref
19. Navarro, A, Valero, A, Julia, B, Quirce, S. Coexistence of asthma and allergic rhinitis in adult patients attending allergy clinics: ONEAIR study. J Investig Allergol Clin Immunol. 2008;18:233-238.
Google Scholar | ISI
20. Ciprandi, G, Tosca, MA, Signori, A, Cirillo, I. Bronchial hyperreactivity in patients with allergic rhinitis: forced expiratory flow between 25 and 75% of vital capacity might be a predictive factor. Allergy Asthma Proc. 2011;32:4-8.
Google Scholar | Crossref | ISI
21. Jeffery, CC, Bhutani, M, Vliagoftis, H, Wright, ED, Seikaly, H, Cote, DW. Association between allergic rhinitis and asthma in a Northern Alberta cohort. J Otolaryngol Head Neck Surg. 2013;42:58.
Google Scholar | Crossref

1 σχόλιο:

  1. I want to share with you all on how Dr Itua saves my life with his powerful Herbal medicines, I was diagnosed of Oral/Ovarian Cancer which i suffered from for 5 years with no positive treatment until when My son came to me in the hospital when i was laying down on my dying bed waiting for god to call out my name to join him in heaven.
    My son was so excited that very day he came across Dr Itua on Blogspot, we decided to give him a try although we Americans are so scared to trust Africans but i really have no choice that time to choose life in between so we gave a try to Dr Itua Herbal medicines, god willing he was a good man with a god gift. Dr Itua sent us the herbal medicine. It was three bottles. I take it for a three weeks instructor and these herbal medicines heal me, cure my Oral/Ovarian Cancer completely. I have been living for 9 months now with a healthy life with no more symptoms.
    I'm sponsoring Dr Itua in LA Advert on Cancer patent seminar which my son will be participating too and other patent Dr Itua has cured from all kind of human disease, also if you are sick from disease like,Epilepsy,Breast Cancer,Prostate Cancer,Throat cancer,Thyroid Cancer,Uterine cancer,Fibroid,Angiopathy, Ataxia,Arthritis,Brain cancer,Hiv,. Vaginal cancer,Herpes,Colon-Rectal Cancer,Chronic Disease.Amyotrophic Lateral Sclerosis,Brain Tumor,Fibromyalgia,Fluoroquinolone Toxicity,Multiple myeloma,Tach Diseases,Leukemia,Liver cancer,
    Esophageal cancer,Gallbladder cancer,,Bladder cancer,Gestational trophoblastic disease,Head and neck cancer,Hodgkin lymphoma
    Intestinal cancer,Kidney cancer,Hpv,Lung cancer,Adrenal cancer.Bile duct cancer,Bone cancer,Melanoma,Mesothelioma,Neuroendocrine tumors
    Non-Hodgkin lymphoma,Cervical Cancer,Oral cancer,Hepatitis,Skin cancer,Soft tissue sarcoma,Spinal cancer,Pancreatic Cancer, Stomach cancer
    Testicular cancer,
    Syndrome Fibrodysplasia Ossificans ProgresS sclerosis,Alzheimer's disease,Chronic Diarrhea,Copd,Parkinson,Als,Adrenocortical carcinoma Infectious mononucleosis,Vulvar cancer,Ovarian cancer,,Sinus cancer, Here Is The Wonderful Healer Contact. Name_ Doctor Itua, Email Contact: drituaherbalcenter@gmail.com, Phone/WhatsApp: +2348149277967

    ΑπάντησηΔιαγραφή

Αρχειοθήκη ιστολογίου

Translate