Editorial
Meet the Team


Correlation of Rhinosinusitis with Bronchial Asthma

ECG Interpretation Skills of Family Physicians: A Comparison with Internists and Untrained Physicians

Efficacy of Chlorhexidine Mouthwash as an Oral Antiseptic - An Invivo Study on 20 Patients.


Facial pain, a common clinical condition, usually missed by clinicians as a psychosomatic disorder


Complementary and Alternative Medicine Training in Medical Schools: Half of Residents and Professors Agree that it Should be Taught

Methods of Management in hospital of Shiraz University of Medical Sciences: the development of suitable pattern


Public health schools in Iraq


Case study - Ethyl malonic aciduria


Urgent medical assistance still required in Pakistan


Avian influenza - situation in Thailand, Indonesia

Avian influenza - new areas with infection in birds

Yellow fever in Senegal


Childhood emergencies


ECG interpretation quiz


 

 


Dr Abdulrazak Abyad
MD,MPH, AGSF
Editorial office:
Abyad Medical Center & Middle East Longevity Institute
Azmi Street, Abdo Center,
PO BOX 618
Tripoli, Lebanon

Phone: (961) 6-443684
Fax:     (961) 6-443685
Email:
aabyad@cyberia.net.lb

 
 

Lesley Pocock
medi+WORLD International
572 Burwood Road,
Hawthorn 3122
AUSTRALIA
Emai
l
: lesleypocock

 


Correlation of Rhinosinusitis with Bronchial Asthma

 
AUTHORS

Dr. Nemer Al-Khtoum, MD
Department of Otolaryngology, Royal Medical Services.

Dr. Amin Al-Qudeh
Department of Medicine, Royal Medical Services.

CORRESPONDENCE

Dr. Nemer Al-khtoum
Department of ENT, RMS, Jordan Armed Forces
Amman, Jordan
PO Box Sweileh 1834
Email: nemer72@gmail.com


ABSTRACT

Objective: To evaluate the predisposition of sinus involvement in asthmatic patients.

Patients and Methods: One hundred cases of bronchial asthma patients of either sex were studied. Age of patients ranged from 18-60 years with mean age of 33.67 years. CT scan of paranasal sinus was performed for all patients.

Results: 58 (58%) patients had symptoms and signs suggestive of sinusitis. The most common symptom was nasal congestion found in 52 (52%) patients. CT Scan PNS showed evidence of sinusitis in 78 (78%) patients whereas 22 (22%) patients had no evidence of sinusitis. Maxillary sinusitis was found in 78 (78%) patient, and 52 (52%) patients had frontal sinusitis. Ethmoid sinusitis was seen in 22 (22%) patients and 8 (8%) patients had sphenoid sinusitis. Maxillary polyp was found in 22 (22%) patients and ostiomeatal complex block in 54 (54%) patients.
Among one hundred patients of bronchial asthma, clinically 58 (58%) patients had evidence of sinusitis whereas CT scan detected sinusitis in 78 (78%) patients.

Conclusion: The association of sinusitis and asthma seems to be more than an epiphenomenon. All asthmatics need to be examined for evidence of sinusitis preferably by CT scan.


INTRODUCTION

The association between sinusitis and asthma has long been appreciated. The incidence of sinusitis in asthmatic subjects is generally stated to range from 40% to 75%.1-7Although these studies strongly suggest that sinusitis triggers or worsens asthma, it could be argued that they merely coexist and represent different end products of the same process (inflammation) occurring in different organ systems.
Perhaps the most direct evidence of a cause-and-effect relationship has been provided by studies that show that appropriate treatment of sinusitis by medical intervention can result in significant improvement of asthma symptoms.[8-10] Additionally, sinus surgery in patients with asthma has been shown to bring about improvement in lower airway disease, although adequate controls have not been incorporated in most studies.

Hypotheses are forwarded that upper and lower airways need to be considered as different stages of unique entity influenced by common mechanisms in the inflammatory process. Sinusitis and asthma therefore, are considered as manifestations of one disease process.

The aim of the present study was to know the incidence of sinusitis in asthmatic populations, and to compare the relevant findings pertaining to sinus involvement obtained by clinical and radiological studies.

MATERIALS & METHODS

The sample of this study was conducted in the period from March 2003 to April 2005, in the Department of Medicine, royal medical services (Amman-Jordan).

After institutional ethical committee clearance and written informed consent one hundred cases of bronchial asthma patients of either sex were studied. Age of patients ranged from 18-60 years with the mean age of 33.67 years.

Asthmatic patients were selected as per the guidelines advocated by the American Thoracic Society in 1995. [11] All these asthmatic patients underwent a detailed history taking and a through general examination, systemic examination and were screened for clinical and radiological evidence of sinusitis. CT scan of paranasal sinus was performed for all patients.

The clinical criteria for diagnosing sinusitis were the presence of: [12]

  1. Nasal congestion/stuffiness
  2. purulent rhinorrhoea
  3. postnasal drainage
  4. Local pain and tenderness overlying the sinuses
  5. Night cough
  6. Unpleasant smell, or taste (Fetor oris)

CT criteria for the diagnosis of sinusitis was the presence of: [13]

  1. Mucosal thickening > 6 mm in children and > 8 mm in adults,
  2. Indistinct bony margins,
  3. Erosion of mucoperiosteum,
  4. Obstruction of ostiomeatal complex.

 

 
RESULTS

As per history and clinical examination 58 (58%) patients had symptoms and signs suggestive of sinusitis. The most common symptom was nasal congestion found in 52 (52%) patients.

CT Scan PNS showed evidence of sinusitis in 78 (78%) patients whereas 22 (22%) patients had no evidence of sinusitis. Maxillary sinusitis was found in 78 (78%) patients, and 52 (52%) patients had frontal sinusitis. Ethmoid sinusitis was seen in 22 (22%) of patients and 8 (8%) of patients had sphenoid sinusitis. Maxillary polyp was found in 22 (22%) of patients and ostiomeatal complex block in 54 (54%) patients.

Among one hundred patients of bronchial asthma, clinically 58 (58%) patients had evidence of sinusitis whereas CT scan detected sinusitis in 78 (78%) patients.

DISCUSSION

In our study, clinically 58 (58%) of patients out of 100 patients of bronchial asthma had signs and symptoms of sinusitis whereas 42 (42%) of patients were asymptomatic for sinusitis.

On CT scan of paranasal sinus, 78 (78%) patients of bronchial asthma showed evidence of sinusitis. All 58 patients, who were clinically symptomatic for sinusitis, had evidence of chronic sinusitis on CT scan PNS.

In addition, on CT scan PNS 20 (47%) more patients were detected to have sinusitis out of 42 clinically asymptomatic patients. 54 (54%) of patients showed evidence of ostiomeatal complex block. The ostiomeatal complex is the common drainage pathway for maxillary, frontal and anterior ethmoid sinuses. CT scan has given newer understanding of how the patient is affected with sinusitis.

Various mechanisms have been proposed to explain the relationship between sinusitis and asthma. The 5 most common are sinonasobronchial reflex [14-25]; inhalation of cold, dry air [26-31]; aspiration of nasal secretions[32-38]; cellular and soluble mediators [39-42], and diminished?-agonist responsiveness.

In one study Weille [43] examined 500 patients with asthma, 72% of whom had concomitant chronic sinus disease. Of 100 patients who underwent sinus surgery, 56 subsequently experienced improvements in chest symptoms; complete resolution of asthma occurred in 10. Twenty-three of 24 patients with simultaneous chronic sinusitis and asthma experienced a 75% or greater improvement in asthma symptoms after surgical drainage in another study.[44] This association is supported by other researchers, including Slavin,[45] who reported that lower airway symptoms were significantly reduced after nasal surgery in patients with severe asthma that often required daily oral corticosteroid therapy. In a follow-up of similar patients, 60% were found to have experienced improved asthma symptoms that persisted for 5 years.

In another study of sinus surgery in patients with asthma, 17 patients were treated with nasal surgery because of severe sinus disease. Fifteen of these patients experienced improved sinus symptoms, and 13 experienced significantly improved asthma symptoms, postoperatively.[46] Most of these patients underwent the Montgomery procedure, in which the mucosal lining of the sinuses is obliterated, and adipose tissue from the abdomen is implanted. This procedure promotes the formation of fibrous tissue, which helps to reduce the recurrence of infection. In one patient, severe asthma symptoms that could not be controlled with high-dose corticosteroids developed after the procedure. When the implant was removed, however, control of the asthma was regained. This phenomenon supports the idea that sinus disease and asthma exacerbations are related.

CONCLUSION

The association of sinusitis and asthma seems to be more than an epiphenomenon.
In our study out of 100 asthmatics evidence for sinusitis was found clinically in 58% cases while CT Scan PNS detected sinusitis in 78% cases. This observation assumes significant clinical importance that all asthmatics need to be examined for evidence of sinusitis preferably by CT scan.

It is very pertinent to mention that ENT specialist must look down into the chest for evidence of bronchospasm and chest physicians should examine asthmatic patients for evidence of rhinosinusitis.

REFERENCES

1. 1. Gottlieb MS. Relation of intranasal sinus disease in the production of asthma. JAMA 1925;85:105-9.
2. Adinoff AD, Wood RW, Buschman D, et al. Chronic sinusitis in childhood asthma: Correlations of symptoms, x-rays, culture, and response to treatment. Pediatr Res 1983;17:264.
3. Rachelefsky GS, Goldberg M, Katz RM, et al. Sinus disease in children with respiratory allergy. J Allergy Clin Immunol 1978;61:310-4.
4. Adinoff AD, Cummings NP. Sinusitis and its relationship to asthma. Pediatr Ann 1989;18:785-90.
5. Katz R. Sinusitis in children with respiratory allergy. J Allergy Clin Immunol 1978;61:190.
6. Friedman R, Ackerman M, Wald E. Asthma and bacterial sinusitis in children. J Allergy Clin Immunol 1984;74:185-9.
7. Fuller C, Richards W, Gilsanz V, Schoettler J, Church JA. Sinusitis in status asthmaticus [abstract]. J Allergy Clin Immunol 1990;85:222.
8. Friedman R, Ackerman M, Wald E, et al. Asthma and bacterial sinusitis in children. J Allergy Clin Immunol 1984;74:185-94.
9. Cummings N, Morris HG, Strunk RC. Failure of children with asthma to respond to daily aspirin therapy. J Allergy Clin Immunol 1983;71:245-9.
10. Rachelefsky G, Katz RM, Siegel SC. Chronic sinus diseases with associated reactive airway disease in children. Pediatrics 1984;73:526-9.
11. American Thoracic Society. Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease & asthma. Am J Respir Crit Care Med. 1995; 152 : S77-S120.
12. Salvin RG. Sinusitis in adults and its relation to allergic rhinitis, asthma and nasal polyps. J Allergy Clin Immunol. 1988; 82 : 950-56.
13. Havas TE, Bery JA, Gullane PJ. Prevalence of incidental abnormalities on computerised tomographic scans of the paranasal sinuses. Arch Otol Head Neck Surg. 1988; 114 : 856-59.
14. Sluder G. Asthma as a nasal reflex. JAMA 1919;73:589-91.
15. Yan K, Salome C. The response of the airways to nasal stimulation in asthmatics with rhinitis. Eur J Respir Dis 1983;64(suppl 128):105-8.
16. Nolte D, Berger. On vagal bronchoconstriction in asthmatic patients by nasal irritation. Eur J Respir Dis 1983;64:110-5.
17. Speizer FE, Frank NR. A comparison of changes in pulmonary flow resistance in healthy volunteers acutely exposed to sulfur dioxide by mouth and by nose. Br J Ind Med 1966;23:75-9.
18. Kaufman J, Wright GW. The effect of nasal and nasopharyngeal irritation of airway resistance in man. Am Rev Respir Dis 1969;100:626-30.
19. Nadel JA, Widdicombe JG. Reflex effects of upper airway irritation on total lung resistance and blood pressure. J Appl Physiol 1962;17:861-5.
20. Kaufman J, Chen JC, Wright GW. The effect of trigeminal resection of reflex bronchoconstriction after nasal and nasopharyngeal irritation in man. Am Rev Respir Dis 1970;101:768-9.
21. Holtzman MJ, Sheller JR, Dimeo M, et al. Effect of ganglionic blockade on bronchial reactivity in atopic subjects. Am Rev Respir Dis 1980;122:17-25.
22. Hoehne JH, Reed CE. Where is the allergic reaction in ragweed asthma? J Allergy Clin Immunol 1971;48:36-9.
23. Rosenberg GL, Rosenthal RR, Norman PS. Inhalation challenge with ragweed pollen in ragweed-sensitive asthmatics. J Allergy Clin Immunol 1983;71:302-10.
 
24. Schumacher MJ, Cota KB, Taussig LM. Pulmonary response to nasal-challenge testing of atopic subjects with stable asthma. J Allergy Clin Immunol 1986;78:30-5.
25. McFadden ER Jr. Nasal-sinus-pulmonary reflexes and bronchial asthma. J Allergy Clin Immunol 1986;78:1-3.
26. Wells R. Effects of cold air on respiratory airflow resistance in patients with respiratory tract disease. N Engl J Med 1960;263:268-73.
27. Lee TH, Assoufi BK, Cromwell O, et al. Exercise-induced asthma and the mast cell. Lancet 1983;2:164.
28. Deal ED Jr, McFadden ER Jr, Ingram RH Jr, et al. Airway responsiveness to cold air and hyperpnea in normal subjects and in those with hay fever and asthma. Am Rev Respir Dis 1980;121:621-8.
29. Wyllie JW, Kern EB, O'Brien PC, et al. Alteration of pulmonary function associated with artificial nasal obstruction. Surg Forum 1976;27:535-7.
30. Togawa K, Ogura JH. Physiologic relationships between nasal breathing and pulmonary function. Laryngoscope 1966;76:30-63.
31. Ogura HJ, Neslon JR, Dammkoehler R, et al. Experimental observations of the relationships between upper airway obstruction and pulmonary function. Ann Otol Rhinol Laryngol 1974;73:381-403.
32. Rachelefsky G, Siegel S, Katz R. Chronic sinus disease with associated reactive airways disease in children. Pediatrics 1984;73:526-9.
33. Quinn LH, Meyer OO. The relationship of sinusitis and bronchiectasis. Arch Otolaryngol Head Neck Surg 1929;10:152-65.
34. Mullin WV, Wyder CT. Experimental lesions of the lungs produced by the inhalation of fluid from the nose and throat. Am Res TB 1920;4:683-7.
35. McLaurin JG. Chest complications of sinus disease. Ann Otol Rhinol Laryngol 1932;41:780-93.
36. Huxley EJ, Viroslav J, Gray WR, Pierce AK. Pharyngeal aspiration in normal adults and patients with depressed consciousness. Am J Med 1978;64:564-8.
37. Winfield JB, Sande MA, Gwaltney JM. Aspiration during sleep. JAMA 1973;233:1288.
38. Bardin PG, Van Heerden BB, Joubert JR. Absence of pulmonary aspiration of sinus contents in patients with asthma and sinusitis. J Allergy Clin Immunol 1990;86:82-8.
39. Gleich GJ. The eosinophil and bronchial asthma: current understanding. J Allergy Clin Immunol 1990;85:422-36.
40. Harlin SL, Ansel DG, Lane SR, et al. A clinical and pathologic study of chronic sinusitis: the role of the eosinophil. J Allergy Clin Immunol 1988;81:867-75.
41. Gleich J, Frigas E, Loegering DA, et al. Cytotoxic properties of the eosinophil major basic protein. J Immunol 1979;123:2925.
42. Stone BD, Georgitis JW, Matthews B. Inflammatory mediators in sinus lavage fluid [abstract]. J Allergy Clin Immunol 1990;85:222.
43. Weille F. Studies in asthma; nose and throat in 500 cases of asthma. N Engl J Med 1936;215:235-6.
44. Davison F. Chronic sinusitis and infectious asthma. Arch Otolaryngol 1969;90:292-307.
45. Slavin R. Relationship of nasal disease and sinusitis to bronchial asthma. Ann Allergy 1982;49:76-9.
46. Spector S, Farr R. Aspirin idiosyncrasy: asthma and urticaria. In: Middleton E, Reed C, Ellis E, editors. Allergy: principles and practice. St Louis: Mosby-Year Book, Inc; 1983. p. 1249-73.