J Med Life. 2014; 7(Spec Iss 2): 83–87. 

PMCID: PMC4391365

PMID: 25870681

Surveys on therapeutic effects of “halotherapy chamber with artificial salt-mine environment” on patients with certain chronic allergenic respiratory pathologies and infectious-inflammatory pathologies

H Lazarescu,* I Simionca,* M Hoteteu,* A Munteanu,* I Rizea,* A Iliuta,* D Dumitrascu,* and  E Dumitrescu*

Author information Copyright and License information Disclaimer

Go to:

Introduction

Halotherapy, derived from speleotherapy in salt mines, is also a drug-free therapeutic method, applied especially on patients with bronchial asthma and chronic bronchitis. Following the “survey for the innovative use of potentially therapeutic salt-mine environment factors, in health and balneoclimateric tourism; modeling solutions”, the conceptual model was elaborated, subsequently converted into an experimental functional model entitled “halotherapy chamber with artificial salt-mine environment”, destined for surface halotherapy and built within the National Institute of Rehabilitation, Physical Medicine and Balneoclimatology. 

This model was followed by surveys in the underground salt-mine environment, destined to assess the presence and quality of factors with speleotherapeutic / halotherapeutic potential, medical-biological multi-discipline surveys, including organismic and cellular-level analysis, before and after the experimental halotherapy treatment, on lab animals – Wistar rats with pathology experimentally induced by sensitization with ovalbumin.

Based on the experimental results acquired [1,2], the “Inception medical indications for the selection of patients with certain chronic respiratory pathologies for experimental halotherapy treatment” were elaborated.

Notably, in the infectious–inflammatory or allergic process, various systems and mechanisms of the body and organismic or cellular components were involved.

The phagocytosis process is one of the promptest defensive mechanisms against infection. The phagocytic cells are generated from precursor cells of bone marrow and they divide into macrophagous and microphagous cells. In blood, macrophagous cells are represented by monocytes, and microphagous cells – by polymorphonuclear neutrophils (PMN), which account for app. 60% of leukocytes and which are also the most significant phagocytic cells [4].

Go to:

Material and Methods

The selection of patients intended for the application of experimental HT treatment in the “halotherapy chamber with artificial salt-mine environment” of INRMFB was made based on medical indications and contraindications obtained, including: 

I. Indications

1. Patient age: 7-60 years old; infants under 10 years must be accompanied by parents. 

2. Gender: female or male.

3. Non-allergic / intrinsic / non-atopic asthma, allergic / extrinsic / atopic asthma, asthmatic bronchitis:

(1) With negative allergological tests or atopic skin tests (for non-allergic / intrinsic / non-atopic asthma) or positive tests (allergic / extrinsic / atopic asthma);

(2) eosinophils (Eo) – high or normal count in blood and ∕ or in expectorated sputum;

(3) relatively non-severe clinical evolution;

(4) asymptomatic period with or without bronchial obstruction, without asthmatic seizures; 

(5) symptomatic period with proven bronchial obstruction, without asthmatic seizures or severe asthmatic conditions; 

4. intermittent bronchial asthma, without medication or with symptomatic medication (patient’s medication):

(1) with no asthmatic seizures or severe asthmatic conditions; 

(2) with no negative evolution (frequent seizures or severe asthmatic conditions) caused by physical stress (Exercise-Induced Asthma);

(3) with no negative evolution (frequent seizures or severe asthmatic conditions) caused by humidity, changes in air temperature, gases of other microclimatic parameters (Airways Asthma);

(4) with or without non-allergic rhinitis;

(5) with or without nasal polyposis; 

(6) with or without sensitiveness to aspirin or other drugs;

5. chronic bronchitis, asymptomatic or symptomatic period without a negative evolution, without medication or with symptomatic medication (patient’s medication);

6. chronic obstructive bronchopneumopathy (BPOC), asymptomatic or symptomatic period without a negative evolution (no aggravation / acute exacerbation, no wheezing respiration, persistent cough with the production of sputum and shortness of breath), without medication or with symptomatic medication (patient’s medication);

7. allergic and chronic, infectious-inflammatory rhinitis and sinusitis, intermittent or slightly persistent, asymptomatic or symptomatic period without a negative evolution, without medication or with symptomatic medication (patient’s medication);

Results

Thus, during the first 3-7 days of HT procedure, occurrence and onset of irritative cough was noticed in 7 patients (5 patients with bronchial asthma, 1 – with chronic bronchitis and 1 – with chronic obstructive bronchopneumopathy) out of the 15 patients from the group subjected to HT treatment. The clinical adaptation of patients to the underground environment condition was found after 5–10 days of HT procedures, depending on the pathology and clinical progress of illness. After 10 days of HT procedures, a scarceness of cases and significant reduction in severity – until full regress – of irritative dry cough was seen in investigated patients, and after 12–15 of specific HT treatment – absence of dry cough and wheezing, and also for 2/3 of investigated patients (suffering from bronchial asthma, chronic bronchitis, chronic obstructive bronchopneumopathy) – rare cases of cough with viscous expectoration (1–3 expectorations in the last HT treatment procedures), and also cough with liquid expectoration and increase of expectorated sputum volume was noticed (in 3 patients with bronchial asthma and 1 patient with obstructive bronchopneumopathy). 

During the treatment period, no severe asthmatic conditions or additional infections occurred. ¼ of the investigated patients were characterized after 15 days of HT procedures, or 5–10 days after the HT treatment was ceased, or after gradually reducing the dose of specific medications (antihistaminic, bronchiolitis drugs, corticosteroids inhalers) to 20-30%. 

The patient with bronchial asthma and duodenal ulcer ceased the halotherapeutic treatment during the 3rd HT procedure, upon recommendation of the INRMFB physician, due to duodenal pains, and another patient with chronic bronchitis – during the 7th HT procedure, due to digestive issues occurred at home before the HT procedure, and resumed treatment after three days. The halotherapeutic treatment was also interrupted in one patient with bronchial asthma, during the 10th HT procedure, on the family doctor’s recommendation, due to acute exacerbation of cervical spondylosis pains. 

The data gathered proved the need for additional specific surveys on patients with chronic infectious-inflammatory and allergic respiratory diseases accompanied by other pathologies.

The average blood count of phagocytes – neutrophils PMN in patients with bronchial asthma and other respiratory allergies, as well as in patients with chronic bronchitis or chronic obstructive bronchopneumopathy was found to be lower compared to the lower limit of “normal (“reference”) values”, cases with lower test values being noted in 9 of 13 patients with bronchial asthma and other allergies (namely, for app. 2/3 of the respective patients group, P<0,05) and in patients with infectious-inflammatory bronchopulmonary diseases (chronic bronchitis, chronic obstructive bronchopneumopathy). The relative count of formasan-positive PMN neutrophil cells (in nitroblue tetrazolium test) was found to be high in blood for most investigated patients (12/13 – cases of bronchial asthma and other allergies P<0,01) and for patients with chronic bronchitis or chronic obstructive bronchopneumopathy. Thus, most of the investigated patients showed a deficit in the phagocytosis activity prior to the halotherapeutic treatment and also a decrease in the oxidative metabolism of phagocytes – granulocytes PMN in blood being noted. 

Based on data acquired after the experimental halotherapy (HT) treatment, the triggering of non-specific resistance parameters of the body was noted (phagocytosis of neutrophils PMN, intra-cellular redox of neutrophils in NBT test) in patients (including infants) subjected to specific halotherapy treatment, compared to “normal values” and to values found in control patients, respectively with chronic respiratory pathology and drug treatment (P>0,05<0,1 and P>0,1).

The results obtained showed the positive effect of experimental halotherapeutic treatment related to the stimulation of phagocytosis process and the increase in non-specific anti-infection resistance of the body, a fact noted based on the ascendant trend of phagocytes PMN in blood and the activation of oxygen-dependent bactericide action of granulocytes PMN (nitroblue-tetrazolium test) in patients with bronchial asthma and allergic rhinitis and in those with chronic bronchitis, chronic obstructive bronchopneumopathy (P>0,1). Still, the fact that the low number of patients with chronic bronchitis and chronic obstructive bronchopneumopathy did not allow the mentioning of significant positive changes should be mentioned, and, therefore, in this case, the extension of the respective surveys is needed.

Go to:

Conclusions

The assessment of results achieved in the investigated patients with bronchial asthma, chronic bronchitis and chronic obstructive bronchopneumopathy, after a specific halotherapy treatment, indicates the triggering of an anti-inflammatory (including anti-allergic mechanisms) mechanism and a decreasing trend of the inflammatory process.

Data acquired indicate a decrease in the body’s sensitiveness and in infectious-inflammatory process in patients with bronchial asthma after HT treatment, and it also proves the need to extend the period or to repeat the halotherapeutic treatment. 

Go to:

References

1. Gorbenko PP, Adamova IV, Sinitsyna TM. Bronchial hyperreactivity to the inhalation of hypo- and hyperosmolar aerosols and its correction by halotherapy. Ter Arkh. 1996;68(8):24–28. [PubMed]

2. Chervinskaya A. II: Halotherapy of respiratory diseases. Physiotherapy, balneology and rehabilitation. Physiotherapy, balneology and rehabilitation. 2003;6:8–15.

3. Simionca I, Hoteteu M, Lazarescu H, Grudnicki N, Stoian G, Enache L, Munteanu C, Mera O, Calin MR. Haloterapia – descendenta a speleoterapiei in minele saline; realitati si perspective de haloterapie stiintifica in Romania. 2012;73:56–57.

4. Olinescu A, Dolganiuc A.  Imunologie Clinica. Viata Medicala Romaneasca; 2001. p. 276.

Articles from Journal of Medicine and Life are provided here courtesy of Carol Davila - University Press

© 2015 Salt Serenity LLC