Product review:

Eleven pharmaceutical brands were analyzed, totaling 44 products (table 2)

The NaCl concentration varies from 0.9% to 2.5% in the most hypertonic solutions, the latter presenting a range between 2 and 2.5%. The solutions without added components differ from each other by their tonicity, by the way or force of application or by the size of the container or applicator. Those with greater force of application or tonicity are usually indicated in older patients. The most common mode of application is spray, although two of the brands also offer single-dose vials for application in drops in younger children.

Regarding the added elements, the use of herbs or plants is frequent, mainly chamomile/chamomile and aloe vera. The addition of other salts (manganese, iron, copper, or potassium) is also common. Lastly, some add other components, such as xylitol (also known as birch sugar) and dexpanthenol (provitamin b5), or show that obtaining seawater in certain geographical locations is an additional value.

It was not possible to obtain objective or comparable data regarding the price of the products since, as they are available free of charge, both the laboratory sale price and the sale price to the public are variable.

Bibliographic citations were only found on the web pages of two products. Sterimar® provides 13 citations, obtaining access to seven of the cited documents. Of the remaining six, three of them are publications from 1989 incahiers d’oto-laryngologie y gazette médicale; uno es una publicación enreview of paediatrydel año 1999; one is a 1999 review of paediatry publication; another shows an incomplete reference that prevents its location, and the last is a review on the non-pharmacological-treatment-of-nasal congestion in pediatrics published in 2014 inminerva pediatrics. Except for the latter, which could not be accessed because they did not have a subscription to the magazine, no other references were found other than those provided by the product's own website. The seven publications reviewed include a randomized controlled clinical trial⁽⁶⁾, an intervention with evaluation by telephone survey⁷, a descriptive-analytic observational study with the same type of evaluation⁸and fourin vitrostudies^9-12.

In the first trial, grasso et al.⁶studied the efficacy of Sterimar Mn® (with manganese salts) for preventing exacerbations of allergic rhinitis in 60 patients over 18 years old. The control group receives "standard treatment" and the experimental group, in addition, four daily puffs of sterimar mn®. After five months of treatment, the experimental group shows a statistically significant decrease in the number of exacerbations compared to the previous year (from 10.67 to 6.33 episodes vs. 9.5 to 9.33 episodes in the group control) and an improvement in quality of life measured according to the visual analogue scale between the third and fifth month of starting the study (in the experimental group, improvement of +0.2 points vs. In the control group, +0.67 points).

The second cited study is an observational, cross-sectional, and multicenter study financed by Reig Jofre S.a.. Sanabria Brassart et al.⁷surveyed 1,350 patients of all ages with various medical conditions to whom their attending physician recommended nasal lavages with seawater in regimens variables according to clinical criteria. Patients report improvement in symptoms compared to previous similar episodes.

The following is an observational study that assesses adherence and tolerance of nasal washes with physiological saline solution (PSS) in the pediatric population. Jeffe et al.⁸select 61 patients (2-16 years) who are prescribed these rinses for nasal congestion and rhinorrhea in different pathologies, showing that the majority of children (93%) tolerate nasal rinses even though their parents (78%) initially think otherwise.

The remaining studies arein vitro ^{( 9-12}. They compare different solutions (saline and seawater in different concentrations) regarding their effects on the healthy or injured epithelium. Their conclusions can be summarized as follows: hypertonic solutions caused cytotoxicity, affected the barrier function and reduced cilia beating, damage that did not occur with isotonic solutions⁹. Compared with conventional PSS, isotonic seawater promoted faster tissue re-epithelialization after mechanical injury¹⁰; being both isotonic, diluted seawater, compared to electrodialyzed, had a more sustained effect on tissue recovery after hypotonic stress¹¹. A last study¹²specifically evaluated sterimar stop & protect cold and flu ® (2.3% hypertonic seawater with hyaluronic acid, eucalyptus oil, copper and manganese salts), not observing cytotoxic or proinflammatory effects and also observing a improvement of mucociliary clearance with respect to untreated tissues and better recovery capacity with respect to the use of pss.

Sinomarin®, for its part, collects five citations. One of them, entitled “utility of the hypertonic solution (Sinomarin®) in rhinology,” was published in the Revista Oficial De La Sociedad Francesa De Otorrinolaringología in 1998 and is not found on the internet. Of the rest, 3 are randomized controlled clinical trials published in 1998¹³, 2002¹³, 2003¹⁵, and the last one could be classified as a narrative review¹⁶. In the latter, published in otolaryngologic clinics of north america (1996), the author exposes the change in management of chronic sinusitis (from an eminently surgical treatment to conservative management) and the usefulness of nasal lavages with saline solution in this pathology. , alleging an unpublished communication of his own and an experimental study also of his own authorship¹⁷.

Since Sinomarin® products are all hypertonic (NaCl 2.3%), the referred studies focus on justifying this characteristic. Shoseyov et al.¹³comparan la aplicación en gotas de SSIversuscompare the application of SSI drops versus hypertonic saline solution (HSS) (3.5%) for the treatment of chronic sinusitis in 30 pediatric patients (3-16 years). After four weeks of treatment, HSS statistically significantly improved the runny nose and cough, as well as the radiological image of the sinuses. The PSS only significantly improved the runny nose.

Using validated scales, Rabago et al.¹⁴studied the long-term effect (six months) of daily nasal lavage with HSS on quality of life and symptom control in 76 adult patients with recurrent sinusitis. Improvement was observed in all the scales in the experimental group with respect to the control (without nasal washings), as well as a reduction in the use of antibiotics.

Finally, Garavello et al.¹⁵included 20 pediatric patients with seasonal allergic rhinitis (6-12 years), in whom they evaluated the efficacy of nasal irrigation with HSS (3%)versusno irrigation for the control of symptoms and reducing the use of antihistamines. He found statistically significant differences in both aspects from the third week of treatment.

A. Sea water versus saline solutions:

Most experimental studies on nasal lavages use conventional saline solutions (not seawater). However, the available evidence in pediatrics can be summarized in the following systematic reviews: Cabaillot et al.¹analyze the efficacy of isotonic solution lavages in upper respiratory tract infections, observing improvement in nasal symptoms, faster resolution of the episode, decrease in the incidence of complications and relapses and less consumption of additional medication (especially antibiotics) compared to therapeutic abstention. In treating allergic rhinitis in the pediatric age group, wang et al.²observe that patients who receive nasal lavages with saline solution show statistically significant clinical improvement compared to therapeutic abstention. No significant differences were observed compared to the use of nasal corticosteroids or when comparing the usual treatment alone (nasal corticosteroids or oral antihistamines) with the addition of lavages as adjuvant treatment. Finally, gallant et al.¹⁸propose a systematic review of nasal washes in children under 18 years of age for the treatment of rhinosinusitis (acute or chronic), but finally only one study on acute rhinosinusitis meets the inclusion criteria. This compares the use of high-dose amoxicillin + SSI washesversusplacebo + lavados con placebo + SSI washes, finding no significant difference between the two groups. As a conclusion of the different reviews, there is great heterogeneity between studies and difficulty for the objective assessment of clinical improvement, so higher quality studies are desirable to obtain more robust evidence^1,2,18.

Studies aimed at proving the efficacy of seawater are much scarcer. Chen et al.³studied the treatment of allergic rhinitis in children, noting that the combination of isotonic seawater spray and intranasal fluticasone showed better clinical and cytological results (decrease in the eosinophil count in nasal secretion) than each. One of them in isolation.

The clinical improvement persisted even after reducing the dose of corticosteroids, making seawater a good adjuvant treatment. For their part, Slapak et al.⁴intend to study the efficacy of seawater both in the treatment and in preventing complications and recurrences of the common cold or flu in children from 6 to 10 years of age. While the control group received standard treatment (symptomatic and antibiotics according to medical indication), the experimental group also received nasal lavages with isotonic seawater (with different modes of administration in different subgroups), which they maintained for 12 weeks. In the acute phase, the group that received seawater showed statistically significant differences in terms of greater improvement in rhinorrhea and nasal obstruction, subjective improvement in general condition, and less use of nasal decongestants and mucolytics. At longer follow-up (up to 12 weeks), continued use of douches reduced sick days, school absences, and complications, as well as the use of antipyretics, nasal decongestants, mucolytics, and antibiotics, suggesting a preventive role for these pathologies. There were no differences between the various seawater subgroups, althoughsprayapplication was better tolerated than irrigation.

Only one study was found that compared the efficacy of saline and seawater. Köksal et al.⁵, in a controlled clinical trial in children under two years of age with upper respiratory tract infection, compare the efficacy of SSIversus2.3% seawater administered as nasal drops for nasal obstruction, without finding statistically significant differences between both intervention groups.

B. Different concetrations:

The already commented review by wang et al.²shows evidence in favor of HSS compared to ISS in treating allergic rhinitis in children, which should not exceed a 3% nacl concentration to avoid local irritation or other adverse effects.

For their part, Kanjanawasee et al.¹⁹carried out a systematic review of this topic, including trials with multiple pathologies. Observes evidence in favor of HSS over SSI, suggesting greater efficacy in the following subgroups: rhinitis (versus rhinosinusitis), under 18 years of age, with "high volumes" of solution and "high pressure" application devices, and with NaCl<5% HSS more frequently produced local irritation, although no major adverse effects were reported.

C. Modes of administration:

In the studies reviewed, both Cabaillot et al.¹and Slapak et al.⁴observe thatsprayapplication is better tolerated and equally effective than irrigation in treating upper respiratory tract infections.

D. Elements added to seawater:

The search for components added to seawater did not return any results regarding the following elements: aloe vera, mint, allium cepa (onion), sabadilla, potassium chloride, iron, and manganese. On the other hand, Sterimar Mn ® and sterimar stop & protect cold and flu ® (with copper and manganese salts, eucalyptus extract and hyaluronic acid) were evaluated in the bibliography provided by this brand^6,12, although by the design of both studies it is not possible to know what part of the observed effect is due to the “added elements” and not only to seawater.

Several interesting studies were found about xylitol, dexpanthenol and hyaluronic acid:

Xylitol is a glycitol that, by promoting the concentration of nitric oxide (no) in epithelial tissue, has an antimicrobial and anti-inflammatory effect. Among the studies reviewed, a clinical trial conducted in adult patients with chronic rhinosinusitis stands out²⁰. The group that received xylitol nasal irrigations had statistically significant differences in the improvement of clinical parameters and in the increase in no concentration in the sinus epithelium compared with the baseline situation and the control group (irrigations with ssi). On the other hand, according to silva et al.²¹irrigations with xylitol can also be beneficial in the postoperative period of endoscopic endonasal surgery.

Dexpanthenol (provitamin b5) is known for its antioxidant effect, cell proliferation promoter, and epithelium protector. Tantilipikorn et al.²²observed a significant improvement in mucociliary clearance and rhinorrhea with the application of dexpanthenol (compared to SSI) in the postoperative period of chronic rhinosinusitis. However, more than in monotherapy, it seems to be of interest in combination with alpha-agonists. In patients with nasal congestion (due to allergic rhinitis or after nasal surgery), Jagade et al.²³obtained better symptomatic control, less rebound effect, and better medication tolerance in the group treated with dexpanthenol + alpha-antagonist nasal drops. In combination than in those patients who only received alpha-antagonists. Mösges et al.²⁴add that this synergism leads to earlier healing in patients with acute rhinitis.

Hyaluronic acid is a high molecular weight glycosaminoglycan present in the respiratory mucosa. Its fragmentation gives rise to smaller molecules that act as proinflammatory mediators. On the contrary, the high molecular weight hyaluronic acid suppresses the immune and inflammatory response and contributes to cell proliferation²⁵. Sfurthermore, its intranasal application decreases the number of neutrophils in the mucosa compared to the use of SSI, in addition to being well tolerated and without adverse effects^25-26.

However, the data regarding its efficacy compared to SSI are not conclusive: while some studies^25-26show a statistically significant (although clinically modest) greater symptomatic improvement in the group treated with hyaluronic acid, others²⁷do not differences were found between both groups.