Cyclamen europaeum improves the effect of oral antibiotics on exacerbations and recurrences of chronic rhinosinusitis: a real-life observational study (CHRONOS)
Chronic rhinosinusitis (CRS) is an inflammatory disease of the nose and paranasal sinuses affecting 11% of the European population. Cyclamen
europaeum plant extract (CE) has demonstrated efficacy in treating acute rhinosinusitis, but its role in CRS exacerbations remains
unknown. In this real-life, prospective, epidemiological, observational study, a total of 317 patients with exacerbations of CRS without
nasal polyps (CRSsNP) of moderate severity were treated using three different options: oral antibiotics, CE extract nasal spray, or the
combination of oral antibiotic with CE extract. The main outcomes were the effect of treatment on sinonasal symptoms and endoscopic
appearance after 6 weeks of therapy, and the number of recurrences of CRS exacerbations after 6 months of follow-up. On the top of oral
antibiotics, CE extract significantly improved sinonasal symptoms and endoscopic findings and caused a 4-fold reduction of CRS recurrences.
When administered in monotherapy, CE extract was at least as effective as antibiotic in monotherapy on relief of both symptoms
and reduction of CRS recurrences. In patients with CRS exacerbation of moderate severity, CE extract nasal spray in monotherapy or added
to standard antibiotic treatment significantly reduces sinonasal symptoms and CRS recurrences compared to antibiotics in monotherapy.
In recent decades, an increase in the prevalence of respiratory diseases, particularly inflammatory diseases of the nose and paranasal sinuses, has been observed 1-3. Chronic rhinosinusitis (CRS) is a complex condition that dramatically affects the patient’s quality of life and has profound effects on health care expenditure 4-6. Management of this disease continues to challenge both patients and physicians. According to the European Position Paper on Rhinosinusitis and Nasal Polyp (EP3OS 2012) 7, the prevalence of CRS is increasing annually, currently being one of the most common chronic diseases. For instance, the prevalence of CRS is 3.4% among Canadian men and 5.7% among women 8, 6% in Belgium 9 and reaching 9.6% in the Scottish population 10. CRS has been reported as high as 10.9% in Europe 11 and 14% in the USA 12.
An exact definition of an acute exacerbation of CRS (AECR) is not available. Usually this condition is defined as a sudden worsening of baseline symptoms (or developing new symptoms) in a patient with an established CRS diagnosis. Triggers leading to CRS disease exacerbation are also not well characterised. Previous epidemiologic studies have focused on identification of risk factors for a diagnosis of CRS rather than on risk factors that lead to disease exacerbation. Empirical definition criteria that were used for AECR are at least one of the following: a prescription for systemic antibiotics, systemic corticosteroids, plans for a semi-urgent surgical intervention, emergency department or urgent care visit, or hospitalisation 13. Patients are approximately twice as likely to present with AECR in winter season when viral infections are known to be prevalent compared with spring, summer, or fall. Age and sex does not significantly affect the seasonal pattern 13 14. According to the EP3OS document, AECR should be treated as acute rhinosinusitis (ARS), i.e. with intranasal corticosteroids and antibiotics, depending on symptom severity 7.
There is good evidence supporting the concept that inflammation, more than infection, is the dominant aetiologic factor in CRS. Unlike ARS, pathogenic microorganisms play a much smaller role in the pathogenesis of CRS 15 17. However, based on the available evidence, oral antibacterial antibiotics (mainly in acute exacerbations) and prolonged macrolide antibiotics are considered therapeutic options in the treatment of CRS 18. Although necessary to control AECR, both so-called “short” and “long-term” courses of antibiotic therapy may interfere with diversity and abundance of the paranasal sinuses microbial community and carry a risk of aggravation of dysbiosis that already exists in chronic inflammatory respiratory diseases like CRS 19 20.
The ineffectiveness of the standard antibiotic therapy and the increased number of resistant strains of causative pathogens 21 22, coupled with some doubts on the efficacy of corticosteroids in CRS without nasal polyps 23 and the inability to achieve a total control with surgery 24, indicate the need to develop new topical therapeutic modalities.
Cyclamen europaeum plant extract (CE) has been used since ancient times as a topical remedy, is devoid of undesirable systemic side effects and in general, is safer than systemically administered drugs. Like other topical remedies, CE might offer a reliable alternative to conventional therapeutic approaches. Sinuforte® is the extract of the fresh tubers of Cyclamen europaeum that belongs to the Primulaceae family. This extract comes from a botanical raw material, a natural extract with many compounds, the active substances being saponins. Tubers of Cyclamen europaeum are lyophilised, without adding any excipient, to obtain 50 mg of the lyophilised extract. A solvent (5 ml of water for injection) is provided for reconstitution of the lyophilised powder. Sinuforte® is administered to each nostril (2.6 mg once daily) for 8 days. Recent studies have confirmed the efficacy of CE in treating ARS 25 26 but its role in AECR is still not known.
The objective of this study was to evaluate efficacy of CE extract in treatment of AECR either as a monotherapy or in combination with an oral antibiotic and to compare its efficacy with standard oral antibiotic therapy.
Materials and methods
From June 2011 to February 2012, we conducted a real-life, prospective, observational study aimed to examine the efficacy of three different medical treatment protocols in patients with AECR without polyps. The study was conducted at 16 clinical centres across the Russian Federation. The study protocol was approved by the Inter-institutional Ethics Committee of the Sechenov First Moscow State Medical University. All the patients signed written informed consent before entering the study. A total of 327 patients aged 18 to 60 years and diagnosed with acute exacerbation of CRSsNP of moderate severity were enrolled. According to EP3OS 2012 criteria 7, a diagnosis of CRS was supported by clinical history, nasal endoscopy and computed tomography (CT) or plain X-rays of the paranasal sinuses.
To be enrolled in the study, patients had to fulfill the following criteria: established diagnosis of CRS (code J32.0-4 and J.32.8-9 according to ICD-10 Version:2010), significant acute aggravation of symptoms (or development of new sinusitis symptom/symptoms) in the last 10 days that forced the patient to see an ENT physician, presence of two or more CRS symptoms and total Visual Analogue Scale (VAS) score of > 3-7 at the time of entering the study, physician’s decision for the need of specific therapy or escalation of the previous management.
Exclusion criteria included patients with CRS with nasal polyps, mild or severe CRSsNP according to VAS, absence of paranasal sinuses opacification on CT scans/plain X-rays, orbital or intracranial complications, the use of systemic or topical antibiotics or corticosteroid therapy during the previous month, severe intercurrent illnesses (immunocompetent diseases, severe endocrine, respiratory or metabolic diseases, etc.) and pregnancy. Patients with concomitant allergic rhinitis were also excluded.
Patients with mild AECR were not included because they did not need antibiotic therapy. Patients with severe forms of AECR (in whom systemic antibiotics were necessary to prevent complications and monotherapy with CE would not be sufficient) were likewise not included.
Ten patients were withdrawn at different stages of the study because they were unable to attend the next visit due to personal reasons; no patient withdrew from the study due to adverse effects or lack of treatment efficacy. Therefore, 317 patients completed the study and were suitable for statistical analysis.
Physicians in all centres had free choice to include patients in one of the three treatment protocols: patients in group 1 were treated with an oral antibiotic plus intranasal CE (Sinuforte® Nasal Spray, Hartington Pharmaceutical, Barcelona, Spain), group 2 with intranasal CE in monotherapy and group 3 with oral antibiotic alone. There were no strict recommendations for empirical antibiotic therapy, and participating physicians selected a first-line oral antibiotic according to their personal clinical experience and institutional guidelines. When used, CE was administered to each nostril (2.6 mg once daily) for 8 days. Patients were free to stop the prescribed therapy and to discontinue their participation in the study at any time.
After start of the treatment, all patients were followed-up for 6 months by regular examination by the responsible observer. Patients from Groups 1 and 3 received systemic antibacterial therapy and the physicians’ choice and dosages completely followed standards of empirical antibiotic therapy presented in rhinosinusitis national guidelines. The most common antibiotics prescribed were amoxicillin (1.0, 3 times daily) and amoxicillin/clavulanate (1.0, 2 times daily) followed by macrolides (clarithromycin 0.25, 2 times daily) and cephalosporins of the I-III generation. Routine antibiotic treatment was for 7 days (according to national guidelines) with some exclusions (for instance, azithromycin 0.5 once daily for 3 days, and moxifloxacin 0.4 once daily for 5 to 6 days). Physicians were encouraged to change the treatment protocol and to prescribe or change antibiotic when necessary. They were also free to use additional treatment options such as systemic or topical corticosteroids, topical antimicrobials, antral tap, sinus lavage, or Proetz replacement irrigations. Any change in the treatment protocol, use of additional therapeutic options and withdrawals were registered in case report forms. After the inclusion visit (T0), patients were visited at day 3 (T1), day 5 (T2), and day 8/end of treatment (T3) and after 6 weeks (T4) of follow-up. After 6 months (T5), patients were interviewed by a telephone call and asked about the number of episodes of AECR after discontinuation of treatment (Table I).
- Nasal symptoms. Treatment efficacy was assessed at visits T1-T4. Assessment was based on the patient’s subjective evaluation of the severity of the four main CRS symptoms (nasal obstruction, nasal discharge, facial pain/pressure, loss of smell or hyposmia) by VAS, (10 cm) as well as the composite evaluation of total nasal symptoms score (TNSS).
- Nasal endoscopic assessment. Treatment efficacy was assessed at visits T1-T4. Semi-quantitative scores were recorded for middle meatal discharge and mucosal oedema. These results were evaluated using an endoscopic appearance score (EAS) 27 28. Discharge was scored after decongestion as follows: 0, no discharge; 1, moderate amount of mucous or purulent discharge; and 2, large amount of thick, purulent discharge. Mucosal oedema was scored before decongestion as follows: 0, absent; 1, moderate, and 2, severe.
- Patient’s self-perception of treatment efficacy was assessed at visits T3 and T4. The patient’s assessment was scored as excellent, good, well/moderate, no effect, or bad/worsening.
With the help of a medical statistician (SSS), the results were entered into a computerised database and processed using the statistical software package SPSS version 17.0 for Windows. For each group of patients, the data distribution was identified, the frequency and scores were described and 95% confidence intervals were defined. Median, mode, standard error of the mean and standard deviation of the average, the minimum and maximum (variability), the interquartile range values, ANOVA analysis of variance (Levene Statistic) and ANCOVA analysis of covariance across treatment groups and Wilcoxon signed-rank test were used to compare variables between the groups to determine statistical significance at various time points. Values were presented as mean ± standard deviation (SD). Changes within and between the groups were considered statistically significant when p values were < 0.05.
A total of 317 patients with AECR (135 men and 182 women) aged from 18 to 60 years (mean 46.4 ± 5.0) were included in the study: CE plus antibiotic (group 1, N = 128), CE in monotherapy (group 2, N = 90) and antibiotic in monotherapy (group 3, N = 99). Baseline characteristics of patients are presented in Table II.
Assessment of symptoms
Total Nasal Symptom Score (TNSS). At baseline (T0), TNSS was higher in group 1 than in group 2 (p < 0.01). Starting from day 3 (T1) and at all consecutive time points, either oral antibiotic plus CE or CE in monotherapy induced a significantly (p < 0.001) higher resolution of TNSS compared to oral antibiotic alone. After 6 weeks (T4) of treatment initiation, TNSS was significantly reduced from 8.80±0.29 at baseline to 0.78 ± 0.16 by antibiotic plus CE, from 7.93 ± 0.25 to 0.76 ± 0.12 by CE alone and from 8.23 ± 0.34 to 1.70 ± 0.22 by antibiotic alone) (Fig. 1).
Individual Nasal Symptom Score. At baseline (T0), scores for nasal congestion, facial pain/pressure and hyposmia were similar in all treatment groups, while score for nasal discharge in group 1 was higher than in groups 2 and 3 (p = 0.001). Either oral antibiotic plus CE or CE in monotherapy induced a significantly (p < 0.001) higher resolution of nasal congestion and nasal discharge from day 5 (T2) to week 6 (T4) and from day 8 (T3) to week 6 (T4) than antibiotics in monotherapy (Fig. 2 a-d). All three treatment options improved hyposmia during the treatment period but with no significant differences between the groups. No significant difference was found between oral antibiotic plus CE and CE in monotherapy for all individual symptom improvements.
Nasal endoscopy assessment. At baseline (T0), EAS for middle meatus discharge, but not for oedema, was significantly (p < 0.01) worse in group 1 than in groups 2 and 3. Either oral antibiotic plus CE or CE in monotherapy induced a significant (p < 0.001) reduction of the middle meatus mucosal oedema from day 3 (T1) to week 6 (T4) (Fig. 3). Regarding the score for middle meatus discharge, there was no significant difference between groups at T1-T3 visits, however, at visit T4 the score in group 3 (oral antibiotic alone) was significantly (p < 0.05) higher than in group 2 (CE alone). No statistical difference was found between groups 1 and 2 at T1-T4 visits.
Patient self-evaluation of treatment efficacy. After 8 days of active treatment (T3), no patient in any group reported that they feel “worse/bad”; an absence of effect was revealed more frequently in group 3 (oral antibiotic alone) and least in group 2 (CE) (p = 0.013). The number of “well/moderate” assessments was not significantly different between the three groups; “good effect” assessment in group 3 (oral antibiotic alone) was three times less frequent than in group 1 (oral antibiotic +CE) and group 2 (CE alone) (p = 0.001); the same number of “excellent” results according to patient assessment was recorded in all groups (Fig. 4a). Six weeks after (T4), a “bad effect” was reported by a few patients in groups 2 and 3; “no effect” and “well/moderate” was observed in the same number of patients; a “good” effect was more often reported in group 1 than in group 2 (p = 0.023) and six times less frequently in group 3 (p = 0.007) (Fig. 4b).
Recurrence rate assessment
When interviewed by telephone 6 months (T5) after the start of the therapy, patients treated with antibiotic and CE reported significantly less (p < 0.01) AECR than those treated with either CE or antibiotic in monotherapy (Fig. 5). Only 3.9% (N = 5) of patients treated with antibiotic plus CE reported exacerbations (4 patients with one episode and 1 patient with two episodes) compared to 23.3% (N = 21) of patients treated with CE alone (14 patients with one episode and 7 patients with two episodes) or 20.2% (N = 20) of patients treated with antibiotic alone (14 patients with one episode, 3 patients with 2 episodes, 2 patients with 3 episodes and 1 patient with 4 episodes).
Changes to therapeutic protocols
In group 1, the selected antibiotic was not replaced in any patient. In group 2, CE was supplemented with an antibiotic in 5.5% of patients. In group 3, the selected antibiotic was replaced due to lack of clinical efficacy with a second-line antibiotic in 5% of patients. In no case were systemic or topical corticosteroids added to initial therapy in any study group. Antral puncture and sinus lavage, as adjunct to initial therapy, was performed after 3 or 5 days of therapy in 3.1% and 13.1% of patients from group 1 and group 3, respectively, but in no patients in group 2. Proetz nasal lavage, as adjunct to initial therapy, was conducted after 3 or 5 days in 2.3% of patients from group 1, 4.4% of patients from group 2 and 9.1% of patients from group 3. Therefore, in terms of the need for alternative therapeutic options, physician satisfaction with treatment efficacy was significantly (p < 0.05) higher in groups 1 and 2 (both with CE extract) than in group 3.
Adverse events. No severe adverse events were reported in this study. Only 7 patients (5 in group 1 and 2 in group 2) reported mild adverse effects (itching, sneezing, burning of the nose or throat irritation) after CE extract nasal spray, which did not require changes in the protocol or study withdrawal.
While systemic antibiotics (for severe bacterial disease) and intranasal corticosteroids (for moderate to severe disease) remain a mainstay in treatment of ARS and AECR, several studies have been carried out in recent years to find alternative therapies to improve the symptoms and severity of rhinosinusitis. In particular, two randomised controlled studies assessed the efficacy of herbal compounds in treatment of ARS. One study showed that Pelargonium sidoides might be effective in alleviating symptoms of ARS in adults 29. The other randomised multicentre study assessed the efficacy of Myrtol in the treatment of ARS. The results showed a statistically significant difference in improvement of TNSS between active treatment and placebo. The need for antibiotic therapy after Myrtol was 23%, compared to 40% for placebo 30.
The tuber of Cyclamen europaeum (Cyclamen purpurascens), a member of the Primulaceae family, has been used in herbal medicine since ancient times as a topical remedy for a range of indications. An extract of the tuber has been used for sinusitis in the form of nasal spray. The chemical composition of CE has not been thoroughly studied. The most examined active components of CE are triterpenoid saponins that belong to the group of organic glycosides. The saponin fraction of CE stimulates nasoparanasal secretions. When delivered to the nasal cavity, CE with its saponin fraction causes irritation of the trigeminal nerve endings in the nasal mucosa through cholinergic pathways, leading to rapid and abundant discharge of inflammatory sinus exudates through the nose and subsequent decongestion lasting approximately 30 min 31. Saponins also possess a direct osmotic effect and are able to stimulate mucociliary clearance by triggering mucus secretion 32. Our previous study has shown that CE application increases microcirculation in the nasal mucosa and dilates blood vessels supplying the mucus glands 33 34.
Two recent randomised, double-blind, placebo-controlled trials, conducted in Europe 27 and the US 28, reported the improvement by CE of facial pain, endoscopic signs (middle meatus mucosal oedema and secretion), reduction of sinus opacification and increase of both investigator and patient treatment satisfaction in patients with ARS. These two studies with level of evidence Ib have confirmed CE is a suitable therapeutic option for ARS recommended by international guidelines (EP3OS 2012) 7. Few non-controlled, non-blinded studies have reported on the efficacy of CE in larger cohorts of patients with both ARS and CRS. When added to antibiotic treatment, CE therapy caused an increased reduction of ARS symptoms in adults compared to antibiotic alone 32 35.
Our real-life observational study is the first to show that CE alone or in combination with an oral antibiotic is significantly more effective in treating AECR than antibiotics alone in terms of relieving nasal symptoms (TNSS, nasal congestion, nasal discharge, and facial pain/pressure) as well as decreasing middle meatus mucosal oedema.
Furthermore, the combination of a course of oral antibiotic and CE showed the best results in terms of prevention of CRS recurrence after 6 months of follow-up. The number of AECR was 4 times less than in patients receiving oral antibiotic or CE in monotherapy. In addition, an increased number of AECR where physicians replaced a first-line antibiotic with a different one or used alternative treatment options due to insufficient efficacy of initial therapy was mainly observed in group 3 (antibiotic in monotherapy). These findings are in line with the results of previous observational study, which showed that adding CE to oral antibiotic increased the ARS success rate by 15% as well as CE on top of the combination of oral antibiotic plus topical corticosteroid, which increased the rate of clinical recovery by 24% 36.
Among the limitations of the present study, we may firstly highlight the lack of randomisation since allocation of a patient to the treatment group in this real-life observational investigation was based on the physician’s choice. Worse initial TNSS in the group 1, as well as the higher initial middle meatus discharge score in this group might be explained by the physicians’ intention to reserve combined therapy for patients with relatively more severe symptoms. Secondly, blinding was not used for either patients when receiving the treatment protocol and additional therapy or for physicians when grading endoscopic findings. Thirdly, patients were selected from the group of moderate severity probably discarding those with common cold exacerbations (mild) and those with bacterial rhinosinusitis (severe). All these factors could be theoretically a potential bias for both the physicians and patients. Moreover, like ARS, AECR is a self-limited disease and about 90% of cases improve spontaneously.
However, a multicentre (16 independent clinical centres around the Russian Federation) observational study was performed among three potential therapeutic protocols in a real-life design whose aim was to evaluate clinical outcomes for 6 weeks after treatment of AECR and recurrences during 6-month follow-up. The relatively short duration of oral antibiotic therapy (7 days) could be also considered a controversial issue in the study. Although longer courses are used to treat AECR in Western Europe and the US 7, the design of the study tried, however, to follow the recommendations endorsed in the Russian Federation, where one-week course of antibiotic therapy is recommended for treatment of ARS and AECR 37.
The results of this observational study suggest that in AECR of moderate severity, both CE in monotherapy or added to oral antibiotics induces an increased symptom relief and prevents long-term CRS recurrences compared to antibiotics in monotherapy. Thus, intranasal CE may be considered as an alternative to standard antibiotic therapy in the treatment of non-complicated non-severe AECR and potentially help to reduce costs of disease 36 as well as to reduce antibiotic abuse and the consequent increase in antibiotic resistance.
Figures and tables
|Day 1||Day 3||Day 5||Day 8||6 weeks||6 months|
|Visit 0||Visit 1||Visit 2||Visit 3||Visit 4: Primary endpoint||End of follow-up: Secondary endpoint|
|Sign informed consent||x||-||-||-||-||-|
|Filling CRF, collecting medical history: concomitant diseases, inclusion/exclusion criteria, previous therapies||x||-||-||-||-||-|
|Evaluation of symptoms severity (VAS)||x||x||x||x||x||-|
|General ENT examination||x||x||x||x||x||-|
|CT/plain X-rays of paranasal sinuses||x||-||-||-||-||-|
|Selecting treatment protocol||x||-||-||-||-||-|
|Checking patient adherence||-||x||x||x||-||-|
|Adverse events registration||-||x||x||x||-||-|
|Evaluation of treatment efficacy||-||x||x||x||x||-|
|Group 1(antibiotic + CE)||Group 2(CE in monotherapy)||Group 3(antibiotic in monotherapy)||Allpatients|
|Patients, N (%)||128 (40.3%)||90 (28.4%)||99 (31.3%)||317 (100%)|
|Gender (female), N (%)||74 (57.8%)||53 (58.9%)||55 (55.6%)||182 (57.4%)|
|Age, years (mean±SD)||49.7 ± 4.7||47.3 ± 5.3||42.3 ± 4.9||46.4 ± 5.0|
|TNSS, VAS (mean±SD)||8.80 ± 0.29*||7.93 ± 0.25||8.23 ± 0.34||8.32 ± 0.29|
|EAS, middle meatus discharge (mean±SD)||2.35 ± 0.09||2.07 ± 0.10||2.11 ± 0.12||2,18 ± 0.1|
|EAS, middle meatus mucosal edema (mean±SD)||2.55 ± 0.07||2.49 ± 0.08||2.59 ± 0.11||2.54 ± 0.09|
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