Characteristics of representative corticosteroids .
During the last 15 years, cochlear implantation became available as a method of treatment for different types of hearing impairment. Leading, specialized centers have now introduced the analysis of the nonsurgical factors that could contribute to improve rates of hearing preservation in preoperative period, during surgery, or in postoperative period in patients who suffer from partial deafness. One of the approaches is using pharmacotherapy (glucocorticoids) as a factor that may improve hearing functions. Preservation of hearing in patients who suffered from partial deafness and underwent cochlear implantation by using two different regimes of corticosteroid therapy was the aim of the study carried out by the World Hearing Center (WHC). Forty-six patients were enrolled in the trial and divided into three subgroups. Hearing preservation (HP) was evaluated using pure tone audiometry (PTA) (11 frequencies ranging from 125 to 8000 Hz). The impact of administrated substances was evaluated by pure tone audiometry during six different periods: before cochlear implant surgery, during activation of audio processor, and 1, 6, 9, and 12 months after activation of audio processor in comparison with control group. According to hearing preservation (HP) classification, patients from the second group, to whom combined glucocorticoid therapy was administrated, achieved the best HP results. The complete hearing preservation index was observed in the highest percentage of patients from the second subgroup. The dispersion of measured values was lesser than in other subgroups. According to the results, administration of glucocorticoids (dexamethasone and prednisone or dexamethasone only) to the patients, who suffered from partial deafness and underwent cochlear implantation surgery, may be important in stabilization of hearing thresholds and in protection of hearing.
- partial deafness treatment
- cochlear implant
In the past cochlear implantation was a “gold standard” treatment method for patients who suffer from hearing impairment and dedicated only for patients totally deaf. During the last 15 years, cochlear implantation became available also as a treatment for different types of hearing impairment. Regardless of surgical technique for cochlear implantation (cochleostomy or an approach through the round window), specialized centers have now introduced the comprehensive analysis of the nonsurgical factors that could contribute to improve rates of hearing preservation in preoperative, during surgery, or in postoperative period in patients who suffer from partial deafness. One of the approaches of many leading research centers is using pharmacotherapy (glucocorticoids) as a factor which may improve hearing functions following cochlear implantation [1, 2]. Glucocorticoids play an important role in pharmacotherapy of many different otorhinolaryngological diseases, such as Meniere’s disease, sudden sensorineural hearing loss (SSNHL), and tinnitus, and as a part of otorhinolaryngological procedures in surgeries (e.g., cochlear implantation) [3, 4]. The effects of treatment listed diseases are different and mainly depend on treatment results, adverse effects of used medications, and additional pharmacological treatment that was used during treatment. Unfortunately, the side effects of glucocorticoids are serious, and as the result, sometimes pharmacotherapy has to be stopped, and discontinuation of therapy is the only solution.
On the one hand, insertion of specific electrode of cochlear implant requires perfection in surgical techniques, but on the other it is difficult to do perfectly. Clinically approved algorithm of corticosteroid therapy (local or systematic) is discussed as one factor in reducing oxidative stress, an inflammatory reaction, and as a result apoptosis of hearing cells. A major challenge in effective administration and delivery medicines is the
1.1 Characteristic: glucocorticoids
The adrenal cortex synthesizes two classes of steroids: corticosteroids (mineralocorticoids and glucocorticoids) and androgens. One of the differences is the number of carbon atoms. Corticosteroids have 21 carbon atoms, and androgens have 19 carbon atoms. In the human body, the main glucocorticoid is cortisol, and the main mineralocorticoid is aldosterone .
Glucocorticoid receptor (GR) is located in the cytoplasm in inactive form until it binds with the molecule of glucocorticoid. This action results in activation of receptor and translocation complex:
|Anti-inflammatory activity||Biological half-life t1/2 (h)|
|Cortisol||1||Short: t1/2 = 8–12|
|Cortisone||0.8||Short: t1/2 = 8–12|
|Fludrocortisone||10||Intermediate: t1/2 = 12–36|
|Prednisone||4||Intermediate: t1/2 = 12–36|
|Prednisolone||4||Intermediate: t1/2 = 12–36|
|6α-methylprednisone||5||Intermediate: t1/2 = 12–36|
|Triamcinolone||5||Intermediate: t1/2 = 12–36|
|Betamethasone||25||Long: t1/2 = 36–72|
|Dexamethasone||25||Long: t1/2 = 36–72|
1.2 Functions and activity of glucocorticoids
The two key roles glucocorticoids play as biological and pharmaceutical compounds are anti-inflammatory and immunosuppressive roles. Glucocorticoids also affect:
Carbohydrate and protein metabolism. Glucocorticoids stimulate the liver to form glucose in biochemical reaction (gluconeogenesis) from amino acids and glycerol or/and stimulate the liver to release glucose from glycogen. At the same time, the diminishing of glucose is reduced, reaction of lipolysis and protein breakdown increases, and as a result the blood glucose level rises. Patients suffering from diabetes or other forms of hyperglycemia during glucocorticoid therapy should be under special control. Glucocorticoids induce increased protein metabolism and deliver compounds such as amino acids for further reactions.
Lipid metabolism. One effect of therapy with corticosteroids is redistribution of fat tissue known as Cushing’s syndrome.
Water and electrolyte balance. Glucocorticoids exert negatively on metabolism of Ca2+ due to reduction of absorption from the digestive system and increased excretion via kidneys. Prophylaxis of osteoporosis requires supplementation of Ca2+ ions and physical activity adequate to possibilities of patient. Additionally, glucocorticoids reduce activity of osteoclasts and stimulate the activity of osteoblasts. Glucocorticoid therapy sometimes may cause increased retention of Na+ ions and decrease in concentration of K+ ions because of interaction with receptor for mineralocorticoids. The deterioration in ion level may affect the cardiovascular system.
Impaired wound healing. Due to reduction of synthesis of collagen, glycosaminoglycans and disturbance in fibroblast function problem with healing wound may occur.
Anti-inflammatory and immunosuppressive activity. Glucocorticoids can suppress or prevent inflammatory reactions in different ways: reduction in diapedesis of granulocytes and proliferation of lymphocytes Th, inhibition/reduction of activation of macrophages, neutrophils, mast cells and cytokines (interleukins 1, 2, 3, 4, 5, 6, 8), and tumor necrosis factor alpha (TNF-α); reduction in the expression of cyclooxygenase 2 (COX-2) resulting in dropping of production of a few prostanoids; intensification of activity of catechol amines; and reduction in production of histamine by basophils [7, 8].
Sometimes glucocorticoid treatment in the otorhinolaryngological diseases requires high doses or long time of therapy. It may cause adverse effects. Some of them are listed below:
Repression in responding on infections and injuries
Propensity to opportunistic infections
Propensity to hyperglycemia
Glaucoma (mostly in patients genetically predisposed)
Acute discontinuation of treatment may cause adrenocortical insufficiency, especially when therapy was long-term. It is important to reduce the dose of glucocorticoids slowly, not suddenly .
1.3 Pharmacokinetics of glucocorticoids and studies on animal model
Many factors have an impact on pharmacokinetics of drugs. Pharmacokinetics is described by acronym
In a study published in 2017, authors in animal model (guinea pig) compared dexamethasone with saline. Both substances were administrated intravenously 60 min before implantation. As a final conclusion, authors stressed that dexamethasone could reduce scarring process as the electrode negotiated the hook region or near the electrode tip, but they did not observe the relation between dexamethasone and reduction of fibrosis relating to cochleostomy . In vitro studies showed the correlation between reduction (loss) of auditory cells after exposure to
Research carried out on animal model proved that prolonged steroid therapy could significantly improve hearing preservation rate (including pharmacokinetic and morphological analysis) when the electrode of cochlear implants was covered with dexamethasone (special formulation with controlled drug release) . However, Honeder et al. did not confirm that steroids could have a positive impact on residual hearing in a guinea pig model. One reason why both authors gain different results may lie in different types of steroid therapy. In the first study, dexamethasone was used on the contrary to the second study where triamcinolone was administrated . Douchement et al. investigated the effects of steroids using a gerbil animal model. Animals were implanted with an electrode with controlled dexamethasone delivery (1 and 10% concentration of dexamethasone) on one side and a conventional electrode on the contralateral side. Hearing levels were established based on the tone bursts on auditory brain stem responses at 4–6-week postimplantation and at 1-year postimplantation period for older gerbils. A 1-year observation period showed significantly improved results obtained for the high auditory frequencies, but the results for the low frequencies were ambiguous .
Cho et al. analyzed the efficacy of preoperative and intraoperative schemes of administration of steroids for hearing preservation. Dexamethasone was administrated systematically at the dose of 5 mg/ml in the preoperative period and then topically (off-label) during cochlear implantation surgery. Pure tone audiometry (PTA) was measured in four frequencies: 250, 500, 1000, and 2000 Hz. Statistically significant differences were observed between the steroid group and the control group, supporting the observation and beneficial impact of administration steroid treatment .
1.4 Glucocorticoid administration: the possibilities
During treatment of otologic diseases, two routes of administration of glucocorticoids are possible: local and systemic. Local administration (e.g., transtympanic injection) allows to achieve high concentration of glucocorticoid in the middle ear, but due to presence of Eustachian tube, the medication may be partly evacuated. Local drug administration to the middle and inner ear avoids “the first pass effect.” The main advantages of local drug delivery are as follows:
Reduction dose of medicine
Achieving high concentration
Better effects of treatment
Reducing possibility of adverse effects
Bypassing of the blood-labyrinth barrier (BLB)
Local drug administration may involve intracochlear administration (e.g., stem cell, gene therapy) or extracochlear administration (e.g., intratympanic injection). A combination of both routes of drug delivery to the ear is also possible . According to publications, systemic administration in treatment of otorhinolaryngological diseases is known as noninvasive route of drug delivery, due to lack of damaging of tympanic membrane. Adverse effects of systemic delivery may be one of the purposes of discontinuation of the therapy. The presence of
1.5 The experience in using glucocorticoids in PDT patients
This study was the first study which was carried out in the Institute of Physiology and Pathology of Hearing World Hearing Center and will be continued with different groups of patients and different implants and algorithms of glucocorticoid administration. The aim of the study was to evaluate different regimes of administration of glucocorticoids: dexamethasone and dexamethasone/prednisone to
During activation of audio processor
One month after activation of audio processor
Six months after activation of audio processor
Nine months after activation of audio processor
One year (12 months) after activation of audio processor
Forty-six patients were enrolled to the trial and then divided randomly into three subgroups. Patients from the first subgroup underwent intravenous steroid therapy (Figure 1). According to the scheme, 30 min before implantation, dexamethasone at the dose of 0.1 mg/kg body mass was administrated intravenously to patients from the first subgroup. For the next 3 consecutive days in every 12 h, dexamethasone was administrated intravenously at the same dose to each patient.
Patients from the second subgroup underwent prolonged (combined) steroid therapy: oral and intravenous. Three days prior to the surgery, prednisone was administrated orally at a dose of 1 mg/kg body mass/day. Then, 30 min before the cochlear implantation surgery, dexamethasone was administrated intravenously at a dose of 0.1 mg/kg body mass. For the next 3 consecutive days in every 12 h, dexamethasone was administrated intravenously (the same as in the first subgroup). For the next 3 days, prednisone was administrated orally at the dose of 1 mg/kg body mass/day. After this period, the dose of prednisone was reduced (10 mg per every day) till complete reduction of dose, due to reducing the risk of adverse effects. The algorithm of administration of glucocorticoids to patients form the second subgroup is presented below (Figure 2).
The third subgroup was a control group and underwent standard cochlear implantation procedure .
1.6 Administrated glucocorticoids
According to the protocol of this study, two different algorithms of administration with two different glucocorticoids were proposed in the study. Although both substances belong to the same pharmacological group, both of them have different pharmacokinetics and pharmacodynamic properties. Dexamethasone is a synthetic glucocorticoid (
Prednisone is a synthetic glucocorticoid (derivative of cortisone) and classified according to the
1.7 Methodology of the study: primary and secondary outcomes and inclusion and exclusion criteria
The primary outcome variables were mean values of hearing thresholds averaged across all 11 frequencies (125–8000 Hz). The secondary outcome variable was hearing preservation (HP). Hearing preservation (HP) was calculated by comparing hearing thresholds in the 1-year postoperative period with the preoperative hearing thresholds, according to the hearing preservation (HP) formula (below) and converted to three levels: minimal, partial, and complete hearing preservation.
In this equation,
The protocol of this prospective clinical trial was approved by the Bioethics Commission. Patients enrolled to the study suffered from severe-to-profound hearing loss and were classified according to Prof. H. Skarżyński
Inclusion and exclusion criteria were in accordance with the consensus of the international
Hearing sound levels in the range of 10–120 decibels (dB) and sound frequencies of 125–250 hertz (Hz)
Hearing sound levels of 35–120 dB and frequencies of 500–1000 Hz
Hearing sound levels of 75–120 dB and frequencies of 2000–8000 Hz 
Exclusion criteria included suffering from severe diseases when the steroid treatment could worsen the patient’s condition or when there would be a possibility of interaction between medication intake by patients and steroids. Nonparametric tests were used in the study due to discrepancies in the number of participants between all subgroups, small number of participants in the study, and violation of normal distribution of pure tone audiometry results .
1.8 Main results and observations
Preoperative hearing threshold levels of patients from the first, the second, and the control subgroup were similar. The difference between patients from the three subgroups was not statistically significant, which means that hearing thresholds in preoperative period of all participants, who were enrolled to the study, were similar.
The deterioration of average hearing thresholds (measured by pure tone audiometry) was observed from the first point of observation—the activation period. A significant difference was observed between two groups: patients from the second subgroup (combined steroid therapy, prednisone + dexamethasone) and the control subgroup. Patients from the second subgroup had better pure tone audiometry (PTA) results considering low frequencies in comparison with the results of patients from the control group. Similar observation was done in 1, 6, 9, and 12 months after activation follow-up periods. The results of the study may be even more a promise and beneficial for patients. The hearing of participants of the study, to whom combined (prolonged) glucocorticoid therapy was administrated, remained stable during all observed follow-up periods (
The hearing preservation (HP) rate is calculated using hearing preservation formula by comparing hearing threshold in the 12-month postoperative period with the preoperative hearing thresholds. Then the results were divided, according to the hearing preservation (HP) formula, into minimal HP, partial HP, and complete HP according to Table 2. The smallest variability of results was observed in the second subgroup (patients to whom prednisone and dexamethasone were administrated) as well as the highest overall HP rate. Patients from the second subgroup (prolonged steroid therapy) and nearly 69% of the patients from the first subgroup had partial or complete hearing preservation. The majority of patients from the control group had minimal hearing preservation (Table 2 and Figure 5).
|Minimal (0–25%)||Partial (26–75%)||Complete (≤75%)|
|Subgroup No 1||5 (31.2)||7 (43.8)||4 (25.0)|
|Subgroup No 2||0 (0.0)||8 (61.5)||5 (38.5)|
|Control group||12 (70.6)||3 (17.6)||2 (11.8)|
1.9 Final conclusion
This study is the first study to report the results of two different regimes of steroid administration in human subjects who underwent cochlear implantation in comparison with the control group. As it was said in the previous paragraph, the findings of this study have shown that glucocorticoid therapy not only stabilizes hearing thresholds but also preserves hearing ability in adult patients. The combination of