INTERDISCIPLINARY

Cele mai frecvente complicaţii otorinolaringologice în diabetul zaharat de tip 2

 Most common otorhinolaryngologic complications of type 2 diabetes mellitus

First published: 03 martie 2023

Editorial Group: MEDICHUB MEDIA

DOI: 10.26416/ORL.58.1.2023.7651

Abstract

It is well known that diabetes represents an important glo­bal health issue. The disease can generate multiple micro- or macrovascular complications, but also oto­rhi­no­la­ryn­go­logic disorders. At the same time, the disease in­crea­ses the risk of infections. The possible factors involved are represented by altered cellular and humoral immune de­fense mechanisms, poor vascular flow to sites of infection, and microvascular complications. Several studies have shown that diabetic patients have an increased risk of deep neck infection. Other studies have also reported that dia­be­tic patients have a higher incidence of sensorineural hearing loss than the general population. The relationship between dia­be­tes and hearing loss is not completely elucidated. The in­volved risk factors in hearing loss in diabetic patients may be represented by the duration of the affliction, glycemic con­trol, microangiopathy, neuropathy, or medications used to treat comorbidities. The link between type 2 diabetes mel­li­tus, deep neck infection and auditory disorders thus po­ses great interest for both diabetologists, as well as oto­la­ryn­go­lo­gists. This article is a brief review of the information available about the most common oto­rhi­no­la­ryn­go­lo­gic complications in diabetes, based on articles published on PubMed and Google Academic.
 

Keywords
diabetes mellitus, deep neck infection, sensorineural hearing loss

Rezumat

Este bine cunoscut că diabetul reprezintă o problemă im­por­­tan­­tă de sănătate publică la nivel mondial. Afec­ţiunea poa­te genera mul­ti­ple complicaţii micro- şi ma­cro­vas­­cu­­la­re, precum şi pa­to­lo­gii otorinolaringologice. În ace­laşi timp, afecţiunea creşte ris­cul infecţiilor. Posibilii fac­tori implicaţi sunt reprezentaţi de mecanisme de apă­ra­re ce­lu­la­ră şi umorală deficiente, vas­cu­la­ri­za­ţia săracă a zo­ne­lor in­fectate şi de complicaţii mi­cro­vas­cu­la­re. Numeroase stu­­dii au arătat că pacienţii dia­be­tici au un risc crescut pen­tru infecţii cervicale pro­fun­de. Alte studii au raportat o incidenţă mai crescută a hi­po­acu­ziei neurosenzoriale la pacienţii diabetici, faţă de po­pu­la­ţia generală. Re­la­ţia dintre diabet şi hipoacuzie nu este complet elu­ci­da­tă. Factorii de risc implicaţi pot fi reprezentaţi de durata ex­­pu­­ne­­rii la zgomot, controlul gli­ce­miei, micro­an­gio­patie, neu­ro­patie sau de medicamentele utilizate pentru co­mor­bi­­di­­tă­­ţi­le asociate. Legătura dintre dia­be­tul zaharat, in­fec­ţiile cervicale profunde şi tulburările au­di­ti­ve suscită in­te­re­sul atât al diabetologilor, cât şi al me­di­ci­lor oto­ri­no­la­rin­­go­­logi. Acest articol este o scurtă tre­ce­re în revistă a informaţiilor disponibile în bazele de date PubMed şi Google Academic referitoare la cele mai frec­ven­te com­pli­ca­ţii ORL prezente în diabet.
 

Introduction

Type 2 diabetes mellitus (T2DM) is an important global health issue. According to the International Diabetes Federation (IDF), 537 million adults were living with diabetes in 2021. The predictions for future years are worrying. According to the same organization, the number of patients diagnosed with this condition will reach 643 million by 2030 and 783 million by 2045(1). Several studies have shown that diabetic patients have an increased risk of infection. The possible factors involved are represented by altered cellular and humoral immune defense mechanisms, poor vascular flow to sites of infection, and microvascular complications(2). The disease can generate numerous complications, including otorhinolaryngologic disorders. This article presents an overview of the available information based on articles published on PubMed and Google Academic.

Otorhinolaryngologic infections disease

Type 2 diabetes mellitus is a risk factor for deep neck infection. Peritonsillar abscesses is a common disease, being defined by the localized polymicrobial infections between the fibrous capsule of the tonsil and the superior pharyngeal constrictor muscle(3). In the etiopathogenesis of the disease, a polymicrobial mixture of aerobes and anaerobes is involved. Some theories suggest that Weber glands, infection, periodontal disease and smoking contribute to the formation of peritonsillar abscesses(4-6).

Wu et al. investigated the risk, prognosis and complications of peritonsillar abscesses in 67,852 patients with T2DM. The results were compared with those obtained from a control group made up of 135,704 subjects without type 2 diabetes mellitus. The results of the study showed that, in patients with T2DM, the incidence of peritonsillar abscesses was relatively high, being 1.73 times higher compared to the one of subjects without type 2 diabetes mellitus. The patients with T2DM should be particularly careful about this condition within one to five years after the diagnosis(7).

In 2017, Pascual et al. published in the Brazilian Journal of Otorhinolaryngology the results of a retrospective study of 330 patients with deep neck infections and peritonsillar infections. In this study, the authors found that systemic comorbidities like diabetes mellitus are bad prognostic factors(8). Similar conclusions were presented in 2014 by Jin and Zhang in a retrospective study of 142 patients with deep neck infection. The authors specify that “the most common underlying systemic disease was diabetes mellitus”(9).

The influence of diabetes on deep neck infection was also evaluated by Lin et al. in a retrospective study of 131 patients. The results of the study showed that deep neck infections were significantly more prevalent in diabetic patients over 60 years old than in nondiabetic subjects of similar age. The diabetic group had a higher complication rate, longer hospital stays and a higher tracheotomy rate compared to the control group(10). In most situations, diabetic patients’ bacteriological investigations highlighted a higher prevalence of culture identification for Klebsiella pneumoniae and a lower prevalence of anaerobes and Streptococcus pneumoniae(11).

Malignant external otitis is an invasive infection that can affect the external auditory canal and the skull base(12-14). The condition affects patients with impaired immune systems and diabetes. The most common symptoms and clinical signs include deep otalgia, chronic otorrhea and cranial nerve involvement(15). Lee et al. performed a retrospective study on prognostic factors in malignant external otitis. Twenty-eight patients diagnosed and treated with this condition were evaluated. Twelve patients who experienced complete remission from malignant external otitis were included in the control group, and the other 16 patients either survived with the disease or died from this condition. Twenty-three patients (82.1%) had diabetes. The results of the study showed that the duration of diabetes and the presence of inflammatory markers influenced the prognosis of malignant external otitis(15).

Franco-Vidal et al. performed a retrospective study, reviewing a series of 46 patients with necrotizing external otitis. Of these, 30 patients had diabetes(16).

Joshua et al. aimed at identifying the risk factors for malignant external otitis in 75 patients hospitalized between 1990 and 2003. The results of the study showed that malignant external otitis “affected mostly diabetic patients and were characterized by granulations and discharge in the external ear, severe prolonged pain, soft tissue involvement and bone destruction on computed tomographic scan, and growth of Pseudomonas aeruginosa in culture”(17).

In 2022, Peled et al. published in the European Archives of Oto-Rhino-Laryngology the results of a study on diabetes and glycemic control in necrotizing otitis externa. Eighty-nine patients were included in the study, of which 83 patients had diabetes. Pre-admission average value of glycated hemoglobin (HbA1c) was 8.13%, and 49 patients had mean glucose above 140 mg/dL. The duration of diabetes was 157.88 months among patients who required surgery and 127.6 months among patients who were treated conservatively. The authors concluded that the value of “HbA1c at admission is associated with longer hospitalization duration” among necrotizing external otitis patients(18).

Auditory acuity in diabetic patients

The incidence of acquired sensorineural hearing loss has increased and may result in permanent hearing disability(19). The affliction occurs due to damage to the inner ear, the auditory nerve or the brain. Other proposed mechanisms are inflammation, oxidative stress and blood flow blood alteration in the inner ear(19,20).

Several studies have reported that diabetic patients have a higher incidence of sensorineural hearing loss than general subjects. This risk has been assessed by Lin et al. in a study that included 26,556 patients with diabetes mellitus and 26,556 nondiabetic patients. The results of the study showed that the incidence of sensorineural hearing loss was 1.54 times higher in the diabetic group compared to the control group. An increased risk of developing sensorineural hearing loss was observed in diabetic patients with comorbidities, as well as retino­pathy and renal insufficiency(21).

Krishnappa and Naseeruddin performed a cross-sectional study on 106 patients with T2DM and 90 subjects without diabetes mellitus. The patients and subjects were evaluated by tone audiometry and blood investigations (HbA1c, fasting and postprandial glucose, serum creatinine levels). The results of the study showed that the prevalence of hearing loss was 73% in diabetic patients. The authors concluded that “diabetes mellitus was associated with higher hearing loss compared to presbycusis and hearing threshold was seen to affect all frequencies, but significantly the higher frequencies in diabetics. As the duration of diabetes increased, the severity also increased. Poorer the HbA1c, more severe was the hearing loss”(22).

The incidence of sensorineural hearing loss in patients with type 2 diabetes mellitus was evaluated by Rajendan et al. The study included 60 patients with ages between 40 and 50 years old, with T2DM, and 60 subjects without diabetes mellitus, with matching ages and sexes. The patients and subjects were evaluated by tone audiometry and blood investigations (HbA1c, fasting and postprandial glucose, serum creatinine levels). The results of the study showed a very stark difference in the prevalence of hearing loss: 73.3% in diabetic patients compared to only 6.7% in the control group. The authors mention that the glycemic status and duration of diabetes have no significant correlation with this condition(23).

Hearing loss in T2DM has also been evaluated by Pemmaiah and Srinivas in a cross-sectional study involving 110 patients. Forty-eight patients (43.6%) had bilateral sensorineural hearing loss. Of these, seven patients exhibited severe hearing loss, 16 exhibited moderately severe hearing loss and 25 exhibited moderate hearing loss. The duration of the patients’ diabetes and sensorineural hearing loss revealed a statistically significant correlation(24).

The relationship between diabetes and hearing loss is not completely elucidated. The involved risk factors may be represented by age, duration of the affliction, glycemic control, microangiopathy, neuropathy, and medications used to treat comorbidities. Ototoxic effects can represent side effects of medications such as antibiotics, psychotropics, anticancer agents, antihypertensive and antiarrhythmics, nonsteroidal anti-inflammatory drugs and loop diuretics(25,26). In a review published in 2005 by Maia and Campos, about the hearing loss in diabetic patients, the authors mention that “there are many different types of hearing loss found in diabetic patients. One of them is progressive, gradual bilateral sensorineural loss, affecting especially high frequencies and the elderly. It would be similar to presbycusis, but with more severe losses than those expected by aging. Conversely, there are authors that report the possibility of having early sensorineural loss and others that reported hearing loss in low and medium frequencies. Some studies described diabetes as the possible cause of unilateral sudden loss, but other authors did not find the same association”(25).

This led some researchers to investigate the effects of antidiabetic therapy on hearing loss. Metformin is the most used oral hypoglycemic agent in the treatment of type 2 diabetes mellitus and remains the first choice when treating the affection. A 14-year follow-up study conducted by Chen et al. demonstrated an association between the treatment with metformin and the lower incidence of hearing loss among patients with T2DM(27). Similar results were reported by Miwa et al.(28)

Conclusions

While the link between type 2 diabetes mellitus, deep neck infection and auditory disorders was highlighted in numerous publications, its exact nature and the influencing factors have not yet been elucidated, remaining a keen interest for diabetologists and otolaryngologists alike.

Conflict of interest: none declared

Financial support: none declared

This work is permanently accessible online free of charge and published under the CC-BY.
sigla CC-BY

Bibliografie

  1. Sun H, Saeedi P, Karuranga S, et al. IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Res Clin Pract. 2022;183:109119. doi:10.1016/j.diabres.2021.109119. 

  2. Pozzilli P, Leslie RD. Infections and diabetes: mechanisms and prospects for prevention. Diabet Med. 1994;11:935-941.10.1111/j.1464-5491.1994.tb00250.x.

  3. Galioto NJ. Peritonsillar abscess. Am Fam Physician. 2008;77(2):199-202.

  4. Klug TE, Rusan M, Fuursted K, Ovesen T. Peritonsillar abscess: complication of acute tonsillitis or Weber’s glands infection. Otolaryngol Head Neck Surg. 2016;155(2):199–207.

  5. Powell EL, Powell J, Samuel JR, Wilson JA. A review of the pathogenesis of adult peritonsillar abscess: time for a re-evaluation. J Antimicrob Chemother. 2013;68(9):1941-1950.

  6. Hidaka H, Kuriyama S, Yano H, Tsuji I, Kobayashi T. Precipitating factors in the pathogenesis of peritonsillar abscess and bacteriological significance of the Streptococcus milleri group. Eur J Clin Microbiol Infect Dis. 2011;30(4):527-532.

  7. Wu CL, Tsai MS, Lee TJ, Wang YT, Liu CY, Yang YH, Tsai YT, Hsu CM, Wu CY, Chang PJ, Chang GH. Type 2 Diabetes Mellitus Increases Peritonsillar Abscess Susceptibility: Real-World Evidence. Clin Exp Otorhinolaryngol. 2021;14(3):347–354. doi:10.21053/ceo.2020.02257.

  8. Pascual PM, Martinez PP, FriedlanderE, Oviedo CM, Yurrita BS. Peritonsillar and deep neck infections: a review of 330 cases. Braz J Otorhinolaryngol. 2017;84(3):305–310. doi:10.1016/j.bjorl.2017.03.008.

  9. Jin L, Zhang T. Deep neck infections: A retrospective study of 142 patients. B-ENT. 2014;10(2):127-32. 

  10. Lin HT, Tsai CS, Chen YL, Liang JG. Influence of diabetes mellitus on deep neck infection. J Laryngol Otol. 2006;120(8):650-654.

  11. Hidaka H, Yamaguchi T, Hasegawa J, Yano H, Kakuta R, Ozawa D, Nomura K, Katori Y. Clinical and bacteriological influence of diabetes mellitus on deep neck infection: Systematic review and meta-analysis. Head Neck. 2015;37(10):1536-1546. doi: 10.1002/hed.23776.

  12. Marina S, Giutham MK, Rajeshwary A, Vadisha B, Devika T. A retrospective review of 14 cases of malignant otitis externa. J Otology. 2019;14(2):63–66.

  13. Amaro CE, Espiney R, Radu L, Guerreiro F. Malignant (necrotizing) externa otitis: the experience of a single hyperbaric centre. Eur Arch Otorhinolaryngol. 2019;276(7):1881–1887.

  14.  Singh A, Al Khabori M, Hyder MJ. Skull base ostemyelitis: Diagnostic and therapeutic challenges in atypical presentation. Otolaryngol Head Neck Surg. 2005;133(1):121–125. 

  15. Lee SK, Lee SA, Seon SW, Jung JH, Lee JD, Choi JY, Kim BG. Analysis of Prognostic Factors in Malignant External Otitis. Clin Exp Otorhinolaryngol. 2017;10(3):228–235.

  16. Franco-Vidal V, Blanchet H, Bebear C, Dutronc H, Darrouzet V. Necrotizing external otitis: a report of 46 cases. Otol Neurotol. 2007;28(6):771–773.

  17. Joshua BZ, Sulkes J, Raveh E, Bishara J. Predicting outcome of malignant external otitis. Otology & Neurotology. 2008;29(3):339-343.

  18. Peled C, Sadeh R, El-Saied S, Novack V, Kaplan DM. Diabetes and glycemic control in necrotizing otitis externa (NOE). Eur Arch Otorhinolaryngol. 2022;279(3):1269-1275. 

  19. Alexander TH, Harris JP. Incidence of sudden sensorineural hearing loss. Otol Neurotol. 2013;34:1586–1589.

  20. Herrera M, García Berrocal JR, García Arumí A, Lavilla MJ, Plaza G. Update on consensus on diagnosis and treatment of idiopathic sudden sensorineural hearing loss. Acta Otorrinolaringol Esp. 2019;70:290–300.

  21. Lin SW, Lin YS, Weng SF, Chou CW. Risk of developing sudden sensorineural hearing loss in diabetic patients: a population-based cohort study. Otol Neurotol. 2012;33(9):1482-1488.

  22. Krishnappa S, Naseeruddin K. A clinical study of age related hearing loss among diabetes patients. Indian J Otol. 2014;20:160-165.

  23. Rajendran S, Anandhalakshmi MB, Viswanatha R. Evaluation of the incidence of sensorineural hearing loss in patients with Type 2 diabetes mellitus. Int J Biol Med Res. 2011;2(4):982–987.

  24. Pemmaiah KD, Srinivas DR. Hearing loss in Diabetes Mellitus. International Journal of Collaborative Research on Internal Medicine & Public Health. 2011;3(10):725-731.

  25. Maia CAS, Campos CAH. Diabetes mellitus as etiological factor of hearing loss. Braz J Otorhinolaryngol. 2005;71(2):208–214. 

  26. Rizk HG, Lee JA, Liu YF, Endriukaitis L, Isaac JL, Bullington WM. Drug-Induced Ototoxicity: A Comprehensive Review and Reference Guide. Pharmacotherapy. 2020;40:1265–1275.

  27. Chen HC, Chung CH, Lu CH, Chien WC. Metformin decreases the risk of sudden sensorineural hearing loss in patients with diabetes mellitus: a 14-year follow-up study. Diabetes Vasc Dis Res. 2019;16:324–327.

  28. Miwa T, Kita T, Yamaguchi T, Sakamoto T. Metformin Reduces the Incidence of Sensorineural Hearing Loss in Patients with Type 2 Diabetes Mellitus: A Retrospective Chart Review. Cureus. 2022;14(10):e30406. doi:10.7759/cureus.30406. 

Articole din ediţiile anterioare

CERVICAL PATHOLOGY | Ediţia 3 64 / 2024

Supuraţiile cervicale la pacientul diabetic – o provocare permanentă pentru chirurgul ORL

Mihail Tuşaliu, Elena-Mădălina Vulpe, Elena-Monica Tudor, Cristian Bucur, Iulia Tiţă, Camelia Iancu, Elena-Alexandra Gherghe

Supuraţiile cervicale reprezintă un capitol re­du­ta­bil de patologie, constituind o urgenţă medico-chirurgicală ma­jo­ră, caracterizată printr-un ...

20 septembrie 2024
AUDIOLOGIE | Ediţia 4 41 / 2018

Infecţia congenitală cu CMV şi hipoacuzia

Mădălina Georgescu

Infecţia cu citomegalovirus (CMV) este cea mai obişnuită in­fec­ţie congenitală, cu o prevalenţă la naştere între 0,48% şi 1,3% în ultimele decenii...

30 noiembrie 2018
OTOLOGY | Ediţia 3 56 / 2022

Studiu retrospectiv al schwanomului vestibular în Republica Moldova

M. Buracovschi, A. Sandul, Oleg Borysenko, Grigore Zapuhlîh, V. Moraru, Iulian Glavan

Schwanomul vestibular este o tumoare benignă, intracraniană, a nervului vestibulocohlear. Incidenţa schwanomului vestibular este de 3-5,2 cazuri la...

20 septembrie 2022