ISSN: 0443-511
e-ISSN: 2448-5667
Usuario/a
Idioma
Herramientas del artículo
Envíe este artículo por correo electrónico (Inicie sesión)
Enviar un correo electrónico al autor/a (Inicie sesión)
Tamaño de fuente

Open Journal Systems

Association between depression and hearing loss in patients with type 2 diabetes

How to cite this article: Zamora-Vega O, Gómez-Díaz RA, Delgado-Solís M, Vázquez-Estupiñán F, Vargas-Aguayo AM, Wacher-Rodarte NH. [Association between depression and hearing loss in patients with type 2 diabetes]. Rev Med Inst Mex Seguro Soc. 2016;54 Suppl 2:S140-7.

PubMed: http://www.ncbi.nlm.nih.gov/pubmed/27561017


ORIGINAL CONTRIBUTIONS


Received: November 2nd 2015

Judged: May 2nd 2016


Association between depression and hearing loss in patients with type 2 diabetes


Omar Zamora-Vega,a Rita Angélica Gómez-Díaz,a Margarita Delgado-Solís,b Felipe Vázquez-Estupiñán,c Alejandro Martín Vargas-Aguayo,d Niels H. Wacher-Rodartea


aUnidad de Investigación en Epidemiología Clínica

bEspecialista en Audiometría y Foniatría

cServicios de Atención Psiquiátrica, Secretaría de Salud

dEx Jefe del Servicio de Otorrinolaringología


a,b,dHospital de Especialidades, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de México, México


Communication with: Rita Angélica Gómez Díaz

Telephone: 55 5627 6900, extension 21481

Email: ritagomezdiaz@yahoo.com.mx


Background: The association between diabetes, hearing loss and depression is unknown, and needs to be understood clearly and precisely. Our objective was to estimate the association between depression and hearing loss in patients with type 2 diabetes.

Methods: Cross-sectional analytical study. Patients of 40 years or older with type 2 diabetes were studied. Anthropometric measurements and biochemical parameters were recorded. The Beck Depression Inventory and a pure tone audiometry were applied. Groups were compared with chi squared test and logistic regression for confounders.

Results: 150 patients were included (76 % women). Average age was 56 ± 9.3 years, with 12.4 ± 6.5 years of progression of diabetes, weight 67.4 ± 11.6 kg; 31 % were obese; 25.5 % hypertensive (126.3 ± 19.3/79.4 ± 19.7 mm Hg) and 80.7 % had poor metabolic control (HbA1c ≥ 7 %). Of all the patients, 45.3 % presented hearing loss and 32.4 % depression. Diagnosis of depression in patients with hearing loss remained significant after adjusting for confounders (odds ratio [OR] = 2.3; 95 % confidence interval [CI] = 1.051-5.333, p = 0.037). Women had greater risk of depression, difference that remained significant (OR = 3.2; 95 % CI = 1.268-8.584, p = 0.014) after adjustment.

Conclusions: Almost half of the patients with diabetes presented hearing loss and more than three times the risk of depression. Subjects with depression and diabetes presented more hearing loss (> 20 dB) than those without diabetes and/or without depression.

Keywords: Type 2 diabetes mellitus; Hearing loss; Depression


Patients with diabetes are more prone to atherosclerotic disease than the general population. Many of the complications of the elderly appear earlier in patients with diabetes. 1 According to the World Health Organization (WHO), for 2025 it is estimated that 25% of adults aged 65 to 75 years and between 70 and 80% of those over 75 will suffer from sensorineural hearing loss.2 Diabetes can cause hearing loss by microcirculation compromise, neuropathic factors, and chronic hyperglycemia, with deleterious effects on the organ of Corti, 3-5 causing varying degrees of sensorineural hearing loss. 6-8 The most common form of hearing loss in patients with type 2 diabetes is progressive, sensorineural, bilateral, and symmetrical, particularly affecting the high frequencies, but with more severe losses especially in elderly patients. 9 The evaluation of hearing loss by audiometry is a rapid, accessible, and non-invasive method, taking into account the type, degree, and configuration of hearing loss.

On the other hand, a strong relationship is found between hearing loss and depression. 10 This is the mood characterized by loss of interest and the ability to enjoy things, decreased activity levels, and tiredness following minimal exertion, for two or more consecutive weeks. 11 To establish a diagnosis of depression one must have at least two of the following symptoms: decreased attention and concentration; loss of self-confidence and feelings of inferiority; ideas of guilt and of being useless; bleak future outlook; thoughts or acts of suicide and self-harm; sleep disturbances; and loss of appetite. Certain questionnaires are used to identify and quantify the intensity of depressive symptoms or to evaluate treatment. Among them is the Beck questionnaire. 12

The association of diabetes and depression causes poor adherence to treatment, poor metabolic control, increased presence of complications, and increased mortality. If left untreated, these conditions contribute to deteriorating health. The association between diabetes and depression is bidirectional.13 Depression and hearing loss are diseases that lead to life with disabilities. Furthermore, the comorbidity of depression and diabetes increases health costs if compared with diabetes only. 14

The presence of diabetes increases the incidence of depression around 20%, while depression is associated with a 60% increase in the risk of new cases of type 2 diabetes. 15

According to the above, diabetes, like other comorbidities, such as hypertension, cardiovascular disease, sleep disorders, cancer, etc., has been strongly associated with hearing loss and depression. 16

As suggested by Petrak et al., multidisciplinary collaboration between medical and psychological specialties is needed to improve the treatment of patients with diabetes, hearing loss, and depression. 17

Therefore, the aim of our study was to estimate the strength of association between depression and hearing loss in patients with type 2 diabetes.

Methods

This is an analytical cross-sectional design. Patients attending their scheduled appointments at the Unidad de Investigación en Epidemiología Clínica of the Hospital de Especialidades of the Centro Médico Nacional Siglo XXI of the Instituto Mexicano del Seguro Social Institute over 12 months (from January to December 2014) were invited to participate.

Patients of both sexes with type 2 diabetes and non-diabetic subjects, 40 years of age or older, who agreed to sign the informed consent were included. The study did not include patients with previous otologic surgeries or illnesses or those under antipsychotic/antidepressant treatment; nor those with a history of acute otologic disease in the last three months, or those who work in noisy environments without the use of hearing protection equipment, or subjects with a history of mental illness or prior diagnosis of depression.

Subjects who did not answer the questionnaires were excluded, as well as those who had no audiometry test or with incomplete data.

After informed consent, an interview and complete clinical examination were performed, recording age, weight, height, sex, and blood pressure. The body mass index (BMI) was calculated according to the Quetelet index (weight/height 2). A peripheral venous blood sample was taken to determine the fraction of A1c glycated hemoglobin (HbA1C), fasting glucose, creatinine, and lipid profile. The Beck questionnaire was applied to diagnose depression; patients were also taken the Otolaryngology department for audiometry.

The cutoff point for depression with the Beck questionnaire was ≥ 12 points according to the total score.

Regarding the statistical analysis, quantitative results are reported as mean and standard deviation; qualitative data were expressed as a percentage. The analysis used Chi-squared or Fisher's exact test according to the type and distribution of the variable. The variables (age, gender, socioeconomic status, HbA1c, and time of disease progression) were categorized and multiple logistic regression analysis was done. A p-value < 0.05 was considered statistically significant.

Results

150 subjects were included. 76% were women (n = 114). The average age and average weight of the total population were 56 ± 9.3 years and 60.6 ± 10.0 kg, respectively. 75 patients had diabetes and had 12.4 ± 6.5 years of disease progression. The average BMI calculated in subjects with diabetes was 28.8 ± 4.4 kg/m2, versus 26.91 ± 3.6 kg/m2 for subjects without diabetes (p = 0.005) (Table I).


Table I Anthropometric characteristics of study subjects
Variable Diabetes
( = 75)
No diabetes
( = 75)
Total
(n = 150)
p
n % n % n %
Female 56 74.7 58 77.3 114 76 0.702
Mean ± SD Mean ± SD Mean ± SD
Age (in years) 56 ± 9.3 57 ± 9.4 57 ± 9.3 0.597
Weight (in kg) 69.24 ± 12.8 65.73 ± 10.04 67.4 ± 11.6 0.064
Height (in m) 1.54 ± 0.09 1.56 ± 0.07 1.55 ± 0.08 0.343
BMI (in kg/m2) 28.8 ± 4.4 26.91 ± 3.6 27.87 ± 4.20 0.005
Med IR Med IR Med IR
SBP (in mm Hg) 125 118-130 120 110-130 120 113-130 0.068
DBP (in mm Hg) 80 71-85 80 70-85 80 70-85 0.307
SD = standard deviation; BMI = body mass index; Med = medium; IR = interquartile range; SBP = systolic blood pressure; DBP = diastolic blood pressure

As expected, a significant difference (p < 0.001) was observed when comparing glucose values ​​and HbA1c in subjects without diabetes (86.7 mg/dL and 5.7%), with subjects with diabetes (177.1 mg/dL and 7.9%), respectively. Also, lower mean HDL cholesterol values ​​were noted in subjects with diabetes (46.1 ± 12.5 mg/dL) than in those without diabetes (50.5 ± 14.4 mg/dL) (p = 0.031). The same was observed with triglyceride values (164 mg/dL) versus (128.5 mg/dL) (p = 0.001) Table II.  


Table II Biochemical characteristics of study participants
Variables Diabetes
(n = 75)
No diabetes
(n = 75)
p
Mean ± SD Mean ± SD
Glucose (in mg/dL) 177.1 ± 72.9 86.7 ± 9.9 < 0.001
Total cholesterol (in mg/dL) 191.3 ± 46.1 192.7 ± 40.6 0.658
HDL cholesterol (in mg/dL) 46.1 ± 12.5 50.5 ± 14.4 0.031
LDL cholesterol (in mg/dL) 126.4 ± 37.5 135.0 ± 33.4 0.701
Median IR Median IR
HbA1c (%) 7.9 6.58-10.1 5.7 5.5-6.0 < 0.001
Creatinine (in mg/dL) 0.73 0.66-0.88 0 81 0.70-0.89 0.130
Triglycerides (in mg/dL) 164.0 123.2-209.5 128.5 102.5-159.2 < 0.001
SD = standard deviation; HDL cholesterol = high-density cholesterol; LDL cholesterol = low-density cholesterol; HbA1c = A1c glycosylated hemoglobin; IR = interquartile range

34 patients with diabetes presented hearing loss (45.3%), i.e., that condition was 17.3% more frequent than in subjects without diabetes (28%). The hearing loss was moderate in 6.6% vs. 8% of patients with and without diabetes (p = 0.103), respectively.

21.3% of patients with diabetes (n = 16) presented depression (Beck questionnaire ≥ 12 points), while only 14.7% (n = 11) of those without diabetes had it (p = 0.288). 9.3% of patients with diabetes (n = 7) and 10.6% without diabetes (n = 8) had a score ≥ 17 (0.415). When comparing patients with and without diabetes, 37.3% (n = 28) versus 16% (n = 12) (p = 0.007) presented obesity, respectively- Table III.


Table III Social and special characteristics of patients
Variable Diabetes
(n = 75)
No diabetes
(n = 75)
p
n % n %
Diagnosis of hearing loss
Yes 34 45.3 21 28 0.028
No 41 54.7 54 72
Socioeconomic level
Low 28 37.3 26 34.7 0.734
Medium 47 62.7 49 65.3
Depression 16 21.3 11 14.7 0.288
Degree of hearing loss
No hearing loss 41 54.7 54 72 0.103
Mild 29 38.7 15 20
Moderate hearing loss or more 5 6.6 6 8
Obesity/overweight
Normal 14 18.7 25 33.3 0.007
Overweight 33 44 38 50.7
Obesity 28 37.3 12 16

The risk of depression in subjects who had hearing loss and diabetes was 3.44 (95% confidence interval [CI] = 1.05-11.2). In subjects with diabetes with low socioeconomic status, the odds ratio (OR) was 3.7 (95% CI = 1.19-12.03).

When the risk was calculated adjusted for sex, age, obesity, years of diabetes diagnosis, and degree of metabolic control, the risk in patients with diabetes and hearing loss increased with an OR of 5.4; also for those who had low socioeconomic status and diabetes, OR increased to 5.91- Table IV.


Table IV Odds ratio describing the association between depression and hearing loss in patients with and without diabetes
Variable No diabetes No diabetes Diabetes Diabetes
Raw OR 95% CI Adjusted OR 95% CI Raw OR 95% CI Adjusted OR 95% CI
Hearing lossa 0.95 0.22-4.02 0.73 0.15-3.4 3.44 1.05-11.2 5.4 1.25-23.28
Low socio-economic statusb 2.6 0 72-9.6 3.03 0.75-12.2 3.7 1.19-12.03 5.91 1.45-24.1
Womenc 3.33 0.39-28.1 3.3 0.38-29 9 6.5 0.80-53.7 8.85 0.93-83.9
Age ≥ 60 yearsd 1.01 0.26-3.8 0.96 0.22-4.1 1 92 0.61-5.9 1.72 0.40-7.3
Obesitye 0.85 0.22-3.2 0.76 0.18-3.1 0.61 0.16-2.2 0.53 0.10-2.8
Evolution ≥ 14 yearsf --- --- --- --- 1.4 0.43-4.5 1.22 0.28-5.3
≥ 7% HbA1cg --- --- --- --- 1.5 0.43-5.3 0.75 0.16-3.4
Compared with the variable tono hearing loss, b medium socioeconomic status, cman, d< 60 years old, enot obese, f< 14 years evolution, gHbA1c < 7%

Logistic regression analysis was made using depression according to the Beck questionnaire (≥ 12 points) as a dependent variable. After adjusting for age, gender, BMI, time of evolution, HbA1c, HDL-C, LDL-C, and triglycerides, the independent association between hearing loss and depression was confirmed (beta = 0.748, OR 2.113, 95% CI = 1.003-4.449; p = 0.049). Gender had a borderline association (beta 0.703 with OR 2.20 [p = 0.082, 95% CI .914-4.464]) Table IV


Table V Logistic regression analysis for the association between hearing loss and related variables
Depression
Beta * Exp-beta 95% CI p
Hearing loss 0.748 2.113 1.003-4.449 0.049
Gender 0.703 2.020 0.914-4.464 0.082
* The beta coefficient of depression includes Beck questionnaire scoring with a value ≥ 12 and is adjusted for each variable (age, gender, body mass index, time of evolution, HbA1c, HDL-C, LDL-C and triglycerides)
Exp-beta = beta exponent; CI = confidence interval; BMI = body mass index;
HDL-C = high-density cholesterol; LDL-C = low-density cholesterol; HbA1c = A1c glycosylated hemoglobin

Overt hearing loss was observed in subjects with depression (Beck questionnaire ≥ 12 points), with a predominance in the left ear in subjects with diabetes, compared with those without diabetes (Annex 1).


Annex 1 Comparison of average audiometry values ​​by ear by subgroup


Discussion

Our results demonstrate the independent association between depression and hearing loss in people over 40 years with type 2 diabetes. Both comorbidities are common and may go unnoticed if they are not looked for intentionally. Depression and hearing loss diminish the quality of life and are barriers to adherence in the management of chronic diseases. The strength of the association justifies the search for both conditions when either is detected. In addition, they should be considered in the evaluation of therapeutic barriers that can be resolved in the management of diabetes.

Nearly half of patients with diabetes had hearing loss and three times the risk of depression. In subjects with diabetes and depression, the presence of hearing loss had greater predominance in the left ear than those without diabetes or without depression.

Several studies have correlated diabetes with hearing loss, but there is still controversy about this, and its association with depression has only been studied separately. 18-21 The present study evaluated the association between depression and hearing loss in patients with type 2 diabetes.

Diabetes affects a growing number of Mexicans over 40 years. 22 Its presence is associated with loss of years of quality life and premature disability. The effectiveness of the available therapy in the health sector is lower than that reported in other countries. Identifying the conditions that limit the quality of life and efficacy of treatment should be part of the systematic evaluation of people with diabetes. These include depression and hearing loss, so their deliberate search should be part of the initial evaluation of patients with diabetes.

In our study, the group of patients with diabetes showed hearing loss in almost all hearing frequencies, compared to those without diabetes. The prevalence of hearing loss was 45.3%; the value is unexpected since patients were asymptomatic. The severity of hearing loss was moderate in 6.6%, enough to have a negative impact on quality of life. These results are consistent with the studies of Hernandez et al.5 and Bainbridge et al. 9

The frequency of hearing loss in women was found in three-quarters of people with diabetes, close to that reported by Imarai et al., who found 64% hearing loss in females.23

There is three times the risk of depression in subjects with hearing loss and diabetes. The American Diabetes Association categorizes depression and hearing loss as common comorbid conditions that may complicate the management of diabetes, and therefore recommends that they be part of the initial evaluation of patients with this disease.24 A study of 93 diabetic patients in Spain found a higher prevalence than ours (42.8% mild unilateral hearing loss and 57.1% bilateral moderate, predominantly in the right ear in 59.1% and 40.9% in the left). Unlike that reported by Sambola, 25 our patients with depression had overt bilateral hearing loss, predominantly observed in the left ear.

Our data confirm the high prevalence of depression in people with diabetes (21.3%). Multiple reports show that depression is one of the most common barriers to adherence in people with diabetes. 14-17 Our data confirm that cases with depression have higher levels of HbA1c and glucose levels than the rest of the participants in the study who had diabetes.

Our data also show that there is an independent association between depression and hearing loss in people with diabetes. Of the confounding variables analyzed, only age had a borderline role, probably because the patients are younger and have less time of evolution of the disease. This is opposite to what was reported by Michikawa et al., who support a causal role between hyperglycemia and age-related hearing loss, which turned out to be associated with the degree of control of HbA1c.26

However, the risk of depression for those who have diabetes and low socioeconomic status is increased almost six times. Furthermore, the severity of hearing loss was significantly higher when it coexisted with depression.

We recognize the limitations of this study, which has to do with the small size of our sample, plus the fact that causality cannot be established because the design is transversal. It is necessary to make an intentional search for patients with depression and hearing loss to begin management early and thereby slow related complications.

Conclusions

Nearly half of patients with diabetes had hearing loss and more than three times the risk of depression. Subjects with depression and diabetes showed greater hearing loss (> 20 dB) than those without diabetes or without depression. Hearing loss and depression are conditions that must be looked for intentionally in people with diabetes.

Acknowledgments

To Master of Science Rafael Mondragón González for his support in the laboratory, to Ricardo Saldaña Espinoza for his support with data management, and to Drs Aline Berenice Herrera Rangel and Leticia del Carmen Cruz Hernandez, for their role in the inclusion of patients in the protocol.

References
  1. Biessels GJ, van der Heide LP, Kamal A, Bleys RL, Gispen WH. Ageing and diabetes: implications for brain function. Eur J Pharmacol. 2002 Apr 19;441(1-2):1-14.
  2. World Health Organization (WHO). Active ageing a policy framework. A contribution of the World Health Organization to the Second United Nations World assembly on ageing. Madrid, Spain: WHO; 2002. Available from: http://whqlibdoc.who.int/hq/2002/WHO_NMH_NPH_02.8.pdf
  3. Maia CAS, de Campos CAH. Diabetes mellitus as etiological factor of hearing loss. Rev Bras Otorrinolaringol. 2005;71(2):208-14.
  4. Hruban RH, Iacobuzio-Donahue C. The pancreas. In Robbins and Cotran pathologic basis of disease. Robbins SL, Kumar V, Cotran RS, editors. 8th ed. Philadelphia, PA: Saunders / Elsevier; 2010. pp. 1709-37.
  5. Diniz TH, Guida HL. Hearing loss in patients with diabetes mellitus. Braz J Otorhinolaryngol. 2009 Jul-Aug;75(4):573-8.
  6. Cummings CW, Flint PW, Haughey BH, Lund VJ, Niparko JK, Richardson MA, et al. Otolaryngology: Head & Neck Surgery. 5th ed. Philadelphia, PA: Mosby Elsevier; 2010.
  7. American Speech-Language-Hearing Association (ASHA). Audiology Information Series: Type, Degree, and Configuration of Hearing Loss. ASHA. 2011;7976(16):1-2.
  8. Mathers C, Smith A, Concha M. Global Burden of Hearing Loss in the Year 2000. Global Burden of Disease. Geneva: World Health Organization; 2003: 1-30. Available from: http://www.who.int/healthinfo/statistics/bod_hearingloss.pdf
  9. Bainbridge KE, Hoffman HJ, Cowie CC. Diabetes and hearing impairment in the United States: audiometric evidence from the National Health and Nutrition Examination Survey, 1999 to 2004. Ann Intern Med. 2008;149(1):1-10.
  10. Bot M, Pouwer F, Zuidersma M, van Melle JP, de Jonge P. Association of coexisting diabetes and depression with mortality after myocardial infarction. Diabetes Care. 2012 Mar;35(3):503-9. doi: 10.2337/dc11-1749.
  11. Espinosa-Aguilar A, Caraveo-Anduaga J, Zamora-Olvera M, Arronte-Rosales A, Krug-Llamas E, Olivares-Santos R, et al. Guía de práctica clínica para el diagnóstico y tratamiento de depresión en los adultos mayores. Salud Mental. 2007;30(6):69-80.
  12. Sanz J, Perdigón AL, Vázquez C. Adaptación española del Inventario para la Depresión de Beck-II (BDI-II). Propiedades psicométricas en población general. Clínica y Salud. 2003;14(3):249-80.
  13. Fiske A, Wetherell JL, Gatz M. Depression in Older Adults. Annu Rev Clin Psychol. 2009;5:363-89. doi: 10.1146/annurev.clinpsy.032408.153621.
  14. Bosmans JE, Adriaanse MC. Outpatient costs in pharmaceutically treated diabetes patients with and without a diagnosis of depression in a Dutch primary care setting. BMC Health Services Research. 2012;12(46):1-8.
  15. Li CM, Zhang X, Hoffman HJ, Cotch MF, Themann CL, Wilson MR. Hearing impairment associated with depression in US adults, National Health and Nutrition Examination Survey 2005-2010. JAMA Otolaryngol Head Neck Surg. 2014 Apr;140(4):293-302. doi: 10.1001/jamaoto.2014.42.
  16. Moulton CD, Pickup JC, Ismail K. The link between depression and diabetes: the search for shared mechanisms. Lancet Diabetes Endocrinol. 2015 Jun;3(6):461-71. doi: 10.1016/S2213-8587(15)00134-5.
  17. Petrak F, Baumeister H, Skinner TC, Brown A, Holt RI. Depression and diabetes: treatment and health-care delivery. Lancet Diabetes Endocrinol. 2015;3(6):472-85.
  18. Gutiérrez JP, Rivera-Dommarco J, Shamah-Levy T, Villalpando-Hernández S, Franco A, Cuevas-Nasu L, Romero-Martínez M, et al. Encuesta Nacional de Salud y Nutrición 2012. Resultados Nacionales. Cuernavaca, México: Instituto Nacional de Salud Pública (Mx); 2012.
  19. Cullen JR, Cinnamond MJ. Hearing loss in diabetics. J Laryngol Otol. 1993;107(3):179-82.
  20. Austin DF, Konrad-Martin D, Griest S, McMillan GP, McDermott D, Fausti S. Diabetes-related changes in hearing. Laryngoscope. 2009 Sep;119(9):1788-96. doi: 10.1002/lary.20570.
  21. Ren J, Zhao P, Chen L, Xu A, Brown SN, Xiao X. Hearing loss in middle-aged subjects with type 2 diabetes mellitus. Arch Med Res. 2009 Jan;40(1):18-23. doi: 10.1016/j.arcmed.2008.10.003.
  22. Mitchell P, Gopinath B, McMahon CM, Rochtchina E, Wang JJ, Boyages SC, et al. Relationship of Type 2 diabetes to the prevalence, incidence and progression of age-related hearing loss. Diabet Med. 2009 May;26(5):483-8. doi: 10.1111/j.1464-5491.2009.02710.x.
  23. Imarai B, Aracena C, Contreras M. Relación entre hipoacusia y diabetes mellitus tipo 2. Rev Otorrinolaringol Cir Cabeza Cuello. 2013;73:157-63.
  24. American Diabetes Association. Initial evaluation and diabetes management planning. Sec. 3. In Standards of Medical Care in Diabetesd2015. Diabetes Care. 2015;38 (Suppl. 1):S17-19.
  25. Sambola-Cabrer I. Otoemisiones acústicas en pacientes diabéticos no insulinodependientes. OEA & Diabetes (Barcelona) 17 de mayo de 2006. Available from: www.tdx.cat/bitstream/handle/10803/4290/isc1de1pdf?sequence=1
  26. Michikawa T, Mizutari K, Saito H, Takebayashi T, Nishiwaki Y. Glycosylated hemoglobin level is associated with hearing impairment in older Japanese: the Kurabuchi Study. J Am Geriatr Soc. 2014;62:1231-7.

Conflict of interest statement: The authors have completed and submitted the form translated into Spanish for the declaration of potential conflicts of interest of the International Committee of Medical Journal Editors, and none were reported in relation to this article.

Enlaces refback

  • No hay ningún enlace refback.