Automatic detection of reverse-triggering related asynchronies during mechanical ventilation in ARDS patients using flow and pressure signals.

Asynchrony due to reverse-triggering (RT) may appear in ARDS patients. The objective of this study is to validate an algorithm developed to detect these alterations in patient-ventilator interaction. We developed an algorithm that uses flow and airway pressure signals to classify breaths as normal, RT with or without breath stacking (BS) and patient initiated double-triggering (DT). The diagnostic performance of the algorithm was validated using two datasets of breaths, that are classified as stated above. The first dataset classification was based on visual inspection of esophageal pressure (Pes) signal from 699 breaths recorded from 11 ARDS patients. The other classification was obtained by vote of a group of 7 experts (2 physicians and 5 respiratory therapists, who were trained in ICU), who evaluated 1881 breaths gathered from recordings from 99 subjects. Experts used airway pressure and flow signals for breaths classification. The RT with or without BS represented 19% and 37% of breaths in Pes dataset while their frequency in the expert's dataset were 3% and 12%, respectively. The DT was very infrequent in both datasets. Algorithm classification accuracy was 0.92 (95% CI 0.89-0.94, P < 0.001) and 0.96 (95% CI 0.95-0.97, P < 0.001), in comparison with Pes and experts' opinion. Kappa statistics were 0.86 and 0.84, respectively. The algorithm precision, sensitivity and specificity for individual asynchronies were excellent. The algorithm yields an excellent accuracy for detecting clinically relevant asynchronies related to RT.

High-Flow Nasal Cannula and Standard Oxygen in Acute Hypoxemic Respiratory Failure Due to COVID-19.

BACKGROUND: The evidence regarding benefits of high-flow nasal cannula (HFNC) in patients with COVID-19 is controversial. The aim of this study was to evaluate the impact of HFNC in comparison with standard oxygen therapy on the frequency of endotracheal intubation at 28 d in subjects with acute hypoxemic respiratory failure (AHRF) secondary to SARS-CoV-2 infection. METHODS: A retrospective, age- and sex-matched-paired, cohort study was conducted in subjects with moderate-to-severe AHRF. Intervention group was treated with HFNC, and control group was treated with standard oxygen therapy. Baseline characteristics and clinical evolution were analyzed. Mantel-Haenszel test was used for categorical variables. Paired samples Wilcoxon test was used for quantitative variables. Multivariate analysis was performed using conditional multiple logistic regression. RESULTS: Eighty-four subjects were included. The median time from admission to progression of oxygen therapy to FIO2 ≥ 0.5 or HFNC was 1 (interquartile range [IQR] 0-3) d. PaO2 /FIO2 at the time of oxygen therapy progression showed a median of 150.5 (IQR 100.0-170.0) for the entire sample and was lower in HFNC group compared with control group (median 135 [IQR 96-162] vs median 158 [IQR 132-174], respectively, P = .02). Endotracheal intubation at 28 d was observed in 54.8% HFNC and 73.8% standard oxygen (unadjusted odds ratio 0.38 [95% CI 0.13-1.07], P = .069). In the multivariate analysis, presence of dyspnea at hospital admission, Sequential Organ Failure Assessment score, and PaO2 /FIO2 at time of progression of oxygen therapy to FIO2 ≥ 0.5 was identified as confounding factors for the association between the intervention group and the outcome. Use of HFNC was not an independent predictor of endotracheal intubation frequency after adjusting confounders (odds ratio 0.26 [95% CI 0.04-1.51], P = .13). CONCLUSIONS: In this study, HFNC therapy in subjects with AHRF secondary to COVID-19 was not an independent predictor of endotracheal intubation, compared with standard oxygen therapy, after adjusting for confounders.

Prevalence of Reverse Triggering in Early ARDS: Results From a Multicenter Observational Study.

BACKGROUND: The prevalence of reverse triggering (RT) in the early phase of ARDS is unknown. RESEARCH QUESTION: During early ARDS, what is the proportion of patients affected by RT, what are its potential predictors, and what is its association with clinical outcomes? STUDY DESIGN AND METHODS: This was prospective, multicenter, and observational study. Patients who met the Berlin definition of ARDS with less than 72 h of mechanical ventilation and had not been paralyzed with neuromuscular blockers were screened. A 30-min recording of respiratory signals was obtained from the patients as soon as they were enrolled, and the number of breaths with RT were counted. RESULTS: One hundred patients were included. ARDS was mild to moderate in 92% of them. The recordings were obtained after a median of 1 day (interquartile range, 1-2 days) of ventilation. Fifty patients had RT, and most of these events (97%) were not associated with breath stacking. Detecting RT was associated with lower tidal volume (Vt) and less opiate infusion. The presence of RT was not associated with time to discontinuation of mechanical ventilation (subdistribution hazard ratio, 1.03; 95% CI, 0.6-1.77), but it possibly was associated with a reduced hospital mortality (hazard ratio, 0.65; 95% CI, 0.57-0.73). INTERPRETATION: Fifty percent of patients receiving assist-control ventilation for mild or moderate ARDS, sedated and nonparalyzed, demonstrate RT without breath stacking on the first day of mechanical ventilation. RT may be associated with low VTS and opiate doses. TRIAL REGISTRY: ClinicalTrials.gov; No.: NCT02732041; URL: www.clinicaltrials.gov.

High-flow nasal cannula in the treatment of acute hypoxemic respiratory failure in a pregnant patient: case report. / Oxigenoterapia a alto flujo con cánula nasal en el tratamiento de la falla respiratoria aguda hipoxémica en una paciente embarazada: reporte de un caso.

Little evidence exists to support the use of noninvasive mechanical ventilation for acute hypoxemic respiratory failure. However, considering the complications associated with endotracheal intubation, we attempted to implement noninvasive mechanical ventilation in a 24-year-old patient who was 32 weeks pregnant and was admitted to the intensive care unit with acute hypoxemic respiratory failure and sepsis secondary to a urinary tract infection. Lack of tolerance to noninvasive mechanical ventilation led us to use an alternative method to avoid endotracheal intubation. The use of high-flow nasal cannula allowed to overcome this situation, wich supports this technique as a treatment option for critical obstetric patients that is safe for both the mother and fetus.

Existe poca evidencia que avale el uso de ventilación mecánica no invasiva en falla respiratoria aguda hipoxémica. Sin embargo, considerando las complicaciones asociadas a la intubación endotraqueal, se intentó implementar ventilación mecánica no invasiva en una paciente de 24 años cursando 32 semanas de gestación, que ingresó a la unidad de cuidados intensivos con falla respiratoria aguda hipoxémica y sepsis a foco urinario. La falta de tolerancia a la ventilación mecánica no invasiva, nos indujo a utilizar un método alternativo con el fin de evitar la intubación endotraqueal. La implementación de terapia con oxígeno a alto flujo a través de cánula nasal permitió superar la situación, presentando a ésta técnica como una opción de tratamiento en pacientes obstétricas críticas, segura tanto para la madre como para el feto.

Effects of High-Flow Nasal Cannula on End-Expiratory Lung Impedance in Semi-Seated Healthy Subjects.

BACKGROUND: High-flow nasal cannula (HFNC) enables delivery of humidified gas at high flow while controlling the FIO2 . Although its use is growing in patients with acute respiratory failure, little is known about the impact of HFNC on lung volume. Therefore, we aimed to assess lung volume changes in healthy subjects at different flows and positions. METHODS: This was a prospective physiological study performed in 16 healthy subjects. The changes in lung volumes were assessed by measuring end-expiratory lung impedance by using electrical impedance tomography. All the subjects successively breathed during 5 min in these following conditions: while in a supine position without HFNC (T0) and 3 measurements in a semi-seated position at 45° without HFNC (T1), and with HFNC at a flow of 30 L/min (T2), and 50 L/min (T3). RESULTS: Compared with the supine position, the values of end-expiratory lung impedance significantly increased with the subjects in a semi-seated position. End-expiratory lung impedance significantly increased after HFNC initiation in subjects in a semi-seated position and further increased by increasing flow at 50 L/min. When taking the end-expiratory lung impedance measurement in subjects in a semi-seated position (T1) as reference, the differences among the medians of global end-expiratory lung impedance were statistically significant (P < .001), which amounted to 1.05 units in T1; 1.12 units in T2; and 1.44 units in T3 (P < .05 for all comparisons, Wilcoxon test). The breathing frequency did not differ between the supine and semi-seated position (T0 and T1) but significantly decreased after initiation of HFNC and further decreased at high flow. T0 and T1 were not different (P = .13); whereas there was a statistically significant difference among T1, T2, and T3 (P < .05, post hoc test with Bonferroni correction). CONCLUSIONS: In healthy subjects, the semi-seated position and the use of HFNC increased end-expiratory lung impedance globally. These changes were accompanied by a significant decrease in the breathing frequency.

Effect of tracheostomy tube on work of breathing: Comparison of pre- and post-decannulation.

OBJECTIVE: To describe and compare the work of breathing (WOB) during spontaneous breathing under four conditions: (1) breathing through a tracheostomy tube with an inflated cuff, (2) breathing through the upper airway (UA) with a deflated cuff and occluded tube, (3) breathing through the UA with an occluded cuffless tube, and (4) postdecannulation. PATIENTS AND METHODS: Patients who tolerated an occluded cuffless tube were included. Ventilatory variables and esophageal pressure were recorded. The pressure-time product (PTP), PTP/min, and PTP/min/tidal volume (PTP/min/VT) were measured. Each condition was measured for 5 min with a 15 min time interval between evaluations. Quantitative data are expressed as mean ± standard deviation. Single-factor analysis of variance was used, and the Games-Howell test was used for post hoc analysis of comparisons between group means (P ≤ 0.05). RESULTS: Eight patients were studied under each of the four conditions described above. Statistically significant differences were found for PTP, PTP/min, and PTP/min/VT. In the post hoc analysis for PTP, significant differences among all conditions were found. For PTP/min, there was no significant difference between Conditions 2 and 4 (P = 0.138), and for PTP/min/VT, there was no significant difference between Conditions 1 and 2 (P = 0.072) or between Conditions 2 and 3 (P = 0.106). A trend toward a higher PTP, PTP/min, and PTP/min/VT was observed when breathing through a cuffless tracheostomy tube. CONCLUSION: The four conditions differed with respect to WOB. Cuff inflation could result in a reduced WOB because there is less dead space. Cuffless tracheostomy tubes generate increased WOB, perhaps due to the material deformity caused by body temperature.

Oxigenoterapia a alto flujo con cánula nasal en el tratamiento de la falla respiratoria aguda hipoxémica en una paciente embarazada: reporte de un caso / High-flow nasal cannula in the treatment of acute hypoxemic respiratory failure in a pregnant patient: case report

RESUMEN Existe poca evidencia que avale el uso de ventilación mecánica no invasiva en falla respiratoria aguda hipoxémica. Sin embargo, considerando las complicaciones asociadas a la intubación endotraqueal, se intentó implementar ventilación mecánica no invasiva en una paciente de 24 años cursando 32 semanas de gestación, que ingresó a la unidad de cuidados intensivos con falla respiratoria aguda hipoxémica y sepsis a foco urinario. La falta de tolerancia a la ventilación mecánica no invasiva, nos indujo a utilizar un método alternativo con el fin de evitar la intubación endotraqueal. La implementación de terapia con oxígeno a alto flujo a través de cánula nasal permitió superar la situación, presentando a ésta técnica como una opción de tratamiento en pacientes obstétricas críticas, segura tanto para la madre como para el feto.

ABSTRACT Little evidence exists to support the use of noninvasive mechanical ventilation for acute hypoxemic respiratory failure. However, considering the complications associated with endotracheal intubation, we attempted to implement noninvasive mechanical ventilation in a 24-year-old patient who was 32 weeks pregnant and was admitted to the intensive care unit with acute hypoxemic respiratory failure and sepsis secondary to a urinary tract infection. Lack of tolerance to noninvasive mechanical ventilation led us to use an alternative method to avoid endotracheal intubation. The use of high-flow nasal cannula allowed to overcome this situation, wich supports this technique as a treatment option for critical obstetric patients that is safe for both the mother and fetus.

Ventilación mecánica en pacientes con falla respiratoria aguda hipoxémica / Mechanical ventilation in patients with acute hypoxemic respiratory failure

Objetivo: Describir las características clínicas de los pacientes internados en la UCI con requerimiento de VMi con FRAH-No SDRA. Evaluar la asociación de la mortalidad con diferentes variables. Diseño: Cohorte de comienzo. Ámbito: Estudio realizado en 2 UCIs argentinas del ámbito privado de la salud, entre el 01/07/2013 y 31/12/2014. Pacientes: De una muestra consecutiva de 2526 pacientes, se incluyeron a 229 mayores de 18 años, que ingresaron a la UCI con requirimiento de VMi por más de 24hs desarrollando FRAH-No SDRA. Variables de interés principales: Se registraron variables demográficas, estadía en VMi y en UCI, variables de programación inicial del respirador, variables de monitoreo y evolución al alta. También se registraron el número y tipo de complicaciones desarrolladas durante el periodo de VMi Resultados: El 70,7% de los ingresos fue por causa médica. El SAPS II fue de 42. El tiempo de VMi y de estadía en UCI fue mayor en los pacientes con delirio (p < 0,0001 en ambos). En el modelo de regresión logística ajustado por severidad de la hipoxemia, la edad (OR 1,02; IC95% 1,002-1,04: p = 0,033) y el shock (OR 2,37; IC95% 1,12-5: p = 0,023) resultaron predictores independientes de mortalidad. Conclusiones: En este grupo de pacientes que requirieron VMi por más de 24 hs y desarrollaron FRAH-No SDRA se encontró una distribución demográfica similar a la descripta por otros reportes. La mortalidad no se relacionó con la severidad de la hipoxemia, mientras que el shock y la edad fueron predictores independientes de mortalidad.

Mechanical ventilation in patients with acute hypoxemic respiratory failure

Objective: To describe the clinical characteristics of patients with AHRF (without ARDS) hospitalized in the ICU who require IMV. To evaluate the association between mortality and different variables. Design: Inception cohort. Scope: This study was conducted in two Argentine ICUs from the private health sector between 07/01/2013 and 12/31/2014. Patients: From a consecutive sample of 2526 patients, 229 individuals aged 18 and upwards were included in the study; they were admitted to the ICU requiring IMV for over 24 hours and developed AHRF (without ARDS). Primary endpoints: Demographic variables and variables associated with the number of days with IMV and at the ICU were documented, as well as the initial setting of the respirator, monitoring variables and evolution at discharge. Likewise, the number and type of complications developed during the period of IMV were documented. Results: 70.7% of admissions were for medical reasons. SAPS II score was 42. The period of IMV and at the ICU was higher in patients with delirium (p<0.0001 in both). In the logistic regression model adjusted by the severity of hypoxemia, age (OR 1.02; 95% CI 1.002-1.04: p = 0.033) and shock (OR 2.37; 95% CI 1.12-5: p = 0.023) acted as independent predictors of mortality. Conclusions: In this group of patients who required IMV for over 24 hours and who developed AHRF (without ARDS) there was a demographic distribution similar to that described in other reports. Mortality was not associated with the severity of hypoxemia, whereas shock and age were independent predictors of mortality.

[Cross-cultural adaptation and validation of the Dizziness Handicap Inventory: Argentine version]. / Adaptación cultural y validación del Dizziness Handicap Inventory: versión Argentina.

INTRODUCTION AND OBJECTIVES: The Dizziness Handicap Inventory is a useful tool for quantifying self-perceived handicap in patients with vertigo, dizziness or unsteadiness and its impact on daily living activities. The Dizziness Handicap Inventory identifies functional, physical and emotional disorders related to balance disturbance. Our objective was to cross-culturally adapt the Peninsular Spanish version of the Dizziness Handicap Inventory for use in Argentina and validate the adapted Argentinian version. METHODS: We included both healthy subjects and patients with vertigo, dizziness or unsteadiness, aged 18 to 85 years, native Spanish-speaking Argentinians. We introduced linguistic and cultural modifications to the Peninsular Spanish version to obtain the Argentinian one. This version was given twice to 108 patients, 24 to 72 h apart. Internal consistency, test-retest reliability and construct validity were assessed using a visual analogue scale, the Romberg test, the tandem Romberg test and the tandem gait test. RESULTS: We found high internal consistency (α=0.87) and very high test-retest reliability for the total Dizziness Handicap Inventory score (intraclass correlation coefficient: 0.98) and its subscales. The total Dizziness Handicap Inventory and the functional subscale were found to correlate significantly with the Romberg and tandem Romberg tests. The emotional subscale showed a significant correlation with the Romberg test and the eyes-open tandem Romberg test (P<.05) CONCLUSIONS: The Argentinian version of the Dizziness Handicap Inventory proved to be a reliable and valid tool to quantify self-perceived handicap resulting from vertigo, dizziness or unsteadiness.

Factores de riesgo para el fracaso de destete en una población de pacientes con EPOC en ventilación mecánica prolongada / Risk Factors for Weaning Failure in Patients with Chronic Obstructive Pulmonary Disease in Prolonged Mechanical Ventilation

Introducción: Los pacientes con EPOC experimentan episodios de falla respiratoria que requieren de asistencia ventilatoria mecánica (AVM). Debido al compromiso pulmonar, muscular y nutricional, experimentan dificultad en el destete. Hay escasa información de los factores que puedan predecir el fracaso del destete en pacientes con EPOC en VM prolongada (VMP). El objetivo de este trabajo es encontrar factores de riesgo para el fracaso del destete en pacientes con EPOC y evaluar mortalidad según éxito o fracaso en el destete. Materiales y Métodos: El estudio se realizó en un centro de weaning (CW) y se incluyeron pacientes internados en una unidad de terapia intensiva (UTI) por reagudización de su EPOC derivados a nuestro CW traqueostomizados con requerimiento de AVM. Resultados: Se recolectaron los datos de 40 pacientes, de los cuales 21 finalizaron AVM de manera exitosa y 19 fracasaron. El análisis univariado arrojó 4 variables asociadas al fracaso del destete: Pimax (p = 0.035), días de AVM en el CW (p = 0.005), pH (p = 0.039) y la PaCO2 (p = 0.002). Sin embargo, solo la PaCO2 a las 12hs de la prueba de respiración espontánea (PRE) fue predictor de fracaso de destete (p = 0.007). No se encontraron predictores de mortalidad. Conclusión: Encontrar factores de riesgo que permitan identificar el fracaso en la desvinculación de la VM puede contribuir en la decisión de insistir con el destete, o bien, plantear un programa de internación domiciliaria con la finalidad de mejorar la calidad de vida. La única variable asociada al fracaso de destete fue la PaCO2 a las 12hs de comenzada la PRE.

Introduction: Patients suffering from chronic obstructive pulmonary disease (COPD) have an airflow limitation and require mechanical ventilation (MV). Because of deteriorated lung function, respiratory muscles weakness and malnutrition, patients also present difficulties in the weaning process. Information on the factors that can predict weaning failure in patients with COPD after prolonged MV is scarce. To identify risk factors for weaning failure in patients with COPD and evaluate the mortality depending on weaning success or failure. Materials and Methods: This study was carried out at a weaning center in Buenos Aires, Argentina. We evaluated patients admitted to an intensive care unit (ICU) and referred to the weaning center as a result of COPD exacerbation, after tracheostomy and in need of mechanical ventilation. Results: Data from 40 patients were collected; 21 were successfully weaned from MV and 19 failed the weaning process. Univariate analysis showed 4 variables associated with weaning failure: maximum inspiratory pressure (MIP) (p = 0.035), length of MV at weaning center (p = 0.005), pH (p = 0.039) and PaCO2 (p = 0.002). However, only PaCO2 twelve hours after the spontaneous breathing trial (SBT) was a predictor of weaning failure (p=0.007). Mortality predictors were not found. Conclusion: The only predictive variable associated with weaning failure was PaCO2 twelve hours after SBT. Finding risk factors for failure in discontinuing MV may provide information to decide whether to insist in the weaning process or choose home MV to improve life quality.

Decanulación después de la estadía en UCI: Análisis de 181 pacientes traqueotomizados / Decannulation after the ICU Stay. Analysis of 181 Tracheostomized Patients

Objetivo: Encontrar predictores de decanulación en pacientes traqueostomizados y desvinculados de la asistencia ventilatoria mecánica. Analizar la mortalidad en el centro de weaning y supervivencia al alta. Materiales y métodos: Estudio retrospectivo. Se revisaron historias clínicas de pacientes que ingresaron al centro de weaning entre enero de 2004 y junio de 2011. Se estudiaron diferentes variables como posibles predictores de decanulación. Se analizó la mortalidad y se realizó seguimiento al alta. Resultados: Se incluyeron 181 pacientes con una media de 62 años. Se logró decanular al 44.2% de los pacientes (mediana 20 días). El análisis univariado encontró 6 variables asociadas al fracaso de decanulación: sexo masculino, antecedentes respiratorios, antecedentes cardiovasculares, albúmina al ingreso al centro de weaning, días de internación en centro de weaning y días de internación en Unidad de Cuidados Intensivos + centro de weaning. La regresión logística encontró como predictores independientes: sexo masculino y antecedentes respiratorios. En el análisis de regresión logística la decanulación fue un factor protectivo con respecto a la mortalidad. El 80% de los pacientes decanulados y el 15,8% de los no decanulados obtuvieron alta médica. La mediana de supervivencia de los decanulados fue de 45.47 meses y los no decanulados de 10.87. Conclusiones: Los pacientes de sexo masculino y aquellos con antecedentes respiratorios se asocian con fracaso de decanulación. Los pacientes decanulados tienen menor riesgo de muerte durante la internación.

Objective: Find predictors of decannulation in tracheostomized patients and without mechanical ventilation. A secondary objective was the analysis of mortality in the weaning center and survival at discharge. Material and methods: We reviewed, retrospectively, the medical records of patients admitted to the weaning center with tracheostomy and without mechanical ventilation between January 2004 and June 2011. Different variables as possible predictors of decannulation were studied. Mortality at weaning center and outcomes during follow up after discharge were analyzed. Results: We included 181 patients with an average age of 62 years old. Decannulation was carried out in 44.2% of the patients. The decannulation process took 20 days. The univariate analysis found six variables associated with decannulation failure: male gender, respiratory or cardiovascular history, albumin at admission to the weaning center, days of hospitalization in the weaning center and admission to intensive care units plus the weaning center. Logistic regression analysis found that male sex and respiratory history were independent predictors. Regarding mortality during hospitalization, logistic regression analysis found that decannulation was a protective factor. Another finding was that 80% of patients decannulated were discharged; only 15.8% of the group was not decannulated. The average survival was 45.47 months among the decannulated patients and 10.87 months for the non decannulated patients. Conclusions: We found that male sex and a history of respiratory failure were factors associated with unsuccessful decannulation. Decannulated patients had lower risk of death during hospitalization.

Adaptación cultural y validación del Dizziness Handicap Inventory: versión Argentina / Cross-cultural adaptation and validation of the Dizziness Handicap Inventory: Argentine version

Introducción y objetivos: El Dizziness Handicap Inventory es una herramienta útil para cuantificarla autopercepción de la discapacidad en pacientes con vértigo, mareo o inestabilidad y su impacto en actividades de la vida diaria. El Dizziness Handicap Inventory identifica problemas de orden funcional, físico y emocional relacionados con trastornos del equilibrio. Nuestro objetivo es realizar la adaptación cultural y validación del Dizziness Handicap Inventory al castellano argentino a partir de la versión española. Métodos: Se incluyeron personas sanas y pacientes con vértigo, mareo o inestabilidad, de 18 a 85 años, argentinos nativos capaces de comprender castellano. Sobre la versión española se realizaron modificaciones lingüísticas y culturales para obtenerla versión argentina. Esta versión se administró a un grupo de 108 pacientes, 2 veces, en un lapso de 24 a 72 h. Se evaluó consistencia interna, confiabilidad test-retest y validez de constructo a través de: Escala Visual Análoga, Romberg, Romberg en tándem y marcha en tándem. Resultados: Se encontró una alta consistencia interna (Alfa=0,87), y muy alta confiabilidad testretest del Dizziness Handicap Inventory total (coeficiente de correlación intraclase: 0,98) y sus subescalas. Se encontraron correlaciones significativas entre Romberg y el Romberg en tándemcon el Dizziness Handicap Inventory total y la subescala funcional. La subescala emocional mostró una correlación significativa cuando se comparó con Romberg y Romberg en tándem ojos abiertos (p < 0,05).Conclusiones: La versión argentina del Dizziness Handicap Inventory mostró ser una herramienta confiable y válida para cuantificar la autopercepción de la discapacidad debida a vértigo, mareo o inestabilidad(AU)

Introduction and objectives: The Dizziness Handicap Inventory is a useful tool for quantifying self-perceived handicap in patients with vertigo, dizziness or unsteadiness and its impact on daily living activities. The Dizziness Handicap Inventory identifies functional, physical and emotional disorders related to balance disturbance. Our objective was to cross-culturally adapt the Peninsular Spanish version of the Dizziness Handicap Inventory for use in Argentina and validate the adapted Argentinian version. Methods: We included both healthy subjects and patients with vertigo, dizziness or unsteadiness, aged 18 to 85 years, native Spanish-speaking Argentinians. We introduced linguistic and cultural modifications to the Peninsular Spanish version to obtain the Argentinian one. This version was given twice to 108 patients, 24 to 72 h apart. Internal consistency, test-retest reliability and construct validity were assessed using a visual analogue scale, the Romberg test, the tandem Romberg test and the tandem gait test. Results: We found high internal consistency (Alfa=0.87) and very high test-retest reliability for the total Dizziness Handicap Inventory score (intraclass correlation coefficient: 0.98) and its subscales. The total Dizziness Handicap Inventory and the functional subscale were found to correlate significantly with the Romberg and tandem Romberg tests. The emotional subscales howed a significant correlation with the Romberg test and the eyes-open tandem Romberg test(P<.05)Conclusions: The Argentinian version of the Dizziness Handicap Inventory proved to be a reliable and valid tool to quantify self-perceived handicap resulting from vertigo, dizziness or unsteadiness(AU)