Evidence of validity of the Brazilian version of the Cancer Behavior Inventory - Brief Version / Evidencia de validez de la versión brasileña del Cancer Behavior Inventory - Brief Version / Evidências de validade da versão brasileira do Cancer Behavior Inventory - Brief Version

ABSTRACT Objective: To analyze the validity evidence of the Brazilian version of the Cancer Behavior Inventory - Brief Version. Method: Methodological study, conducted between November and December 2021, with 140 patients undergoing hospital cancer treatment in João Pessoa, Paraíba, Brazil. Psychometric analyses were performed in the adapted version, using exploratory factor analysis and correlation with correlated constructs. Results: A two-factor and 10-item model was evidenced. The cumulative variance explained about 61% the shared variance of the items. Satisfactory values were observed for the factors in the analyses of composite reliability (0.89 and 0.91, respectively), internal consistency (0.86 and 0.91, respectively) and ORION (0.89 and 0.85, respectively). The expected correlations of self-efficacy with quality of life (convergent) and with anxiety and depression (divergent) were evident. Conclusion: The Brazilian version of the instrument showed evidence of validity, being considered reliable to assess the self-efficacy of patients undergoing cancer treatment.

RESUMEN Objetivo: Analizar las evidencias de validez de la versión brasileña del Cancer Behavior Inventory - Brief Version. Método: Estudio metodológico, realizado entre noviembre y diciembre de 2021, con 140 pacientes en tratamiento oncológico hospitalario en João Pessoa, Paraíba, Brasil. Se realizaron análisis psicométricos en la versión adaptada, mediante análisis factorial exploratorio y correlación con constructos correlacionados. Resultados: Se evidenció un modelo de 2 factores y 10 ítems. La varianza acumulada explicó alrededor del 61% de la varianza compartida de los ítems. Se observaron valores satisfactorios para los factores en el análisis de confiabilidad compuesta (0,89 y 0,91, respectivamente), consistencia interna (0,86 y 0,91, respectivamente) y ORION (0,89 y 0,85, respectivamente). Se evidenciaron las correlaciones esperadas de la autoeficacia con la calidad de vida (convergente) y con la ansiedad y la depresión (divergente). Conclusión: La versión brasileña del instrumento mostró evidencias de validez, siendo considerado confiable para evaluar la autoeficacia de pacientes en tratamiento oncológico.

RESUMO Objetivo: Analisar as evidências de validade da versão brasileira do Cancer Behavior Inventory - Brief Version. Método: Estudo metodológico, realizado entre os meses de novembro e dezembro de 2021, com 140 pacientes em tratamento oncológico hospitalar em João Pessoa, Paraíba, Brasil. Foram realizadas análises psicométricas na versão adaptada, mediante a análise fatorial exploratória e correlação com constructos correlacionados. Resultados: Evidenciou-se um modelo de 2 fatores e 10 itens. A variância acumulada explicou cerca de 61% da variância compartilhada dos itens. Foram observados valores satisfatórios para os fatores nas análises de confiabilidade composta (0,89 e 0,91, respectivamente), consistência interna (0,86 e 0,91, respectivamente) e ORION (0,89 e 0,85, respectivamente). Evidenciaram-se as correlações esperadas da autoeficácia com a qualidade de vida (convergente) e com a ansiedade e depressão (divergente). Conclusão: A versão brasileira do instrumento mostrou evidências de validade, sendo considerada como confiável para avaliar a autoeficácia dos pacientes em tratamento oncológico.

Instrumento de Avaliação Fonológica: evidências de validade de construto / Phonological Assessment Instrument: evidence of construct validity

RESUMO Objetivo Investigar evidências de validade de construto para um Instrumento de Avaliação Fonológica para o Português Brasileiro, baseadas nos dados de diagnóstico gerados por sua própria aplicação a partir da análise contrastiva e do grau de severidade de fala. Método A amostra foi composta por dados de 176 crianças, com idades entre cinco até nove anos. Foram avaliadas pelo Instrumento de Avaliação Fonológica e classificadas em com transtorno fonológico ou em desenvolvimento fonológico típico, comparando tais resultados aos critérios para o transtorno no DSM-5. A busca por evidências da validade de construto contou com a concordância entre os dois métodos de avaliação, aplicando o Coeficiente Kappa. Para a diferenciação entre os grupos, utilizou-se o teste t de Student para amostras independentes. Buscou-se a investigação dos índices do instrumento pela estatística da Curva de Receiver Operating Characteristic para obter valores de área, ponto de corte, sensibilidade, especificidade, acurácia, valor preditivo positivo e negativo. Resultados O instrumento apresentou concordância e diferenciação significativa entre as classificações. Quanto aos parâmetros de desempenho, exibe ponto de corte para diagnóstico com resultados iguais ou maiores do que 96,17%, excelente valor de área sob a curva, assim como percentuais satisfatórios para as outras análises investigadas. Conclusão O conjunto de dados encontrados indicam evidências para validade de construto do Instrumento de Avaliação Fonológica, apresentando uma contribuição útil e válida ao arsenal de avaliação clínica e de pesquisa envolvendo diagnóstico de Transtorno Fonológico e, com seu resultado de acurácia, contribuiu as propriedades de desempenho dos instrumentos utilizados na Fonoaudiologia.

ABSTRACT Purpose To investigate evidence of construct validity for a Phonological Assessment Instrument for Brazilian Portuguese, based on the diagnostic data generated by its application from contrastive analysis and speech severity. Methods The sample consisted of 176 children, aged between five to nine years old. They were evaluated with the Phonological Assessment Instrument and then classified as having Speech Sound Disorder or in typical phonological development, comparing these results to the criteria described for the disorder in the DSM-5. The search for evidence of construct validity relied on the agreement between the two assessment methods while applying the Kappa Coefficient. To differentiate between groups, Student's t-test was used for independent samples. We sought to investigate the instrument indexes using the Receiver Operating Characteristic Curve statistics to obtain values for area, cut-off point, sensitivity, specificity, accuracy, and positive and negative predictive value. Results The instrument showed agreement and significant differentiation between the classifications. As for the performance parameters, it shows a cut-off point for diagnosis with results equal to or greater than 96.17%, an excellent area under the curve, as well as satisfactory percentages for the other analyses investigated. Conclusion The data indicated evidence for the construct validity of the Phonological Assessment Instrument, presenting a useful and valid contribution to the arsenal of clinical assessment and research involving the diagnosis of Speech Sound Disorder and, with its accuracy result, contributed to the properties of performance of instruments used in Speech, Language and Hearing Sciences.

Instrumento de Avaliação Fonológica: evidências de validade de conteúdo e de processos de resposta / Phonological Assessment Instrument: evidence of content validity and response processes

RESUMO Objetivo evidenciar validade de conteúdo e validade de processos de resposta de um instrumento destinado à avaliação fonológica de crianças. Método validade realizada em duas etapas por dois diferentes grupos de juízes, grupo de especialistas e grupo de não-especialistas. O primeiro grupo composto por três juízes especialistas avaliaram os 123 itens lexicais após a elaboração do instrumento, julgando a aplicabilidade das figuras no contexto da avaliação infantil e sugerindo ajustes para compor o conteúdo. A partir das observações, o instrumento foi adequado e direcionado ao grupo de juízes não-especialistas que, por meio da aplicação do instrumento, tiveram suas respostas avaliadas conforme a facilidade ou dificuldade de elicitação dos itens do instrumento. Resultados As avaliações obtiveram resultados de teor positivo para as validades de conteúdo e de processos de resposta. Conclusão o estudo permitiu aprimorar os itens de teste de forma mais criteriosa, beneficiando o uso clínico e científico.

ABSTRACT Purpose to demonstrate the validity of content and the validity of response processes of an instrument intended for the phonological assessment of children. Methods validation was carried out in two stages by two different groups of judges, a group of specialists and a group of non-specialists. The first group, composed of three expert judges, evaluated the 123 lexical items after creating the instrument, judging the applicability of the figures in the context of child assessment, and suggesting adjustments to compose the content. From the observations, the instrument was adapted and directed to the group of non-specialist judges who, through the application of the instrument, had their responses evaluated according to the ease or difficulty of eliciting the instrument's items. Results The predictions obtained positive results for content validity and response processes. Conclusion the study allowed to improve the test items more judiciously, benefiting clinical and scientific use.

The intra- and inter-rater reproducibility of bone level measurements at strategic mini-implants using dental panoramic radiography

Abstract Objectives: This experimental study focused on the intra- and inter-rater reproducibility of vertical bone level (VBL) measurements at strategic mini-implants (MI) using digital panoramic radiographs (PR). Study design: VBLs of 152 MIs for removable partial denture stabilization at 50 randomly chosen PRs from a clinical trial were digitally evaluated by three ratters. Rater deviations exceeding 0.5 mm were re-examined. The intra-class correlation coefficient (ICC) was applied to estimate reliability. The smallest detectable change (SDC) was interrelated to the minimal clinically important change of 0.2 mm. Results: The first measurement round revealed intra- and inter-rater ICCs of > 0.8. However, 28 sites (9 %) were unreadable, and 97 sites (32 %) revealed differences between observers of ≥ 0.5 mm. Following a consensus session and re-training, an additional 8 sites were excluded and all remaining VBL differences were ≤ 0.5 mm. Thus, the SDCs with 95 % credibility were improved from 0.73 to 0.31 mm in the intra-rater and from 1.52 to 0.34 mm in the interrater statistics. Given a 50 % credibility for this special setting, both the intra- and inter-rater SDCs were 0.11 mm. Conclusions: Digital PR can be reliably utilized to determine VBLs around MIs under conditions of at least two trained observers, mutual calibration sessions, and exclusion of unquantifiable radiographs. German Clinical Trials Register ID:DRKS00007589, www.germanctr.de

Reliability and validity of remote Life Space Assessment: LSA in persons with chronic stroke / Confiabilidade e validade da escala Life Space Assessment aplicada remotamente: LSA em pacientes com AVC crônico

Abstract Background StepWatch Activity Monitor (SAM) is used to measure the mobility of chronic hemiparetic patients and the Life Space Assessment (LSA) scale was developed to assess the displacement of hemiparetic patients in different contexts through self-reporting. Studies that apply the LSA remotely and correlate it with the number of steps measured by the SAM were not found. Objective To evaluate the measurement properties of the LSA applied remotely and to evaluate the correlation between the LSA scale score and the number of steps measured by the SAM in post-stroke chronic hemiparetic patients. Methods Nineteen patients participated in the study. The LSA scale was applied remotely and later, face to face. The SAM measured the steps taken by the participants over a period of three consecutive days. The correlation between the LSA and the SAM was performed using Pearson's correlation. The measurement properties calculated of remote LSA were the intraclass correlation coefficient (ICC), Cronbrach's alpha, standard error of measurement (SEM), and smallest real difference (SRD). Results The reproducibility of the LSA scale between remote and face-to-face applications was considered excellent with ICC = 0.85 (IC 95% 0.62-0.94); SEM = 8.4; SRD = 23.2, and Cronbach's alpha = 0.85. The correlation between SAM and LSA was positive, considered moderate (r = 0.51) and significant (p = 0.025). Conclusion The LSA is a reproducible measure for post-stroke chronic hemiparetic patients even if applied remotely and can be used as a remote measurement for mobility in a real-world environment for people with chronic hemiparesis after stroke.

Resumo Antecedentes O StepWatch Activity Monitor (SAM) é utilizado para medir a mobilidade de pacientes hemiparéticos crônicos e a escala Life Space Assessment (LSA) avalia o deslocamento de pacientes hemiparéticos em diferentes contextos por meio de autorrelato. Não foram encontrados estudos que tenham aplicado a LSA remotamente nem que a correlacionam com o número de passos mensurados pelo SAM. Objetivo Avaliar as propriedades de medida da LSA aplicada remotamente e avaliar a correlação entre o escore da escala LSA e o número de passos mensurados pelo SAM em pacientes com hemiparesia crônica pós-AVC. Métodos Dezenove participantes responderam a LSA remotamente e, posteriormente, presencialmente. O SAM mediu os passos dados pelos participantes durante um período de três dias consecutivos. A correlação entre a LSA e o SAM foi realizada por meio da correlação de Pearson. As propriedades de medida calculadas da LSA aplicada remotamente foram o coeficiente de correlação intraclasse (ICC), alfa de Cronbrach, erro do padrão de medida (SEM) e menor diferença real (SRD). Resultados A reprodutibilidade da escala LSA entre as aplicações remotas e presenciais foi considerada excelente com ICC = 0,85 (IC 95% 0,62-0,94); SEM = 8,4; SRD = 23,2 e alfa de Cronbrach = 0,85. A correlação entre SAM e a LSA foi positiva, considerada moderada (r = 0,51) e significativa (p= 0,025). Conclusão A LSA é uma medida reprodutível para pacientes hemiparéticos crônicos pós-AVC mesmo se aplicada remotamente e pode ser usada como uma medida remota de mobilidade em ambiente real para pessoas com hemiparesia crônica após AVC.

Research progress on dental materials for preventing root caries / 口腔疾病防治

@#The high incidence and untreated rate of root caries, a common and frequently occurring oral disease with challenging treatment in elderly individuals, is the main cause of tooth loss among elderly people, as rapid development results in pulpitis and periapical periodontitis or residual crown and root, which has been regarded as one of the common chronic oral diseases seriously affecting the quality of life of elderly people. Thus, early intervention and prevention are important. Traditional dental materials for preventing root caries have been widely used in clinical practice; however, they have the disadvantages of tooth coloring, remineralization and low sterilization efficiency. A series of new dental materials for preventing root caries have gradually become a research hotspot recently, which have the advantages of promoting the mineralization of deep dental tissue, prolonging the action time and enhancing adhesion. Future caries prevention materials should be designed according to the characteristics of root surface caries and the application population and should be developed toward simplicity, high efficiency and low toxicity. This review describes current research regarding anti-caries prevention material application, serving as a theoretical underpinning for the research of root caries prevention materials, which is important for both promotion in the effective prevention of root caries and improvement in the status of oral health and the quality of life among old people.

Psychometric properties of the Providers Survey in the Brazilian context of mental health: a validation study

ABSTRACT BACKGROUND: Precisely determining the aspects related to an instrument's validity and reliability measures allows for greater assurance of the quality of the results. OBJECTIVES: To analyze the psychometric properties of The Providers Survey in the Brazilian context of mental health services. DESIGN AND SETTING: The instrument validation study was conducted in Montes Claros, Minas Gerais, Brazil. METHODS: The validation study was conducted using the Consensus-based Standards for the Selection of Health Measurement Instruments checklist to analyze its validity and reliability. RESULTS: A committee of expert judges performed content validation after which the Content Validity Index was calculated. Construct validation took place through Exploratory Factor Analysis using the Kaiser-Meyer-Olkin Test criterion and Bartlett's Sphericity Test. Reliability was verified using test-retest reliability. The significance level adopted for the statistical tests was 5% (P < 0.05). The final instrument comprised 54 questions. The Content Validity Index was 97%. Exploratory Factor Analysis identified a Kaiser-Meyer-Olkin index of 0.901 and Bartlett's Sphericity Test with P < 0.001. We obtained a Cronbach's alpha coefficient of 0.95 and an intraclass correlation coefficient of 0.849. CONCLUSIONS: The Providers Survey, translated and adapted into Portuguese, was named the Work Assessment Instrument for the Recovery of Mental Health. It presented adequate psychometric properties for evaluating work-related practices for the recovery of psychosocial care network users.

Efficacy of Roncolab mobile application for diagnosing the primary sign of sleep-disordered breathing (snoring) in children / Eficacia de la aplicación móvil Roncolab para el diagnóstico de signo primario de trastorno respiratorio del sueño (ronquido) en niños

ABSTRACT Sleep-disordered breathing (SDB) is a group of disorders associated with breathing anomalies during sleep. Easily detectable by sound, snoring is one of the most common manifestations and the main sign of SDB. Snoring is characteristic of breathing sound during sleep, without apnea, hypoventilation, or interrupted sleep. It may reduce the percentage of sleep and increase microarousals due to breathing effort or gas exchange. A range of questionnaires have been validated and adapted to the pediatric population to screen for patients who require laboratory testing. The Pediatric Sleep Questionnaire (PSQ) screens for SDB and identifies primary signs such as snoring. RoncoLab is a mobile application that records and measures snoring intensity and frequency Aim To compare the RoncoLab app and the PSQ regarding how efficiently they diagnose snoring Materials and Method This was an observational, analytical study of 31 children aged 7 to 11 years who visited the pediatric dental clinic at Benemérita Universidad Autónoma de Puebla, Mexico (BUAP). The PSQ was applied to diagnose SDB. Guardians were then instructed on how to download and use the mobile application to record data while the child was sleeping at home. Agreement between RoncoLab and the PSQ was analyzed statistically by Cohen's Kappa index at 95% confidence level Results The Kappa index for identification of primary snoring was 0.743 (p<0.05). App sensitivity was 0.92, and specificity 0.82 Conclusion There is good agreement between PSQ and RoncoLab for diagnosing primary snoring, with acceptable sensitivity and specificity.

RESUMEN Los trastornos respiratorios del sueño (TRS) son un grupo de padecimientos asociados con anormalidades respiratorias del sueño. Una de las manifestaciones más comunes es el ronquido; signo fácil de detectar por el ruido que emite y se considera como el signo principal. Este trastorno es característico del ruido respiratorio durante el sueño, sin apneas, hipoventilación, ni interrupciones del sueño. Este puede ocasionar disminución del porcentaje del sueño y aumentar los microdespertares, esto debido al esfuerzo respiratorio o al intercambio de gases. En la actualidad existen cuestionarios validados y adaptados para la población pediátrica útiles como herramienta clínica para el tamizaje y selección de pacientes que requieran pruebas de laboratorio. El Pediatric Sleep Questionnaire (PSQ) permite el cribado de TRS e identificación de signos primarios como el ronquido. RoncoLab es una aplicación móvil que registra y mide la intensidad y frecuencia del ronquido. Objetivo Comparar la eficacia del diagnóstico del ronquido por medio del RoncoLab contrastado con el PSQ Materiales y Método Estudio observacional, analítico, en el cual se incluyeron 31 niños de 7 a 11 años, que acudieron a la clínica de odontopediatría de la Benemérita Universidad Autónoma de Puebla, México (BUAP) Se aplicó el PSQ a los 31 niños para el diagnóstico de TRS, después se le instruyó al tutor como descargar y utilizar la aplicación móvil para registrar los datos obtenidos en las horas de sueño en casa. El análisis estadístico de concordancia entre los instrumentos diagnósticos se realizó con el Índice Kappa de Cohen a un nivel de confianza del 95% Resultados El Índice de Kappa para la identificación de los ronquidos primarios fue de 0.743 (p<0.05). La sensibilidad de la aplicación fue de 0.92, mientras la especificidad fue de 0.82 Conclusión Existe buena concordancia entre el PSQ y el RoncoLab en el diagnóstico de ronquido primario, con sensibilidad y especificidad aceptable.

La reproducibilidad de la alineación dental en medidas digitales y manuales

Introducción: La incorporación de modelos digitales ofrece al ortodoncista una alternativa a los modelos de estudio de yeso que se utilizan habitualmente. Estos son un componente estándar de los registros de ortodoncia y son fundamentales para el diagnóstico y la planificación del tratamiento. No obstante, es importante indagar sobre la confiabilidad de las nuevas tecnologías. Objetivo: Evaluar la reproducibilidad de las medidas digitales y manuales de alineación dental en modelos iniciales de pacientes de ortodoncia. Métodos: Se realizó un estudio de evaluación de tecnología diagnóstica, con 80 modelos de yeso, que fueron digitalizados con el escáner Ineos X5. Una vez obtenidos los modelos en yeso y sus imágenes digitales, el investigador que obtuvo el mejor resultado en la calibración inter e intra examinador realizó la medición de la alineación dental. Las medidas manuales se tomaron con un calibrador digital, y las digitales fueron tomadas en el software Nemocast. El análisis incluyó el cálculo del coeficiente de correlación intraclase (CCI) y los límites de acuerdo de Bland y Altman. Un valor de p < 0,05 fue considerado como estadísticamente significativo. Resultados: Los valores de CCI oscilaron entre 0,643 y 0,874. Más de la mitad de las mediciones obtuvieron valores de CCI superiores a 0,81, lo que se consideró una reproducibilidad "casi perfecta", según la interpretación sugerida por Landis y Koch. Se obtuvo un promedio de las diferencias entre -0,2 a -0,4, con límites de acuerdo estrechos. Conclusiones: Se encontró una reproducibilidad "casi perfecta" y un promedio de las diferencias cercano a cero entre las medidas manuales y digitales.

Introduction: The incorporation of digital models offers the orthodontist an alternative to the plaster study models that are commonly used. These are a standard component of orthodontic records and are critical to diagnosis and treatment planning. It is important to inquire about the reliability of new technologies. Objective: To evaluate the reproducibility of digital and manual measurements of dental alignment in initial models of orthodontic patients. Methods: A diagnostic technology evaluation study was carried out with 80 plaster models that were digitized with the Ineos X5 Scanner. Once the plaster models and digital images of them were obtained, the researcher who obtained the best result in the inter and intra examiner calibration performed the dental alignment measurement. Manual measurements were taken with a digital caliper, and digital ones were taken in the Nemocast software. The analysis included the calculation of the Intraclass Correlation Coefficient (ICC) and the Bland and Altman limits of agreement. A value of p <0.05 was considered statistically significant. Results: ICC values ​​ranged between 0.643 and 0.874, more than half of the measurements obtained ICC values ​​higher than 0.81, which was considered "almost perfect" reproducibility according to the interpretation suggested by Landis and Koch. Differences between -0.2 to -0.4 were averaged with narrow limits of agreement. Conclusions: An "almost perfect" reproducibility was found and an average of the differences close to zero between manual and digital measurements.

Análisis ecocardiográfico de la variabilidad de la presión sistólica arterial pulmonar en la hipertensión pulmonar / Echocardiographic analysis of pulmonary arterial systolic pressure in pulmonary hypertension

Resumen Introducción: La confiabilidad de la presión sistólica arterial pulmonar por ecocardiografía transtorácica se encuentra limitada por su variabilidad para definir la hipertensión pulmonar. Objetivo: Conocer la variabilidad en la presión sistólica arterial pulmonar estimada por ecocardiografía en la hipertensión pulmonar. Métodos: En el periodo 2016-2020 se captaron sujetos con hipertensión pulmonar que tuvieron estimada la presión sistólica de la arteria pulmonar por ecocardiografía transtorácica y por cateterismo cardiaco derecho. Se obtuvieron sus variables demográficas. Los datos se analizaron con el estadístico descriptivo de Bland-Altman y el coeficiente de correlación intraclase (intervalo de confianza al 95%). Resultados: Se estudiaron 152 sujetos, edad 60 ± 12 años. Índice de masa corporal 27.64 ± 4.69 kg/m2. La presión sistólica de la arteria pulmonar por ecocardiografía transtorácica 58.99 ± 18.62 vs. cateterismo cardiaco 55.43 ± 16.79. Diferencia media (sesgo) -3.6 (29.1, -36.2) y coeficiente de correlación intraclase 0.717 (0.610, 0.794). Conclusiones: La variabilidad es amplia y el acuerdo es sustancial con la presión sistólica de la arteria pulmonar. Se aconseja estimarla solo como tamizaje de la hipertensión pulmonar.

Abstract Introduction: The reliability of pulmonary arterial systolic pressure by transthoracic echocardiography is limited by its variability to define pulmonary hypertension. Objective: To know the variability of pulmonary arterial systolic pressure estimated by echocardiography in pulmonary hypertension. Their demographic variables were obtained. Methods: From 2016-2020 subjects with pulmonary hypertension were recruited, with pulmonary artery systolic pressure estimated by transthoracic echocardiography and by right heart catheterization. Data were analyzed using the Bland-Altman descriptive statistic and the intraclass correlation coefficient (95% confidence interval). Results: 152 subjects, age 60 ± 12 years, were studied. Body mass index 27.64 ± 4.69 kg/m2. The pulmonary artery systolic pressure estimated by transthoracic echocardiography 58.99 ± 18.62 vs. cardiac catheterization 55.43 ± 16.79 mmHg. Mean difference (bias) -3.6 (29.1, -36.2) and intraclass correlation coefficient 0.717 (0.610, 0.794). Conclusions: Variability is wide, and agreement is substantial for pulmonary artery systolic pressure. It is recommended to estimate only as screening for pulmonary hypertension.

Perfil de rendimiento de las pertiguistas del equipo nacional cubano

La investigación fue realizada con el objetivo de proponer una variante de perfil de rendimiento o deportograma para el salto con pértiga femenino, a partir del comportamiento de los principales indicadores de rendimiento físico-técnico de esta prueba, para el equipo nacional cubano. Fue realizada una revisión bibliográfica de los principales antecedentes de deportogramas empleados previamente, para el salto con pértiga y los indicadores que los conformaron. Se realizaron mediciones de tipo cuantitativo a 11 indicadores físico-técnicos que fueron correlacionados con el resultado del salto con pértiga en un grupo de estudio integrado por 14 pertiguistas de la selección nacional de Cuba, con un rango de edad entre los 15 y los 32 años (media ± desviación típica: 25,20 ± 3,5). Se utilizaron métodos teóricos como el análisis-síntesis y la inducción-deducción; como métodos empíricos, la revisión de documentos, la entrevista, la medición y, estadístico-matemáticos que facilitaron el proceso investigativo. Los resultados aportaron un nuevo perfil de rendimiento o deportograma para el salto con pértiga femenino con una correlación significativa entre los nuevos indicadores propuestos y el resultado en salto con pértiga.

A pesquisa foi realizada com o objetivo de propor uma variante de perfil de desempenho ou esportograma para o salto com vara feminino, com base no comportamento dos principais indicadores de desempenho físico-técnico desse evento, para a equipe nacional cubana. Foi realizada uma revisão bibliográfica dos principais esportogramas utilizados anteriormente para o salto com vara e dos indicadores que os compunham. Foram realizadas medições quantitativas de 11 indicadores físico-técnicos que foram correlacionados com o resultado do salto com vara em um grupo de estudo formado por 14 saltadores com vara da equipe nacional de Cuba, com uma faixa etária entre 15 e 32 anos (média ± desvio padrão: 25,20 ± 3,5). Foram usados métodos teóricos como análise-síntese e indução-dedução; como métodos empíricos, revisão de documentos, entrevista, medição e métodos estatístico-matemáticos que facilitaram o processo de pesquisa. Os resultados forneceram um novo perfil de desempenho ou esportograma para o salto com vara feminino com uma correlação significativa entre os novos indicadores propostos e o resultado do salto com vara.

The research was carried out with the objective of proposing a variant of performance profile or deportogram for the female pole vault, based on the behavior of the main physical-technical performance indicators of this test, for the Cuban national team. A bibliographic review of the main antecedents of deportograms previously used for pole vaulting and the indicators that comprised them was carried out. Quantitative measurements were made to 11 physical-technical indicators that were correlated with the result of the pole vault in a study group made up of 14 pole vaulters from the Cuban national team, with an age range between 15 and 32 years (mean ± standard deviation: 25.20 ± 3.5). Theoretical methods such as analysis-synthesis and induction-deduction were used; as empirical methods, the review of documents, the interview, the measurement and, statistical-mathematical that facilitated the research process. The results provided a new performance profile or deportogram for the female pole vault with a significant correlation between the new proposed indicators and the pole vault result.

Validación facial, confiabilidad y comprensibilidad del cuestionario principal usado en el estudio PLATINO, Colombia 2021

Introducción: es fundamental garantizar que los instrumentos de medición al ser usados en contextos distintos a los que fueron desarrollados se ajusten en su lenguaje y compresibilidad; el cuestionario principal usado en el estudio PLATINO, en el cual se estableció la prevalencia de enfermedad pulmonar obstructiva crónica en áreas metropolitanas de Latinoamérica por la Asociación Latinoamericana del Tórax, sin incluir población colombiana. Objetivo: realizar validación facial, confiabilidad y comprensibilidad del cuestionario principal usado en el estudio PLATINO para la identificación de personas sin enfermedad respiratoria en Colombia, 2021. Metodología: estudio psicométrico que incluyó validez facial por juicio de expertos, prueba de compresibilidad y confiabilidad; la validación facial valoró la coherencia, relevancia y pertinencia de cada ítem, la aplicación del instrumento se hizo en prueba preliminar de compresibilidad, tras la cual se calculó su confiabilidad. Resultados: la validación facial obtuvo concordancia alta, requiriendo mejoras en redacción del instrumento (Kappa de Fleiss: 0,8569; p=0,000). De los 88 participantes, la mayoría eran hombres (n: 75; 85 %), con edad promedio de 23 años (DS: 6,8), el 25 % con antecedentes de enfermedad pulmonar y el 21 % de tabaquismo. La versión ajustada del cuestionario obtuvo una comprensibilidad global del 94 % y un alfa de Cronbach de 0,82. Conclusiones: se obtiene una versión abreviada y adaptada del cuestionario principal usado en el estudio PLATINO para la identificación de personas sanas respiratorias en población colombiana, con adecuadas propiedades psicométricas en términos de su validación facial, su confiabilidad y su comprensibilidad.

Introduction: It is essential to guarantee that the measurement instruments, when used in contexts other than those in which they were developed, adjust in their language and comprehensibility. The main questionnaire used in the PLATINO study was developed to establish the prevalence of Chronic Obstructive Pulmonary Disease in metropolitan areas of Latin America by the Latin American Thorax Association, without including the Colombian population. Objective: To perform face validity, reliability and comprehensibility of the main questionnaire used in the PLATINO study for the identification of people without respiratory disease in Colombia, 2021. Materials and methods: Psychometric study that included face validity by expert judgment, compressibility and reliability test. The face validity valued the coherence, relevance and pertinence of each item. The application of the instrument was made in a preliminary compressibility test after which its reliability was calculated. Results: Face validity obtained high concordance requiring improvements in the writing of the document (Fleiss Kappa: 0,8569; p=0,000). Ofthe 88 participants, the majority were men (n: 75; 85%) with a mean age of 23 years (SD: 6.8), 25% with a history of lung disease and 21% with a history of smoking. The adjusted version of the questionnaire obtained a global comprehensibility of 94% and a Cronbach's alpha of 0.82. Conclusions: An abbreviated and adapted version of the main questionnaire used in the PLATINO study for the identification of respiratory healthy people in the Colombian population was obtained with adequate psychometric properties in terms of its face validity, reliability and comprehensibility.

Introdução: é fundamental garantir que os instrumentos de medição ao ser usados em contextos diferentes aos que foram desenvolvidos se adequam em sua linguagem e compressibilidade; o questionário principal usado no estudo PLATINO se desenvolveu para estabelecer a prevalência de doença pulmonar obstrutiva crónica em áreas metropolitanas de Latino américa pela Associação Latino-americana do Tórax, sem incluir população colombiana. Objetivo: realizar validação facial, confiabilidade e compreensibilidade do questionário principal usado no estudo PLATINO para a identificação de pessoas sem doença respiratória na Colômbia, 2021. Metodologia: estudo psicométrico que inclui validez facial por juízo de expertos, teste de compressibilidade e confiabilidade; a validação facial valorou a coerência, relevância e pertinência de cada item, a aplicação do instrumento se fez em teste preliminar de compressibilidade, pela qual se calculou sua confiabilidade. Resultados: a validação facial obteve concordância alta, requirindo melhoras em redação do instrumento (Kappa de Fleiss: 0,8569; p=0,000). Dos 88 participantes, a maioria eram homens (n:75; 85 %), com idade média de 23 anos (DS: 6,8), o 25 % com antecedentes de doença pulmonar e o 21 % de tabaquismo. A versão ajustada do questionário obteve uma compreensibilidade global do 94 % e um alfa de Cronbach de 0,82. Conclusões: Obteve-se uma versão abreviada e adaptada do questionário principal usado no estudo PLATINO para a identificação de pessoas sanas sem doenças respiratórias na população colombiana, com adequadas propriedades psicométricas em termos de sua validação facial, sua confiabilidade e sua compreensibilidade.

Formulación de conclusiones de investigación

Este artículo trata sobre la metodología de formulación de las conclusiones de una investigación. De forma inicial, se distingue y descarta que los comentarios, las síntesis de resultados, la reiteración de datos y la descripción de las actividades realizadas no son propiamente conclusiones de una investigación. En segundo lugar, se define lo que constituyen las conclusiones, las condiciones, las actividades de formulación y la estructura que se sigue en su exposición. También se sugieren las actividades de evaluación de la investigación, así como la forma y los aspectos sobre los cuales realizar las recomendaciones respectivas en torno al estudio realizado.

This article deals with the methodology for formulating the conclusions of an investigation. Initially, it is distinguished and ruled out that the comments, the synthesis of results, the reiteration of data and the description of the activities carried out are not properly conclusions of an investigation. Secondly, it defines what constitutes the conclusions, the conditions, the formulation activities and the structure that is followed in their presentation. Research evaluation activities are also suggested, as well as the form and aspects on which to make the respective recommendations regarding the study carried out.

Este artigo trata da metodologia para formular as conclusões de uma investigação. Inicialmente, distingue-se e exclui-se que os comentários, a síntese de resultados, a reiteração de dados e a descrição das atividades realizadas não sejam propriamente conclusões de uma investigação. Em segundo lugar, define o que constituem as conclusões, as condições, as atividades de formulação e a estrutura que se segue na sua apresentação. São também sugeridas actividades de avaliação da investigação, bem como a forma e os aspectos sobre os quais fazer as respectivas recomendações relativamente ao estudo realizado.

Confiabilidade teste-reteste de um protocolo de coleta do sinal eletromiográfico do músculo masseter em indivíduos com disfunção temporomandibular / Test-retest reliability of a protocol for recording the electromyographic signal from the masseter muscle on patients with temporomandibular disorders

Introdução: A eletromiografia (EMG) tem sido utilizada para avaliar alterações no sistema mastigatório proporcionada pela disfunção temporomandibular (DTM). Objetivos: Verificar a confiabilidade teste-reteste de um protocolo de coleta do sinal EMG do músculo masseter em indivíduos com DTM. Métodos: Estudo transversal composto por 20 indivíduos com DTM. Os testes foram realizados em duas sessões com 7 dias de intervalo. O sinal EMG foi avaliado pelas variáveis integral (iEMG) e a raiz quadrada da média do sinal (RMS). Resultados: Na análise intradia a confiabilidade para o RMS (ICC2,k: 0.85 a 0.96 ) e iEMG ICC2,k: 0.85 a 0.95) foi excelente, enquanto que a confiabilidade teste/reteste foi pobre para ambas as variáveis RMS (ICC2,1: 0.03 a 0.29) e iEMG (ICC2,1: 0.08 a 0.39). Conclusões: O protocolo de coleta do sinal EMG do músculo masseter em indivíduos com DTM demonstrou que os dados são reprodutíveis somente na mesma sessão de coletas enquanto que, para coletas em dias alternados a confiabilidade foi pobre.

Introduction: Electromyography (EMG) has been used to assess alterations in the masticatory system caused by temporomandybular disorders (TMD). Objectives: The aim of this study was to verify the test-retest reliability of a protocol for recording the EMG signal from masseter muscle in TMD patients. Methods: This is a cross-sectional study comprising 20 individuals with TMD. Tests were performed in two sessions 7 days apart. The EMG signal was evaluated by the variables integral (iEMG) and the root mean square of the signal (RMS). Results: In the intraday analysis the reliability for the RMS (ICC2,k: 0.85 to 0.96) and iEMG (ICC2,k: 0.85 to 0.95) was excellent, while the test/retest reliability was poor for both RMS (ICC2,1: 0.03 to 0.29) and iEMG (ICC2,1: 0.08 to 0.39) variables. Conclusions: The protocol for collecting the EMG signal from the masseter muscle in an individual with TMD demonstrated that the data are reproducible only in the same recording session, whereas for c recording on alternate days, the reliability was poor.

Reproducibilidad del cuestionario POIBA-¿Cómo nos movemos?, en escolares colombianos de tercer grado de primaria / Reproducibility of the "POiBA-How do we Move?" Questionnaire in Colombian Third-Grade Elementary Schools / Reprodutibilidade do questionário POiBA-(como nos movemos?) em estudantes colombianos da terceira série do ensino fundamental

Introducción: disponer de instrumentos reproducibles que midan la actividad física y los comportamientos sedentarios es una prioridad para la vigilancia y promoción de estilos de vida saludables en niños y niñas. En esta investigación se evaluó la reproducibilidad prueba-reprueba del cuestionario POIBA-¿Cómo nos movemos? en escolares colombianos. Materiales y métodos: participaron 125 estudian- tes de tercer grado de primaria de una institución educativa colombiana. En dos ocasiones se aplicó el cuestionario POIBA-¿Cómo nos movemos?, que evalúa la actividad física realizada para transportarse a la institución educativa y desde esta, durante el tiempo escolar (clases de educación física y recreo), extraescolar (deportiva, con entrenador) y libre. Se emplearon índices kappa y kappa ponderado en los ítems categóricos y el coeficiente de correlación intraclase con modelo de efectos mixtos en los ítems con escala cuantitativa. Resultados: en los ítems sobre actividad física en el ámbito escolar y deportivo predominaron kappas superiores a 0.70. Las preguntas sobre el transporte a la institución educativa y desde esta tuvieron coeficientes kappa cercanos a 0.90. Los ítems de tiempo frente a pantallas alcanzaron coeficientes kappa alrededor de 0.5, y los correspondientes a la hora de acostarse y levantarse obtuvieron coeficientes de correlación intraclase entre 0.40 y 0.72. Conclusiones: el cuestionario POIBA-¿Cómo nos movemos? es una opción para evaluar la actividad física de escolares en el contexto latinoamericano. Los ítems sobre actividad física de transporte, en el ámbito escolar y deportivo, tuvieron los mayores índices de reproducibilidad.

Introduction: Reproducible instruments measuring physical activity and sedentary behaviors are a priority for monitoring and promoting healthy lifestyles for boys and girls. This study evaluated the test-retest reproducibility of the "Prevención de la Obesidad Infantil en Barcelona (Childhood Obesity Prevention in Barcelona) [POIBA]-How do we move?" questionnaire in Colombian school children. Materials and methods: One hundred twenty-five third-grade primary students from a public educational institution in Colombia participated in the "POIBA-How do we move?" questionnaire, which was conducted twice. The survey measured physical activity during travel to and from school, school hours (physical education classes and recess), extracurricular activities (sports with a coach), and leisure time. To assess reproducibility, categorical questions and questions with a quantitative scale were evaluated using kappa and weighted kappa indices and an intraclass correlation coefficient with a mixed-effects model. Results: In the questions about physical activity at school and sports practice, kappas higher than 0.70 predominated. The questions about commuting to and from school had kappa coefficients close to 0.90. The kappa coefficients for the screen-time questions were around 0.5, and the intraclass correlation coefficients for questions about going to bed and getting up were between 0.40 and 0.72. Conclusions: The "POIBA-How do we move?" questionnaire is a valuable tool for evaluating the physical activity of school children in a Latin American context. The questions concerning physical activity during commuting to and from school, school hours, and sports environment had the highest reproducibility indices.

Introdução: dispor de instrumentos reprodutíveis que meçam a atividade física e os comportamentos sedentários é uma prioridade para a monitorização e promoção de estilos de vida saudáveis em meninos e meninas. Nesta pesquisa, a reprodutibilidade teste-reteste do Questionário POIBA ­ (como nos movemos?) foi avaliada em estudantes colombianos. Materiais e métodos: participaram do estudo 125 alunos da terceira série do ensino fundamental de uma instituição educacional colombiana. Foi aplicado o questionário POIBA ­ (como nos movemos?) em dois momentos, que avalia a atividade física realizada para o transporte de e para a instituição de ensino, no horário escolar (aulas de educação física e recreio), extracurricular (esportes, com treinador) e no tempo livre. Para avaliar a reprodutibi- lidade, foram utilizados os índices Kappa e Kappa ponderado para itens categóricos e o coeficiente de correlação intraclasse com modelo de efeitos mistos para itens com escala quantitativa. Resultados: nos itens sobre atividade física no ambiente escolar e esportivo predominaram Kappas superiores a 0.70. As questões sobre transporte de ida e volta para a instituição de ensino apresentaram coeficientes Kappa próximos a 0.90. Os itens tempo de tela atingiram coeficientes Kappa em torno de 0.5, e os correspondentes a hora de dormir e acordar obtiveram coeficientes de correlação intraclasse entre 0.40 e 0.72. Conclusões: o questionário POIBA ­ (como nos movemos?) é uma opção para avaliação da atividade física de estudantes no contexto latino-americano. Os itens sobre atividade física de transporte, no ambiente escolar e esportivo apresentaram os maiores índices de reprodutibilidade

Validation of the Brazilian version of the Hip Sports Activity Scale (HSAS) for patients with femoroacetabular impingement: a cross-sectional study

ABSTRACT BACKGROUND: The Hip Sports Activity Scale (HSAS) is a hip-specific instrument for assessing the present levels of physical activity among patients with femoroacetabular impingement (FAI) syndrome. When evaluating treatment outcomes in patients with FAI syndrome, it is necessary to use joint-specific instruments and ones that can evaluate the levels of physical activity in these patients, such as the HSAS-Brazil. OBJECTIVE: To validate the HSAS-Brazil among a group of physically active patients after arthroscopic treatment of FAI syndrome. DESIGN AND SETTING: Cross-sectional research of quantitative and qualitative types using data obtained from July 2018 to October 2019. METHODS: A total of 58 patients of both genders diagnosed with FAI syndrome and who had undergone hip arthroscopy participated in this research. To establish reliability and validity, patients first answered the Brazilian versions of the 12-Item Short-Form Health Survey (SF-12), Nonarthritic Hip Score (NAHS), and HSAS; after a 48-hour interval, they answered the HSAS-Brazil again. RESULTS: For test-retest reliability, the interclass correlation was 0.908 (P < 0.001). The HSAS-Brazil correlated to the NAHS-Brazil (r = 0.63, P < 0.001), as well as the SF-12 (Physical Health) (r = 0.42, P = 0.001). CONCLUSION: The HSAS-Brazil was validated and proved to be a reliable and valid scale to assess sports activity levels in physically active patients with FAI syndrome after arthroscopic treatment.

Violência contra pessoa idosa: análise da consistência interna de instrumentos* / Abuse against the elderly person: analysis of the internal consistency of instruments* / Violencia contra los ancianos: análisis de la coherencia interna de los instrumentos*

RESUMO: Objetivo: avaliar a consistência interna de instrumentos utilizados no Brasil para mensuração de situações de violência contra pessoa idosa em dois estados. Método: estudo de corte transversal, desenvolvido com 481 idosos, em duas amostras, estados e recorte temporal diferentes. Foram aplicados dois instrumentos de mensuração de violência contra pessoa idosa. Os dados foram analisados, e a consistência interna entre os itens foi medida pelo coeficiente de Alfa de Cronbach. Resultados: o Hwalek-Sengstock Elder Abuse Screening Test apresentou o coeficiente de α = 0,08 para amostra coletada na Paraíba, enquanto, em Pernambuco, foi α = 0,57. A Conflict Tactics Scale apresentou alta precisão para definição da violência com coeficiente de α = 0,81 e α = 0,80 para as duas amostras. Conclusões: apenas a Conflict Tactics Scale apresentou-se confiável e estável para determinação da violência de natureza física e psicológica entre idosos, contribuindo assim, como uma possibilidade de desvelar o fenômeno.

ABSTRACT Objective: to evaluate the internal consistency of instruments used in Brazil to measure situations of violence against the elderly in two states. Method: a cross-sectional study with 481 elderly people in two different samples, states, and time periods. Two instruments were used to measure violence against the elderly person. The data was analyzed and the internal consistency between the items was measured by the Cronbach's alpha coefficient. Results: the Hwalek-Sengstock Elder Abuse Screening Test showed a coefficient of α = 0.08 for the sample collected in Paraíba, while in Pernambuco it was α = 0.57. The Conflict Tactics Scale was highly accurate in defining violence, with a coefficient of α = 0.81 and α = 0.80 for the two samples. Conclusions: only the Conflict Tactics Scale turned out to be reliable and stable for determining physical and psychological violence among the elderly, thus contributing as a way of uncovering the phenomenon.

RESUMEN Objetivo: Evaluar la consistencia interna de instrumentos utilizados en Brasil para medir situaciones de violencia contra ancianos en dos estados. Método: Estudio transversal realizado con 481 ancianos en dos muestras, estados y periodos de tiempo diferentes. Se utilizaron dos instrumentos para medir la violencia contra ancianos. Se analizaron los datos y se midió la consistencia interna entre los ítems mediante el coeficiente alfa de Cronbach. Resultados: el Hwalek-Sengstock Elder Abuse Screening Test presentó un coeficiente de α = 0,08 para la muestra recogida en Paraíba, mientras que en Pernambuco fue de α = 0,57. La Escala de Tácticas de Conflicto fue altamente precisa en la definición de violencia, con coeficientes de α = 0,81 y α = 0,80 para ambas muestras. Conclusiones: sólo la Escala de Tácticas de Conflicto demostró ser fiable y estable para determinar la violencia física y psicológica entre ancianos, contribuyendo así a desvelar el fenómeno.

Implantación coclear en pacientes de edad avanzada: Resultados auditivos

Introducción: El envejecimiento de la población, así como la ampliación en las indicaciones de implantación, hace que cada día haya más pacientes implantados mayores de 65 años, lo que supone un reto a nivel de ajuste y optimización auditiva. Se ha constatado que la implantación coclear en pacientes de edad avanzada generalmente conduce a una mejoría, tanto auditiva como en la neurocognición, la depresión, el aislamiento social, la actividad física y la calidad de vida. Objetivo: Los objetivos de este estudio son valorar las características de los pacientes implantados a partir de 65 años en un centro terciario, analizar los beneficios e identificar particularidades clínicas en este grupo de pacientes. Material y Método: Se llevó a cabo un estudio retrospectivo con un seguimiento de 5 años postcirugía de pacientes con implante MED-EL y se realizó una visita preoperatoria y un seguimiento con audiometría en campo libre y audiometría verbales postquirúrgica al año, 3 años y 5 años postquirúrgico. Resultados: Se incluyó a 16 pacientes implantados unilateralmente. La edad media inicio pérdida fue de 36,75 años. La edad media de cirugía fue de 71,44 años. Los resultados auditivos fueron satisfactorios, con una media de audiometría en campo libre de 44,33 dB al año, 43,33 dB a los 3 años y 41,66 dB a los 5 años. El resultado en las audiometrías verbales (test de bisílabos y test de frases) fue mejor en el grupo de pacientes con adaptación bimodal. Conclusión: En nuestra experiencia, la implantación coclear en ≥65 años sí que logra mejorar las capacidades auditivas medidas, tanto en audiometría de campo libre como en pruebas verbales. La adaptación bimodal mejora los resultados auditivos, a pesar de la dificultad de procesamiento de los dos estímulos diferentes.

Introduction: The aging of the population, as well as the expansion in the indications for implantation means that every day there are more implanted patients over 65 years of age, which represents a challenge in terms of hearing adjustment and optimization. Cochlear implantation in elderly patients has been found to generally lead to improvements in hearing and neurocognition, depression, social isolation, physical activity, and quality of life. Aim: The objectives of this study are to assess the characteristics of patients over 65 years of age implanted in a tertiary center, analyze the benefits and identify clinical particularities in this group of patients. Material and Method: A retrospective study was carried out with a 5-year post-surgery follow-up of patients with a MED-EL implant, and a preoperative visit and follow-up with free-field audiometry and post-surgical speech audiometry were performed at one year, 3 years and 5 years post-surgery. Results: Sixteen unilaterally implanted patients were included. The mean age at onset of loss was 36.75 years. The mean age at surgery was 71.44 years. Hearing results were satisfactory, with a mean free field audiometry of 44.33 dB at one year, 43.33 dB at 3 years, and 41.66 dB at 5 years. The result in the verbal audiometries (disyllable test and sentence test) was better in the group of patients with bimodal adaptation. Conclusión: In our experience, cochlear implantation in patients ≥ 65 years of age does manage to improve hearing capacities measured both in free-field audiometry and in verbal tests. Bimodal adaptation improves auditory results, despite the difficulty ofprocessing the two different stimuli.

Validation and reliability of the Glittre-ADL test to evaluate functional capacity in older adults

INTRODUCTION: The decline in functional capacity (FC) interferes with the functional independence of older adults, so it is important to assess the FC and use appropriate instruments for this. OBJECTIVE: To investigate the Glittre Activities of Daily Living (ADL) test's validity and reliability for assessing functional capacity in older adults. METHODS: Cross-sectional study with a sample of 100 elderly (68 ± 5.16 years). To assess the convergent validity, the Six-Minute Walk Test (6MWT) and the Timed Up and Go Test (TUG) were performed. The intra-examiner test-retest of the Glittre-ADL test was performed on the same day with a 30-minute interval between repetitions and inter-examiner reliability with an interval of seven days. RESULTS: There was a strong correlation between the Glittre-ADL test and the 6MWT (r=-0,75; p<0.001) and the TUG (r=0.77; p<0.001). The intra-examiner and inter-examiner reliability was excellent (ICC)=0.91 and 95% CI=0.14-0.97; p<0.001 and ICC=0.91; 95% CI: 0.86-0.94; p<0.001, respectively). CONCLUSION: The Glittre-ADL test demonstrated that it is valid and that its reliability is adequate to assess functional capacity in older adults.

Calculation of the Minimal Important Clinical Difference of the Lysholm and IKDC Scores After Anterior Cruciate Ligament Reconstruction / Cálculo da mínima diferença clínica importante dos escores Lysholm e IKDC após reconstrução do ligamento cruzado anterior

Abstract Objective To calculate the minimal important clinical difference (MICD) value for the Lysholm and International Knee Documentation Committee (IKDC) scores in a sample of patients submitted to anterior cruciate ligament reconstruction. Methods Primary, observational, retrospective, analytical study of participants submitted to anterior cruciate ligament reconstruction from March 2019 to December 2020 by the same surgeon, with a minimum follow-up of 6 months, analysis of knee function in the pre- and postoperative period by the Lysholm and IKDC scores, and answer to an anchor question at 6 months postoperatively for the calculation of the MICD of each score. Results A total of 59 patients participated in the study, with a mean age of 27.1 ± 5.7 years old. In the comparison between pre- and postoperative scores of all groups, there was an increase in values with statistical significance after intervention. The MICD was 5.5 for the Lysholm score, and the MICD value for the IKDC score could not be determined. Conclusion For the Lysholm score, the calculation of the MICD value by the anchor question method in the sample evaluated was 5.5. It was not possible to determine the value of the MICD for the IKDC score.

Resumo Objetivo Calcular o valor da mínima diferença clinicamente importante (MDCI) para os escores de Lysholm e International Knee Documentation Commitee (IKDC) na amostra de pacientes submetidos a reconstrução de ligamento cruzado anterior. Métodos Estudo primário, observacional, retrospectivo, analítico, de participantes submetidos a reconstrução do ligamento cruzado anterior no período de março de 2019 a dezembro de 2020, pelo mesmo cirurgião, com seguimento mínimo de 6 meses, análise da função do joelho no período pré e pós-operatório pelos escores de Lysholm e IKDC, e resposta a uma pergunta âncora aos 6 meses de seguimento pós-operatório, para o MDCI de cada escore. Resultados Participaram do estudo 59 pacientes, com média de idade de 27,1 ± 5,7 anos. Na comparação dos escores pré- e pós-operatórios de todos os grupos, observa-se aumento dos valores com significância estatística após a intervenção. A MDCI foi de 5,5 para o escore de Lysholm, não tendo sido possível determinar o valor para o IKDC. Conclusão O cálculo do valor da MDCI pelo método da pergunta âncora, na amostra avaliada, foi de 5,5 para o escore de Lysholm. Não foi possível determinar o valor da MDCI para o IKDC.