Does total knee arthroplasty affect pelvic movements? A prospective comparative study

SUMMARY OBJECTIVE: Pathology in any segment of the spine-pelvis-lower extremity may impair the global postural balance, leading to compensatory alterations in other parts. The aim of this study was to compare the pelvic movements of patients suffering from knee osteoarthritis with patients who underwent total knee arthroplasty and healthy controls. METHODS: This study was performed at the Department of Orthopedics and Traumatology Clinic of a Cankiri State Hospital between April 2021 and February 2022. This study included 84 participants. Of them, 31 patients who underwent total knee arthroplasty between 2018 and 2020 years were selected as the total knee arthroplasty group, while 28 patients with knee osteoarthritis were selected as the knee osteoarthritis group. In the control group, there were 25 healthy individuals. Exclusion criteria from the study included any kind of neurological disease, an inability to walk a distance of 100 m unassisted, or a history of surgery to the lower limb. Pelvic movements (i.e., tilt, rotation, and obliquity) and gait parameters (i.e., "gait velocity," "cadence," and "stride length") were assessed using a wireless tri-axial accelerometer. RESULTS: Total knee arthroplasty and control groups had decreased minimum anterior tilt of the pelvis, decreased maximum anterior tilt, and decreased oblique range of the pelvis compared with the knee osteoarthritis group. In comparison with the control group, gait velocity and length of stride during gait were remarkably lower in both knee osteoarthritis and total knee arthroplasty groups. CONCLUSION: In this study, total knee arthroplasty was found to affect pelvic movements. It was thought that total knee arthroplasty changed these variables, probably owing to the frontal and sagittal plane alignment correction through surgery.

ASSESSMENT OF THE USE OF TRANEXAMIC ACID AFTER TOTAL KNEE ARTHROPLASTY.

OBJECTIVE: To evaluate the profile of blood loss and blood transfusions after the introduction of Tranexamic acid (TXA) in a tertiary university hospital in Brazil. METHODS: 173 patients were retrospectively divided into two groups: the ones who received TXA and the control group. Hemoglobin levels (Hb), drain output, transfusion rates, and thromboembolic events were measured. RESULTS: Among the patients included in this study, 82 cases received TXA. Blood transfusion occurred in 3 cases of the TXA group (3.7%), and in 27 control group cases (29.7%; p < 0.001). The average Hb decrease was 2.7 g/dl (± 1.39) and the median drain output was 270 mL in the TXA group. In the control group, the values were 3.41 g/dl (± 1.34; p < 0.001) and 460 mL (p < 0.001), respectively. Thromboembolic events occurred in 2 TXA group cases (2.4%) and in 3 control group cases (3.3%; p > 0.999). CONCLUSION: TXA was effective in reducing blood transfusion rates, Hb decrease, and drain output on the 1st postoperative day without increasing thromboembolic events. Level of evidence III, Retrospective comparative study.

OBJETIVO: Avaliar o perfil de perda sanguínea e hemotransfusões após a introdução da prática do uso de ácido tranexâmico (ATX) em um serviço terciário universitário brasileiro. MÉTODOS: 173 pacientes foram separados retrospectivamente em dois grupos: uso do ATX e controle. Foram analisados valores da hemoglobina (Hb), débito do dreno, necessidade transfusional e complicações tromboembólicas. RESULTADOS: Dentre os pacientes admitidos no estudo, 82 fizeram uso do ATX. Hemotransfusão ocorreu em 3 casos do grupo ATX (3,7%) e em 27 controles (29,7%, p < 0,001). A queda de Hb teve média de 2,7 g/dl (± 1,39) e o débito do dreno, mediana de 270 ml no grupo ATX. No grupo controle, os valores foram de 3,41 g/dl (± 1,34; p < 0.001) e de 460 ml (p < 0.001), respectivamente. Eventos tromboembólicos ocorreram em 2 casos (2,4%) no grupo ATX e em 3 no controle (3,3%, p > 0.999). CONCLUSÃO: o uso do ATX foi efetivo em reduzir hemotransfusões, queda de Hb e débito drenado no 1° dia pós-operatório, sem aumentar eventos tromboembólicos. Nível de evidência III, Estudo retrospectivo comparativo.

Assessment of the use of tranexamic acid after total knee arthroplasty / Avaliação do uso do ácido tranexâmico durante a artroplastia total do joelho

ABSTRACT Objective: To evaluate the profile of blood loss and blood transfusions after the introduction of Tranexamic acid (TXA) in a tertiary university hospital in Brazil. Methods: 173 patients were retrospectively divided into two groups: the ones who received TXA and the control group. Hemoglobin levels (Hb), drain output, transfusion rates, and thromboembolic events were measured. Results: Among the patients included in this study, 82 cases received TXA. Blood transfusion occurred in 3 cases of the TXA group (3.7%), and in 27 control group cases (29.7%; p < 0.001). The average Hb decrease was 2.7 g/dl (± 1.39) and the median drain output was 270 mL in the TXA group. In the control group, the values were 3.41 g/dl (± 1.34; p < 0.001) and 460 mL (p < 0.001), respectively. Thromboembolic events occurred in 2 TXA group cases (2.4%) and in 3 control group cases (3.3%; p > 0.999). Conclusion: TXA was effective in reducing blood transfusion rates, Hb decrease, and drain output on the 1st postoperative day without increasing thromboembolic events. Level of evidence III, Retrospective comparative study.

RESUMO Objetivo: Avaliar o perfil de perda sanguínea e hemotransfusões após a introdução da prática do uso de ácido tranexâmico (ATX) em um serviço terciário universitário brasileiro. Métodos: 173 pacientes foram separados retrospectivamente em dois grupos: uso do ATX e controle. Foram analisados valores da hemoglobina (Hb), débito do dreno, necessidade transfusional e complicações tromboembólicas. Resultados: Dentre os pacientes admitidos no estudo, 82 fizeram uso do ATX. Hemotransfusão ocorreu em 3 casos do grupo ATX (3,7%) e em 27 controles (29,7%, p < 0,001). A queda de Hb teve média de 2,7 g/dl (± 1,39) e o débito do dreno, mediana de 270 ml no grupo ATX. No grupo controle, os valores foram de 3,41 g/dl (± 1,34; p < 0.001) e de 460 ml (p < 0.001), respectivamente. Eventos tromboembólicos ocorreram em 2 casos (2,4%) no grupo ATX e em 3 no controle (3,3%, p > 0.999). Conclusão: o uso do ATX foi efetivo em reduzir hemotransfusões, queda de Hb e débito drenado no 1° dia pós-operatório, sem aumentar eventos tromboembólicos. Nível de evidência III, Estudo retrospectivo comparativo.

Blood level changes in total knee arthroplasty with and without a tourniquet.

OBJECTIVE: To evaluate the difference between the total blood loss in patients undergoing primary total knee arthroplasty with and without the use of tourniquet. METHODS: A retrospective cohort study, with analysis of medical records of patients undergoing primary total knee arthroplasty in 2015, with and without the use of a tourniquet. Comparison was performed of hemoglobin (HB) and hematocrit (HT) variation in the complete blood count (CBC) during the pre- and post-operative period between the two groups. RESULTS: There were 117 patients undergoing primary total knee arthroplasty included, minimum age of 33 and maximum of 86 years, with a mean of 67 years. 64.1% of the surgeries used a tourniquet and 35.9% did not. The mean preoperative HB in Group 1 was 13.08 and 12.97 in Group 2 (p = 0.435). The mean postoperative HB in Group 1 was 11.64 and 10.93 in Group 2 (p = 0.016). The variation of HB in Group 1 was 1.44 and 2.04 in Group 2 (p = 0.025). The mean preoperative HT in Group 1 was 38.96 and 39.01 in Group 2 (p = 0.898). The mean postoperative HT in Group 1 was 34.47 and 32.19 in Group 2 (p = 0.005). The variation of HT in Group 1 was 4.49 and 6.82 in Group 2 (p = 0.001). A total of 21 patients received transfusions RCC (red cell concentrates), as a result of HB below 8 g/dL or clinical symptoms, respectively, representing seven of Group 1 (9.3% of total intra-group) and 14 of Group 2 (33.3% of total intra-group), with p = 0.001. CONCLUSION: In patients undergoing primary total knee arthroplasty using a tourniquet, a lower variance in the hematimetric indices was observed and fewer blood transfusions were necessary.

OBJETIVO: Avaliar a diferença entre a perda sanguínea total em pacientes submetidos à artroplastia total do joelho com e sem o uso de garrote. MÉTODOS: Estudo de coorte retrospectivo, com análise dos prontuários de pacientes submetidos a artroplastia primária total de joelho em 2015, com e sem o uso de garrote. Comparou-se a variação de hemoglobina (HB) e hematócrito (HT) no pré- e pós-operatório entre os dois grupos. RESULTADOS: Foram incluídos 117 pacientes submetidos a artroplastia total de joelho primária, idade mínima de 33 e máxima de 86 anos, com média de 67; em 64,1% das cirurgias, foi usado garrote e em 35,9%, não. No pré-operatório, a média da HB no Grupo 1 foi de 13,08; no Grupo 2, 12,97 (p = 0,435). No pós-operatório, a média da HB no Grupo 1 foi de 11,64; no Grupo 2, 10,93 (p = 0,016). A variação da HB no Grupo 1 foi de 1,44; no Grupo 2, de 2,04 (p = 0,025). No pré-operatório, a média do HT no Grupo 1 foi de 38,96; no Grupo 2, de 39,01 (p = 0898). No pós-operatório, a média do HT no Grupo 1 foi de 34,47; no Grupo 2, de 32,19 (p = 0,005). A variação do HT no Grupo 1 foi de 4,49; no Grupo 2, de 6,82 (p = 0,001). Dos pacientes, 21 receberam transfusão de CH (concentração de hemácias), por HB abaixo de 8 ou sintomas clínicos, sete do Grupo 1 (9,3% do total intragrupo) e 14 do Grupo 2 (33,3% do total intragrupo) com p = 0,001. CONCLUSÃO: Nos pacientes submetidos a artroplastia total de joelho primária com o uso de garrote, ocorreu uma menor variância dos índices hematimétricos e um menor número de transfusões sanguíneas foi necessário.

Blood level changes in total knee arthroplasty with and without a tourniquet / Variação sanguínea nas artroplastias de joelho com e sem o uso de garrote

ABSTRACT OBJECTIVE: To evaluate the difference between the total blood loss in patients undergoing primary total knee arthroplasty with and without the use of tourniquet. METHODS: A retrospective cohort study, with analysis of medical records of patients undergoing primary total knee arthroplasty in 2015, with and without the use of a tourniquet. Comparison was performed of hemoglobin (HB) and hematocrit (HT) variation in the complete blood count (CBC) during the pre- and post-operative period between the two groups. RESULTS: There were 117 patients undergoing primary total knee arthroplasty included, minimum age of 33 and maximum of 86 years, with a mean of 67 years. 64.1% of the surgeries used a tourniquet and 35.9% did not. The mean preoperative HB in Group 1 was 13.08 and 12.97 in Group 2 (p = 0.435). The mean postoperative HB in Group 1 was 11.64 and 10.93 in Group 2 (p = 0.016). The variation of HB in Group 1 was 1.44 and 2.04 in Group 2 (p = 0.025). The mean preoperative HT in Group 1 was 38.96 and 39.01 in Group 2 (p = 0.898). The mean postoperative HT in Group 1 was 34.47 and 32.19 in Group 2 (p = 0.005). The variation of HT in Group 1 was 4.49 and 6.82 in Group 2 (p = 0.001). A total of 21 patients received transfusions RCC (red cell concentrates), as a result of HB below 8 g/dL or clinical symptoms, respectively, representing seven of Group 1 (9.3% of total intra-group) and 14 of Group 2 (33.3% of total intra-group), with p = 0.001. CONCLUSION: In patients undergoing primary total knee arthroplasty using a tourniquet, a lower variance in the hematimetric indices was observed and fewer blood transfusions were necessary.

RESUMO OBJETIVO: Avaliar a diferença entre a perda sanguínea total em pacientes submetidos à artroplastia total do joelho com e sem o uso de garrote. MÉTODOS: Estudo de coorte retrospectivo, com análise dos prontuários de pacientes submetidos a artroplastia primária total de joelho em 2015, com e sem o uso de garrote. Comparou-se a variação de hemoglobina (HB) e hematócrito (HT) no pré- e pós-operatório entre os dois grupos. RESULTADOS: Foram incluídos 117 pacientes submetidos a artroplastia total de joelho primária, idade mínima de 33 e máxima de 86 anos, com média de 67; em 64,1% das cirurgias, foi usado garrote e em 35,9%, não. No pré-operatório, a média da HB no Grupo 1 foi de 13,08; no Grupo 2, 12,97 (p = 0,435). No pós-operatório, a média da HB no Grupo 1 foi de 11,64; no Grupo 2, 10,93 (p = 0,016). A variação da HB no Grupo 1 foi de 1,44; no Grupo 2, de 2,04 (p = 0,025). No pré-operatório, a média do HT no Grupo 1 foi de 38,96; no Grupo 2, de 39,01 (p = 0898). No pós-operatório, a média do HT no Grupo 1 foi de 34,47; no Grupo 2, de 32,19 (p = 0,005). A variação do HT no Grupo 1 foi de 4,49; no Grupo 2, de 6,82 (p = 0,001). Dos pacientes, 21 receberam transfusão de CH (concentração de hemácias), por HB abaixo de 8 ou sintomas clínicos, sete do Grupo 1 (9,3% do total intragrupo) e 14 do Grupo 2 (33,3% do total intragrupo) com p = 0,001. CONCLUSÃO: Nos pacientes submetidos a artroplastia total de joelho primária com o uso de garrote, ocorreu uma menor variância dos índices hematimétricos e um menor número de transfusões sanguíneas foi necessário.