RESUMEN
BACKGROUND: Intraoperative fluids are still poorly studied in veterinary medicine. In humans the dosage is associated with significant differences in postoperative outcomes. OBJECTIVES: The aim of this study is to verify the influence of three different fluid therapy rates in dogs undergoing video-assisted ovariohysterectomy. METHODS: Twenty-four female dogs were distributed into three groups: G5, G10, and G20. Each group was given 5, 10, and 20 mL·kg-1·h-1 of Lactate Ringer, respectively. This study evaluated the following parameters: central venous pressure, arterial blood pressure, heart rate, respiratory rate, temperature, acid-base balance, and serum lactate levels. Additionally, this study evaluated the following urinary variables: urea, creatinine, protein to creatinine ratio, urine output, and urine specific gravity. The dogs were evaluated up to 26 h after the procedure. RESULTS: All animals presented respiratory acidosis during the intraoperative period. The G5 group evidenced intraoperative oliguria (0.80 ± 0.38 mL·kg-1·h-1), differing from the G20 group (2.17 ± 0.52 mL·kg-1·h-1) (p = 0.001). Serum lactate was different between groups during extubation (p = 0.036), with higher values being recorded in the G5 group (2.19 ± 1.65 mmol/L). Animals from the G20 group presented more severe hypothermia at the end of the procedure (35.93 ± 0.61°C) (p = 0.032). Only the members of the G20 group presented mean potassium values below the reference for the species. Anion gap values were lower in the G20 group when compared to the G5 and G10 groups (p = 0.017). CONCLUSIONS: The use of lactated Ringer's solution at the rate of 10 mL·kg-1·h-1 seems to be beneficial in the elective laparoscopic procedures over the 5 or 20 mL·kg-1·h-1 rates of infusion.
Asunto(s)
Perros/cirugía , Fluidoterapia/veterinaria , Histerectomía/veterinaria , Ovariectomía/veterinaria , Lactato de Ringer/uso terapéutico , Cirugía Asistida por Video/veterinaria , Animales , Relación Dosis-Respuesta a Droga , Histerectomía/rehabilitación , Ovariectomía/rehabilitaciónRESUMEN
BACKGROUND AND OBJECTIVES: Modern crystalloid and colloid solutions are balanced solutions which are increasingly used in perioperative period. However, studies investigating their negative effect on whole blood coagulation are missing, and vivid debate is going on about which solution has the minimal coagulopathy effect. The aim of our study was to assess the effect of modern fluid solutions on whole blood coagulation using rotational thromboelastometry. METHODS: Blood samples were obtained from 30 patients during knee arthroscopy before and after administration of 500mL of crystalloid, Hydroxyethyl Starch and gelatin according to the randomization. Rotational thromboelastometry (Extem, Intem and Fibtem tests) was used to assess negative effect of fluid solutions on whole blood coagulation. RESULTS: In Extem test, the initiation phase of fibrin clot formation represented by CT parameter was not influenced by any fluid solution (p>0.05). The speed of clot formation represented by CFT and α angle was impaired by Hydroxyethyl Starch and gelatin but not by crystalloids (p<0.05). The strength of formatted coagulum represented by MCF parameter was impaired both in Extem and Fibtem test by HES and in Fibtem also by crystalloids (p<0.05). Intem test was not negatively influenced by any crystalloid or colloid solution in any parameter (p>0.05). CONCLUSION: Extem test appears to be sensitive to coagulopathy effect of modern colloids and crystalloids. Hydroxyethyl starch has the most obvious negative effect on clot formation followed by gelatin and finally by crystalloids. Intem test seems to be insensitive to adverse effect of modern colloids and crystalloids.
Asunto(s)
Soluciones Cristaloides/administración & dosificación , Gelatina/administración & dosificación , Derivados de Hidroxietil Almidón/administración & dosificación , Tromboelastografía/métodos , Adulto , Artroscopía/métodos , Coagulación Sanguínea/efectos de los fármacos , Pruebas de Coagulación Sanguínea , Coloides/administración & dosificación , Femenino , Humanos , Articulación de la Rodilla/cirugía , Masculino , Persona de Mediana Edad , Sustitutos del Plasma/administración & dosificaciónRESUMEN
Abstract Background and objectives Modern crystalloid and colloid solutions are balanced solutions which are increasingly used in perioperative period. However, studies investigating their negative effect on whole blood coagulation are missing, and vivid debate is going on about which solution has the minimal coagulopathy effect. The aim of our study was to assess the effect of modern fluid solutions on whole blood coagulation using rotational thromboelastometry. Methods Blood samples were obtained from 30 patients during knee arthroscopy before and after administration of 500 mL of crystalloid, Hydroxyethyl Starch and gelatin according to the randomization. Rotational thromboelastometry (Extem, Intem and Fibtem tests) was used to assess negative effect of fluid solutions on whole blood coagulation. Results In Extem test, the initiation phase of fibrin clot formation represented by CT parameter was not influenced by any fluid solution (p > 0.05). The speed of clot formation represented by CFT and α angle was impaired by Hydroxyethyl Starch and gelatin but not by crystalloids (p < 0.05). The strength of formatted coagulum represented by MCF parameter was impaired both in Extem and Fibtem test by HES and in Fibtem also by crystalloids (p < 0.05). Intem test was not negatively influenced by any crystalloid or colloid solution in any parameter (p > 0.05). Conclusion Extem test appears to be sensitive to coagulopathy effect of modern colloids and crystalloids. Hydroxyethyl starch has the most obvious negative effect on clot formation followed by gelatin and finally by crystalloids. Intem test seems to be insensitive to adverse effect of modern colloids and crystalloids.
Resumo Justificativa e objetivos Os cristaloides e coloides modernos são soluções balanceadas e cada vez mais utilizadas no período perioperatório. No entanto, não há estudos que avaliem seu efeito negativo na coagulação do sangue total e o intenso debate sobre a solução que cause um efeito mínimo na coagulopatia permanece. O objetivo de nosso estudo foi avaliar o efeito das soluções líquidas modernas na coagulação do sangue total com o uso da tromboelastometria rotacional. Métodos De acordo com a randomização, amostras de sangue foram colhidas de 30 pacientes durante a artroscopia de joelho, antes e após a administração de 500 mL de cristaloides, hidroxietilamido e gelatina. A tromboelastometria rotacional (testes Extem, Intem e Fibtem) foi utilizada para avaliar o efeito negativo das soluções líquidas na coagulação do sangue total. Resultados No teste Extem, a fase de iniciação da formação de coágulos de fibrina representada pelo parâmetro CT não foi influenciada por qualquer solução líquida (p > 0,05). A velocidade da formação de coágulos representada pelo CFT e pelo ângulo α foi prejudicada pelo hidroxietilamido e pela gelatina, mas não pelos cristaloides (p < 0,05). A força do coágulo formatado representado pelo parâmetro MCF foi prejudicada tanto no teste Extem quanto no teste Fibtem pelo HES e no teste Fibtem também pelos cristaloides (p < 0,05). O teste Intem não foi influenciado negativamente por nenhuma solução cristaloide ou coloide em nenhum parâmetro (p > 0,05). Conclusão O teste Extem parece ser sensível ao efeito de coagulopatia dos coloides e cristaloides modernos. O hidroxietilamido apresentou o efeito negativo mais óbvio na formação do coágulo, seguido pela gelatina e finalmente pelos cristaloides. O teste Intem parece ser insensível ao efeito adverso dos coloides e cristaloides modernos.
Asunto(s)
Humanos , Masculino , Femenino , Adulto , Tromboelastografía/métodos , Soluciones Cristaloides/administración & dosificación , Gelatina/administración & dosificación , Artroscopía/métodos , Coagulación Sanguínea/efectos de los fármacos , Pruebas de Coagulación Sanguínea , Derivados de Hidroxietil Almidón/administración & dosificación , Sustitutos del Plasma/administración & dosificación , Coloides/administración & dosificación , Articulación de la Rodilla/cirugía , Persona de Mediana EdadRESUMEN
Abstract Background and objectives: Hypothermia occurs in about 60% of patients under anesthesia and is generally not managed properly during short lasting surgical procedures. Hypothermia is associated with adverse clinical outcomes. The current study is designed to assess the effects of crystalloid warming on maternal and fetal outcomes in patients undergoing elective cesarean section with spinal anesthesia. Methods: In this prospective randomized controlled trial, sixty parturients scheduled for elective cesarean section with spinal anesthesia were randomly allocated to receive crystalloid at room temperature or warmed at 37 °C. Spinal anesthesia was performed at L3-L4 interspace with 10 mg of hyperbaric bupivacaine without adding opioids. Core temperature, shivering, and hemodynamic parameters were measured every minute until 10th minute and 5-min intervals until the end of operation. The primary outcome was maternal core temperature at the end of cesarean section. Results: There was no difference for baseline tympanic temperature measurements but the difference was significant at the end of the operation (p = 0.004). Core temperature was 36.8 ± 0.5 °C at baseline and decreased to 36.3 ± 0.5 °C for isothermic warmed crystalloid group and baseline tympanic core temperature was 36.9 ± 0.4 °C and decreased to 35.8 ± 0.7 °C for room temperature group at the end of the operation. Shivering was observed in 43.3% in the control group. Hemodynamic parameter changes and demographic data were not significant between groups. Conclusions: Isothermic warming crystalloid prevents the decrease in core temperature during cesarean section with spinal anesthesia in full-term parturients. Fetal Apgar scores at first and fifth minute are higher with isothermic warming.
Resumo Justificativa e objetivos: A hipotermia ocorre em cerca de 60% dos pacientes sob anestesia e geralmente não é tratada adequadamente durante procedimentos cirúrgicos de curta duração. A hipotermia está associada a desfechos clínicos adversos. O presente estudo teve como objetivo avaliar os efeitos do aquecimento de cristaloides nas condições maternas e fetais em pacientes submetidas à cesariana eletiva com raquianestesia. Métodos: Neste estudo prospectivo, randômico e controlado, 60 parturientes agendadas para cesárea eletiva com raquianestesia foram distribuídas aleatoriamente para receber cristaloides à temperatura ambiente ou aquecidos a 37 °C. A raquianestesia foi realizada no interespaço L3-L4 com 10 mg de bupivacaína hiperbárica sem adição de opioides. Temperatura central, tremores e parâmetros hemodinâmicos foram medidos a cada minuto até o décimo minuto e em intervalos de 5 min até o fim da operação. O desfecho primário foi a temperatura central materna ao final da cesárea. Resultados: Não houve diferença nas mensurações basais da temperatura timpânica, mas a diferença foi significativa no fim da operação (p = 0,004). A temperatura central foi de 36,8 ± 0,5 °C na fase basal e diminuiu para 36,3 ± 0,5 °C no grupo com aquecimento isotérmico de cristaloides e a temperatura basal timpânica foi de 36,9 ± 0,4 °C e diminuiu para 35,8 ± 0,7 °C no grupo sem aquecimento das soluções no fim da operação. Tremores foram observados em 43,3% no grupo controle. Alterações nos parâmetros hemodinâmicos e dados demográficos não foram significantes entre os grupos. Conclusões: O aquecimento isotérmico de cristaloides previne a redução da temperatura central durante a cesariana com raquianestesia em parturientes a termo. Os escores de Apgar para os fetos no primeiro e quinto minutos são maiores com o aquecimento isotérmico.
Asunto(s)
Humanos , Femenino , Embarazo , Adolescente , Adulto , Adulto Joven , Temperatura Corporal/efectos de los fármacos , Cesárea , Método Doble Ciego , Feto/efectos de los fármacos , Soluciones Cristaloides/uso terapéutico , Hipotermia/terapia , Anestesia Obstétrica/efectos adversos , Anestesia Raquidea/efectos adversos , Estudios Prospectivos , Soluciones Cristaloides/farmacología , Hipertermia Inducida/métodos , Persona de Mediana EdadRESUMEN
BACKGROUND AND OBJECTIVES: Hypothermia occurs in about 60% of patients under anesthesia and is generally not managed properly during short lasting surgical procedures. Hypothermia is associated with adverse clinical outcomes. The current study is designed to assess the effects of crystalloid warming on maternal and fetal outcomes in patients undergoing elective cesarean section with spinal anesthesia. METHODS: In this prospective randomized controlled trial, sixty parturients scheduled for elective cesarean section with spinal anesthesia were randomly allocated to receive crystalloid at room temperature or warmed at 37°C. Spinal anesthesia was performed at L3-L4 interspace with 10mg of hyperbaric bupivacaine without adding opioids. Core temperature, shivering, and hemodynamic parameters were measured every minute until 10th minute and 5-min intervals until the end of operation. The primary outcome was maternal core temperature at the end of cesarean section. RESULTS: There was no difference for baseline tympanic temperature measurements but the difference was significant at the end of the operation (p=0.004). Core temperature was 36.8±0.5°C at baseline and decreased to 36.3±0.5°C for isothermic warmed crystalloid group and baseline tympanic core temperature was 36.9±0.4°C and decreased to 35.8±0.7°C for room temperature group at the end of the operation. Shivering was observed in 43.3% in the control group. Hemodynamic parameter changes and demographic data were not significant between groups. CONCLUSIONS: Isothermic warming crystalloid prevents the decrease in core temperature during cesarean section with spinal anesthesia in full-term parturients. Fetal Apgar scores at first and fifth minute are higher with isothermic warming.
Asunto(s)
Anestesia Obstétrica , Anestesia Raquidea , Temperatura Corporal/efectos de los fármacos , Cesárea , Soluciones Cristaloides/uso terapéutico , Feto/efectos de los fármacos , Hipertermia Inducida , Hipotermia/terapia , Adolescente , Adulto , Anestesia Obstétrica/efectos adversos , Anestesia Raquidea/efectos adversos , Soluciones Cristaloides/farmacología , Método Doble Ciego , Femenino , Humanos , Hipertermia Inducida/métodos , Hipotermia/etiología , Persona de Mediana Edad , Embarazo , Estudios Prospectivos , Adulto JovenRESUMEN
BACKGROUND: Tetrastarch solution (TS) can impair coagulation but the clinical relevance of this impairment is unclear in veterinary medicine. OBJECTIVE: Compare the effects of volume replacement (VR) with lactated Ringer's solution (LRS) or 6% TS on coagulation in hemorrhaged dogs. ANIMALS: Six healthy English Pointer dogs (19.7-35.3 kg). METHODS: Prospective crossover study. Dogs were anesthetized without hemorrhage and VR (control). Two weeks later, dogs were hemorrhaged under anesthesia on 2 occasions (8-week washout intervals) and randomly received VR with LRS or TS at 3:1 or 1:1 of shed blood, respectively, aiming to decrease the hematocrit to 33%. Rotational thromboelastometry and other coagulation variables were determined before 0.5, 2, and 4 hours after VR during anesthesia and 24 hours after VR (conscious dogs). RESULTS: Buccal mucosal bleeding time did not differ between treatments after VR. Activated partial thromboplastin time increased from controls 4 hours after TS (P = 0.045). Clot formation time (CFT) and alfa-angle increased from controls from 0.5 to 4 hours after LRS (CFT, P ≤ 0.0001-0.02; alpha angle, P = 0.0001-0.02) and from 0.5 to 2 hours after TS (CFT, P = 0.0002-0.01; alpha angle, P = 0.0005-0.02). The maximum clot firmness decreased from controls from 0.5 to 4 hours after LRS (P ≤ 0.0001-0.01) and TS (P ≤ 0.0001-0.04). CONCLUSIONS AND CLINICAL RELEVANCE: Tetrastarch does not impair primary hemostasis and induces transient dilutional coagulopathy that is similar to LRS because, when compared to a 3 times higher volume of LRS in hemorrhaged dogs, it does not cause greater interference on the viscoelastic properties of the coagulum.
Asunto(s)
Coagulación Sanguínea/efectos de los fármacos , Enfermedades de los Perros/tratamiento farmacológico , Hemorragia/veterinaria , Derivados de Hidroxietil Almidón/uso terapéutico , Lactato de Ringer/uso terapéutico , Animales , Estudios Cruzados , Enfermedades de los Perros/sangre , Perros , Femenino , Hematócrito/veterinaria , Hemorragia/sangre , Hemorragia/tratamiento farmacológico , Masculino , Estudios Prospectivos , Distribución Aleatoria , Tromboelastografía/veterinariaRESUMEN
BACKGROUND: Tetrastarch can cause acute kidney injury (AKI) in humans with sepsis, but less likely to result in tissue edema than lactated Ringer's solution (LRS). OBJECTIVES: Compare effects of volume replacement (VR) with LRS and 6% tetrastarch solution (TS) on extravascular lung water (EVLW) and markers of AKI in hemorrhaged dogs. ANIMALS: Six healthy English Pointer dogs (19.7-35.3 kg). METHODS: Prospective crossover study. Animals underwent anesthesia without hemorrhage (Control). Two weeks later, dogs hemorrhaged under anesthesia on 2 occasions (8-week washout intervals) and randomly received VR with LRS or TS at 3 : 1 or 1 : 1 of shed blood, respectively. Anesthesia was maintained until 4 hour after VR for EVLW measurements derived from transpulmonary thermodilution cardiac output. Neutrophil gelatinase-associated lipocalin (NGAL) and creatinine concentrations in plasma and urine were measured until 72 hour after VR. RESULTS: The EVLW index (mL/kg) was lower at 1 hour after TS (10.0 ± 1.9) in comparison with controls (11.9 ± 3.4, P = 0.04), and at 4 hour after TS (9.7 ± 1.9) in comparison with LRS (11.8 ± 2.7, P = 0.03). Arterial oxygen partial pressure-to-inspired oxygen fraction ratio did not differ among treatments from 0.5 to 4 hour after VR. Urine NGAL/creatinine ratio did not differ among treatments and remained below threshold for AKI (120,000 pg/mg). CONCLUSIONS AND CLINICAL IMPORTANCE: Although TS causes less EVLW accumulation than LRS, neither fluid produced evidence of lung edema (impaired oxygenation). Both fluids appear not to cause AKI when used for VR after hemorrhage in healthy nonseptic dogs.
Asunto(s)
Agua Pulmonar Extravascular/efectos de los fármacos , Derivados de Hidroxietil Almidón/farmacología , Soluciones Isotónicas/farmacología , Anestésicos por Inhalación/administración & dosificación , Animales , Gasto Cardíaco/efectos de los fármacos , Creatinina/sangre , Creatinina/orina , Estudios Cruzados , Perros , Femenino , Hemorragia , Derivados de Hidroxietil Almidón/efectos adversos , Isoflurano/administración & dosificación , Soluciones Isotónicas/efectos adversos , Lipocalina 2/sangre , Lipocalina 2/orina , Masculino , Sustitutos del Plasma/efectos adversos , Sustitutos del Plasma/farmacología , Estudios Prospectivos , Lactato de RingerRESUMEN
Sepse, definida pela Síndrome da Resposta Inflamatória Sistêmica (SRIS) secundária a um agente infeccioso, é uma afecção comum em cães e gatos e está relacionada a altos índices de morbidade e mortalidade nestas espécies. Sua patogenia é complexa e multifatorial, mas a instabilidade hemodinâmica tem sido apontada como fator relevante para o alto índice de óbito nos pacientes, pois gera hipóxia e subsequente disfunção de múltiplos órgãos. O tratamento é baseado na terapia guiada por metas e tem como objetivo restaurar o equilíbrio circulatório pela infusão de grandes quantidades de fluido, sendo que a escolha da fluidoterapia adequada é ainda muito controversa. Assim, esta revisão descreve a fisiopatogenia da sepse e compara resultados do uso de coloides e cristaloides apresentados nos periódicos consultados.
Defined by the Systemic Inflammatory Response Syndrome (SIRS), which is secondary to an infectious agent, sepsis is a common affection in dogs and cats, being related to high morbidity and mortality rates in these species. The pathogenesis is multifactorial and complex. Hemodynamic instability is being identified as a key factor for the high mortality rate, since it causes hypoxia and subsequent multiple organ dysfunction. The treatment consists of goal-oriented therapy and the primary objective is to restore the circulatory balance through the infusion of large amounts of fluid. However, choosing the adequate fluid therapy is still very controversial. Thus, the objective of this review is to describe the pathophysiology of sepsis and to compare the results of the use of the colloids and crystalloids presented in the scientific articles analyzed.
Asunto(s)
Animales , Coloides , Cristales Líquidos , Sepsis/fisiopatología , Sepsis/terapia , Sepsis/veterinaria , Choque Séptico/terapia , Choque Séptico/veterinaria , Soluciones Farmacéuticas/uso terapéuticoRESUMEN
Sepse, definida pela Síndrome da Resposta Inflamatória Sistêmica (SRIS) secundária a um agente infeccioso, é uma afecção comum em cães e gatos e está relacionada a altos índices de morbidade e mortalidade nestas espécies. Sua patogenia é complexa e multifatorial, mas a instabilidade hemodinâmica tem sido apontada como fator relevante para o alto índice de óbito nos pacientes, pois gera hipóxia e subsequente disfunção de múltiplos órgãos. O tratamento é baseado na terapia guiada por metas e tem como objetivo restaurar o equilíbrio circulatório pela infusão de grandes quantidades de fluido, sendo que a escolha da fluidoterapia adequada é ainda muito controversa. Assim, esta revisão descreve a fisiopatogenia da sepse e compara resultados do uso de coloides e cristaloides apresentados nos periódicos consultados.(AU)
Defined by the Systemic Inflammatory Response Syndrome (SIRS), which is secondary to an infectious agent, sepsis is a common affection in dogs and cats, being related to high morbidity and mortality rates in these species. The pathogenesis is multifactorial and complex. Hemodynamic instability is being identified as a key factor for the high mortality rate, since it causes hypoxia and subsequent multiple organ dysfunction. The treatment consists of goal-oriented therapy and the primary objective is to restore the circulatory balance through the infusion of large amounts of fluid. However, choosing the adequate fluid therapy is still very controversial. Thus, the objective of this review is to describe the pathophysiology of sepsis and to compare the results of the use of the colloids and crystalloids presented in the scientific articles analyzed.(AU)
Asunto(s)
Animales , Sepsis/fisiopatología , Sepsis/terapia , Sepsis/veterinaria , Cristales Líquidos , Coloides , Choque Séptico/terapia , Choque Séptico/veterinaria , Soluciones Farmacéuticas/uso terapéuticoRESUMEN
Resumen OBJETIVO Evaluar cómo se atendieron las pacientes con hemorragia obstétrica, qué recursos se utilizaron y los costos directos relacionados con el tratamiento de pacientes con placenta previa, con o sin placenta acreta, en quienes se indicó Floseal® como parte de las medidas de control e inhibición de la hemorragia en comparación con quienes solo recibieron los cuidados convencionales. MATERIALES Y MÉTODOS Estudio retrospectivo, observacional y comparativo de los expedientes clínicos de pacientes adultas con más de 20 semanas de gestación y placenta previa tratadas entre septiembre y noviembre del 2012 en la Unidad Médica de Alta Especialidad 23 en Monterrey, México. Los resultados clínicos y costos se compararon con pruebas paramétricas y no paramétricas. RESULTADOS Se analizaron 29 expedientes (15: Floseal® coadyuvante, 14: solo con tratamiento convencional). El grupo tratado con Floseal® tuvo menos reintervenciones (0 vs 57.1%, p 0.0010), días de estancia hospitalaria [2(2-4) vs 6(4-11), p 0.0048] y cuidados intensivos (2.4 ± 1.5 vs 4.5 ± 2.1, p 0.0048). El costo promedio por remuestreo fue de 109,172.00 pesos mexicanos (IC95%: 80,153.10-139,073.71 pesos) para Floseal® vs 224,289.00 pesos mexicanos (IC95%: 181,881.48-269,061.23 pesos) para el tratamiento convencional a expensas de un número de piezas mayor de Tisseel®, crioprecipitados, cristaloides y retiro quirúrgico de compresas. CONCLUSIONES El uso coadyuvante de Floseal® se asoció con menor número de reintervenciones, días de estancia hospitalaria y atención en cuidados intensivos. Se registraron menores costos promedio y total asociados con la atención. Para corroborar estos resultados en población mexicana se requieren análisis de largo seguimiento y con muestras más grandes.
Abstract OBJECTIVE To evaluate the clinical outcomes and direct costs related to treatment of placenta previa with Floseal® hemostatic matrix as part of the treatment of obstetric hemorrhage in comparison with conventional management only. METHODS Clinical records of patients with hemorrhagic hemorrhage, with more than 20 weeks of pregnancy and placenta previa were reviewed, all patients were adults and treated within September and November of 2012 in the "Unidad Médica de Alta Especialidad 23" of the Mexican Institute of Social Security, Monterrey, México. Costs where estimated using the Diario Oficial de la Federación 2013) and a resampling was performed. Clinical and costs outcomes where compared with parametric and non-parametric tests. RESULTS 29 clinical records (15: Adjuvant Floseal®, 14: conventional treatment only). Floseal® group resulted in less re-interventions (0% vs 57.1%, p 0.0010), days of hospital stay [2(2-4) vs 6(4-11), p 0.0048] and days in the intensive care unit (2.4 ± 1.5 vs 4.5 ± 2.1, p 0.0048). Average cost by resampling was $109,172.00 [CI95% (80,153.10-139,073.71 mexican pesos)] for Floseal® vs 224,289.00 mexican pesos [IC95% (181,881.48-269,061.23)] for conventional treatment at the expense greater number of pieces of Tisseel®, cryoprecipitate, crystalloids and surgical removal of compresses. CONCLUSIONS The adjuvant use of Floseal® was associated with fewer re-interventions, days of hospital stay and intensive care. Lower average and total costs associated with treatment were also estimated. Future long-term analyzes and larger sample sizes are necessary to corroborate these results in the Mexican population.
RESUMEN
OBJECTIVE: To test the hypothesis that resuscitation with balanced fluids (lactated Ringer [LR]) is associated with improved outcomes compared with normal saline (NS) in pediatric sepsis. STUDY DESIGN: We performed matched analyses using data from 12 529 patients <18 years of age with severe sepsis/septic shock at 382 US hospitals between 2000 and 2013 to compare outcomes with vs without LR as part of initial resuscitation. Patients receiving LR were matched 1:1 to patients receiving only NS (NS group), including separate matches for any (LR-any group) or exclusive (LR-only group) LR use. Outcomes included 30-day hospital mortality, acute kidney injury, new dialysis, and length of stay. RESULTS: The LR-any group was older, received larger crystalloid volumes, and was less likely to have malignancies than the NS group. After matching, mortality was not different between LR-any (7.2%) and NS (7.9%) groups (risk ratio 0.99, 95% CI 0.98, 1.01; P = .20). There were no differences in secondary outcomes except longer hospital length of stay in LR-any group (absolute difference 2.4, 95% CI 1.4, 5.0 days; P < .001). Although LR was preferentially used as adjunctive fluid with large-volume resuscitation or first-line fluid in patients with lower illness severity, outcomes were not different after matching stratified by volume and proportionate LR utilization, including for patients in the LR-only group. CONCLUSIONS: Balanced fluid resuscitation with LR was not associated with improved outcomes compared with NS in pediatric sepsis. Although the current practice of NS resuscitation is justified, selective LR use necessitates a prospective trial to definitively determine comparative effectiveness among crystalloids.
Asunto(s)
Mortalidad Hospitalaria/tendencias , Soluciones Isotónicas/administración & dosificación , Resucitación/métodos , Sepsis/mortalidad , Sepsis/terapia , Adolescente , Factores de Edad , Estudios de Casos y Controles , Causas de Muerte , Niño , Preescolar , Estudios de Cohortes , Soluciones Cristaloides , Bases de Datos Factuales , Femenino , Fluidoterapia/métodos , Fluidoterapia/mortalidad , Humanos , Lactante , Unidades de Cuidado Intensivo Pediátrico , Masculino , Pronóstico , Resucitación/mortalidad , Estudios Retrospectivos , Lactato de Ringer , Medición de Riesgo , Sepsis/diagnóstico , Factores Sexuales , Choque Séptico/diagnóstico , Choque Séptico/mortalidad , Choque Séptico/terapia , Cloruro de Sodio/administración & dosificación , Análisis de SupervivenciaRESUMEN
A hipotensão arterial é intercorrência frequente na rotina clínica e cirúrgica de pequenos animais, provocando graves consequências, como injúria renal aguda ou mesmo disfunção de múltiplos órgãos. Entender a fisiopatologia e conhecer as opções diagnósticas e terapêuticas dessa intercorrência são condições fundamentais para uma correta abordagem nesses casos. O objetivo deste estudo foi revisar a fisiopatologia da hipotensão arterial, mas principalmente descrever os principais métodos de diagnóstico e as recentes diretrizes de seu tratamento. A atual terapia guiada por metas direciona o profissional para o entendimento da necessidade de uma ação terapêutica precoce a partir do diagnóstico da hipotensão. Dessa forma, por meio de um rápido restabelecimento da pressão arterial, espera-se reduzir ou mesmo prevenir sequelas dessa síndrome clínica potencialmente fatal.
Hypotension is an usual event in small animals clinics, which can impact severely the clinical outcome of patients by causing acute kidney injury or multiple organ failure. It is fundamental to understand the physiopathology of this condition and to know the main diagnosis and therapeutic options to deal correctly with such cases. Therefore, the aim of this study was to briefly review the physiopathology of hypotension and to describe the main diagnostic methods, as well as the most recent treatment guidelines. The current goal-based therapy helps the professional to understand the need for an early therapeutic action as soon hypotension is diagnosed. Thus, one expects to decrease or even prevent major sequelae through a rapid return to normal blood pressure in this potentially fatal clinical syndrome.
La hipotensión es una complicación frecuente en la clínica y cirugía de pequeños animales que tiene consecuencias graves como la insuficiencia renal aguda o la falia de múltiples órganos. La comprensión de la fisiopatología y el reconocimiento de las opciones diagnósticas y terapêuticas de esta complicación son fundamentales para el correcto manejo de estos casos. EI objetivo de este trabajo fue revisar la literatura relacionada con la fisiopatología de la hipotensión arterial, describiendo, principalmente, los métodos más importantes para su diagnóstico, y las directrices recientes en cuanto al tratamiento. La terapêutica actual a través de metas guía al profesional en la comprensión de la necesidad de una acción terapêutica precoz a partir dei diagnóstico de la hipotensión. De esa forma, a través de uma recuperación rápida de la presión arterial, se espera reducir o prevenir las posibles secuelas de este síndrome clínico potencialmente fatal.
Asunto(s)
Animales , Gatos , Perros , Hipotensión/diagnóstico , Hipotensión/terapia , Hipotensión/veterinaria , Choque/veterinaria , Hipovolemia/veterinariaRESUMEN
A hipotensão arterial é intercorrência frequente na rotina clínica e cirúrgica de pequenos animais, provocando graves consequências, como injúria renal aguda ou mesmo disfunção de múltiplos órgãos. Entender a fisiopatologia e conhecer as opções diagnósticas e terapêuticas dessa intercorrência são condições fundamentais para uma correta abordagem nesses casos. O objetivo deste estudo foi revisar a fisiopatologia da hipotensão arterial, mas principalmente descrever os principais métodos de diagnóstico e as recentes diretrizes de seu tratamento. A atual terapia guiada por metas direciona o profissional para o entendimento da necessidade de uma ação terapêutica precoce a partir do diagnóstico da hipotensão. Dessa forma, por meio de um rápido restabelecimento da pressão arterial, espera-se reduzir ou mesmo prevenir sequelas dessa síndrome clínica potencialmente fatal.(AU)
Hypotension is an usual event in small animals clinics, which can impact severely the clinical outcome of patients by causing acute kidney injury or multiple organ failure. It is fundamental to understand the physiopathology of this condition and to know the main diagnosis and therapeutic options to deal correctly with such cases. Therefore, the aim of this study was to briefly review the physiopathology of hypotension and to describe the main diagnostic methods, as well as the most recent treatment guidelines. The current goal-based therapy helps the professional to understand the need for an early therapeutic action as soon hypotension is diagnosed. Thus, one expects to decrease or even prevent major sequelae through a rapid return to normal blood pressure in this potentially fatal clinical syndrome.(AU)
La hipotensión es una complicación frecuente en la clínica y cirugía de pequeños animales que tiene consecuencias graves como la insuficiencia renal aguda o la falia de múltiples órganos. La comprensión de la fisiopatología y el reconocimiento de las opciones diagnósticas y terapêuticas de esta complicación son fundamentales para el correcto manejo de estos casos. EI objetivo de este trabajo fue revisar la literatura relacionada con la fisiopatología de la hipotensión arterial, describiendo, principalmente, los métodos más importantes para su diagnóstico, y las directrices recientes en cuanto al tratamiento. La terapêutica actual a través de metas guía al profesional en la comprensión de la necesidad de una acción terapêutica precoz a partir dei diagnóstico de la hipotensión. De esa forma, a través de uma recuperación rápida de la presión arterial, se espera reducir o prevenir las posibles secuelas de este síndrome clínico potencialmente fatal.(AU)
Asunto(s)
Animales , Gatos , Perros , Hipotensión/veterinaria , Hipotensión/diagnóstico , Hipotensión/terapia , Choque/veterinaria , Hipovolemia/veterinariaRESUMEN
The measurement of serum parameters during general anesthesia procedures are subject to variations due to differences in protocol, splenic storage, and by the instituted fluid therapy. The aim of this study was to assess the hematocrit changes promoted by controlled fluid therapy and general anesthesia. Six mongrel female dogs underwent an anesthetic protocol with acepromazine (0.03 mg kg-1) and tramadol (5 mg kg-1) for premedication, induction with propofol (3 mg kg-1), and maintained with isoflurane and mechanical ventilation for 120 minutes. After induction, they were infused with 10 ml kg hr-1 of Ringers lactate solution. Hematocrit measurements were performed from the start until 72 hours from anesthesia and evaluated statistically to check if there were significant changes over time. The fluid therapy, the acepromazine and propofol in the anesthetic protocol promotes a significant reduction of hematocrit up to four hours after general anesthesia.(AU)
A mensuração de parâmetros séricos durante procedimentos dependentes de anestesia geral são passíveis de variações devido a diferenças do protocolo utilizado, armazenamento esplênico e também da fluidoterapia instituída. O objetivo deste trabalho foi avaliar o hematócrito buscando evidenciar as alterações flutuantes promovidas por fluidoterapia controlada e anestesia geral em cães submetidos a ovariohisterectomia laparoscópica. Seis cadelas sem raça definida foram submetidas a um protocolo anestésico com acepromazina (0,03 mg kg-1) e tramadol (5,0 mg kg-1) como medicação pré-anestésica, indução com propofol (3,0 mg kg-1) e mantidas com isoflurano e ventilação mecânica durante 120 minutos. Após a indução, receberam a infusão de 10,0 ml kg hr-1 de solução Ringer com lactato. Foram realizadas aferições de hematócrito do início (ou antes?) até 72 horas após a anestesia, sendo avaliadas estatisticamente para verificar se houve alterações relevantes durante os tempos. A fluidoterapia e o uso de acepromazina e propofol no protocolo anestésico para esta técnica cirúrgica promoveram uma redução de hematócrito significativa até quatro horas após a anestesia geral.(AU)
Asunto(s)
Animales , Perros , Enfermedades de los Perros , Lactato de Ringer/administración & dosificación , Anestesia General/veterinaria , Hematócrito/veterinariaRESUMEN
Several clinical trials on Goal directed fluid therapy (GDFT) were carried out, many of those using colloids in order to optimize the preload. After the decision of European Medicines Agency, there is such controversy regarding its use, benefits, and possible contribution to renal failure. The objective of this systematic review and meta-analysis is to compare the use of last-generation colloids, derived from corn, with crystalloids in GDFT to determine associated complications and mortality. A bibliographic research was carried out in MEDLINE PubMed, EMBASE and Cochrane Library, corroborating randomized clinical trials where crystalloids are compared to colloids in GDFT for major non-cardiac surgery in adults. One hundred thirty references were found and among those 38 were selected and 29 analyzed; of these, six were included for systematic review and meta-analysis, including 390 patients. It was observed that the use of colloids is not associated with the increase of complications, but rather with a tendency to a higher mortality (RR [95% CI] 3.87 [1.121-13.38]; Because of the limitations of this meta-analysis due to the small number of randomized clinical trials and patients included, the results should be taken cautiously, and the performance of new randomized clinical trials is proposed, with enough statistical power, comparing balanced and unbalanced colloids to balanced and unbalanced crystalloids, following the protocols of GDFT, considering current guidelines and suggestions made by groups of experts.
Foram feitos múltiplos ensaios clínicos em fluidoterapia guiada por objetivos (FGO), muitos deles com o uso de coloides para aprimoramento da pré-carga. Após a decisão da Agência Europeia de Medicamentos, existe ainda controvérsia sobre seu uso, seus benefícios e sua possível contribuição para a falência renal. O objetivo desta revisão sistemática e metanálise é comparar o uso de coloides de última geração, derivados de milho, com cristaloides em FGO para determinar as complicações e a mortalidade associadas. Busca bibliográfica em Medline, Pubmed, Embase e Biblioteca Cochrane de ensaios clínicos aleatórios nos quais se comparam cristaloides com coloides dentro de FGO para cirurgia não cardíaca de grande porte em adultos. Foram obtidas 130 referências das quais se selecionaram 38 e 29 foram analisadas; dessas, seis foram incluídas para revisão sistemática e metanálise, incluindo 390 pacientes. Observou-se que o uso de coloides não está associado a um aumento de complicações, mas sim a uma tendência a maior mortalidade (RR [IC 95%] 3,87 [1,121-13,38]; I2 = 0,0%; p = 0,635). Devido às limitações desta metanálise em decorrência do número escasso de ensaios clínicos aleatórios e pacientes incluídos, os resultados devem ser usados com cautela e propõe-se a feitura de novos ensaios clínicos aleatórios, com potência estatística suficiente naqueles em que se comparam coloides balanceados e não balanceados com cristaloides balanceados e não balanceados, dentro de protocolos de FGO, que respeitem as indicações atuais e as sugestões emitidas pelos grupos de especialistas.
Se han realizado múltiples ensayos clínicos en fluidoterapia guiada por objetivos (FGO), muchos de ellos con el uso de coloides para la optimización de la precarga. Tras la decisión de la Agencia Europea del Medicamento, existe cierta controversia en cuanto a su utilización, beneficios y su posible contribución al fallo renal. El objetivo de esta revisión sistemática y metaanálisis es comparar el uso de coloides de última generación, derivados del maíz, con cristaloides en FGO para determinar las complicaciones y la mortalidad asociadas. Se realiza una búsqueda bibliográfica en MEDLINE Pubmed, EMBASE y Cochrane Library comprobando ensayos clínicos aleatorizados en los que se comparan cristaloides con coloides dentro de FGO para cirugía mayor no cardíaca de adultos. Se obtuvieron 130 referencias de las que se seleccionaron 38 y 29 fueron analizadas; de ellas 6 fueron incluidas para revisión sistemática y metaanálisis, incluyendo a 390 pacientes. Se apreció que el uso de coloides no se asocia con un aumento de complicaciones pero sí con una tendencia a mayor mortalidad (RR [IC 95%] 3,87 [1,121-13,38]; I2 = 0,0%; p = 0,635). Debido a las limitaciones de este metaanálisis por el escaso número de ensayos clínicos aleatorizados y pacientes incluidos, los resultados deben tomarse con cautela, y se propone la realización de nuevos ensayos clínicos aleatorizados, con suficiente potencia estadística en los que se comparen coloides balanceados y no balanceados con cristaloides balanceados y no balanceados, dentro de protocolos de FGO, respetando las indicaciones actuales y las sugerencias emitidas por los grupos de expertos.
Asunto(s)
Humanos , Adulto , Coloides/administración & dosificación , Fluidoterapia/métodos , Soluciones Isotónicas/administración & dosificación , Procedimientos Quirúrgicos Operativos/métodos , Ensayos Clínicos Controlados Aleatorios como Asunto , Coloides/efectos adversos , Fluidoterapia/efectos adversos , Soluciones Cristaloides , Soluciones Isotónicas/efectos adversosRESUMEN
INTRODUCTION: Several clinical trials on Goal directed fluid therapy (GDFT) were carried out, many of those using colloids in order to optimize the preload. After the decision of European Medicines Agency, there is such controversy regarding its use, benefits, and possible contribution to renal failure. The objective of this systematic review and meta-analysis is to compare the use of last-generation colloids, derived from corn, with crystalloids in GDFT to determine associated complications and mortality. METHODS: A bibliographic research was carried out in MEDLINE PubMed, EMBASE and Cochrane Library, corroborating randomized clinical trials where crystalloids are compared to colloids in GDFT for major non-cardiac surgery in adults. RESULTS: One hundred thirty references were found and among those 38 were selected and 29 analyzed; of these, six were included for systematic review and meta-analysis, including 390 patients. It was observed that the use of colloids is not associated with the increase of complications, but rather with a tendency to a higher mortality (RR [95% CI] 3.87 [1.121-13.38]; I(2)=0.0%; p=0.635). CONCLUSIONS: Because of the limitations of this meta-analysis due to the small number of randomized clinical trials and patients included, the results should be taken cautiously, and the performance of new randomized clinical trials is proposed, with enough statistical power, comparing balanced and unbalanced colloids to balanced and unbalanced crystalloids, following the protocols of GDFT, considering current guidelines and suggestions made by groups of experts.
Asunto(s)
Coloides/administración & dosificación , Fluidoterapia/métodos , Soluciones Isotónicas/administración & dosificación , Adulto , Coloides/efectos adversos , Soluciones Cristaloides , Fluidoterapia/efectos adversos , Humanos , Soluciones Isotónicas/efectos adversos , Ensayos Clínicos Controlados Aleatorios como Asunto , Procedimientos Quirúrgicos Operativos/métodosRESUMEN
INTRODUCTION: Several clinical trials on Goal directed fluid therapy (GDFT) were carried out, many of those using colloids in order to optimize the preload. After the decision of European Medicines Agency, there is such controversy regarding its use, benefits, and possible contribution to kidney failure. The objective of this systematic review and meta-analysis is to compare the use of last-generation colloids, derived from corn, with crystalloids, in GDFT, to determine complications and mortality associated associated. METHODS: A bibliographic research was carried out in Medline, Pubmed, Embase and Cochrane Library, corroborating randomized clinical trials in those crystalloids are compared to colloids in GDFT for mayor non-cardiac surgery in adults. RESULTS: One hundred thirty references were found, among those 38 were selected, and 29 analyzed; of these, 6 were included for systematic review and meta-analysis, including 390 patients. It was perceived that the use of colloids it not associated with the increase of complications, but rather with a tendency to a higher mortality (RR [95% IC] 3.87 [1.121, 13, 38]); I(2)=0.0%; p=0.635). CONCLUSIONES: Due to this meta-analysis' limitations for small number of randomized clinical trials and patients included, the results should be taken cautiously, and it is proposed to carry out new randomized clinical trials, with enough statistical power, comparing balanced and non-balanced colloids to balanced and non-balanced crystalloids, following the protocols of GDFT, respecting current guidelines and suggestions made by groups of experts.
RESUMEN
The measurement of serum parameters during general anesthesia procedures are subject to variations due to differences in protocol, splenic storage, and by the instituted fluid therapy. The aim of this study was to assess the hematocrit changes promoted by controlled fluid therapy and general anesthesia. Six mongrel female dogs underwent an anesthetic protocol with acepromazine (0.03 mg kg-1) and tramadol (5 mg kg-1) for premedication, induction with propofol (3 mg kg-1), and maintained with isoflurane and mechanical ventilation for 120 minutes. After induction, they were infused with 10 ml kg hr-1 of Ringers lactate solution. Hematocrit measurements were performed from the start until 72 hours from anesthesia and evaluated statistically to check if there were significant changes over time. The fluid therapy, the acepromazine and propofol in the anesthetic protocol promotes a significant reduction of hematocrit up to four hours after general anesthesia.
A mensuração de parâmetros séricos durante procedimentos dependentes de anestesia geral são passíveis de variações devido a diferenças do protocolo utilizado, armazenamento esplênico e também da fluidoterapia instituída. O objetivo deste trabalho foi avaliar o hematócrito buscando evidenciar as alterações flutuantes promovidas por fluidoterapia controlada e anestesia geral em cães submetidos a ovariohisterectomia laparoscópica. Seis cadelas sem raça definida foram submetidas a um protocolo anestésico com acepromazina (0,03 mg kg-1) e tramadol (5,0 mg kg-1) como medicação pré-anestésica, indução com propofol (3,0 mg kg-1) e mantidas com isoflurano e ventilação mecânica durante 120 minutos. Após a indução, receberam a infusão de 10,0 ml kg hr-1 de solução Ringer com lactato. Foram realizadas aferições de hematócrito do início (ou antes?) até 72 horas após a anestesia, sendo avaliadas estatisticamente para verificar se houve alterações relevantes durante os tempos. A fluidoterapia e o uso de acepromazina e propofol no protocolo anestésico para esta técnica cirúrgica promoveram uma redução de hematócrito significativa até quatro horas após a anestesia geral.
Asunto(s)
Animales , Perros , Anestesia General/veterinaria , Enfermedades de los Perros , Hematócrito/veterinaria , Lactato de Ringer/administración & dosificaciónRESUMEN
BACKGROUND: In the later stages of circulatory shock, monitoring should help to avoid fluid overload. In this setting, volume expansion is ideally indicated only for patients in whom the cardiac index (CI) is expected to increase. Crystalloids are usually the choice for fluid replacement. As previous studies evaluating the hemodynamic effect of crystalloids have not distinguished responders from non-responders, the present study was designed to evaluate the duration of the hemodynamic effects of crystalloids according to the fluid responsiveness status. METHODS: This is a prospective observational study conducted after the initial resuscitation phase of circulatory shock (>6 h vasopressor use). Critically ill, sedated adult patients monitored with a pulmonary artery catheter who received a fluid challenge with crystalloids (500 mL infused over 30 min) were included. Hemodynamic variables were measured at baseline (T0) and at 30 min (T1), 60 min (T2), and 90 min (T3) after a fluid bolus, totaling 90 min of observation. The patients were analyzed according to their fluid responsiveness status (responders with CI increase >15% and non-responders ≤15% at T1). The data were analyzed by repeated measures of analysis of variance. RESULTS: Twenty patients were included, 14 of whom had septic shock. Overall, volume expansion significantly increased the CI: 3.03 ± 0.64 L/min/m(2) to 3.58 ± 0.66 L/min/m(2) (p < 0.05). From this period, there was a progressive decrease: 3.23 ± 0.65 L/min/m(2) (p < 0.05, T2 versus T1) and 3.12 ± 0.64 L/min/m(2) (p < 0.05, period T3 versus T1). Similar behavior was observed in responders (13 patients), 2.84 ± 0.61 L/min/m(2) to 3.57 ± 0.65 L/min/m(2) (p < 0.05) with volume expansion, followed by a decrease, 3.19 ± 0.69 L/min/m(2) (p < 0.05, T2 versus T1) and 3.06 ± 0.70 L/min/m(2) (p < 0.05, T3 versus T1). Blood pressure and cardiac filling pressures also decreased significantly after T1 with similar findings in both responders and non-responders. CONCLUSIONS: The results suggest that volume expansion with crystalloids in patients with circulatory shock after the initial resuscitation has limited success, even in responders.
RESUMEN
La administración de fluidos intravenosos, es uno de los pilares de la reanimación del paciente en shock y su beneficio es mayor cuanto antes se inicie. Los fluidos más utilizados para tal objeto son las soluciones cristaloides (solución salina y Ringer Lactato) y los coloides (albumina, gel, dextrán y almidones). Estudios fisiológicos y clínicos han demostrado que los coloides y los cristaloides tienen diferentes efectos y perfiles de seguridad. Por otra parte, ambos tipos de fluidos administrados en exceso o a destiempo pueden tener efectos perjudiciales. Estudios clínicos recientes parecen coincidir que, en general, los coloides no ofrecen mayor beneficio clínico que los cristaloides y se asocian a mayor tasa de eventos adversos. Por tanto, el presente artículo pretende describir las ventajas y limitaciones de los tipos de soluciones que se utilizan para la reanimación de los pacientes críticos en base a literatura más reciente.
The administration of intravenous fluids, is a mainstay of patient resuscitation in shock and your benefit is greater the earlier it starts. The fluids commonly used for this purpose are crystalloid solutions (saline and Ringer Lactate) and colloids (albumin, gel, dextran and starch). Physiological and clinical studies have shown that colloids and crystalloids have different effects and safety profiles. Moreover, both ty-pes of fluids administered in excess or untimely can have detrimental effects. Recent clinical studies seem to agree that, in general, colloids offer no greater clinical benefit than crystalloids and are associated with increased rate of adverse events. Therefore, this article aims to describe the advantages and limitations of the types of solutions used for resuscitation of critically ill patients based on recent literature.