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1.
Clinics ; 69(6): 372-377, 6/2014. tab
Article in English | LILACS | ID: lil-712703

ABSTRACT

OBJECTIVE: Laryngoscopy and stimuli inside the trachea cause an intense sympatho-adrenal response. Remifentanil seems to be the optimal opioid for rigid bronchoscopy due to its potent and short-acting properties. The purpose of this study was to compare bolus propofol and ketamine as an adjuvant to remifentanil-based total intravenous anesthesia for pediatric rigid bronchoscopy. MATERIALS AND METHODS: Forty children under 12 years of age who had been scheduled for a rigid bronchoscopy were included in this study. After midazolam premedication, a 1 µg/kg/min remifentanil infusion was started, and patients were randomly allocated to receive either propofol (Group P) or ketamine (Group K) as well as mivacurium for muscle relaxation. Anesthesia was maintained with a 1 µg/kg/min remifentanil infusion and bolus doses of propofol or ketamine. After the rigid bronchoscopy, 0.05 µg/kg/min of remifentanil was maintained until extubation. Hemodynamic parameters, emergence characteristics, and adverse events were evaluated. RESULTS: The demographic variables were comparable between the two groups. The decrease in mean arterial pressure from baseline values to the lowest values during rigid bronchoscopy was greater in Group P (p = 0.049), while the reduction in the other parameters and the incidence of adverse events were comparable between the two groups. The need for assisted or controlled mask ventilation after extubation was higher in Group K. CONCLUSION: Remifentanil-based total intravenous anesthesia with propofol or ketamine as an adjuvant drug along with controlled ventilation is a viable technique for pediatric rigid bronchoscopy. Ketamine does not provide a definite advantage over propofol with respect to hemodynamic stability during rigid bronchoscopy, while propofol seems more suitable during the recovery period. .


Subject(s)
Child , Child, Preschool , Female , Humans , Male , Anesthetics, Combined/administration & dosage , Anesthetics, Intravenous/administration & dosage , Bronchoscopy/methods , Ketamine/administration & dosage , Piperidines/administration & dosage , Propofol/administration & dosage , Anesthesia, Intravenous/methods , Anesthetics, Combined/adverse effects , Blood Pressure/drug effects , Drug Administration Schedule , Heart Rate/drug effects , Ketamine/adverse effects , Piperidines/adverse effects , Propofol/adverse effects
2.
Acta cir. bras ; 28(1): 26-32, jan. 2013. tab
Article in English | LILACS | ID: lil-662344

ABSTRACT

PURPOSE: To comparatively study the efficacy and maternal and fetal side-effects of two doses of bupivacaine associated with morphine and clonidine, administered by the subarachnoid route for cesarean section. METHODS: The study included 66 pregnant women at term, distributed into two groups. GI: bupivacaine 8.0 mg (1.6mL) + clonidine 75µg (0.5mL) + morphine 100µg (1.0mL) and GII: bupivacaine 10mg (2.0mL) + clonidine 75µg (0.5mL) + morphine 100µg (1.0mL). The following parameters were assessed: onset and maximum level of sensory block; quality of intraoperative and postoperative analgesia; degree and duration of motor block; maternal repercussions and Apgar score. RESULTS: The onset of sensory block, quality of intraoperative analgesia and total duration of analgesia were similar in both groups; maximum extent of sensory block predominated in T4; maximum degree of motor block (Bromage 3); time motor block regression was significantly longer in GII; Hemodynamic, respiratory repercussions, adverse maternal effects and Apgar scores were similar between groups. In both groups, there was a predominance of drowsy or sleeping patients. CONCLUSION: The addition of morphine and clonidine to low doses of hyperbaric bupivacaine produced adequate anesthesia for cesarean section and good postoperative analgesia, without any maternal and fetal repercussions.


Subject(s)
Adult , Female , Humans , Pregnancy , Young Adult , Anesthesia, Spinal/methods , Anesthetics, Combined/administration & dosage , Bupivacaine/administration & dosage , Cesarean Section/methods , Clonidine/administration & dosage , Morphine/administration & dosage , Anthropometry , Adjuvants, Anesthesia/administration & dosage , Adjuvants, Anesthesia/adverse effects , /administration & dosage , /adverse effects , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/adverse effects , Anesthetics, Combined/adverse effects , Anesthetics, Local/administration & dosage , Anesthetics, Local/adverse effects , Bupivacaine/adverse effects , Clonidine/adverse effects , Epidemiologic Methods , Morphine/adverse effects , Pain, Postoperative , Elective Surgical Procedures/methods , Time Factors
3.
Acta cir. bras ; 25(2): 181-189, Mar.-Apr. 2010. graf, tab
Article in English | LILACS | ID: lil-540495

ABSTRACT

Purpose: To evaluate hemodynamics and bispectral index (BIS) in bitches anesthetized with ketamine and midazolam in combination with dexmedetomidine or medetomidine and submitted to ovariohysterectomy. Methods: Twenty bitches pretreated with levomedetomidine and buprenorphine were anesthetized with 5 mg.kg-1 ketamine and 0.2 mg.kg-1 midazolam i.v. Continuous infusion of 0.4 mg.kg-1.h-1 midazolam and 20 mg.kg-1.h-1 ketamine was initiated in combination with DEX (n=10): 20 µg.kg-1.h-1 dexmedetomidine or MED (n=10): 30 µg.kg-1.h-1 medetomidine over 30 minutes. A pharmacokinetic study provided dexmedetomidine plasma concentration, set to be 3.0 ng.mL-1. Results: BIS decreased in both groups (P<0.05), but it was lower in DEX (P<0.05) as compared to MED. No differences were found in hemodynamic parameters (heart rate, systolic, diastolic and mean arterial pressure) between groups (P>0.05), but heart rate decreased in both groups, as compared to control values (P<0.05). Respiratory rate decreased (P<0.05) and expired end tidal CO2 increased progressively (P<0.05) and similarly in both groups. Anesthetic recovery period was similar between groups (P<0.05) with no adverse effects. Conclusion: Continuous administration of dexmedetomidine with calculated plasma concentration equal to 3 ng.mL-1 in combination with midazolam and ketamine provides suitable anesthesia for spay surgery in bitches, hemodynamic stability and calm awakening with no adverse effects.


Objetivo: Verificar o comportamento hemodinâmico e o índice bispectral de cadelas anestesiadas com cetamina e midazolam associados à dexmedetomidina ou medetomidina. Métodos: Vinte cadelas receberam pré-tratamento com levomepromazina e buprenorfina e foram anestesiadas com cetamina, 5 mg.kg-1 i.v., e midazolam, 0,2 mg.kg-1 i.v., seguidos da administração contínua de midazolam, 0,4 mg.kg-1.h-1, e cetamina, 20 mg.kg-1.h-1, associados, conforme o grupo, à: DEX (n=10): dexmedetomidina 20 µg.kg-1.h-1 ou MED (n=10): medetomidina 30 µg.kg-1.h-1, mantidos por 30 minutos. A dose de dexmedetomidina foi obtida por meio de estudo farmacocinético planejando-se concentração plasmática de 3,0 ng.mL-1. Resultados: Os valores do BIS diminuíram em ambos os grupos (P<0,05), mas foram menores no grupo DEX (P<0,05), em comparação com o grupo MED. Não houve diferença significativa nos atributos hemodinâmicos (frequência cardíaca, pressão arterial sistólica, diastólica e média) entre os grupos, mas a frequência cardíaca diminuiu em ambos os grupos em relação ao momento controle (P<0,05). A frequência respiratória diminuiu (P<0,05) e o CO2 expirado aumentou progressivamente em ambos os grupos (P<0,05). O tempo de recuperação anestésica foi semelhante entre os grupos (P>0,05), sem a presença de efeitos adversos. Conclusão: A administração contínua de dexmedetomidina em concentração plasmática calculada de 3 ng.mL-1, em combinação com midazolam e cetamina, resulta em plano anestésico adequado para castração de cadelas, estabilidade hemodinâmica e despertar tranquilo, sem efeitos adversos.


Subject(s)
Animals , Dogs , Female , Anesthetics, Combined/administration & dosage , Hemodynamics/drug effects , Hypnotics and Sedatives/administration & dosage , Hysterectomy/veterinary , Ovariectomy/veterinary , Anesthetics, Combined/adverse effects , Dexmedetomidine/administration & dosage , Dexmedetomidine/blood , Electromyography/veterinary , Hypnotics and Sedatives/adverse effects , Hysterectomy/methods , Ketamine/administration & dosage , Medetomidine/administration & dosage , Midazolam/administration & dosage , Monitoring, Intraoperative/veterinary , Ovariectomy/methods
4.
Rev. bras. anestesiol ; 59(6): 649-664, nov.-dez. 2009. tab, graf
Article in Portuguese | LILACS | ID: lil-533877

ABSTRACT

Justificativa e objetivos: A anestesia para artroplastia total do quadril (ATQ) constitui desafio devido à idade avançada e às doenças associadas dos pacientes. O objetivo do estudo foi avaliar se o bloqueio do plexo lombar combinado à anestesia geral se equivale à anestesia peridural lombar quanto à eficácia do bloqueio nociceptivo, efeitos hemodinâmicos secundários, dificuldade na sua execução e influência no sangramento operatório...


Background and objectives: Anesthesia for total hip arthroplasty (THA) is a challenge due to the advanced age and associated diseases of patients. The objective of this study was to evaluate whether the efficacy of the nociceptive blockade, secondary hemodynamic effects, difficulty to execute the technique, and influence in intraoperative bleeding of lumbar plexus block combined with general anesthesia is equivalent to epidural lumbar...


Justificativa y objetivos: La anestesia para la artroplastia total de la cadera (ATC), constituye un reto a causa de la edad avanzada y de las enfermedades asociadas a los pacientes. El objetivo del estudio, fue evaluar si el bloqueo del plexo lumbar combinado con la anestesia general, equivale a la anestesia epidural lumbar en cuanto a la eficacia del bloqueo nociceptivo, efectos hemodinámicos secundarios, dificultad en su ejecución e influencia en el sangramiento operatorio...


Subject(s)
Humans , Anesthesia, Epidural/standards , Anesthesia, General/standards , Anesthetics, Combined/adverse effects , Anesthetics, Combined/standards , Hemodynamics , Arthroplasty, Replacement, Hip , Lumbosacral Plexus
5.
Arq. bras. cardiol ; 93(5): 430-472, nov. 2009. graf, tab
Article in English, Spanish, Portuguese | LILACS | ID: lil-536212

ABSTRACT

FUNDAMENTO: Os efeitos da anestesia local em odontologia com lidocaína e epinefrina, sobre parâmetros cardiovasculares de gestantes portadoras de valvopatias e seus conceptos, não estão esclarecidos. OBJETIVO: Avaliar e analisar parâmetros da cardiotocografia, de pressão arterial e eletrocardiográficos da gestante portadora de doença valvar reumática, quando submetida à anestesia local com 1,8 ml de lidocaína 2 por cento sem vasoconstritor e com epinefrina 1:100.000, durante procedimento odontológico restaurador. MÉTODOS: Realizamos monitorização ambulatorial da pressão arterial, eletrocardiografia ambulatorial materna e cardiotocografia de 31 portadoras de cardiopatia reumática, entre a 28ª e 37ª semana de gestação, divididas em dois grupos conforme presença ou não do vasoconstritor RESULTADOS: Demonstrou-se redução significativa dos valores de frequência cardíaca materna nos dois grupos, durante o procedimento, quando comparado aos demais períodos (p < 0,001). Houve ocorrência de arritmia cardíaca em 9 (29,0 por cento) pacientes, das quais 7 (41,8 por cento) pertencentes ao grupo de 17 gestantes que recebeu anestesia com adrenalina. A pressão arterial materna não apresentou diferença quando comparamos períodos ou grupos (p > 0,05). O mesmo ocorreu (p > 0,05) com número de contrações uterinas, nível e variabilidade da linha de base e número de acelerações da frequência cardíaca fetal. CONCLUSÃO: O uso de 1,8 ml de lidocaína 2 por cento associado à adrenalina mostrou-se seguro e eficaz em procedimento odontológico restaurador durante a gestação de mulheres com cardiopatia valvar reumática.


BACKGROUND: The effects of local dental anesthesia with lidocaine and epinephrine on cardiovascular parameters of pregnant women with heart valve diseases and their fetuses are not fully understood. OBJECTIVES: To assess and analyze cardiotocographic, blood pressure and electrocardiographic parameters of pregnant women with rheumatic heart valve disease undergoing local anesthesia with 1.8mL of lidocaine 2 percent with or without epinephrine 1:100,000 during restorative dental treatment. METHODS: Maternal ambulatory blood pressure and electrocardiographic monitoring as well as cardiotocography of 31 patients with rheumatic heart disease were performed between the 28th and 37th week of gestation. The patients were divided into two groups, those with or without vasoconstrictor. RESULTS: A significant reduction in maternal heart rate was shown in both groups during the procedure in comparison with the other periods (p<0.001). Cardiac arrhythmia was observed in nine (29.0 percent) patients, of which seven (41.8 percent) were from the group of 17 pregnant women who received anesthesia plus epinephrine. No difference in maternal blood pressure was observed when periods or groups were compared (p>0.05). The same occurred (p>0.05) with the number of uterine contractions, baseline level and variability, and number of accelerations of fetal heart rate. CONCLUSION: The use of 1.8mL of lidocaine 2 percent in combination with epinephrine was safe and efficient in restorative dental procedures during pregnancy in women with rheumatic heart valve disease.


FUNDAMENTO: Los efectos de la anestesia local en odontología con lidocaína y epinefrina, sobre los parámetros cardiovasculares de gestantes portadoras de valvulopatías y sus conceptos, no son claros. OBJETIVO: Evaluar y analizar parámetros de la cardiotocografía, de la presión arterial y electrocardiográficos de la gestante portadora de enfermedad valvular reumática, al someterse a anestesia local con 1,8 ml de lidocaína 2 por ciento sin vasoconstrictor y con epinefrina 1:100.000, durante procedimiento odontológico restaurador. MÉTODOS: Realizamos monitoreo ambulatorio de la presión arterial, electrocardiografía ambulatoria materna y cardiotocografía de 31 portadoras de cardiopatía reumática, entre la 28ª y la 37ª semana de gestación, divididas en dos grupos según la presencia o no del vasoconstrictor. RESULTADOS: Se observó reducción significativa de los valores de frecuencia cardíaca materna en los dos grupos, durante el procedimiento, al compararlo con los demás períodos (p < 0,001). Se registró ocurrencia de arritmia cardíaca en 9 (29,0 por ciento) pacientes, de las cuales 7 (41,8 por ciento) pertenecían al grupo de 17 gestantes que recibió anestesia con adrenalina. La presión arterial materna no presentó diferencia al comparar períodos o grupos (p > 0,05). Lo mismo ocurrió (p > 0,05) con el número de contracciones uterinas, nivel de variabilidad de la línea de base y número de aceleraciones de la frecuencia cardíaca fetal. CONCLUSIÓN: El uso de 1,8 ml de lidocaína 2 por ciento asociado a la adrenalina se mostró seguro y eficaz en procedimiento odontológico restaurador durante la gestación de mujeres con cardiopatía valvular reumática.


Subject(s)
Adolescent , Adult , Female , Humans , Pregnancy , Young Adult , Anesthesia, Dental/adverse effects , Anesthetics, Local/adverse effects , Epinephrine/adverse effects , Lidocaine/adverse effects , Pregnancy Complications/physiopathology , Rheumatic Heart Disease/physiopathology , Analysis of Variance , Anesthetics, Combined/administration & dosage , Anesthetics, Combined/adverse effects , Anesthetics, Local/administration & dosage , Arrhythmias, Cardiac/chemically induced , Blood Pressure/drug effects , Cardiotocography , Epinephrine/administration & dosage , Gestational Age , Heart Rate, Fetal/drug effects , Lidocaine/administration & dosage , Monitoring, Ambulatory/methods , Statistics, Nonparametric , Vasoconstrictor Agents/administration & dosage , Vasoconstrictor Agents/adverse effects , Young Adult
6.
Rev. bras. anestesiol ; 58(6): 593-601, nov.-dez. 2008. graf, tab
Article in English, Portuguese | LILACS | ID: lil-497047

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: Adição de clonidina subaracnóidea (±-agonista) prolonga a ação analgésica da combinação sufentanil e bupivacaína isobárica em analgesia combinada para o trabalho de parto Õ. O objetivo deste estudo foi comparar a qualidade de analgesia e a prevalência de efeitos colaterais após a adição de clonidina subaracnóidea à solução anestésica em gestantes durante trabalho de parto. MÉTODO: Após aprovação da Comissão de Ética, 22 gestantes em trabalho de parto receberam aleatoriamente no espaço subaracnóideo 2,5 mg de bupivacaína hiperbárica 0,5 por cento (grupo CLON/HIPER; n = 11) ou 2,5 mg de bupivacaína isobárica 0,5 por cento (grupo CLON/ISO; n = 11) em associação ao sufentanil 2,5 µg e à clonidina 30 µg. A dor avaliada pela Escala Analógica Visual, a freqüência cardíaca e a pressão arterial média foram estudadas a cada 5 minutos nos primeiros 15 minutos e, a seguir, a cada 15 minutos até o nascimento. Foi avaliada a prevalência de efeitos colaterais (náusea, vômito, prurido e sedação). O estudo foi encerrado no momento em que foi necessária complementação analgésica peridural (dor > 3 cm) ou ao nascimento. A análise estatística foi realizada pelos testes t de Student, Qui-quadrado, Fisher e ANOVA de duas vias para medidas repetidas, considerando como significativo p < 0,05. RESULTADOS: Os grupos CLON/HIPER e CLON/ISO foram semelhantes com relação a dados antropométricos, duração da analgesia (70,9 ± 32,9 vs. 85,4 ± 39,5), freqüência cardíaca, ocorrência de prurido, sedação, náusea e vômitos. No grupo CLON/ISO houve diminuição significativa da pressão arterial média com relação ao grupo CLON/HIPER nos momentos 15, 30 e 45 minutos (p < 0,05). CONCLUSÕES: Nas condições estudadas, a adição de clonidina em baixa dose (30 »g), associada ao sufentanil, determinou maior ocorrência de hipotensão quando administrada com soluções isobáricas de anestésico local. Com relação aos demais efeitos colaterais, as soluções hiperbáricas...


BACKGROUND AND OBJECTIVES: The addition of subarachnoid clonidine (α-agonist) prolongs the analgesia produced by the combination of sufentanil and isobaric bupivacaine in combined labor analgesiaÕ. The objective of this study was to compare the quality of analgesia and the prevalence of side effects after the addition of subarachnoid clonidine to the anesthetic solution in labor analgesia. METHODS: After approval by the Ethics Commission, 22 pregnant women in labor were randomly assigned to the subarachnoid administration of either 2.5 mg of 0.5 percent hyperbaric bupivacaine (CLON/HYPER Group; n = 11) or 2.5 mg of 0.5 percent isobaric bupivacaine (CLON/ISO Group; n = 11) associated with 2.5 µg of sufentanil and 30 µg of clonidine. Pain, evaluated by the Visual Analogue Scale, heart rate, and mean arterial pressure were assessed every 5 minutes during the first 15 minutes, and then every 15 minutes afterwards until delivery. The prevalence of side effects (nausea, vomiting, pruritus, and sedation) was evaluated. The study was terminated whenever the patient needed supplemental epidural analgesia (pain > 3) or upon delivery of the fetus. The Student t test, Chi-square test, Fisher exact test, and two-way ANOVA for repeated measurements were used in the statistical analysis and a p < 0.05 was considered significant. RESULTS: Anthropometric data, duration of analgesia (70.9 ± 32.9 vs. 85.4 ± 39.5), heart rate, and the incidence of pruritus, sedation, nausea, and vomiting were similar in both groups. Mean arterial pressure was significantly lower in the CLON/ISO Group than in the CLON/HYPER Group at 15, 30, and 45 minutes (p < 0.05). CONCLUSIONS: Under the conditions of the present study, the association of a small dose of clonidine (30 µg) with sufentanil caused a higher incidence of hypotension when the isobaric solution of the local anesthetic was used. For all other side effects, both hyperbaric and isobaric solutions...


JUSTIFICATIVA Y OBJETIVOS: La adición de la clonidina subaracnoidea (±-agonista), prolonga la acción analgésica de la combinación sufentanil y bupivacaína isobárica en analgesia combinada para el trabajo de parto Õ. El objetivo de este estudio fue comparar la calidad de analgesia y la prevalencia de los efectos colaterales, después de la adición de clonidina subaracnoidea a la solución anestésica en gestantes durante el parto. MÉTODO: Después de la aprobación de la Comisión de Ética, 22 gestantes en trabajo de parto recibieron aleatoriamente en el espacio subaracnoideo 2,5 mg de bupivacaína hiperbárica 0,5 por ciento (grupo CLON/HIPER; n = 11) o 2,5 mg de bupivacaína isobárica 0,5 por ciento (grupo CLON/ISO; n = 11) en asociación con el sufentanil 2,5 µg y la clonidina 30 µg. El dolor evaluado por la Escala Analógica Visual, la frecuencia cardíaca y la presión arterial promedio, fueron estudiados a cada 5 minutos en los primeros 15 minutos y a continuación, a cada 15 minutos hasta el nacimiento. Fue evaluada la prevalencia de efectos colaterales (náusea, vómito, prurito y sedación). El estudio fue terminado en el momento en que se hizo necesaria la complementación analgésica epidural (dolor > 3 cm) o al nacimiento. El análisis estadístico fue realizado a través de los tests t de Student, Chi-cuadrado, Fisher y ANOVA de dos vías para medidas repetidas, considerando como significativo p < 0,05. RESULTADOS: Los grupos CLON/HIPER y CLON/ISO fueron similares con relación a los datos antropométricos, duración de la analgesia (70,9 ± 32,9 vs. 85,4 ± 39,5), frecuencia cardíaca, incidencia de prurito, sedación, náusea y vómitos. En el grupo CLON/ISO hubo una disminución significativa de la presión arterial promedio con relación al grupo CLON/HIPER en los momentos 15, 30, y 45 minutos (p < 0,05). CONCLUSIONES: En las condiciones estudiadas, la adición de clonidina en baja dosis (30 »g), asociada al sufentanil, determinó una mayor incidencia de...


Subject(s)
Humans , Female , Pregnancy , Anesthetics, Combined/adverse effects , Anesthetics, Combined/pharmacology , Bupivacaine/pharmacology , Clonidine/adverse effects , Clonidine/pharmacology , Sufentanil/pharmacology , Labor, Obstetric , Anesthesia, Epidural/methods
7.
Journal of Veterinary Science ; : 151-155, 2004.
Article in English | WPRIM | ID: wpr-128638

ABSTRACT

This study was performed to compare the effect of intratesticular (IT) injection of xylazine/ketamine combination for canine castration with those of intramuscular (IM) or intravenous (IV) injection. Xylazine and ketamine was administered simultaneously via intratesticularly (IT group), intramuscularly (IM group) or intravenously (IV group) at doses of 2 and 10 mg/kg, respectively. Pain response at the time of injection, mean induction time, mean arousal time, mean walking time and cardiopulmonary function during anesthesia were monitored after the xylazine and ketamine administration. In IV and IM groups, heart rates were significantly decreased 30 and 45 min after xylazine and ketamine administration, respectively (p < 0.05). Respiratory rates were significantly decreased in the IV group (p < 0.05). In the IT group, there was no significant changes in heart and respiratory rates. The occurrence of cardiac arrhythmias was less severe in IT group compared with those in IM and IV groups. The route of administration did not affect rectal temperature. Mean induction time was significantly (p < 0.05) longer in IT group than in IM and IV groups. On the contrary, mean arousal time and mean walking time were shortened in IT group. Clinical signs related to pain response at the time of injection and vomiting were less observed in IT group than in IM group, and head shaking was less shown in IT group than in IM and IV groups during recovery period. These results indicated that intratesticular injection of xylazine/ketamine for castration has several advantages such as less inhibition of cardiopulmonary function and fast recovery from anesthesia without severe complications, and would be an effective anesthetic method for castration in small animal practice.


Subject(s)
Animals , Dogs , Male , Anesthesia, Intravenous/veterinary , Anesthetics, Combined/adverse effects , Anesthetics, Dissociative/adverse effects , Body Temperature/drug effects , Castration/veterinary , Drug Administration Routes/veterinary , Electrocardiography/drug effects , Heart Rate/drug effects , Injections/veterinary , Injections, Intramuscular/veterinary , Ketamine/adverse effects , Pain, Postoperative , Pulmonary Ventilation/drug effects , Testis/drug effects , Vomiting/chemically induced , Xylazine/adverse effects
8.
Rev. argent. anestesiol ; 60(2): 92-112, mar.-abr. 2002. tab
Article in Spanish | LILACS | ID: lil-318013

ABSTRACT

A pesar de la amplia seguridad y difusión internacional que tienen las técnicas de analgesia y anestesia en obstetricia, aún persisten dudas en algunos aspectos, por lo que es importante promover el conocimiento de los conceptos básicos relacionados con el dolor de parto, sus características y mecanismos de acción, así como los fenómenos relativos a la neurotransmisión de los mismos. Para ello se hace necesario conocer los elementos anatómicos, físicos y químicos involucrados en la transmisión del dolor de parto y su repercusión sistémica, tanto materna como fetal. Igualmente importante resulta la actualización de conocimientos sobre los medios y métodos más utilizados en la actualidad, especialmente en nuestro país, para el alivio del dolor de parto y para la operación cesárea. Numerosos investigadores han demostrado la superioridad de la analgesia peridural sobre otras formas de analgesia para disminuir el dolor, el consumo de O2 y la acidosis materna y fetal. El trabajo de parto produce dolor severo en la mayoría de las mujeres. La técnica ideal de analgesia de parto debería reducir el dolor y permitir a la madre participar activamente en el nacimiento. En suma, la mejor de las técnicas de analgesia será la que produzca mínimos efectos sobre el feto y sobre la evolución del trabajo de parto.


Subject(s)
Humans , Pregnancy , Infant, Newborn , Analgesia, Obstetrical , Analgesia, Obstetrical/methods , Analgesia, Obstetrical , Anesthesia, Obstetrical/history , Anesthesia, Obstetrical/methods , Anesthesia, Obstetrical/trends , Anesthesia, Epidural , Cesarean Section/methods , Pain , Pain Threshold , Parturition , Anesthetics, Combined/administration & dosage , Anesthetics, Combined , Anesthetics, Combined/adverse effects , Anesthetics, Combined/pharmacokinetics , Neurotransmitter Agents
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