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1.
Bol. méd. postgrado ; 35(2): 7-13, Jul.-Dec. 2019. tab
Article in Spanish | LILACS, LIVECS | ID: biblio-1120190

ABSTRACT

Con el objetivo de evaluar la eficacia del sulfato de magnesio como coadyuvante en la analgesia postoperatoria en pacientes sometidos a colecistectomía abierta que ingresaron al Hospital Central Universitario Dr. Antonio María Pineda durante el período mayo­agosto de 2018, se realizó un ensayo clínico controlado simple ciego cuya muestra estuvo formada por 50 pacientes asignados aleatoriamente en dos grupos (relación 1:1): grupo experimental quienes recibieron sulfato de magnesio a una dosis de 50 mg/kg vía intravenoso (IV) más ketoprofeno 100 mg IV y grupo control a quienes se les administró solo ketoprofeno 100 mg IV. La intensidad del dolor se estimó a través de la escala visual análoga (EVA). La intensidad basal del dolor fue menor en el grupo experimental. Las dosis analgésicas de rescate requeridas fueron superiores en el grupo control (p  0,05) mientras que las náuseas se presentaron sólo en el grupo control. El 62,5% de los pacientes del grupo control con EVA > 4 ameritó medicación de rescate entre 30 minutos a 12 horas post-cirugía y el 37,5% de los pacientes del grupo experimental la requirió entre 8 a 24 horas (p < 0,05). Los resultados evidencian que el sulfato de magnesio es una alternativa efectiva en el tratamiento del dolor postoperatorio.


In order to evaluate the efficacy of magnesium sulphate as a coadjuvant in postoperative analgesia in patients undergoing open cholecystectomy admitted to the Hospital Central Universitario Dr. Antonio Maria Pineda during the May - August 2018 period, we performed a controlled single blind study with a sample of 50 patients randomly assigned to two groups (1:1 ratio): experimental group which received 50 mg/kg intravenous magnesium sulfate plus ketoprofen 100 mg IV and control group which only received ketoprofen 100 mg IV. The intensity of pain was estimated through the visual analogue scale (VAS). Basal pain intensity was less in the experimental group. Analgesic rescue doses were higher in the control group (p  0.05) while nausea was only seen in this group. 62.5% of patients of the control group with VAS > 4 required rescue medication between 30 minutes and 12 hours post-surgery while 37.5% of patients of the experimental group received rescue medication between 8 to 24 hours post-surgery (p < 0.05). The results show that magnesium sulphate is an effective alternative in the treatment of postoperative pain.


Subject(s)
Humans , Male , Female , Cholecystectomy , Analgesia , Magnesium Sulfate/administration & dosage , Magnesium Sulfate/therapeutic use , Pain, Postoperative , Perioperative Care , Pain Management
2.
Rev. bras. cir. cardiovasc ; 33(5): 448-453, Sept.-Oct. 2018. tab, graf
Article in English | LILACS | ID: biblio-977448

ABSTRACT

Abstract Objective: Cardiac arrhythmias are a common challenge following open-heart surgeries. Hypomagnesemia is believed to be correlated with this condition. Prophylactic intravenous magnesium supplementation has been practiced for a long time in patients undergoing CABG. This study was designed in an attempt to compare the efficacy of oral versus intravenous routes in the prevention of hypomagnesemia and arrhythmia. Methods: In this interventional clinical study, 82 patients were randomly assigned to 2 groups. All patients were evaluated for baseline serum magnesium level and arrhythmias. One group received 1,600 mg of oral magnesium hydroxide through nasogastric (NG) tube prior to surgery, while the other group received 2 g of magnesium sulfate during the induction of anesthesia. The serum magnesium level was monitored for 48 hours after the operation. The difference in preoperative hypomagnesemia was non-significant (Sig: 0.576). Results: During the operation, the serum magnesium level peaked around 4 mg/dL, and no hypomagnesemia was detected in any patient. Although the curve of oral group declined parallel and below that of intravenous (IV) group, no significant differences were detected during postoperative monitoring. In addition, a prevalence of arrhythmia of 13.9% and 6.5% was noticed in IV and oral groups, respectively (OR: 0.428). Conclusion: Providing 1,600 mg of oral magnesium supplement to patients is as effective as 2,000 mg of magnesium sulfate IV in preventing hypomagnesemia and arrhythmia after CABG. Thus, the authors introduce this treatment regimen as a promising and cost-effective method.


Subject(s)
Humans , Male , Female , Middle Aged , Arrhythmias, Cardiac/prevention & control , Postoperative Complications/prevention & control , Coronary Artery Bypass/adverse effects , Magnesium/administration & dosage , Magnesium/blood , Magnesium Hydroxide/administration & dosage , Arrhythmias, Cardiac/etiology , Time Factors , Coronary Artery Disease/surgery , Administration, Intravenous , Magnesium Sulfate/administration & dosage
3.
Acta ortop. mex ; 31(5): 217-221, sep.-oct. 2017. tab, graf
Article in Spanish | LILACS | ID: biblio-886570

ABSTRACT

Resumen: Antecedentes: Las fracturas de radio distal constituyen hasta 15% de todas las lesiones óseas en los adultos. La rehabilitación es clave en la recuperación de la movilidad y la capacidad funcional. El sulfato de magnesio intraarticular ha sido utilizado para control postoperatorio del dolor; el objetivo fue determinar la mejoría del dolor y la capacidad funcional de los pacientes con fractura de radio distal usando sulfato de magnesio intraarticular. Material y métodos: Pacientes con fractura de radio distal tratados con clavos percutáneos e inmovilización fueron incluidos al azar en dos grupos. Grupo 1 infiltrado con 1.0 ml de sulfato de magnesio y 1.5 ml de agua estéril; en el grupo 2 esta última fue sustituida por 1 ml de bupivacaína (5 mg/ml). La infiltración se realizó al retiro de la inmovilización. El dolor, funcionalidad y rangos de movimiento fueron evaluados. Resultados: 20 pacientes, ocho masculinos y 12 femeninos con edad promedio de 53 años (± 17 DE) fueron evaluados. Se encontró disminución significativa en el dolor al primer minuto y a los tres minutos después de la infiltración en el grupo 2 (p < 0.05). Ambos grupos presentaron una mejoría significativa en la funcionalidad articular a las dos semanas (p < 0.05), así como una mejoría gradual en la movilidad articular en ese mismo período (p < 0.05). Conclusiones: La infiltración de sulfato de magnesio en combinación con bupivacaína ayuda a disminuir el dolor.


Abstract: Background: The distal radius fracture represent until 15% of all bone injuries in adults. The key in the recovery of mobility and functional outcomes are rehabilitation. The intra-articular application of magnesium sulphate has been used for postoperative pain. The objective was to determinate the improvement in pain and functional outcome of patients with distal radius fracture using intra-articular magnesium sulphate. Material and methods: Patients with distal radius fracture treated with percutaneous pinning and cast immobilization was included and randomized into two groups. The group 1 was applied 1.0 ml of magnesium sulphate and 1.5 ml of injectable water; meanwhile the group 2, the water was replaced with 1 ml of bupivacaine (5 mg/ml). The intra-articular infiltration was applied at the end of immobilization. Pain, functionality and movement of the wrist was evaluated for two weeks. Results: Twenty patients, 8 male and twelve females, with a mean age of 53 years (± 17 SD) was evaluated. A significative reduction of pain during the first minute and at three minutes after intra-articular infiltration in group 2 (p < 0.05). Both groups presented better articular outcomes at the two weeks (p < 0.05), and a better articular movement at same point (p < 0.05). Conclusions: The intra-articular infiltration of magnesium sulphate plus bupivacaine help to reduces the pain.


Subject(s)
Humans , Male , Female , Adult , Pain, Postoperative/prevention & control , Radius Fractures/surgery , Bupivacaine/administration & dosage , Fracture Fixation, Internal , Analgesics/administration & dosage , Magnesium Sulfate/administration & dosage , Pilot Projects , Treatment Outcome , Middle Aged
4.
Rev. bras. anestesiol ; 67(1): 50-56, Jan.-Feb. 2017. tab, graf
Article in English | LILACS | ID: biblio-843357

ABSTRACT

Abstract Background and objectives: Hemodynamic response to airway stimuli is a common phenomenon and its management is important to reduce the systemic repercussions. The objective of this study is to compare the efficacy of intravenous magnesium sulfate versus lidocaine on this reflex hemodynamics after laryngoscopy and tracheal intubation. Methods: This single-center, prospective, double-blind, randomized study evaluated 56 patients ASA 1 or 2, aged 18-65 years, scheduled for elective surgeries under general anesthesia with intubation. The patients were allocated into two groups: Group F received 30 mg·kg-1 of magnesium sulphate and Group L, 2 mg·kg-1 of lidocaine, continuous infusion, immediately before the anesthetic induction. Blood pressure (BP), heart rate (HR), and bispectral index (BIS) were measured in both groups at six different times related to administration of the study drugs. Results: In both groups there was an increase in HR and BP after laryngoscopy and intubation, compared to baseline. Group M showed statistically significant increase in the values of systolic and diastolic blood pressure after intubation, which was clinically unimportant. There was no difference in the BIS values between groups. Among patients receiving magnesium sulfate, three (12%) had high blood pressure versus only one among those receiving lidocaine (4%), with no statistical difference. Conclusion: Magnesium sulfate and lidocaine have good efficacy and safety for hemodynamic management in laryngoscopy and intubation.


Resumo Justificativa e objetivos: A resposta hemodinâmica aos estímulos das vias aéreas é um fenômeno comum e seu controle é importante para diminuir as repercussões sistêmicas. O objetivo deste trabalho é comparar os efeitos da administração endovenosa de sulfato de magnésio versus lidocaína na hemodinâmica desse reflexo após a laringoscopia e intubação orotraqueal. Métodos: Este estudo duplamente encoberto, aleatorizado, unicêntrico e prospectivo avaliou 56 pacientes, ASA 1 ou 2, entre 18 e 65 anos, escalados para cirurgias eletivas sob anestesia geral com intubação orotraqueal. Foram alocados em dois grupos, o M recebeu 30 mg·kg-1 de sulfato de magnésio e o L, 2 mg·kg-1 de lidocaína, em infusão contínua, imediatamente antes da indução anestésica. Os valores de pressão arterial (PA), frequência cardíaca (FC) e índice biespectral (BIS) foram aferidos nos dois grupos em seis momentos relacionados com a administração dos fármacos do estudo. Resultados: Em ambos os grupos houve aumento na FC e PA após a laringoscopia e intubação, em relação aos valores basais. No Grupo M observou-se elevação estatisticamente significativa, mas clinicamente pouco importante, nos valores das pressões arteriais sistólica e diastólica após a intubação. Não houve diferença nos valores de BIS entre os grupos. Dos pacientes que receberam o sulfato de magnésio, 3 (12%) apresentaram episódio de hipertensão, ao passo que apenas um dos que receberam lidocaína (4%) apresentou esse sinal, sem diferença estatística. Conclusão: Sulfato de magnésio e a lidocaína apresentam boa eficácia e segurança no controle hemodinâmico à laringoscopia e intubação.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Aged , Young Adult , Hemodynamics/drug effects , Intubation, Intratracheal/adverse effects , Laryngoscopy/adverse effects , Lidocaine/pharmacology , Magnesium Sulfate/pharmacology , Blood Pressure/drug effects , Infusions, Intravenous , Double-Blind Method , Prospective Studies , Treatment Outcome , Elective Surgical Procedures , Heart Rate/drug effects , Lidocaine/administration & dosage , Magnesium Sulfate/administration & dosage , Middle Aged
5.
J. pediatr. (Rio J.) ; 93(supl.1): 19-25, 2017. graf
Article in English | LILACS | ID: biblio-894082

ABSTRACT

Abstract Objectives: To describe the role of intravenous magnesium sulfate (MgSO4) as therapy for acute severe asthma in the pediatric emergency department (ED). Source: Publications were searched in the PubMed and Cochrane databases using the following keywords: magnesium AND asthma AND children AND clinical trial. A total of 53 publications were retrieved using this criteria. References of relevant articles were also screened. The authors included the summary of relevant publications where intravenous magnesium sulfate was studied in children (age <18 years) with acute asthma. The NAEPP and Global Initiative for Asthma expert panel guidelines were also reviewed. Summary of the data: There is a large variability in the ED practices on the intravenous administration of MgSO4 for severe asthma. The pharmacokinetics of MgSO4 is often not taken into account with a consequent impact in its pharmacodynamics properties. The cumulative evidence points to the effectiveness of intravenous MgSO4 in preventing hospitalization, if utilized in a timely manner and at an appropriate dosage (50-75 mg/kg). For every five children treated in the ED, one hospital admission could be prevented. Another administration modality is a high-dose continuous magnesium sulfate infusion (HDMI) as 50 mg/kg/h/4 h (200 mg/kg/4 h). The early utilization of HDMI for non-infectious mediated asthma may be superior to a MgSO4 bolus in avoiding admissions and expediting discharges from the ED. HDMI appears to be cost-effective if applied early to a selected population. Intravenous MgSO4 has a similar safety profile than other asthma therapies. Conclusions: Treatment with intravenous MgSO4 reduces the odds of hospital admissions. The use of intravenous MgSO4 in the emergency room was not associated with significant side effects or harm. The authors emphasize the role of MgSO4 as an adjunctive therapy, while corticosteroids and beta agonist remain the primary acute therapeutic agents.


Resumo Objetivos: Descrever o papel do sulfato de magnésio intravenoso (MgSO4) como terapia para asma grave aguda em serviço de emergência pediátrica (SE). Fonte: As publicações foram pesquisadas nos bancos de dados PubMed e Cochrane com as seguintes palavras-chave: magnésio E asma E crianças E ensaio clínico. Foram encontradas 53 publicações. As referências de artigos relevantes também foram examinadas. Incluímos o resumo de publicações relevantes quando o sulfato de magnésio intravenoso foi estudado em crianças (idade < 18 anos) com asma aguda. Revisamos também as diretrizes do Programa Nacional para a Educação e Prevenção da Asma (NAEPP) e do painel de especialistas da Iniciativa Global para Asma. Resumo dos dados: Há uma grande variabilidade nas práticas do SE na administração intravenosa do MgSO4 para asma grave. A farmacocinética do MgSO4 normalmente não leva em conta um impacto posterior em suas propriedades farmacodinâmicas. A comprovação cumulativa aponta para a eficácia do MgSO4 intravenoso na prevenção da internação, se usado quando necessário e em uma dosagem adequada (50-75 mg/kg). Uma internação hospitalar pode ser evitada para cada cinco crianças tratadas no SE. Outra modalidade de administração é a infusão prolongada de alta dose de sulfato de magnésio (HDMI) a 50 mg/kg/hora/4 horas (200 mg/kg/4 horas). O uso precoce da HDMI, para asma não infecciosa mediada, pode ser superior a um MgSO4 em bólus para evitar internações e antecipar as altas do SE. A HDMI parece ter bom custo-benefício se aplicada precocemente em uma população selecionada. O MgSO4 intravenoso tem um perfil de segurança semelhante a outras terapias de asma. Conclusões: O tratamento com MgSO4 intravenoso reduz as chances de internações hospitalares. O uso de MgSO4 intravenoso no pronto socorro não é associado a efeitos colaterais ou danos significativos. Enfatizamos o papel do MgSO4 como uma terapia adjuvante, ao passo que os corticosteroides e as beta-agonistas continuam os agentes terapêuticos agudos primários.


Subject(s)
Humans , Child , Asthma/drug therapy , Magnesium Sulfate/administration & dosage , Severity of Illness Index , Infusions, Intravenous , Acute Disease , Emergency Service, Hospital , Hospitalization
6.
Rev. chil. pediatr ; 87(4): 261-267, ago. 2016. ilus, tab
Article in Spanish | LILACS | ID: lil-796812

ABSTRACT

Introducción: El empleo de sulfato de magnesio para neuroprotección fetal es un tratamiento cada vez más frecuente. Objetivo: Estudiar la asociación entre sulfato de magnesio administrado a la gestante y la necesidad de reanimación neonatal. Pacientes y método: Estudio prospectivo de un grupo de prematuros menores de 32 semanas expuestos al sulfato de magnesio como neuroprotector y otro grupo retrospectivo inmediatamente anterior al inicio de este tratamiento. En ambos grupos se descartaron los casos que no habían recibido maduración pulmonar con corticoides. Se analizaron y compararon el porcentaje de reanimación y diferentes comorbilidades. Resultados: Se incluyó a 107 prematuros, 56 expuestos al sulfato de magnesio. El porcentaje de reanimación avanzada fue similar en ambos grupos. No se encontraron diferencias en mortalidad, ventilación mecánica invasiva, tiempo de la primera deposición y otras comorbilidades. Conclusiones: El sulfato de magnesio para neuroprotección no aumenta de forma significativa la necesidad de reanimación de los prematuros menores de 32 semanas.


Introduction: Magnesium sulphate administration is recommended for foetal neuroprotection in pregnant women at imminent risk of early preterm birth. Objective: To evaluate the relationship between intrapartum magnesium sulphate for foetal neuroprotection and delivery room resuscitation of preterm infants less 32 weeks. Patients and method: A prospective observational study was conducted on preterm infants less 32 weeks exposed to magnesium sulphate for neuroprotection, and a comparison made with another historic group immediately before starting this treatment. Cases in both groups that had not reached lung maturity with corticosteroids were rejected. The rates of resuscitation, morbidity and mortality for each of the groups were analysed and compared. Results: There was a total of 107 preterm, with 56 exposed to magnesium sulphate. Rate of advanced resuscitation were similar between the two groups. There were no other differences in mortality, invasive mechanical ventilation, time to first stool, and other comorbidities. Conclusions: Intrapartum magnesium sulphate for foetal neuroprotection was not associated with an increased need for intensive delivery room resuscitation and other morbidities in these cohorts of less than 32 weeks preterm infants.


Subject(s)
Humans , Male , Female , Pregnancy , Infant, Newborn , Adult , Young Adult , Prenatal Care/methods , Resuscitation/statistics & numerical data , Neuroprotective Agents/administration & dosage , Magnesium Sulfate/administration & dosage , Infant, Premature , Prospective Studies , Neuroprotective Agents/adverse effects , Magnesium Sulfate/adverse effects
7.
J. coloproctol. (Rio J., Impr.) ; 36(2): 119-121, Apr-Jun. 2016.
Article in English | LILACS | ID: lil-785860

ABSTRACT

Coloprep is a bowel preparatory solution given before endoscopic procedures to get a unobscured internal vision. It has among its constituent's sodium sulphate, potassium sulphate and magnesium sulphate which produce an osmotic effect in the bowel. However, the use of such agents in hyponatremic and patients predisposed to seizures can have adverse ramifications. The current case outlines manifestation of absence seizure in a 52-year-old male patient who was administered Coloprep for colonoscopy. There was absence of other predisposing factors and the symptoms were ameliorated using timely identification and rectification of the underlying derangements.


Coloprep é uma solução preparatória intestinal administrada antes de procedimentos endoscópicos, com o objetivo de se ter uma visão interna não obscurecida. Entre os constituintes de Coloprep, observa-se sulfato de sódio, sulfato de potássio e sulfato de magnésio, que provocam efeito osmótico no intestino. Mas o uso de tais agentes em pacientes hiponatrêmicos e com predisposição para convulsões pode ter ramificações adversas. O caso em tela delineia uma manifestação de convulsão de ausência em paciente do gênero masculino com 52 anos e que recebeu Coloprep para colonoscopia. Não havia outros fatores predisponentes e os sintomas melhoraram graças à oportuna identificação e correção dos transtornos subjacentes.


Subject(s)
Humans , Male , Middle Aged , Seizures/complications , Sulfates/administration & dosage , Cathartics/adverse effects , Colonoscopy/adverse effects , Sodium Compounds/administration & dosage , Potassium Compounds/administration & dosage , Magnesium Sulfate/administration & dosage , Seizures , Sulfates/analysis , Sulfates/adverse effects , Sulfates/therapeutic use , Cathartics/administration & dosage , Cathartics/therapeutic use , Sodium Compounds/analysis , Sodium Compounds/adverse effects , Sodium Compounds/therapeutic use , Potassium Compounds/analysis , Potassium Compounds/adverse effects , Potassium Compounds/therapeutic use , Hyponatremia , Magnesium Sulfate/analysis , Magnesium Sulfate/adverse effects , Magnesium Sulfate/therapeutic use
8.
RELAMPA, Rev. Lat.-Am. Marcapasso Arritm ; 28(1): 27-30, jan.-mar.2015.
Article in Portuguese | LILACS | ID: lil-773029

ABSTRACT

A síndrome do QT longo induzida por fármacos é uma condição potencialmente fatal, capaz decausar morte súbita como primeira manifestação clínica. Relatamos o caso de paciente jovem que evoluiu comparada cardiorrespiratória em fibrilação ventricular durante internação hospitalar, 24 horas após nefrolitotripsiaextracorpórea. Durante a avaliação foi observado intervalo QT corrigido aumentado de 580 ms e uso de fórmulapara emagrecer que continha fluoxetina 30 mg. Após suspensão da medicação houve normalização do QT,optando-se pelo uso de cardiodesfibrilador implantável pelo alto risco de recorrência da fibrilação ventricular.A síndrome do QT longo pode se manifestar após o uso de fármacos para o tratamento de outras afecções,ressaltando a importância da anamnese rigorosa em busca de antecedentes de morte súbita, assim como darealização de eletrocardiografia antes da introdução de fármacos específicos, de forma a identificar possíveis casosassintomáticos de síndrome do QT longo.


Drug-induced long QT syndrome is a potentially fatal condition that can cause sudden death as a firstclinical manifestation. We report the case of a young patient evolved with cardiorespiratory arrest in ventricularfibrillation during hospitalization, 24 hours after extracorporeal nephrolithotripsy. The patient had an increasedcorrected QT interval of 580 ms and was on weight loss medication containing fluoxetine 30 mg. The QT intervalnormalized after withdrawal of the medication and we chose to use an implantable cardioverter defibrillator dueto the high risk of reoccurrence of ventricular fibrillation. Long QT syndrome may manifest after drug therapyfor other diseases, highlighting the importance of obtaining a through family history of sudden death as well asan ECG before using specific drugs, to identify possible asymptomatic cases of long QT syndrome.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Stress, Psychological/therapy , Long QT Syndrome/diagnosis , Tachycardia, Ventricular/complications , Electrocardiography, Ambulatory/nursing , Fluoxetine/adverse effects , Fluoxetine/pharmacology , Lidocaine/administration & dosage , Magnesium Sulfate/administration & dosage
9.
SJA-Saudi Journal of Anaesthesia. 2014; 8 (1): 78-82
in English | IMEMR | ID: emr-138063

ABSTRACT

Spinal anesthesia is an established mode of anesthesia for lower limb orthopedic surgeries. The limitations of the technique are short duration of action and limited post-operative analgesia. Concomitant use of intravenous infusion of magnesium sulfate may have an effect on the block characteristics and duration of action of intrathecal bupivacaine. A total of 80 American Society of Anesthesiologists I and II patients, either sex, 20-60 years of age scheduled for elective orthopedic fixation of fracture of long bones of lower limbs under spinal anesthesia were included. Spinal anesthesia administered with 2.5 ml heavy bupivacaine mixed with 10 mcg fentanyl. The groups were then divided to receive an infusion of injection magnesium sulfate 50 mg/kg/h over 15 min followed by 15 mg/kg/h until the end of the surgery [Group M] and 15 ml of Normal Saline over 15 min followed by 100 ml/h until the end of surgery [Group S]. Onset, duration of sensory and motor block and amount of post-operative analgesic were noted. A total of 6 patients [Group M] and seven patients [Group S] had inadequate block and excluded from the study. Mean block height was T6. Time required to achieve block height was 8.82 min versus 7.42 min in Groups M and S respectively [P = 0.04]. Mean duration of motor block was longer in group M [160.63 +/- 17.76 min] compared with Group S [130.12 +/- 20.70 min] [P = 0.000]. Time for regression of sensory block to T12/L1was 206.88 +/- 20.96 min [Group M] and 163.88 +/- 15.46 min [Group S] [P = 0.000]. Hemodynamic parameters were similar and statistically not significant. Need for first analgesic requirement was after 262.88 +/- 21.11 min in group M and 193.25 +/- 17.74 min in the group S [P = 0.000]. Mean dosage of tramadol needed in first 24 h was less in group M [190 +/- 30.38 mg vs. 265 +/- 48.30 mg, P = 0.000]. Use of intravenous magnesium with spinal anesthesia reduces post-operative pain and analgesic consumption


Subject(s)
Humans , Female , Male , Magnesium Sulfate , Magnesium Sulfate/administration & dosage , Prospective Studies , Pain, Postoperative/prevention & control
10.
Femina ; 41(3)maio-jun.. ilus
Article in Portuguese | LILACS | ID: lil-730207

ABSTRACT

A paralisia cerebral é a causa mais comum de deficiência motora na infância. É uma doença complexa e de caráter não progressivo, que se caracteriza por distúrbios motores secundários alesões cerebrais ou a anomalias oriundas das fases iniciais de desenvolvimento do cérebro. O fator de risco mais importante para paralisia cerebral é o nascimento pré-termo, cuja incidência tem aumentado significativamente. Como consequência, a ocorrência da paralisia cerebral também tem aumentado, a despeito da melhoria da sobrevida dos fetos pré-termos. O risco da paralisia cerebral é tanto maior quanto menores a idade gestacional e o peso ao nascimento. Dessa forma, estratégias que se mostrarem efetivas para reduzir a paralisia cerebral nesses recém-nascidos deveriam ser implementadas com o objetivo de diminuir os seus efeitos danosos nos indivíduos e suas famílias, nos serviços de saúde e na sociedade como um todo. O sulfato de magnésio tem se mostrado como um promissor agente neuroprotetor fetal. Desde a década de 1990, estudos resultantes das suas indicações para prevenção das convulsões eclâmpticas ou para tocólise têm evidenciado uma redução nas taxas de paralisia cerebral e leucomalácia periventricular em prematuros. Publicações mais recentes, incluindo diretrizes internacionais, têm avançado na recomendação sobre os regimes terapêuticos e na construção de algoritmos para utilização do sulfato de magnésio como agente neuroprotetor fetal.


Cerebral palsy is the most common cause of motor disability in childhood.It is a complex and non-progressive disorder, which is characterized by motor disturbances secundary to brain injuries or anomalies resulting from the early stages of brain development. The most important risk factor forthe occurrence of cerebral palsy is preterm birth, which has increased significantly. As a result, the incidence of cerebral paralysis has also increased despite the improvement in the survival of preterm fetuses. The risk of cerebral palsy increases with the reduction of gestational age and birth weight. Thus, strategies that have proved effective in reducing cerebral palsy in these infants should be implemented in order to decrease their harmful effects on individuals and their families, on health services and society as a whole. Magnesium sulfate has been shown as a promising fetal neuroprotective agent. Since the 1990s, studies arising from its indications for prevention of eclamptic seizures or tocolysis have shown a reduction in the rates of cerebral palsy and periventricular leukomalacia in preterm infants. More recent publications, including international guidelines,have advanced in the recommendation on treatment regimens and the construction of algorithms for use of magnesium sulfate as a fetal agent.


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Fetal Diseases/prevention & control , Neuroprotective Agents/therapeutic use , Premature Birth , Cerebral Palsy/prevention & control , Magnesium Sulfate/therapeutic use , Clinical Protocols , Nervous System Diseases/prevention & control , Prenatal Care , Magnesium Sulfate/administration & dosage , Tocolytic Agents/administration & dosage , Obstetric Labor, Premature/drug therapy
11.
Gac. méd. Caracas ; 121(1): 40-42, ene.-mar. 2013.
Article in Spanish | LILACS | ID: lil-707542

ABSTRACT

La amaurosis cortical aguda es una complicación dramática y poco común de la preeclampsia. Se presenta un caso de paciente de 29 años con diagnóstico de preeclampsia grave quien describió deterioro de la agudeza visual repentino en el puerperio inmediato. El fondo de ojo fue normal. La paciente identificaba la luz intensa. Las pupilas estaban reactivas y no se observo la presencia de nistagmo. Se le realizó una resonancia magnética cuyos resultados fueron normales, por lo que se realizó el diagnóstico de amaurosis cortical aguda.


Acute cortical blindness is an uncommon and dramatic complication of preeclampsia. We present a case of a 29 years-old patient with diagnosis of severe preeclampsia who described a sudden loss of visual acuity during immediate puerperium. Fundi were normal. Pupils were reactive and there was no nystagmus A magnetic resonance were performed with normal results, because diagnosis of acute cortical blindness was done.


Subject(s)
Humans , Adult , Female , Pregnancy , Visual Acuity/physiology , Blindness, Cortical/complications , Cesarean Section/methods , Uterine Hemorrhage/therapy , Arterial Pressure/physiology , Magnesium Sulfate/administration & dosage , Magnetic Resonance Imaging/methods , Pregnancy Complications , Pre-Eclampsia/prevention & control
12.
Rev. bras. anestesiol ; 63(1): 144-148, jan.-fev. 2013. ilus, tab
Article in Portuguese | LILACS | ID: lil-666126

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: Avaliar os potenciais efeitos neurotóxicos em nível ultraestrutural desulfato de magnésio administrado por via intratecal em dose única ou múltipla. MÉTODOS: Estudo realizado com 24 ratos Sprague-Dawley, peso médio entre 250 e 300 g. Apósjejum de 4 horas, os ratos receberam 10 mg.kg-1 de cloreto de xilazina por via intraperitoneale, em seguida, foram divididos aleatoriamente em três grupos. Grupo I (n = 8) recebeu 0,9% desoro fisiológico normal, Grupo II (n = 8) recebeu uma injeção de 0,02 mL de sulfato de magnésioa 15% por via intratecal e Grupo III (n = 8) recebeu 0,02 mL de sulfato de magnésio a 15% umavez por dia durante sete dias. As injeções foram aplicadas dentro de 0,40x50 milímetros daárea lombar. Após sete dias, os animais foram sacrificados sob anestesia com uma injeção deformaldeído a 10% na aorta e os tecidos foram fixados. A medula espinal foi, então, examinadae histopatologicamente avaliada sob microscópio eletrônico. O teste de Kruskal-Wallis foi usadopara avaliação estatística. Um valor de p < 0,05 foi considerado estatisticamente significativo. RESULTADOS: Neurodegeneração significativa foi detectada nos ratos que receberam uma únicainjeção ou injeções repetidas de sulfato de magnésio, em comparação com o grupo controle. O escore na avaliação histopatológica desse grupo também foi alto. CONCLUSÃO: Com base no exame de microscopia eletrônica, descobrimos que a administraçãointratecal de sulfato de magnésio induziu neurodegeneração.


BACKGROUND AND OBJECTIVES: To assess the potential neurotoxic effects at the ultrastructural level of magnesium sulfate administered intrathecally as a single or multi-dose. METHODS: Our study was conducted with 24 Sprague-Dawley rats that weighed 250-300 g. After a 4-hour fast, the rats were given 10 mg.kg-1 xylazine chloride intraperitoneal and then randomly allocated into three groups. Group I (n = 8) received 0.9% normal saline, Group II (n = 8) was given one intrathecal injection of 0.02 mL of 15% magnesium sulphate, and Group III (n = 8) was given 0.02 mL of 15% magnesium sulphate once a day for seven days. The injections were given within 0.40x50 mm from the lumbar area. After seven days, the animals were sacrificed under anesthesia with an aortic injection of 10% formaldehyde and their tissues were fixed. The medulla spinalis was then examined and histopathologically evaluated under an electron microscope. The Kruskal-Wallis test was used for statistical evaluation. A value of p < .05 was considered to be statistically significant. RESULTS: Significant neurodegeneration was detected in rats given single or repeated magnesium sulphate injections compared to the control group. The histopathological evaluation score of this group was also high. CONCLUSIONS: Based on electron microscopic examination, we found that intrathecal magnesium sulphate administration induced neurodegeneration.


JUSTIFICATIVA Y OBJETIVOS: Evaluar los potenciales efectos neurotóxicos en nivel ultraestructural de sulfuro de magnesio administrado por vía intratecal en dosis única o múltiple. MÉTODOS: Estudio realizado con 24 ratones Spraque-Dawley, con un peso promedio entre los 250 y los 300 g. Después del ayuno de 4 horas, los ratones recibieron 10 mg.kg-1 de cloruro de xilazina por vía intraperitoneal y enseguida fueron divididos aleatoriamente en tres grupos. El grupo I (n = 8) recibió 0,9% de suero fisiológico normal, Grupo II (n = 8) recibió una inyección de 0,02 mL de sulfuro de magnesio al 15% por vía intratecal y Grupo III (n = 8) recibió 0,02 mL de sulfuro de magnesio al 15% una vez por día durante siete días. Las inyecciones fueron aplicadas dentro de 0,40x50 milímetros del área lumbar. Después de siete días, los animales fueron sacrificados con anestesia con una inyección de formaldehido al 10% en la aorta y los tejidos fueron pegados. La médula espinal se examinó y fue histopatológicamente evaluada bajo microscopio electrónico. El test de Kruskal-Wallis fue usado para la evaluación estadística. Un valor de p < 0,05 fue considerado estadísticamente significativo. RESULTADOS: La neurodegeneración significativa fue detectada en los ratones que recibieron una sola inyección o inyecciones repetidas de sulfuro de magnesio, en comparación con el grupo control. El puntaje en la evaluación histopatológica de ese grupo también fue alto. CONCLUSIONES: Basándonos en el examen de microscopía electrónica, descubrimos que la administración intratecal de sulfuro de magnesio indujo a la neurodegeneración.


Subject(s)
Animals , Rats , Anesthetics/adverse effects , Magnesium Sulfate/adverse effects , Neurotoxicity Syndromes/etiology , Spinal Cord/pathology , Spinal Cord/ultrastructure , Anesthetics/administration & dosage , Injections, Spinal , Magnesium Sulfate/administration & dosage , Rats, Sprague-Dawley
13.
Rev. chil. obstet. ginecol ; 78(3): 201-208, 2013. tab
Article in Spanish | LILACS | ID: lil-687160

ABSTRACT

Antecedentes: la prematuridad es importante factor de riesgo para el desarrollo de parálisis cerebral (PC). El Sulfato de Magnesio (MgSO4) se ha planteado como una estrategia para reducir el riesgo de PC en recién nacidos por debajo de las 34 semanas de gestación. Objetivo: precisar con la evidencia disponible, la validez del uso del MgSO4 para protección neuronal prenatal en embarazadas en riesgo de parto pretér-mino (PP) inminente. Método: se revisaron las bases de datos PubMed, ScienceDirect, EBSCOhost, Scielo y OvidSP en búsqueda de estudios clínicos y epidemiológicos, revisiones sistemáticas, consensos y meta análisis. Se realizó revisión temática de los artículos que cumplieron los criterios de selección. Resultados: experimentos en modelos animales mostraron la posibilidad que el MgSO4 fuese protector neuronal. Estudios observacionales señalaron la posible asociación entre la exposición fetal al MgS04 y reducción en morbilidad neurológica en nacidos pretérmino (NP). Cinco ensayos clínicos entre 2002-2008, individualmente no mostraron datos concluyentes. En el 2009 se publicaron tres metaanálisis, basados en esos mismos ensayos y mostraron significativa reducción de PC en NP expuestos prenatalmente al MgSO4. Conclusión: existe evidencia para recomendar MgSO4 para protección neuronal prenatal antes de las 34 semanas de embarazo y con riesgo inminente de PP, aunque no está definida la dosis óptima. Se recomienda aplicar hasta el parto o por 12-24 horas.


Background: prematurity is a leading risk factor for development of cerebral palsy (CP). The use of Magnesium sulphate (MgSO4) has been proposed as a strategy to reduce the risk of cerebral palsy in preterm infants less than 34 weeks of gestation. Aims: to assess the best available evidence in order to validate the use of MgSO4 for prenatal neuroprotection in pregnant women at risk of imminent preterm delivery. Methods: we searched the PubMed, ScienceDirect, EBSCOhost, Scielo and OvidSP databases for clinical and epidemiological studies, systematic reviews, consensus and meta-analysis about the use of Magnesium sulphate to prevent cerebral palsy. Thematic review was conducted of articles that met the selection criteria. Results: experiments in animal models showed properties of MgSO4 for neuroprotection. Observational studies indicated the possible association between fetal exposures to MgS04 and reduced neurological morbidity in PP. Five clinical trials between 2002 and 2008 showed no conclusive data individually. In 2009, three meta-analysis showed significant reduction of cerebral palsy in MgSO4 exposed preterm infants. Conclusion: there is evidence to recommend the use of MgSO4 for prenatal neuroprotection before 34 weeks of pregnancy and imminent risk of preterm birth. It is unclear the optimal dose of MgSO4; is recommended until delivery or by 12-24 hours.


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Neuroprotective Agents/administration & dosage , Obstetric Labor, Premature , Cerebral Palsy/prevention & control , Magnesium Sulfate/administration & dosage , Infant, Premature, Diseases/prevention & control , Neuroprotective Agents/therapeutic use , Infant, Premature , Prenatal Care , Cerebral Palsy/drug therapy , Magnesium Sulfate/therapeutic use
14.
Arq. neuropsiquiatr ; 69(2b): 349-355, 2011. ilus, tab
Article in English | LILACS | ID: lil-588097

ABSTRACT

Magnesium sulfate (MgSO4) has been used to prevent seizures in eclampsia. This study examined the central effects of MgSO4 on different types of pentylenetetrazole (PTZ)-induced seizures. Male Wistar rats were submitted to intracerebroventricular (ICV) administration of MgSO4 at different doses followed by intraperitoneal administration of PTZ. The latency to the onset of the first seizure induced by PTZ was significantly increased by ICV administration of MgSO4 at a dose of 100 µg compared to the control treatment. In addition, the total period during which animals presented with seizures was significantly reduced at this dose of MgSO4. Furthermore, the latency to the onset of the first partial complex seizure was significantly increased by the lowest dose of MgSO4. However, a high dose of MgSO4 had no effect or even potentiated the effect of PTZ. These results suggest that, depending on the dose, MgSO4 may be important in prevention of epileptic seizures.


Sulfato de magnésio (MgSO4) é utilizado para prevenir crises epilépticas na eclampsia. Este estudo examina os efeitos do MgSO4 em diferentes tipos de crise induzidas por pentilenotetrazol (PTZ). Ratos Wistar foram submetidos à administração intracerebroventricular (ICV) de diferentes doses de MgSO4 seguida de administração intraperitoneal de PTZ. A latência para o início da primeira crise induzida por PTZ foi aumentada pela administração ICV de MgSO4 na dose de 100 µg quando comparada ao tratamento controle. Além disso, o período durante o qual os animais apresentaram crises foi reduzido com a mesma dose de MgSO4. A latência para o início da primeira crise parcial complexa também foi aumentada com a dose menor de MgSO4 (32 µg). No entanto, a maior dose (320 µg) de MgSO4 não foi efetiva ou até potencializou os efeitos do PTZ. Esses resultados sugerem que, dependendo da dose, o MgSO4 pode ser útil na prevenção de crises epilépticas.


Subject(s)
Animals , Male , Rats , Anticonvulsants/therapeutic use , Magnesium Sulfate/therapeutic use , Seizures/prevention & control , Anticonvulsants/administration & dosage , Convulsants , Dose-Response Relationship, Drug , Electroencephalography , Injections, Intraventricular , Magnesium Sulfate/administration & dosage , Pentylenetetrazole , Rats, Wistar , Seizures/chemically induced
15.
Article in English | IMSEAR | ID: sea-45904

ABSTRACT

A retrospective study of 68 eclamptic women who received Magnesium sulphate at Koshi Zonal Hospital were analyzed during a one year period (2006-2007 AD). Maternal conditions at admission, associated complications in mothers and babies, delivery outcomes and cause of death were also studied in each case. There were 5240 deliveries during the period of analysis. Of which 4976 were live births, pregnancy induced hypertension was 0.89% (47), 0.74% (39) presented with pre-eclampsia, 0.30 (16) cases with severe pre-eclampsia and 0.43 (23) cases with mild pre-eclampsia. During this period 1.3% (68) of eclampsia presented to the hospital. Of which 67.7% presented with ante-partum eclampsia, 22.1% with intrapartum eclampsia and 10.3% with post partum eclampsia. Majority of women (63.2%) were between 20-25 years of age, while teenage pregnancy contributed 30.88% of eclamptic cases. The diastolic blood pressure was >110 mm of Hg in 45.6% of cases, 90-110 mmHg in 50% of cases and in 4.4% the it was <90 mmHg. 94.1% presented to the hospital in an unconscious state, 79.4% of eclamptic women received the full dose of magnesium sulphate (initial loading plus maintenance dose), while rest failed to receive the full dose. Nine women with severe pre-eclampsia received magnesium sulphate as a prophylactic measure. 17.7% women had home delivery, one patient left against medical advice and one was referred to a tertiary care center. Caesarian Section (Lower Segment) was performed in 35.2% of cases, 30.8% had normal vaginal deliveries and 5.8% had pre term delivery. About 69.6% babies were born alive, 8.7% were still births, 11.6% were neonatal deaths and 4.4% of babies had to be admitted to the neonatal intensive care. Eclamptic women stayed less than one week in the hospital in majority of cases (64.7%), between 1-2 weeks in 32.4% and more than two weeks in 2.9%. Maternal complications included decreased urinary output, pulmonary edema in three cases; chest and wound infection two cases each; post partum psychosis, vulval haematoma, severe headache one case each. There were seven maternal deaths during this period and eclampsia contributed to one of the deaths. Eclampsia is a major cause of maternal and perinatal morbidity and mortality in our setup. Magnesium sulphate is an excellent drug of choice in management of eclampsia and pre-eclampsia. Wider coverage of pre-natal care, timely referral and optimal management of cases of eclampsia with magnesium sulphate in hospitals are key issues to prevent mortality/morbidity associated with it.


Subject(s)
Adolescent , Adult , Cohort Studies , Eclampsia/drug therapy , Female , Humans , Magnesium Sulfate/administration & dosage , Maternal Mortality , Nepal , Pregnancy , Pregnancy Outcome , Retrospective Studies , Tocolytic Agents/administration & dosage , Treatment Outcome , Young Adult
16.
Rev. Assoc. Med. Bras. (1992) ; 54(3): 232-237, maio-jun. 2008. graf, tab
Article in Portuguese | LILACS | ID: lil-485606

ABSTRACT

OBJETIVO: Comparar a relação da artéria umbilical e artéria cerebral média fetal através dos índices dopplervelocimétricos (índice de resistência, índice de pulsatilidade e relação S/D) antes e após a utilização do sulfato de magnésio nas gestantes com pré-eclâmpsia grave (pura ou superposta). MÉTODOS: Foi desenvolvido um estudo do tipo coorte prospectivo, no qual cada sujeito serviu como seu próprio controle. Foram selecionadas 40 gestantes com pré-eclâmpsia grave, submetidas ao exame dopplervelocimétrico antes e após 20 minutos da administração intravenosa de 6 g do sulfato de magnésio. As variáveis estudadas foram os índices dopplervelocimétricos da relação artéria umbilical e cerebral média fetal. A comparação das médias entre as duas medidas (antes e depois) de cada indivíduo foi realizada através do teste t student pareado. A comparação entre a distribuição de freqüência de diagnóstico fetal (normal, redução isolada na resistência da artéria cerebral média e centralizado) foi realizada através do teste Qui quadrado (c²) de Stuart-Maxwell. RESULTADOS: Não foi observada diferença estatisticamente significativa das médias da relação artéria umbilical/cerebral média nos índices dopplervelocimétricos antes e após o sulfato de magnésio. Verificou-se aumento da freqüência de redução isolada na resistência da artéria cerebral média após o sulfato de magnésio (25,0 por cento x 47,5 por cento; p = 0,01). CONCLUSÃO: A administração intravenosa do sulfato de magnésio nas gestantes com pré-eclâmpsia grave resultou em um aumento significativo na freqüência de fetos com diagnóstico de redução da resistência da artéria cerebral média na dopplervelocimetria.


BACKGROUND: To compare the ratio between the fetal middle cerebral artery and the umbilical artery using Doppler flow velocimetry indices (resistance index, pulsatility index and A/B relation) before and after administration of magnesium sulfate to pregnant women with severe preeclampsia (pure or superimposed). METHODS: A prospective cohort study was conducted with each pregnant woman representing her own control. Forty severe preeclamptic women were included and underwent Doppler sonography before and 20 minutes after administration of 6g of magnesium sulfate. Analysis variables were the Doppler flow velocimetry indices evaluating the ratio of the fetal middle cerebral artery to the umbilical artery. To compare the mean indices before and after magnesium sulfate for the same patient, the "t-paired" Student test was used. The Stuart-Maxwell c² was applied to determine the difference of fetal diagnosis (normal, brain-sparing or reduced middle cerebral artery resistance) before and after magnesium sulfate. RESULTS: No significant difference of the mean ratio between the middle cerebral artery and the umbilical artery, before and after administration of magnesium sulfate was observed. After magnesium sulfate (25.0 percent x 47.5 percent; p= 0.01), there was an increased frequency of isolated lower Doppler flow velocimetry indices in the middle cerebral artery. CONCLUSION: Intravenous administration of magnesium sulfate in patients with severe preeclampsia is associated with increased frequency of fetal Doppler diagnosis of reduced resistance in the middle cerebral artery.


Subject(s)
Adolescent , Adult , Female , Humans , Pregnancy , Young Adult , Fetus/blood supply , Magnesium Sulfate/administration & dosage , Middle Cerebral Artery/physiopathology , Pre-Eclampsia/drug therapy , Umbilical Arteries/physiopathology , Vascular Resistance/physiology , Anticonvulsants/administration & dosage , Blood Pressure , Blood Flow Velocity/physiology , Fetus/drug effects , Infusions, Intravenous , Laser-Doppler Flowmetry , Middle Cerebral Artery/drug effects , Middle Cerebral Artery , Prospective Studies , Pre-Eclampsia , Pulsatile Flow/physiology , Ultrasonography, Prenatal , Umbilical Arteries , Vascular Resistance/drug effects , Young Adult
19.
Iranian Journal of Allergy, Asthma and Immunology. 2008; 7 (4): 221-229
in English | IMEMR | ID: emr-143484

ABSTRACT

Though intravenous [IV] Magnesium Sulphate [MgS04] has additive effect to beta-2 agonists, its additive benefit in face of combination therapy with beta-2-agonists and ipratropium [standard therapy of severe acute exacerbation of asthma] remains unaddressed. The aim of this investigation was to evaluate the role of IV MgSO4 when used as an adjunct to standard therapy of severe exacerbations of asthma. Randomized, single blinded, placebo-controlled study was carried out in Emergency Department [ED]. Patients aged 18-60 years presenting with acute asthma and FEV1 < 30% predicted [pred.] were included. All patients received IV Hydrocortisone on arrival. In group1 [controls], patients were nebulised with salbutamol and ipratropium thrice at 20 minutes interval and were given 2g IV MgSO4 at 30 minutes. In group2 patients were nebulised similarly, but were given IV normal saline at 30 minutes for blinding. FEV1 was evaluated at baseline and at 30 minutes intervals. The primary efficacy end point was FEV1%pred. at 120 mins and pooled discharge rate [derived from comparing proportion of groups attaining PEFR >60%pred. and relief in dyspnea at 30, 60, 90, 120 minutes]. Both groups of 30 patients each, were matched with respect to demographic and pulmonary parameters [Baseline FEV1% :22.0+5.1% in group2 vs.22.07+5.2% in group1, p=0.87].At 120 minutes, there was a higher mean FEV1%pred [62.84+4.73% vs. 56.7+4.5%] and%improvement from baseline of [40.7+9.2%vs34.77+7.3%], in group 2 as compared to group1 [Mean Difference= 6.07%, C.I.1.87-10.62., p<0.01].The pooled discharge rate in group2 with respect to group1 was positive and significant [log rank.=6.8, p<0.05]. Thus IV MgSO4 improves pulmonary function and discharge rates, when used as an adjunct to standard therapy in severe acute asthma. Magnesium sulfate as an adjunct to standard therapy in patients with severe exacerbation of asthma could cause improvement in pulmonary function and decrease in hospital admission


Subject(s)
Humans , Male , Female , Magnesium Sulfate , Magnesium Sulfate/administration & dosage , Treatment Outcome , Respiratory Function Tests , Length of Stay , Acute Disease/drug therapy
20.
Ain-Shams Medical Journal. 2007; 58 (1-3): 321-329
in English | IMEMR | ID: emr-81634

ABSTRACT

To assess whether we can use blood pressure and urine output to adjust the duration at postpartum magnesium sulphate as a prophylaxis against seizures in patients with severe preeclampsia. This is a randomized control single blinded clinical trial held in Suez canal University hospital, Obstetrics and Gynecology Department. The study was carried on 150 of pregnant women attending the emergency delivery ward and are diagnosed as cases of severe preeclampsia distributed in three groups. The first group received magnesium sulphate as a 6 gm intravenous bolus loading dose then 1 gm/hour as a maintenance dose until the delivery time, then the regimen will be continued after delivery spontaneous onset of diuresis and, greater than 50% of the hourly postpartum blood pressures less than 150 mm Hg systolic and, less than 100 mm Hg diastolic [including the hour immediately before medication discontinuation], the second group received magnesium sulphate as a 6 gm intravenous bolus loading dose then 1 gm/hour as a maintenance dose until the delivery time then the regimen continued after delivery until the onset of diuresis only and the third group received a 48 gm of magnesuim sulphate. The results showed that no cases exposed to fits in group 1 and also no cases exposed to fits in group 2;: versus one case [3.3%] exposed to fits in group 3. There was only one as only one case that needed to reinitiate therapy in group 2 versus two cases needed to reinitiate therapy in group which is statistically insignificant. In group 2 there was one case needed to reinitiate therapy, so no effect on blood pressure or the need to reinitiate therapy by increasing the total dose as magnesium sulfate. There were no side effects at all from magnesium sulfate in group 1 and group 2, versus nine cases [30%] suffered from oliguria, two cases [6. 7%] suffered from hyporeflexia and three cases [10%] suffered from arrythmias in group 3. We can depend on diuresis alone as a dependable clinical parameter to withdraw magnesium sulphate safely without giving the patient unnecessary doses of the unsafe magnesium sulfate and without affecting the maternal outcome as no cases had postpartum fits and only one case needed to reinitiate therapy, although depending on diuresis and blood pressure to determine the duration of the therapy carries the same safety margin as diuresis alone and carries no more benefit over diuresis alone as magnesium sulfate not mainly an antihypertensive drug


Subject(s)
Humans , Female , Seizures/drug therapy , Magnesium Sulfate/administration & dosage , Administration, Intravenous , Blood Pressure , Urine
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