RESUMEN
BACKGROUND: This study was undertaken to determine the effect of a restricted versus a standard intravenous fluid regimen on urinary retention and readiness for discharge after surgery for benign anorectal disease. METHODS: A total of 41 ASA I-II patients were randomized into a standard fluid regimen group (group S, n=21) or a restricted fluid regimen group (group R, n=20). Spinal anaesthesia was performed with hyperbaric ropivacaine. Haemodynamic variables were noted. Hypotension, headache, analgesia requirement, nausea and vomiting, thirst and urinary retention were evaluated postoperatively. The Mann-Whitney U and chi-squared tests were used. RESULTS: Patient demographics were comparable between the groups. The area under heart rate versus time curve was higher in group R than in group S (p=0.002). Additional fluid and ephedrine requirements were similar between the groups. First voiding time was longer in group R (p=0.045). CONCLUSION: In minor anorectal surgery under spinal anaesthesia with ropivacaine, standard fluid regimen provides stable haemodynamic variables without urinary retention.
Asunto(s)
Procedimientos Quirúrgicos Ambulatorios/métodos , Anestesia Raquidea/métodos , Fluidoterapia/métodos , Cuidados Preoperatorios/métodos , Enfermedades del Recto/cirugía , Retención Urinaria/prevención & control , Adulto , Femenino , Hemodinámica/fisiología , Humanos , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias/prevención & control , Resultado del Tratamiento , Retención Urinaria/etiología , Urodinámica/fisiologíaAsunto(s)
Cuello/diagnóstico por imagen , Adolescente , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Radiografía , Factores SexualesRESUMEN
BACKGROUND: This randomized, double-blind, prospective, placebo controlled study was planned to determine the effectiveness of selective COX-II inhibitors used preoperatively to alleviate pain after Nissen fundoplication surgery. METHODS: For this study, 60 patients were allocated to four groups at random: group C (celecoxib, 200 mg by mouth), group R (rofecoxib, 50 mg by mouth), group P (placebo, pill), or group D (diclophenac sodium, 75 mg intramuscularly). Postoperative abdominal and shoulder pain experienced by the patient at rest, with motion, and with coughing were assessed. Side effects and postoperative analgesic requirement (tramadol, intramuscular) also were recorded. RESULTS: The median tramadol requirement in the 1st h and total tramadol requirement at the 24th h were higher in group P than in the other study groups (p < 0.01). The pain scores in the first postoperative hour were higher in group P (p < 0.05). CONCLUSIONS: The preoperative use of celecoxib, rofecoxib, or diclophenac in laparoscopic Nissen fundoplication surgery decreases pain intensity and tramadol requirement in the first postoperative hour and has a trarnadol sparing effect in the first 24 h.
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Inhibidores de la Ciclooxigenasa 2/uso terapéutico , Diclofenaco/uso terapéutico , Fundoplicación/efectos adversos , Fundoplicación/métodos , Lactonas/uso terapéutico , Laparoscopía , Dolor Postoperatorio/tratamiento farmacológico , Cuidados Preoperatorios , Pirazoles/uso terapéutico , Sulfonamidas/uso terapéutico , Sulfonas/uso terapéutico , Adulto , Celecoxib , Método Doble Ciego , Femenino , Humanos , Masculino , Estudios ProspectivosRESUMEN
The aim of this study was to evaluate the net changes in bone mineral density (BMD) during the reproductive cycle, and their relation with changes in serum calcium (Ca), phosphorus (P), PTH and calcitonin levels in rats. Twenty-seven female Wistar rats were included in this study. They were divided into three groups as pregnant, lactating and control groups. BMDs of lumbar vertebrates, femoral and tibial bones, and Ca, P, calcitonin and PTH levels were measured at the end of pregnancy, at the end of lactation and in nulliparous controls. In the pregnant group, the BMDs of rats were significantly higher in lumbar vertebrates, femoral and tibia bones than those of the control group (p<0.05). Their PTH and Ca levels were significantly lower than the control group (p<0.05). However, no statistically significant difference was found regarding P and calcitonin levels when compared to those of the control group. In the lactating group, the BMDs were significantly lower in lumbar vertebrates, femoral and tibia bones than those seen in the control and pregnant groups (p<0.05). Ca and PTH levels were significantly higher in lactating rats than in those of pregnant rats (p<0.005). Normal pregnancy increases BMD in rats, whereas lactation decreases it. Change in PTH levels is supposed to contribute to the mineralization and demineralization of the skeleton during pregnancy and lactation, respectively.
Asunto(s)
Densidad Ósea/fisiología , Lactancia/fisiología , Preñez/fisiología , Animales , Resorción Ósea , Calcitonina/sangre , Calcio/sangre , Femenino , Fósforo/sangre , Embarazo , Ratas , Ratas Wistar , Columna Vertebral/química , Tibia/químicaRESUMEN
Gilbert's syndrome (GS) is characterised by the existence of chronic mild unconjugated hyperbilirubinaemia. The value of rifampicin as a provocative test for the diagnosis of GS was evaluated and compared with a fasting test. Twenty-two patients with GS, 15 patients with chronic liver disease and 20 healthy controls were included. Both rifampicin and fasting tests were applied to all subjects. In the fasting test, the subjects were given a 400 calorie/day diet for 24 hours; in the rifampicin test, unconjugated bilirubin levels was measured before and four hours after taking 600 mg of rifampicin. Both tests achieved a significant increase in mean unconjugated bilirubin levels in patients with GS but not in the controls. The sensitivity and specificity of a rifampicin test in the diagnosis of GS were comparable with the fasting test. However, both tests caused a significant increase in unconjugated bilirubin levels in nearly half the patients with chronic liver disease. A rifampicin test may be used in the diagnosis of suspected GS instead of a fasting test, as it is simpler and more practical. However, its specificity for GS is not sufficient, because it also causes an increase in unconjugated bilirubin levels in some patients with chronic liver disease.
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Inhibidores Enzimáticos , Enfermedad de Gilbert/diagnóstico , Hiperbilirrubinemia/diagnóstico , Rifampin , Ayuno , Femenino , Humanos , Masculino , Sensibilidad y EspecificidadRESUMEN
There are no detailed descriptions of the neural structures that may be seen during surgical interventions of the pelvis. Anatomic dissections were performed to see which nerves are endangered in approaches to the anterior sacroiliac joint for plate fixations. Sixty cadavers were dissected bilaterally. Fifty-one were male and nine were female. L4 and L5 nerve roots were followed along the sacroiliac joint from the intervertebral foramen to the entrance into the lesser pelvis. Measurements were made between the nerves and sacroiliac joint from the proximal end of the joint to the pelvic brim. The L4 nerve root and the lumbosacral trunk (and not the L5 nerve root) were the nerves most susceptible to injury because of their course and proximity to the sacroiliac joint. As a result, during the anterior approach and fixation of the sacroiliac joint with plates, extreme care should be taken to identify the L4 nerve root or lumbosacral trunk or both at the anteroinferior third of the joint because the distance between the nerve and the joint is less than 1 cm.
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Plexo Lumbosacro/anatomía & histología , Articulación Sacroiliaca/anatomía & histología , Adulto , Disección , Femenino , Fracturas Cerradas/cirugía , Humanos , Masculino , Persona de Mediana Edad , Huesos Pélvicos/lesiones , Huesos Pélvicos/cirugía , Articulación Sacroiliaca/cirugíaRESUMEN
UNLABELLED: Comparative data on the mechanical properties of epidural catheters used clinically are not available. We performed a controlled laboratory investigation to assess the mechanical performance of three different intact or traumatized catheter types (Polyurethane, clear nylon, and radiopaque nylon catheters, designed for 18-gauge Tuohy needles). We studied a control (intact) and two trauma groups (needle bevel and surgical blade). Catheters were loaded to their breaking points by using a Lloyd LS500 material testing machine (Lloyd, Southampton, UK). Maximal load and extension values before breakage were measured, and modulus of elasticity and toughness values were calculated. Intact polyurethane catheters did not break within the limits of the experimental study (extension up to 3 times the original length of a specimen). The toughness values obtained from polyurethane and clear nylon catheters were significantly higher than those for the radiopaque catheters in intact specimens (P < 0.05). In the traumatized groups, polyurethane catheters had the highest toughness values (P < 0.05). Modulus of elasticity values were higher in both control and trauma groups of the radiopaque catheters when compared with the polyurethane and clear nylon catheters, which indicates a higher stiffness to elastic deformation (P < 0.05). In conclusion, polyurethane catheters are the most durable catheter type to tensile loading, either intact or traumatized. Mechanical properties can be used to predict complications related to the clinical use of these catheters. IMPLICATIONS: Using a computer-assisted material testing machine, we studied the mechanical properties of three different types of epidural catheters, either intact or traumatized, in a blinded, controlled study. This information may be vital to clinicians who implant epidural catheters by helping them choose a catheter that has the lowest probability of failure.
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Anestesia Epidural/instrumentación , Cateterismo , Algoritmos , Elasticidad , Análisis de Falla de Equipo , Agujas , Nylons , Poliuretanos , Estrés Mecánico , Resistencia a la TracciónRESUMEN
Omeprazole combined with 2 antimicrobials has been suggested as a first-line option for Helicobacter pylori eradication in recent years. However, controversy exists regarding the efficacy of this protocol. This open-label, prospective clinical study investigated the efficacy of omeprazole-based triple therapy for H pylori eradication in 518 patients with H pylori-positive functional dyspepsia with or without duodenal ulcer. Amoxicillin, macrolides (clarithromycin or roxithromycin), and nitroimidazoles (metronidazole, ornidazole, or tinidazole) were the antibiotics used in the study. Nonulcer patients were randomly assigned to 1 of 8 different treatment protocols and duodenal ulcer patients were randomly assigned to 1 of 4 different treatment protocols consisting of omeprazole (20 mg once daily for nonulcer patients, 20 mg twice daily for ulcer patients for 14 days) with a combination of 2 of the above antimicrobials (for 10 days). H pylori infection was assessed by histologic findings and a rapid urease test before therapy and 4 weeks after therapy ended. Four hundred fifty-nine patients completed their regimens; 327 had functional dyspepsia (180 men, 147 women; median age, 39 years; range, 18 to 70 years) and 132 had ulcers (81 men, 51 women; median age, 40 years; range, 18 to 70 years). Eradication of H pylori was achieved in 58.8% (270 of 459) of all patients, 58.1% (190 of 327) of nonulcer dyspeptic patients, and 60.6% (80 of 132) of duodenal ulcer patients. The eradication rate varied from 47.2% to 69.4% in different treatment protocols. There were no statistically significant differences in eradication rates in any treatment group. All drugs were generally well tolerated in all groups, and no patient discontinued treatment because of side effects. Therapy with omeprazole and 2 antimicrobials for H pylori had limited efficacy in a Turkish population. The reason for these results, which conflict with those of other studies, is not clear. Further investigations of regimens for the eradication of H pylori in our population are necessary.
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Antibacterianos/uso terapéutico , Antiulcerosos/uso terapéutico , Antitricomonas/uso terapéutico , Infecciones por Helicobacter/tratamiento farmacológico , Omeprazol/uso terapéutico , Adolescente , Adulto , Anciano , Antibacterianos/efectos adversos , Antiulcerosos/efectos adversos , Antitricomonas/efectos adversos , Claritromicina/efectos adversos , Claritromicina/uso terapéutico , Interacciones Farmacológicas , Quimioterapia Combinada , Femenino , Helicobacter pylori/fisiología , Humanos , Masculino , Metronidazol/efectos adversos , Metronidazol/uso terapéutico , Persona de Mediana Edad , Omeprazol/administración & dosificación , Omeprazol/efectos adversos , Ornidazol/efectos adversos , Ornidazol/uso terapéutico , Pacientes Desistentes del Tratamiento , Distribución Aleatoria , Roxitromicina/efectos adversos , Roxitromicina/uso terapéutico , Tinidazol/efectos adversos , Tinidazol/uso terapéutico , TurquíaAsunto(s)
Antagonistas de Dopamina/administración & dosificación , Metoclopramida/administración & dosificación , Médula Espinal/citología , Médula Espinal/efectos de los fármacos , Animales , Perros , Eosina Amarillenta-(YS) , Espacio Epidural , Femenino , Hematoxilina , Inyecciones Epidurales , Masculino , Microscopía Electrónica , Vaina de Mielina/efectos de los fármacos , Adhesión en Parafina , Coloración y Etiquetado/métodosRESUMEN
BACKGROUND AND OBJECTIVES: Postoperative pain management in pediatric strabismus patients is infrequently studied. Pediatric patients can be mobilized earlier if postoperative pain is minimized. In this study, two different regional anesthetic techniques, retrobulbar block and local infiltration, were compared with a "no block" control group for the postoperative management of pain in pediatric patients undergoing elective strabismus surgery. METHODS: Thirty patients were randomly allocated to one of the study groups: group 1 (n=10) control, group 2 (n=10) retrobulbar block, and group 3 (n=10) subconjunctival bupivacaine infiltration. The parameters that were evaluated during the early postoperative period (6 hours) were circulatory, pain scores by Visual Analog Scale (VAS) and Modified Pediatric Objective Pain Scale (MPOPS), additional analgesic requirement, nausea, and vomiting. The parameters that were evaluated after discharge from the hospital (on postoperative days 1 and 2) through questionnaires were additional analgesic requirement, nausea, vomiting, sleep disturbances, activity, and appetite. RESULTS: Group 3 had significantly higher VAS and MPOPS scores at postoperative 120, 180, 240, 300, and 360 minutes than groups 1 and 2 (P < .05). Patients in group 2 seemed to have a higher incidence of nausea and vomiting both in the early (6 hours) and late postoperative (postoperative days 1 and 2) periods; however, the difference was not statistically significant. Group 2 required less analgesic compared with groups 1 and 3 during the late postoperative period. Late postoperative activity and appetite were better in groups 2 and 3. CONCLUSIONS: Because there was no significant difference in terms of postoperative analgesia in the retrobulbar block or subconjunctival local anesthetic infiltration groups compared with the control group, we suggest that conventional methods of pain treatment are adequate for postoperative analgesia in strabismus surgery.
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Analgesia/métodos , Anestesia Local/métodos , Anestésicos Locales/administración & dosificación , Bloqueo Nervioso , Órbita/inervación , Dolor Postoperatorio/prevención & control , Estrabismo/cirugía , Actividades Cotidianas , Analgésicos/administración & dosificación , Analgésicos/uso terapéutico , Apetito/efectos de los fármacos , Bupivacaína/administración & dosificación , Niño , Preescolar , Conjuntiva , Ambulación Precoz , Procedimientos Quirúrgicos Electivos , Femenino , Estudios de Seguimiento , Humanos , Masculino , Dimensión del Dolor , Alta del Paciente , Náusea y Vómito Posoperatorios/etiología , Trastornos del Sueño-Vigilia/etiología , Encuestas y CuestionariosRESUMEN
BACKGROUND: This study was performed to investigate airway complications related to Laryngeal Mask Airway (LMA) use in a selected group of paediatric patients undergoing ophthalmic surgery. METHODS: Ninety-four paediatric patients were enrolled. LMA was inserted under deep general anaesthesia with the standard technique previously described by Brain. Complications during induction, insertion of the LMA, maintenance of anaesthesia, removal of the LMA, emergence and on the first postoperative day were recorded. Failure of insertion, desaturation, laryngospasm, bronchospasm, vomiting, bucking, dislocation of the LMA, breath-holding, and coughing were noted. RESULTS: There was no significant age-related difference in successful insertion ratio of the LMA. In two patients (2%), the LMA could not be inserted with three attempts and tracheal intubation was performed. Laryngospasm was recorded in three patients (3%), leading to desaturation in two patients (SaO2 < 95%) during insertion of the LMA. During maintenance of anaesthesia bucking occurred in one patient (1%). After removal of the LMA, incidence of early desaturation following upper airway suctioning was higher in patients with a history of frequent upper respiratory tract infection (P < 0.01). Five patients (5%) had laryngospasm following the LMA removal; breath-holding and coughing were noted in 21 (22%) patients. Circulatory reactions to insertion and removal of the LMA were minimal. The incidence of sore throat on the first postoperative day was only 1%. CONCLUSION: LMA can be regarded as a safe product for airway maintenance during ophthalmic surgery with a stable circulation and few complications.
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Circulación Sanguínea/fisiología , Oftalmopatías/cirugía , Máscaras Laríngeas , Adolescente , Análisis de Varianza , Periodo de Recuperación de la Anestesia , Anestesia General/efectos adversos , Anestesia General/métodos , Espasmo Bronquial/etiología , Distribución de Chi-Cuadrado , Niño , Preescolar , Tos/etiología , Falla de Equipo , Estudios de Seguimiento , Humanos , Incidencia , Lactante , Intubación Intratraqueal , Máscaras Laríngeas/efectos adversos , Laringismo/etiología , Auditoría Médica , Oxígeno/sangre , Faringitis/etiología , Estudios Prospectivos , Respiración , Infecciones del Sistema Respiratorio/complicaciones , Seguridad , Succión , Vómitos/etiologíaRESUMEN
Urologic lesions accompanying pelvic fractures is a well-known entity, and reports on the correlation of pediatric pelvic fracture type with lower urinary tract injury are few in the literature. We have reviewed 27 records and x-ray films of male pediatric patients who required urologic intervention after trauma to see which type of fracture, classified according to Tile, has a higher predilection of urologic injury. Most of the fractures that were considered to be mechanically stable and mainly localized to the anterior pelvic arch had urologic lesions that were generally confined to the bulbomembranous urethra (48%).
Asunto(s)
Fracturas Óseas/clasificación , Fracturas Óseas/complicaciones , Huesos Pélvicos/lesiones , Uretra/lesiones , Adolescente , Niño , Preescolar , Fracturas Óseas/diagnóstico por imagen , Humanos , Masculino , Huesos Pélvicos/diagnóstico por imagen , Radiografía , Estudios RetrospectivosRESUMEN
In a previous ultrastructural study, the benefit of a single high dose of vitamin D3 on fracture healing in a healthy animal model was demonstrated. This study examined the biomechanical consequences of applying a single high dose of vitamin D3 in a healthy rabbit model subsequent to femoral fracture. The fracture load, the values of energy absorbed until fracture and the flexural rigidity values of the vitamin D group were significantly higher than the corresponding ones of the control group in the case of fracture. On the other hand, for intact bones, those values did not differ significantly between the two groups. It was concluded that single high-dose vitamin D3 application had positive effects on fracture healing in a healthy animal model, as far as the parameters related to mechanical strength are concerned.
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Colecalciferol/farmacología , Fracturas del Fémur/fisiopatología , Fémur/fisiopatología , Curación de Fractura/efectos de los fármacos , Animales , Fenómenos Biomecánicos , Colecalciferol/administración & dosificación , Fémur/efectos de los fármacos , Inyecciones Intramusculares , Masculino , ConejosRESUMEN
Ketamine 3-6 mg kg-1 given by mouth to paediatric patients for anaesthetic premedication was evaluated. Forty-three children, ages 2-9 years were randomly allocated to receive either ketamine (3 or 6 mg kg-1) or placebo (cola 0.2 mL kg-1). Oral use of ketamine made separation from the families easier, gave an increased level of sedation, made acceptance of mask application easier and improved the emotional state in the recovery phase. These improvements were present with ketamine 3 mg kg-1 and 6 mg kg-1 in comparison with the placebo. We conclude that 3 mg kg-1 ketamine given by mouth to premedicate paediatric patients is as effective as 6 mg kg-1 but has a decreased incidence of side effects such as nystagmus and vomiting.