At risk or not: Comparing normative and criterion-referenced Body Mass Index standards among Mexican American children / A riesgo o no: comparando índices de masa corporal normativos e índices basados en criterios en niños méxico-americanos

Most childhood obesity research has classified participants by normative standards for Body Mass Index (BMI) through population percentiles or values corresponding to overweight adults (World Health Organization (WHO), Centers for Disease Control and Prevention (CDC) and the International Obesity Task Force (IOTF)). In 2006, criterion-referenced standards (FitnessGram®) were developed (revised in 2010) which directly associate BMI values with adverse health outcomes. This study assessed agreement between normative and criterion-referenced standards. Participants included 653 Mexican American 3rd to 5th graders living in the U.S.-Mexico border area who participated in a health promotion project. At baseline, agreement was compared between normative and criterion-referenced classifications. At follow-up, agreement between classifications on changes (e.g. from overweight to healthy weight) was assessed. According to FitnessGram® standards, 53.0% of participants were overweight or obese at baseline. Compared to FitnessGram®, the IOTF and CDC standards classified 15% fewer participants as obese/high risk. The WHO standards were closely related to FitnessGram® (kappa=.925) and showed significantly greater agreement with FitnessGram® than the CDC (kappa=.925 versus 0.722, p<.001) and IOTF standards (kappa=.925 versus .682, p<.001). Compared to the FitnessGram® (8.9%), the WHO and CDC (8.6%) were similar, but IOTF standards lower (6.5%) in how many children improved following the health program. Despite acceptable agreement between the different indices, several normative classifications may underestimate the proportion of children who are at risk for BMI-related adverse health consequences.

Muchos de los estudios sobre la obesidad infantil clasifican a los participantes por índices normativas para el índice de masa corporal (IMC) usando valores de percentil de población o valores correspondientes a adultos con sobrepeso (Organización Mundial de la Salud (WHO), Centros para el Control y Prevención de Enfermedades (CDC) y la Comisión International Sobre la Obesidad (OITF)). En 2006, índices con referencias a criterios (Fitness-Gram®) fueron creados asociando valores de IMC directamente a valores de impacto de salud adversos. Este estudio determino las equivalencias de los índices normativos y los con referencias a criterios. Los participantes incluyeron estudiantes (N=653), niveles 3°-5, viviendo en la frontera EEUU-México. Al inicio, se comparó la equivalencia entre el IMC basado en las clasificaciones normativas y los con referencias a criterios. La equivalencia entre las clasificaciones de los cambios fue evaluada. Según las normas Fitness-Gram®, 53.0% tenían sobrepeso o eran obesos aunque las normas OITF y CDC indicaron menos de 15% fueron clasificados con obesidad/alto riesgo. Las normas WHO fueron más cercanamente relacionadas con las de FitnessGram® (kappa=.925) y mostraron significativamente mayor equivalencia con las de FitnessGram® que a las del CDC (kappa= .925 V .722, p<.001) e IOTF (kappa=.925 V .669, p<.001). Los índices FitnessGram® (8.9%), WHO y CDC (8.6%) fueron similares en cuanto el número de niños que mejoraron siguiendo el programa, pero el índice IOTF fue menor (6.3%). Aunque había un acuerdo aceptable entre los índices diferentes, varios pueden subestimar la proporción a riesgo y las consecuencias adversas relacionadas al IMC.

A comparative study of clonidine versus a combination of diazepam and atropine for premedication in orthopaedic patients.

Sixty patients in the age group of 18-60 years of A.S.A. Grade I/II risk, scheduled for elective orthopaedic surgeries under general anaesthesia were studied for pre-medication with either oral clonidine or with combination of effects of diazepam & atropine. Patients in Group A (clonidine group) received tablet clonidine 100 mcg (1 tablet) if less than 50 kg in weight and 200 mcg if weighing more than 50 kg two hours before surgery. Patients in Group B (Diazepam-atropine group) received one tablet of Diazepam (10 mg) orally two hours before surgery and injection atropine-sulphate 0.01 mg/kg half an hour preoperatively by intramuscular route. In our study, the sedative and anti-sialogogue effects of clonidine were comparable to those of diazepam-atropine combination, which are commonly used premedicants. The anti-anxiety effect of clonidine was found to be better than that of diazepam-atropine combination. Clonidine also proved to be a better agent for the attenuation of pressor response to laryngoscopy and intubation. Thus, oral clonidine is a better premedicant compared to atropine-diazepam combination. Also, it is a more acceptable agent because of its oral route of administration.

A comparison of continuous infusion of vecuronium and atracurium in midline and paramedian laparotomies.

This was a study to compare continuous intravenous infusion of atracurium with continuous intravenous infusion of vecuronium for intraoperative muscle relaxation in 62 ASA I / II patients. Scheduled for laparotomies and pelvic surgeries under general anaesthesia. They were randomly allocated in two groups to receive either vecuronium infusion of 50 microg/kg/hour following a bolus dose of 0.1 microg/kg, or atracurium infusion of 400 microg/kg/hour following a bolus dose of 0.5 microg/kg. The mean infusion dose of atracurium was 478 +/- 44.11 microg/kg/hour and that of vecuronium was 63.2 +/- 74 microg/kg/hour for adequate muscle relaxation. The depth of neuromuscular blockade was monitored by using peripheral nerve stimulator so that only one twitch of train of four was present, resistance to ventilation, surgical relaxation and haemodynamic changes. Vecuronium infusions produced more haemodynamic stability than atracurium infusions. Vecuronium produced lesser change in systolic blood pressure (mean change of 3. 46 +/- 3.33%) from baseline values as compared to atracurium (mean change of 5.81 +/- 3.73%) from baseline values ( p < 0.01) which was statistically significant. The difference in mean pulse rate change from baseline value in the atracurium group (4.78 +/- 2.745%) was less than that in the vecuronium group (5.99 +/- 2.67%), which was not statistically significant. Spontaneous recovery was faster with vecuronium (540.94 +/- 76.46 seconds) as compared to atracurium (596. 33 +/- 72.48 seconds). 84.4% of patients who received vecuronium fell within good to very good category of muscle relaxation as compared to 63.3% in atracurium group. There were no cost benefits when either agents were used in infusion form.

Successful management of spontaneous pneumothorax during general anaesthesia in a patient with eosinophilia.

A 10-year-old male patient posted for left elbow arthrolysis developed pneumothorax during general anaesthesia. He had history of upper respiratory tract infection and high eosinophil count, which remained high in spite of treatment. In such patients, it is advisable to use steroid pre-operatively & intraoperatively to produce transient eosinopenia so that complications of eosinophilia are avoided.

Difficult intubation in a case of ankylosing spondylitis: a case report.

A case of severe ankylosing spondylitis involving the entire spine was to be operated for lumbar osteotomy. She had fixed rigidity of the cervical spine with minimal rotational movement, inability to lie down supine and severe restrictive lung disease with hypoxemia (pO2 = 65 mmHg). An awake intubation was performed and the patient was operated under general anaesthesia in the prone position. Intraoperative "wake-up" test was performed to judge whether extent of straightening was excessive. Postoperatively, she was electively ventilated and extubated uneventfully after 24 hours.

Anaesthetic management of bilateral alveolar proteinosis for bronchopulmonary lavage.

The most hazardous manifestation of pulmonary alveolar proteinosis is progressive hypoxia for which bronchopulmonary lavage (BPL) is the single most effective treatment. Unfortunately this procedure under general anesthesia itself increases the risk of hypoxia due to the need for one lung ventilation. It was therefore considered interesting to report the successful anaesthetic management of a patient with pulmonary alveolar proteinosis for Bronchopulmonary lavage.

Comparative study of intrathecal pethidine versus lignocaine as an anaesthetic and a postoperative analgesic for perianal surgery.

100 patients with ASA risk I & II and undergoing perianal surgery were studied for anaesthetic effects and postoperative analgesia following either intrathecal pethidine or lignocaine. Saddle block was performed either with intrathecal pethidine 5% (50 mg/ml) 0.5 mg/kg or 1 ml of 5% lignocaine. Sensory and motor block postoperative analgesia, need for additional analgesia were studied. The onset of sensory and motor blockade with lignocaine was faster than pethidine. However the sensory and motor blockade lasted longer with pethidine. The duration of postoperative analgesia was 15.39 +/- 5.14 hours as against duration of postoperative analgesia with lignocaine which was 1.3 +/- 0.53 hours. Only 10% of patients in the pethidine group required intramuscular analgesic supplementation whereas 30% of patients in the lignocaine group required intramuscular analgesic supplementation.

Use of nitroglycerin ointment to prevent hypertensive response during electroconvulsive therapy--a study of 50 cases.

Fifty patients of either sex, aged between 20 and 60 years undergoing electroconvulsive therapy were included in our study. Each patient was used as his/her own control. We observed the cardiovascular changes without nitroglycerin ointment in the first sitting and in the next sitting with the application of 2 inches of 2% nitroglycerin ointment 45 min before the electroconvulsive therapy. Arterial blood pressure and heart rate increase during electroconvulsive therapy can be effectively attenuated by application of 2 inches of 2% nitroglycerin ointment 45 min before the electroconvulsive therapy (p < 0.001 and p < 0.01 resp.). This may be especially beneficial for patients who are at increased risk of myocardial ischemia and stroke.

Comparative study of oral and intramuscular atropine sulphate as a premedicant in paediatric age group.

The use of atropine sulphate in the paediatric age group as a premedicant orally in a dosage of 0.02 mg/kg body weight 70 minutes prior to surgery was found to be as effective as atropine sulphate given intramuscularly 35 minutes prior to surgery in a dosage of 0.01 mg/kg body weight. This avoids the unpleasant memory of needle prick; The duration of effect as studied in the normal healthy children not subjected to surgery was found to be 2 1/2-3 hours.