Ultrasound guidance provided a 42% reduction in the MEAV of ropivacaine 0.5% required to block the femoral nerve as compared with the nerve stimulation guidance.
SummaryIn this prospective, randomised, observer-blinded study we evaluated whether ultrasound guidance can shorten the onset time of popliteal sciatic nerve block as compared to nerve stimulation with a multiple injection technique. Forty-four ASA I-III patients undergoing posterior popliteal sciatic nerve block with 20 ml of 0.75% ropivacaine were randomly allocated to nerve stimulation or ultrasound guided nerve block. A blinded observer recorded onset of sensory and motor blocks, success rates, the need for fentanyl intra-operatively, the requirement for general anaesthesia, procedure-related pain, patient satisfaction and side-effects. Onset times for sensory and motor blocks were comparable. The success rate was 100% for ultrasound guided vs 82% for nerve stimulation (p = 0.116). Ultrasound guidance reduced needle redirections (p = 0.01), were associated with less procedural pain (p = 0.002) and required less time to perform (p = 0.002). Ultrasound guidance reduced the time needed for block performance and procedural pain. The multiple twitch technique is based on searching and identifying the targeted nerve by eliciting each nerve's motor component with nerve stimulation [1][2][3]. It has been associated with a reduction in sensory and motor block onset and a greater efficacy than a single injection technique [2]. Recently, ultrasound guidance has been introduced in order to improve the efficacy of peripheral nerve blocks, to shorten procedural time, to reduce the minimum local anaesthetic volume required for a successful block and to lower the incidence of complications and side-effects [4][5][6]. Ultrasound guidance may, theoretically, offer an advantage over conventional technique (anatomical landmarks and nerve stimulation) since it allows direct visualisation of nerve structures, needle pathway and local anaesthetic spread in real time [7,8]. Ultrasound guidance for upper limb nerve blocks has been showed to have a greater success rate than nerve stimulation alone and it also allowed a reduction in local anaesthetic dose for femoral nerve block [6]. While its role for proximal sciatic nerve block has been widely described [9], some authors still argue about the feasibility of ultrasound guidance for sciatic block at the popliteal fossa [10,11].We conducted a prospective, randomised, observerblinded study to test the hypothesis that ultrasound guidance can shorten the onset of posterior popliteal sciatic nerve block as compared with nerve stimulation guidance for nerve location when using the multiple injection technique. MethodsWith Local Ethics Committee approval (University of Parma, Parma, Italy) and written informed consent, 44 American Society of Anesthesiologist physical status 1-3 patients undergoing foot and ankle surgery were enrolled in the study in January-March, 2008. Patients with clinically significant coagulopathy, infection at injection site, allergy to local anaesthetics, severe cardiopulmonary disease, body mass index > 35 kg.m 2 , diabetes mellitus, or known neuropathies, as well a...
Coeliac disease is diagnosed by the presence of specific antibodies and a jejunal biopsy showing mucosal atrophy and mononuclear cell infiltration. Mucosal cell-mediated immune response is considered the central event in the pathogenesis of coeliac disease, and untreated coeliac patients show specific features of T-cell activation in the small intestine. Here we describe the use of iodine-123-interleukin-2 scintigraphy in coeliac patients as a non-invasive tool for detection of lymphocytic infiltration in the small bowel and its use for therapy follow-up, and we demonstrate the specificity of binding of labelled-IL2 to activated lymphocytes by ex-vivo autoradiography of jejunal biopsies. 123I-IL2 was administered i.v. [74 MBq (2 mCi)], and gamma camera images were acquired after 1 h. Ten patients were studied with 123I-IL2 scintigraphy at diagnosis and seven were also investigated after 12-19 months of gluten-free diet. Results were expressed as target-to-background radioactivity ratios in six different bowel regions before and after the diet. At the time of diagnosis all patients showed a significantly higher bowel uptake of 123I-IL2 than normal subjects (P < 0.003 in all regions). A significant correlation was found between jejunal radioactivity and the number of IL2R + ve lymphocytes per millimetre of jejunal mucosa as detected by immunostaining of jejunal biopsy (r2 = 0.66; P = 0.008). Autoradiography of jejunal biopsies confirmed that labelled-IL2 only binds to activated T-lymphocytes infiltrating the gut mucosa. After 1 year of the diet, bowel uptake of 123I-IL2 significantly decreased in five out of six regions (P < 0.03), although two patients still had a positive IL2 scintigraphy in one region. We conclude that 123I-IL2 scintigraphy is a sensitive non-invasive technique for assessing in vivo the presence of activated mononuclear cells in the bowel of patients affected by coeliac disease. Unlike jejunal biopsy, this method provides information from the whole intestine and gives a non-invasive measure of the effectiveness of the gluten-free diet.
The data obtained from this study confirm changes in the IGF and cytokine systems at diagnosis of CD which tend to normalize on the gluten-free diet. The two systems show relationships with each other and with linear growth.
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Objective Growth delay is a feature of patients with cystic fibrosis (CF). CF is a condition characterized by chronic inflammation that has been shown to modify the IGF system, which is essential for normal growth, and is related to pulmonary function in CF patients. We aimed to verify whether circulating levels of tumour necrosis factor (TNF)-α , interleukin (IL)-6, insulin and the IGF system were related and/or had relationships with linear growth in children with CF. Design and patients Seventeen prepubertal CF patients (nine males and eight females) in a stable clinical condition were enrolled. Auxological parameters, pulmonary function and the Shwachman-Kulczycki (S-K) score were assessed, and serum samples were drawn at baseline and after 12 months. Measurements TNF-α , IL-6, IGF-I, IGF-II, IGFBP-1, IGFBP-2, IGFBP-3 and insulin were assayed using specific commercial kits. Results At baseline, TNF-α serum concentration was related to serum IGF-I concentration ( R = 0·53), IGF-II bioactivity (IGF-II/IGFBP-3 molar ratio, R = +0·52) and insulin concentration ( R = +0·63). Changes in serum IL-6 and IGFBP-2 concentrations during the 12-month observation were positively correlated ( R = +0·63). Changes in height standard deviation score (Ht SDS) were correlated with IGF-I serum concentrations at baseline ( R = +0·67) and after 12 months ( R = +0·70), with IGF-I bioavailability and with IGFBP-1 serum concentrations ( R = -0·88). Body mass index (BMI) SDS correlated with IGF bioavailability. Conclusions This study showed a relationship between inflammatory status and the IGF system, and an effect of these interactions on longitudinal growth. Moreover, a role for insulin in growth was identified. Better control of inflammation and preservation of insulin secretion could benefit these patients.
To clarify the possible neuroendocrine mechanisms underlying the impairment in growth hormone (GH) secretion present in obesity, the GH response to GH-releasing hormone (GHRH, N = 6), insulin hypoglycemia (N = 6), clonidine (N = 7) and arginine (N = 8) after GHRH pretreatment (1 microgram/kg iv 2 h before the tests) was evaluated in 27 obese peripubertal children and in a group of normal-weight short-normal children (N = 26). Growth hormone-releasing hormone pretreatment and all further stimuli elicited a statistically significant GH response in both obese and short-normal children; in the latter group arginine did not induce a significant GH response. No differences were found among the GH responses after the second stimuli in obese children, while in short-normal children the arginine peak and area values were lower than after GHRH and clonidine. Comparison between the two groups showed similar baseline but higher stimulated GH levels in normal-weight children after all tests except arginine, after which no difference was present. In conclusion, the neuroregulation of GH release seems to be similar qualitatively in normal-weight and obese youngsters; the different behavior observed after arginine, which is supposed to act through somatostatin inhibition, might be due to a chronic increase in somatostatinergic tone responsible for the lower stimulated GH levels in obesity.
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