PubMed · 9379148
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J C Mohs, W P Newton. 1997. Epidural injections for sciatica.. https://pubmed.ncbi.nlm.nih.gov/9379148/
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A fast and efficient multi-residue extraction-purification procedure was developed for 12 corticosteroids in biological matrices (hair, urine and meat), in order to control their illegal use as growth promoters in cattle. Detection and identification of the analytes were achieved using a previously described LC-MS-MS method based on negative electrospray ionisation and a triple quadrupole analyser. The presented procedures included acid (hair) or enzymatic (urine and meat) hydrolysis, C18 reversed-phase SPE, Na2CO3 liquid-liquid clean-up and SiOH normal-phase SPE. The detection limits of the developed methods were between 2.9 and 9.3 pg/mg (ppb) for hair samples and in the 40 - 70 pg/g (ppt) range for the urine or meat samples. The acid hydrolysis used for corticosteroid extraction in hair was optimised using an experimental design and response surface methodology. Achieved performances were linked to a physico-chemical approach based on the corticosteroids specific C17 side-chain. This original multi-residue and multi-matrices analytical methodology will be used for further metabolism studies.
ENDEMIC ZONES: Strongyloidiasis is an intestinal parasitosis which is frequently found in tropical and subtropical regions. RISK: The "autoinfection" cycle during this helminthiasis explains why the infection can be perpetuated without further exposure to exogenous, infective larvae. Hyperinfection may occur by dissemination of Strongyloides stercoralis in immuno-compromised patients, particularly those under corticotherapy. DISSEMINATATED STRONGYLOIDIASIS: Disseminated strongyloidiasis is characterized by severe gastrointestinal and respiratory tract involvement, meningitis, skin rash, or Gram-negative bacteremia. Since disseminated stronglyoidiasis is fatal in 80% of cases it is imperative to diagnose and treat this condition before long-term corticotherapy. Ivermectin is currently recommended because it is effective and well tolerated.
BACKGROUND: Mycophenolate mofetil (MMF) has previously been shown to be significantly better than azathioprine (AZA) in the treatment of first acute renal transplant (Tx) rejection by 6 months after initiation of treatment. This report analyzes the 3-year safety and efficacy data from this cohort of patients. METHODS: Renal Tx recipients with a first rejection episode occurring within 6 months after a first or second cadaver or living donor Tx were randomized, double-blind, to receive MMF (1.5 g b.i.d., n=113) or AZA (1-2 mg/kg, n = 108); both treatment arms also received i.v. corticosteroids (5 mg/kg/day for 5 days) followed by a steroid taper in conjunction with cyclosporine. Patients remained on blinded study medication for 1 year, after which they were converted to open-label study medication at the same dosage. All patients, including those who terminated early (<3 yr) were followed for patient and graft survival, chronic renal allograft dysfunction (CRAD), and malignancy. CRAD was determined by the presence of at least two of the following: a biopsy with chronic rejection, proteinuria >750 mg/day, or an increase in serum creatinine >1 mg/dl over baseline. Patients who continued to receive the assigned medication were followed for additional rejections, renal function, and adverse events including infections. RESULTS: A total of 67 (59.3%) MMF-treated and 56 (51.9%) AZA-treated patients completed the 3-year study; follow-up was available for all randomized patients except one. At 3 years, the cumulative incidence of first subsequent biopsy-proven or presumptive rejection while receiving study drug was 42.2% in the MMF-treated and 68.8% in the AZA-treated patients; a difference of 26.6% (95% confidence interval: 13.4-39.9%). At 3 years, 19.6% of all MMF-treated and 24.1% of all AZA-treated patients lost their Tx or had died. Renal function was similar in both groups. The combined end point of CRAD or Tx loss without CRAD occurred in 23% and 26% of all MMF- and all AZA-treated patients, respectively. Leukopenia, diarrhea, and abdominal pain were the most commonly associated adverse events of MMF treatment. Malignancies (predominantly cutaneous) occurred in 14.2% of MMF-treated patients and 10.2% of AZA-treated patients. Three lymphomas occurred in each treatment arm. CONCLUSION: The addition of MMF at the time of renal Tx rejection reduces the frequency of subsequent rejections without causing new limiting side effects. Although Tx survival was better in the MMF group, comparison with AZA was confounded by the rate of premature terminations in both treatment groups.