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1.
Chinese Journal of Contemporary Pediatrics ; (12): 995-999, 2013.
Article in Chinese | WPRIM | ID: wpr-345662

ABSTRACT

<p><b>OBJECTIVE</b>To study the clinical characteristics of children who suffered from Streptococcus pneumoniae (SP) septicemia and the drug sensitivity of SP strains.</p><p><b>METHODS</b>A retrospective analysis was performed on the clinical data of 25 children with SP septicemia between January 2009 and December 2012.</p><p><b>RESULTS</b>Of the 25 cases, 16 (64%) were aged under 2 years, 5 (20%) were aged 2-5 years, and 4 (16%) were aged over 5 years. Fourteen cases (56%) were complicated by infection of other organs, and 5 cases (20%) had underlying chronic diseases. Fever was the most common clinical manifestation, and the majority presented with remittent fever. Eight patients with pneumonia or pyothorax had pulmonary symptoms. Five patients with purulent meningitis had neurological symptoms, five cases had hepatosplenomegaly and two cases had septic shock. Nineteen cases (76%, 19/25) had significantly elevated white blood cell (WBC) counts, twenty-one cases (84%, 21/25) had significantly elevated serum C-reactive protein (CRP) levels, and eight cases (50%, 8/16) had significantly elevated serum procalcitonin (PCT) levels. The drug sensitivity analysis showed that invasive SP had high resistance rates to penicillin (96%), clindamycin hydrochloride (88%) and erythromycin (84%), and it was completely sensitive to imipenem, vancomycin, levofloxacin and linezolid. The multi-drug resistance rate of invasive SP was up to 88%. Twenty-three cases (92%) were cured or improved after active treatment.</p><p><b>CONCLUSIONS</b>SP septicemia is commonly seen in children aged under 2 years. The most common clinical manifestation is fever, accompanied by elevated WBC count, CRP level and PCT level, and it is usually complicated by pulmonary or brain infection. Resistance to multiple antibiotics is very common in SP strains, so it is important to properly use antibiotics according to drug sensitivity test results. Patients who receive active treatment have a good clinical outcome.</p>


Subject(s)
Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Anti-Bacterial Agents , Therapeutic Uses , Bacteremia , Blood , Drug Therapy , C-Reactive Protein , Calcitonin , Blood , Calcitonin Gene-Related Peptide , Microbial Sensitivity Tests , Pneumococcal Infections , Blood , Drug Therapy , Protein Precursors , Blood , Retrospective Studies , Streptococcus pneumoniae
2.
Chinese Journal of Oncology ; (12): 629-631, 2011.
Article in Chinese | WPRIM | ID: wpr-320155

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the early efficacy of nedaplatin combined with megestrol in concurrent chemoradiotherapy for advanced cervical cancer.</p><p><b>METHODS</b>Forty-two cases of cervical cancer (FIGO IIb to IVa) were divided randomly into two groups: radiotherapy alone (21 cases) and radiation plus chemotherapy (Nedaplatin) group. The same radiotherapy was given to the two groups. Patients of the RT + C group received nedaplatin 30 mg/m2 in intravenous drip infusion once weekly on day 1, for 4 to 5 weeks, and megestrol 160 mg orally every day during the radiation therapy.</p><p><b>RESULTS</b>The early outcome: the complete remission rate was 81.0% and partial remission rate was 19.0% in the RT + C group, significantly better than the CR (38.1%) and PR (42.9%) in the RT group. The 1-year survival rates in the two groups were 100% (21/21) and 81.0% (17/21), respectively, with a significant difference between the two groups (P<0.05).</p><p><b>CONCLUSIONS</b>The combination of nedaplatin and megestrol with concurrent chemoradiotherapy can improve the early outcome of advanced cervical cancer, with somewhat increased but tolerable adverse effects.</p>


Subject(s)
Adult , Female , Humans , Middle Aged , Adenocarcinoma , Drug Therapy , Pathology , Radiotherapy , Alopecia , Anemia , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Brachytherapy , Chemoradiotherapy , Diarrhea , Follow-Up Studies , Iridium Radioisotopes , Therapeutic Uses , Leukopenia , Megestrol , Neoplasm Staging , Organoplatinum Compounds , Particle Accelerators , Radiotherapy, High-Energy , Remission Induction , Survival Rate , Thrombocytopenia , Uterine Cervical Neoplasms , Drug Therapy , Pathology , Radiotherapy
3.
Acta Pharmaceutica Sinica ; (12): 1244-1251, 2009.
Article in Chinese | WPRIM | ID: wpr-344087

ABSTRACT

Diabetes mellitus is a common metabolic disease with a high and growing prevalence affecting 4% of the population worldwide, the development of safe and effective therapeutic drug is the major thrust for chemists and pharmacists. To search for active antidiabetic lead compound, we designed and synthesized some novel beta-amino ketone derivatives containing sulfamethoxazole moiety directly through Mannich reaction of sulfamethoxazole, 4-bromoacetophenone and some aromatic aldehydes catalyzed by concentrated hydogen chloride or iodine in the solution of ethanol at 24-40 degrees C with convenient operation, mild reaction condition and satisfactory yield (32%-90%). Their chemical structures were characterized by 1H NMR, 13C NMR, MS and HR-MS. Biological activity tests showed that, in the range of low concentration (5-10 microg x mL(-1)), these title compounds to a certain degree possess protein tyrosine phosphatase 1B (PTP1B) inhibitory activity and a-glucosidase inhibitory activity, moreover, some could activate peroxisome proliferator-activated receptor response element (PPRE) moderately. The PPRE agonist activities of seven compounds are almost 40% of that of Pioglitazone (the positive control), compound 12 shows the strongest activity (66.35%) among them. Thus, it was found that some of 4-(3-(4-bromophenyl)-3-oxo-1-arylpropylamino)-N-(5-methyl-isoxazol-3-yl) benzenesulfonamide containing sulfamethoxazole moiety exhibited antidiabetic activity for the first time.


Subject(s)
Humans , Glycoside Hydrolase Inhibitors , Hypoglycemic Agents , Chemistry , Pharmacology , Molecular Structure , Oxazoles , Chemistry , Peroxisome Proliferator-Activated Receptors , Protein Tyrosine Phosphatase, Non-Receptor Type 1 , Response Elements , Structure-Activity Relationship , Sulfonamides , Chemistry , Thiazolidinediones , Pharmacology
4.
Journal of Southern Medical University ; (12): 336-339, 2007.
Article in Chinese | WPRIM | ID: wpr-298172

ABSTRACT

<p><b>OBJECTIVE</b>To understand the clinical features and prognosis of IgA nephropathy (IgAN) patients with glomerular crescents.</p><p><b>METHODS</b>The clinical data collected at the time of renal biopsy and the follow-up data of 89 IgAN patients with glomerular crescents were analyzed with 412 IgAN patients without crescents serving as the control group. Follow-up study was conducted in 78 patients with crescents and 198 without it, and the renal survival rate was estimated using Kaplan-Meier survival analysis.</p><p><b>RESULTS</b>The incidence of glomerular crescents was 17.8% in IgAN patients. Clinically, 39 patients with crescents experienced rapidly progressive glomerulonephritis, resulting in a significantly higher rate of this manifestation than that in patients without crescent. Patients with crescents also had more grave pathological changes in the glomerulus and renal tubule interstitium than the control patients. Patients were followed up for an average of 40.3-/+29.6 months in crescent group and 45.1-/+26.9 months in the control group, and the 1-, 3-, 5-year renal survival rate was 95.24%, 80.95%, 61.9% in the former and 100%, 91.67%, 79.17% in the latter, respectively.</p><p><b>CONCLUSION</b>IgAN patients with crescents have severer clinical and pathological manifestations and poorer prognosis than those without crescents.</p>


Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , China , Epidemiology , Follow-Up Studies , Glomerulonephritis, IGA , Mortality , Pathology , Kaplan-Meier Estimate , Kidney Glomerulus , Pathology , Prognosis , Survival Rate
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