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1.
China Pharmacy ; (12): 3297-3301, 2019.
Article in Chinese | WPRIM | ID: wpr-817434

ABSTRACT

OBJECTIVE: To introduce the pharmaceutical care for refractory mycoplasma pneumoniae (MP) pneumonia combined with cerebral infarction in child by clinical pharmacist, and to improve further understanding of MP-induced cerebral infarction and the management level of the clinical pharmacist. METHODS: Clinical pharmacist provided whole course pharmaceutical care for a child case of refractory PM pneumonia complicated with cerebral infarction admitted to the Children’s Hospital of Fudan University in Oct. 2018. The drug use in anti-infection, anti-inflammatory, treatment of cerebral infarction, possible drug interactions and suspected ADR were analyzed during treatment. RESULTS: The child admitted to the hospital for treatment due to MP pneumonia. During the treatment, the child suffered from cerebral infarction symptoms. The child was given a series of treatment programs, such as Azithromycin for injection for anti-infection, Methylprednisolone sodium succinate for injection for anti-inflammation, Nadroparin calcium injection for anticoagulation, Mannitol injection for reducing intracranial pressure, Dextran 40 glucose injection anti-thrombosis, Compound glycyrrhizin injection for protecting liver function, Hydrotalcite tablets for protecting gastric mucosa, intravenous immunoglobulin symptomatic supportive treatment. During the treatment, due to the poor therapeutic effect of Azithromycin for injection, it was considered that the patient may have cerebral infarction caused by refractory MP infection, so the patient’s prognosis was good when Azithromycin injection was replaced with Levofloxacin hydrochloride injection for anti-infection. For the increase of liver enzyme during the treatment, clinical pharmacist suggested that anti-infection combined with liver protection was provided   for the child and then the liver enzyme returned to normal. During the treatment, clinical pharmacist mainly monitored the interaction and possible adverse reactions among anticoagulants, glucocorticoids, liver protecting drugs, drugs for reducing cranial pressure, antipyretic and analgesic drugs, and at the same time, made medication publicity and education for the family members of the child, and inform them of the adverse reactions of drugs to be paid attention to and the precautions for taking stomach protecting drugs, glucocorticoids and other drugs. CONCLUSIONS: Cerebral infarction caused by refractory MP pneumonia in children is because of excessive immune response directly or indirectly mediated by MP. The principle of treatment is to inhibit the inflammatory response, to solve the primary disease, and symptomatic supportive treatment. Multi-drug combination is needed in the course of treatment, so it is more necessary for the clinical pharmacist to participate in the whole process and to manage the drug refinement and ensure the safety of drug use.

2.
Chinese Journal of Epidemiology ; (12): 273-280, 2016.
Article in Chinese | WPRIM | ID: wpr-737469

ABSTRACT

Objective To study the molecular-biologic characteristics and epidemiological status of iatrogenic related Community-acquired methicillin-resistant Staphylococcus (S.) aureus (CA-MRSA) in China through Meta-analysis.Methods Data through systematic searching for peer-reviewed articles published before December 3rd,2015 from 4 main electronic databases including China National Knowledge Infrastructure (CNKI),Wanfang Data,PubMed and Web of Science Core Collection was collected,for this Meta-analysis.PRISMA guidelines were followed and the proportion of MRSA,CA-MRSA,hospital-acquired MRSA (HA-MRSA) and panton-valentine leucocidin (PVL) gene in certain populations were quantitatively analyzed by Stata 13.0 software.Results Average proportion of CA-MRSA from S.aureus was 12% (95%CI:8%-16%).CA-MRSA in MRSA was 18% (95%CI:12%-24%).42.1% (95%CI:20.4%-63.7%) of the CA-MRSA carried a PVL gene,and the number was higher than general MRSA (t =-2.99,P=0.011).Conclusion CA-MRSA was in lower proportion than HA-MRSA,both seen in general MRSA and in S.aureu.s,but under higher proportion of carrying the PVL gene.Transmission of CA-MRSA could be prevented within the general population through conducting effective surveillances and preventive programs.

3.
Chinese Journal of Epidemiology ; (12): 273-280, 2016.
Article in Chinese | WPRIM | ID: wpr-736001

ABSTRACT

Objective To study the molecular-biologic characteristics and epidemiological status of iatrogenic related Community-acquired methicillin-resistant Staphylococcus (S.) aureus (CA-MRSA) in China through Meta-analysis.Methods Data through systematic searching for peer-reviewed articles published before December 3rd,2015 from 4 main electronic databases including China National Knowledge Infrastructure (CNKI),Wanfang Data,PubMed and Web of Science Core Collection was collected,for this Meta-analysis.PRISMA guidelines were followed and the proportion of MRSA,CA-MRSA,hospital-acquired MRSA (HA-MRSA) and panton-valentine leucocidin (PVL) gene in certain populations were quantitatively analyzed by Stata 13.0 software.Results Average proportion of CA-MRSA from S.aureus was 12% (95%CI:8%-16%).CA-MRSA in MRSA was 18% (95%CI:12%-24%).42.1% (95%CI:20.4%-63.7%) of the CA-MRSA carried a PVL gene,and the number was higher than general MRSA (t =-2.99,P=0.011).Conclusion CA-MRSA was in lower proportion than HA-MRSA,both seen in general MRSA and in S.aureu.s,but under higher proportion of carrying the PVL gene.Transmission of CA-MRSA could be prevented within the general population through conducting effective surveillances and preventive programs.

4.
Chinese Journal of General Practitioners ; (6): 650-652, 2013.
Article in Chinese | WPRIM | ID: wpr-437026

ABSTRACT

To explore the effects of nutritional risks on clinical outcomes [length of stay (LOS),hospitalization expense & mortality] in chronic kidney disease (CKD) patients.A total of 127 CKD patients completed the screening of nutritional risks by Nutritional Risk Screening 2002 (NRS-2002) within 24-48 hours of admission.The data of nutritional supports within 2 weeks of admission,LOS,hospitalization expense and mortality were collected.① Among them,the prevalence of nutritional risks was 18.1%.And the values were 8.2%,9.4% and 44.1% in early,middle and advanced CKD groups respectively; ② LOS and hospitalization expense in nutritional risk group were significantly more than the non-nutritional risk group (12.5 d vs.5.2 d,P =0.00 ; 11 806 vs.5311 yuan,P =0.00).There was a positive correlation between NRS score and LOS or hospitalization expense; ③ The nutritional support rate of nutritional risk group was only 17.4%.The progression of CKD increased the nutritional risks leading to greater LOS and hospitalization expense.We should pay more attention to the nutritional risk screening and nutritional intervention in moderate-advanced CKD patients.

5.
Chinese Journal of Microbiology and Immunology ; (12): 302-308, 2012.
Article in Chinese | WPRIM | ID: wpr-428830

ABSTRACT

Objective To examine the therapeutic effect of C Ⅱ TA inhibition in collagen-induced arthritis(CIA),using a delivery system tailored to target C ⅡTA gene by small interfering RNA (siRNA).Methods Mice with collagen-induced arthritis were injected intravenously with C Ⅱ TA siRNA.The clinical score was monitored for up to 4 weeks after treatment.The severity of inflammation of mouse joint was evaluated by histological examination.Real-time PCR was used to determine the cytokine mRNA expression.Cytokine production was measured by ELISA from serum.T cell proliferation was examined by MTT method.Results IFN-γ and IL-17 were elevated in CIA mice,but were iuhibited significantly by C Ⅱ TA siRNA either prevention or intervention of autoimmune arthritis.Collagen specific T cell proliferation was significantly suppressed.Increased level of IL-4 by T cells was observed in C Ⅱ TA siRNA treated group compared with that of control group.Conclusion Our findings indicate that systemic RNAi-mediated C Ⅱ TA gene silencing is effective in the treatment of CIA and regulateds the balance of Th1/Th2 differentiation.

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