1.Constructing a harmonious doctor-patient relationship
Chinese Journal of Hospital Administration 2011;27(2):118-121
Rapid economic development in China gives rise to a growing awareness of patients'rights, resulting in more disputes in medical malpractice between patients and hospitals and deteriorating the once harmonious doctor-patient relationship. The paper discussed the content, influencing factors of a harmonious relationship from both macro and micro perspectives. It focused on the role of governments in building and safeguarding a harmonious relationship, proposing the government should endeavor to create a favorable social environment while the hospital should enhance its management to safeguard a smooth medical process.
2.Integration of Cold-warm Syndrome and Exterior and Interior in Treating Epidemic Hemorrhagic Fever Based on Syndrome Differentiation
China Journal of Traditional Chinese Medicine and Pharmacy 2006;0(09):-
Though the clinical observation of 413 cases of epidemic hemorrhagic fever(EHF) by clinical epidemiological method,we have concluded that the main TCM etiological factors of EHF are damp,toxic heat,blood stasis and deficiency, and the determinant pathogenesis of EHF is the integration of interior and exterior pathogenic factors;the syndrome characteristic of EHF is that the cold,heat,deficiency and excess were intermingled,and the moist heat blood stasis syndrome should be given priority to;its major pathological location is initial YANG and triple warmer;so the therapeutic principle should be the integration of cold-warm syndrome and exterior and interior and paying attention to smoothing the triple warmer all the time.
3.HUANG Hai-long's clinical experience of application of insect drugs
China Journal of Traditional Chinese Medicine and Pharmacy 2005;0(03):-
To introduce HUANG Hai-long's clinical experience of applying insect drugs on treatment of 8 cases of trifacial neuralgia,facial nerve paralysis,lacouna cerebral embolism,sciatica,acne,xerosis cutis and pruritus symptoms of old people,cirrhosis,refractory amenorrhea.The paper reflects the reliabibity and adaptability of insect drug in treating different diseases with the same syndrome,and the flexible application of insect drugs by HUANG Hai-long.
4.Current situation and prospect of liver transplantation in China.
Chinese Journal of Surgery 2007;45(15):1009-1011
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8.Clinical observation of the restoration of vertically fractured molar by insertion fixation:1 case report
Journal of Practical Stomatology 2015;(2):296-297
One cases of vertically fractured molar was treated by following methods:the gap was exparded,the furcation lesion was drained;then a fixed prosthesis was inserted to restore the affected area.No symptom was observed in 2-year follow-up.
9.Investigation of the relationship between serological markers of hepatitis B virus infection and HBV-DNA
International Journal of Laboratory Medicine 2014;(9):1126-1128
Objective To investigate the relationship between serum hepatitis B virus markers (HBV-M ) and HBV-DNA . Methods Enhanced chemiluminescence enzyme immunoassay (ECLIA ) and real-time fluorescent quantitative polymerase chain re-action(FQ-PCR) were employed to detect HBV-M and HBV-DNA in 262 serum samples ,respectively .HBV surface antigen(HB-sAg) ,anti-HBV surface antibody(HBsAb) ,HBV e antigen(HBeAg) ,anti-HBV e antibody(HBeAb) ,anti-HBV core antibody(HB-cAb) were included in HBV-M .Results Compared the positive rates of HBV-DNA ,HBsAg ,HBeAb in HBeAg-negative patients with those in HBeAg-positive patients ,the differences were statistically significant (P< 0 .01) .29(36 .7% ) patients with HBV-DNA logarithm value not less than 5 were found in HBeAg-negative patients .Differences of HBeAg ,HBeAb positive rates among patients with different ages were statistically significant (P<0 .01) .25 patients with HBsAg less than 250 IU/mL were found in HBV-DNA-positive patients ,12(48 .0% ) of which showed HBV-DNA logarithm value not less than 5 .HBV-DNA logarithm value of HBV-DNA-positive patients was positively correlated to HBeAg and HBeAb (r= 0 .542 ,0 .607 ,P< 0 .01) .Conclusion Com-bined detection of HBV-M and HBV-DNA contributes to estimating the HBV infection .
10.Cloning and sequence analysis of human adiponectin gene
Chinese Journal of Tissue Engineering Research 2009;13(28):5519-5522
BACKGROUND: AdiponecUn (apM1) has been a new target for gene therapy of ischemic diseases; apM1 gene cloning is the key of successful apM1 gene therapy. There are two main gene cloning methods: directional cloning and T-A cloning method. Directional cloning method is complicated, while the T-A cloning method is relatively simpler, with higher successful rate. OBJECTIVE: T-A cloning of apM1 gene coding region was applied to verify the sequence in comparison with GenBank. DESIGN, TIME AND SETTING: The gene verification experiment was performed at the laboratories of Fujian Hypertension Research Institute which is in The First Affiliated Hospital of Fujian Medical University and Academy of Integrative Medicine which is in Fujian University of Traditional Chinese Medicine, from June 2006 to December 2008. MATERIALS: Adipose tissue sample of omental fat pad was obtained from a surgical patient in the First Affiliated Hospital of Fujian Medical University. Trizol produced by Invitrogen company; M-,-MLV, Gel Extract Kit produced by PROMEGA company; Taq enzyme produced by TIANGEN company; Restriction Endonucleases BamH Ⅰ and Sal Ⅰ, pMD18-T Vector produced by TAKARAcompany were used in this study.METHODS: Total mRNA was extracted from human greater omentum adipose tissue. The coding region of human apM1 (hapM1) gene was amplified by RT-PCR. The coding region of hapM1 gene was cloned into pMD18-T vector .The recombinant plasmid was identified with restriction enzyme digestion analysis and nucleotide sequencing. MAIN OUTCOME MEASURES: The electrophorasis verification of the recombinant plasmids coding target gene using double enzyme digestion, comparison of the similarity between the sequences of the plasmids and hapM1 in GenBank. RESULTS: Sense and antisense coding region of hapM1 gene were cloned. The sequencing results showed that the sequences of the cloned DNA were completely identical to that of hapM1 in GenBank.CONCLUSION: The coding region of hapM1 gene was successfully cloned.