1.Surgical staging applications with antibiotic graft bone for the treatment of open calcaneal fractures.
Lin-Ru ZENG ; Yang-Hua TANG ; Can-Da XU ; Zhen-Shuang YUE ; Zhi-Jin ZHANG
China Journal of Orthopaedics and Traumatology 2014;27(7):540-544
OBJECTIVETo discuss the effect of surgical staging and using craft bone with vancomycin for the treatment of calcaneal fractures.
METHODSFrom January 2006 to December 2012,13 patients with open calcaneal fractures were treated including 9 males and 4 females with an average of 35.2 years old ranging from 23 to 66. All cases were emergency cases. According to Sanders classification of calcaneal fractures, 2 cases were type II, 7 cases were type III, 4 cases were type IV. According to Gustilo-Anderson soft tissue injury classification, 8 cases were type II, 2 cases were type III A, 2 cases were type III B, 1 case were type III C. Firstly a thorough debridement or VSD procedures were applied,secondly calcaneal fracture were treated with open reduction, plate fixation and bone graft complex with antibiotics. Based on clinical examination, radiographic evaluation, and American Foot and Ankle Surgery Society (AOFAS), ankle function were evaluated after operation.
RESULTSOpen wounds were headed after dressing and repairing,, lateral calcaneal wound were healed during the first period. All patients were followed up for 6 to 36 months (means 14.5 months). Fracture healing time was 14 to 20 weeks (means 16.2 weeks). Last follow-up AOFAS ankle-hindfoot score was (80.0 +/- 7.4) ranging from 55 to 95.
CONCLUSIONFor patients with open fractures, through reasonable clinical evaluation, staging operation, using bone graft with antibiotics can reduce the incidence of postoperative wound infection and promote fracture healing.
Adult ; Aged ; Anti-Bacterial Agents ; administration & dosage ; Bone Transplantation ; methods ; Calcaneus ; injuries ; surgery ; Female ; Fracture Fixation, Internal ; Fracture Healing ; Fractures, Open ; surgery ; Humans ; Male ; Middle Aged
2.An improved method for the isolation of rat hepatic stellate cells.
Jian-chang SHU ; Jing-run ZHAO ; Dong-hua YANG ; Yan SHEN ; Can-can ZHONG
Chinese Journal of Hepatology 2004;12(6):353-355
OBJECTIVETo present an improved method to obtain pure, viable, freshly isolated hepatic stellate cells.
METHODSAdult male SD rats were used. All procedures were performed with the animals under sodium pentobarbital anesthesia. Three days after the single intravenous administration of 1 ml liposome-encapsulated CL2MDP, which has selective cytotoxicity of Kupffer cells, livers were perfused with D-Hank's solution containing 100 U/ml heparin for 10 to 15 minutes, and then with 0.05% collagenase dissolved in D-Hank's solution for 25 to 30 minutes. The liver was then gently homogenized and further incubated in 0.025% collagenase, and 0.005% DNAase I for 30 minutes at 37 degrees C under constant stirring. This suspension was filtered through stainless steel gauze and centrifuged for 2 minutes at 50 x g to remove parenchymal cells. Sinusoidal cells in the supernatant were recovered by centrifugation for 10 minutes at 300 x g. The cells were resuspended in the presence of 28.7% Nycodenz stock solution. The final concentration of Nycodenz at this stage was 11.5%. Following centrifugation for 17 minutes at 1400 x g, The cells at the top of this Nycodenz solution were collected. Cells were resuspended in Dulbecco's modified Eagle medium supplemented with 10% fetal calf serum, The cells were seeded in 50 ml culture flask at a density of 500,000 cells/ml, The cell viability was determined by trypan blue exclusion staining, the purity of hepatic stellate cells was identified by the expression of Desmin using immunocytochemistry method. Endogenous peroxidase staining was used to detect Kupffer cells.
RESULTSThe yield rate of hepatic stellate cells was 3 x 10(7) per rat, the cell viability was more than 95%, the desmin positive cell rate was 90%, no endogenous peroxidase positive cells were detected.
CONCLUSIONThe method for the isolation of hepatic stellate cells was developed without Kupffer cells confusion. The availability of highly purified stellate cells will facilitate the investigation of their functions in primary culture.
Animals ; Cell Culture Techniques ; Cell Separation ; methods ; Kupffer Cells ; cytology ; Liver ; cytology ; Male ; Rats ; Rats, Sprague-Dawley ; Ultracentrifugation ; methods
3.Staple fixation for the treatment of hamate metacarpal joint injury.
Yang-Hua TANG ; Lin-Ru ZENG ; Zhong-Ming HUANG ; Zhen-Shuang YUE ; Da-Wei XIN ; Can-Da XU
China Journal of Orthopaedics and Traumatology 2014;27(3):191-193
OBJECTIVETo investigate the effcacy of the staple fixation for the treatment of hamate metacarpal joint injury.
METHODSFrom May 2009 to November 2012,16 patients with hamate metacarpal joint injury were treated with staple fixation including 10 males and 6 females with an average age of 33.6 years old ranging from 21 to 57 years. Among them, 11 cases were on the fourth or fifth metacarpal base dislocation without fractures, 5 cases were the fourth or fifth metacarpal base dislocation with avulsion fractures of the back of hamatum. Regular X-ray review was used to observe the fracture healing, joint replacement and position of staple fixation. The function of carpometacarpal joint and metacarpophalangeal joint were evaluated according to ASIA (TAM) system evaluation method.
RESULTSAll incision were healed well with no infection. All patients were followed up from 16 to 24 months with an average of (10.0 +/- 2.7) months. No dislocation recurred, the position of internal fixator was good,no broken nail and screw withdrawal were occurred. Five patients with avulsion fracture of the back of hamatum achieved bone healing. The function of carpometacarpal joint and metacarpophalangeal was excellent in 10 cases,good in 5 cases, moderate in 1 case.
CONCLUSIONThe application of the staple for the treatment of hamatometacarpal joint injury has the advantages of simple operation, small trauma, reliable fixation, early postoperative function exercise and other advantages, which is the ideal operation mode for hamatometacarpal joint injury.
Adolescent ; Adult ; Carpal Joints ; injuries ; surgery ; Female ; Fracture Fixation, Internal ; instrumentation ; methods ; Fractures, Bone ; surgery ; Hamate Bone ; injuries ; surgery ; Humans ; Male ; Metacarpal Bones ; injuries ; surgery ; Metacarpophalangeal Joint ; injuries ; surgery ; Middle Aged ; Sutures ; utilization ; Young Adult
4.Antibacterial activity determination of six kinds of natural herbs in yunnan on normal oral predominant.
Yan-hong LI ; Juan LIU ; Li-chuan YANG ; Can-hua ZHANG ; Gang LI
West China Journal of Stomatology 2010;28(2):199-207
OBJECTIVETo determine the antibacterial activity of six kinds of natural herbs in Yunnan on normal oral predominant bacteria in vitro.
METHODSAgar dilution method, the antimicrobial susceptibility testing of anaerobes which was recommended by National Committee for Clinical Laboratory Standard (NCCLs), was used to determine the antimicrobial susceptibility of herbs to 21 kinds of oral model strains and clinical isolates. The results were expressed by minimum inhibitory concentration (MIC).
RESULTSAll six kinds of herbs were effective to the oral predominant bacteria. For the ten kinds of cariogenic bacteria, the MIC of caesalpinia sappan lignum was between 5-10 mg x mL(-1), and the MIC of other herbs was above 20 mg x mL(-1). For the eleven kinds of predominant bacteria which normally involved in pulp periapical disease and periodontitis, the MIC of caesalpinia sappan lignum was below 0.062 5 mg x mL(-1), and the MIC of the terminalia chebula retz was between 10-20 mg x mL(-1), and the others were above 20 mg x mL(-1).
CONCLUSIONThe six kinds of herbs in Yunnan could be used in treatment or prevention of oral bacterial diseases.
Anti-Bacterial Agents ; Bacteria ; China ; Humans ; Microbial Sensitivity Tests ; Mouth ; microbiology
5.Clinical application of free vascularized flaps based on the wrist cutaneous branch of ulnar artery in repairing finger soft tissue defect.
Yang-Hua TANG ; Lin-Ru ZENG ; Zhong-Ming HUANG ; Zhen-Shuang YUE ; Can-Da XU ; Da-Wei XIN
China Journal of Orthopaedics and Traumatology 2014;27(9):778-780
OBJECTIVETo investigate the methods and clinical effects of repairing finger soft tissue defect with free vascularized flaps based on the wrist cutaneous branch of ulnar artery.
METHODSFrom February 2010 to December 2012, 16 patients with finger soft tissue defects were repaired by free vascularized flaps based on the wrist cutaneous branch of ulnar artery, including 10 males and 6 females with an average age of 38.2 years old ranging from 18 to 52 years. Among them, 5 cases caused by hot crush injury, 8 cases caused by machine crush injury, 3 cases caused by firecracker burst injury. The defect area varied from 1.3 cm x 2.3 cm to 2.6 cm x 5.0 cm. The flap area varied from 1.5 cm x 2.5 cm to 2.8 cm x 5.2 cm. The appearance and two-point discrimination of flap were observed after operation.
RESULTSAll flaps survived and wounds healed primarily. No wound infection and skin necrosis were found in donor site and recipient site. Among repair methods, direct suture in forearm donor site had 11 cases and skin graft had 5 cases. All patients were followed up from 6 to 24 months with an average of 10.8 months. The appearance of flap was not fat or clumsy, texture and color were similar to the recipient site, the sensation were good, two-point discrimination was 6 to 9 mm. The appearance of donor site were well complicated with mild scarring without dysfunction obviously.
CONCLUSIONThe free vascularized flaps based on the wrist cutaneous branch of ulnar artery has the advantages of vascular anatomy constant,thickness moderate and carry sensory nerves, etc, which is effective way to repair finger soft tissue defects.
Adolescent ; Adult ; Female ; Finger Injuries ; surgery ; Free Tissue Flaps ; Humans ; Male ; Middle Aged ; Soft Tissue Injuries ; surgery ; Ulnar Artery ; surgery ; Young Adult
6.MRI diagnosis of benign sacrococcygeal teratomas of the infants.
Can LAI ; Shi-zheng ZHANG ; Hua-jun YANG
Journal of Zhejiang University. Medical sciences 2006;35(1):103-107
OBJECTIVETo investigate the value of MR imaging in the diagnosis of benign sacrococcygeal teratomas of the infants.
METHODSMR imaging of benign sacrococcygeal teratomas in 6 cases proved by surgery and pathology was retrospectively reviewed. In all patients, a fast imaging sequence, fast spin echo sequence was employed, together with short time inversion recovery sequence and contrast enhancement scanning by intravenous injection of Gd-DTPA.
RESULTSThere were 6 benign sacrococcygeal teratomas, which were heterogeneous masses and arose from the distal sacrococcygeal region in the pelvis. The MR imaging appearances of the benign sacrococcygeal teratomas were characteristic, T1- and T2-weighted images demonstrated a large mass containing round, well-defined areas of varying signal intensity representing its cystic, solid, and sometimes fat, calcification within the lesions.
CONCLUSIONMR imaging provides definitive information of benign sacrococcygeal teratomas and clearly shows both extra-and intra-pelvic components, and even better anatomic details, which facilitates the surgical planning adequately.
Female ; Humans ; Infant ; Infant, Newborn ; Magnetic Resonance Imaging ; Male ; Retroperitoneal Neoplasms ; diagnosis ; Sacrococcygeal Region ; Teratoma ; diagnosis
7.Protective effect of non-mitogenic haFGF on retinal injury induced by N-methyl-N-nitrosourea in Sprague-Dawley rats.
Hua XU ; Jin-nan YANG ; Qing ZHENG ; Cheng-can YAO ; Yan-ping WANG ; Ji-zhou XIANG ; Xiao-kun LI
Acta Pharmaceutica Sinica 2005;40(4):306-310
AIMTo study the effect of non-mitogenic human acidic fibroblast growth factor (nm-haFGF) on retinal injury induced by N-methyl-N-nitrosourea (MNU) in Sprague-Dawley rats and its mechanism.
METHODSFemale rats of 50-days-old were injected with MNU (60 mg x kg(-1)) intraperitoneally, and three doses of nm-haFGF (1.25 microg, 2.5 microg and 5 microg in one eye of each rat) were injected, separately, into vitreous body of one eye of each rat twice a day at 0 and 12 h after MNU treatment. 24 h later, apoptotic index of photoreceptor cells was detected by TUNEL labeling and the expressions of Bcl-2 and Bax were analyzed by Western blotting. At the 7th day, retinal injury was evaluated based on retinal thickness.
RESULTSCompared with model group, apoptotic index of photoreceptor cells was significantly reduced in nm-haFGF groups at the dose of 1.25 microg and 2.5 microg in one eye of each rat at 24 h, and the total retinal thickness as well as the outer retinal thickness markedly increased 7 days after MNU, respectively. The expressions of Bcl-2 increased and that of Bax decreased adversely after being injected with different doses of nm-haFGF.
CONCLUSIONnm-haFGF partially suppressed retinal injury induced by MNU in Sprague-Dawley rats. The mechanism could be related to up-regulation of Bcl-2 and down-regulation of Bax.
Animals ; Apoptosis ; drug effects ; Female ; Fibroblast Growth Factor 1 ; genetics ; pharmacology ; Methylnitrosourea ; Photoreceptor Cells, Vertebrate ; drug effects ; pathology ; Protective Agents ; pharmacology ; Proto-Oncogene Proteins c-bcl-2 ; metabolism ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Retina ; drug effects ; pathology ; Retinitis Pigmentosa ; chemically induced ; metabolism ; pathology ; bcl-2-Associated X Protein ; metabolism
8.Correlation Analysis between STING Promoter Polymorphism and Susceptibility to Infection after Chemotherapy for Multiple Myeloma
Zhao-Ping HUANG ; Can-Hua YANG
Journal of Experimental Hematology 2024;32(3):927-932
Objective:To investigate the correlation between the stimulator of interferon genes(STING)promoter polymorphism and the susceptibility to infection after chemotherapy for multiple myeloma.Methods:A total of 102 patients who had undergone chemotherapy for multiple myeloma in our hospital from January 2016 to July 2022 were selected.Depending on the presence or absence of infection after chemotherapy,the enrolled patients were divided into infection group(53 cases)and non-infection group(49 cases).The infection sites and distribution characteristics of pathogenic bacteria of the infection group were analyzed.The genotype distribution of STING gene promoter rs587777609 was compared between the two groups,and the risk factors of infection after chemotherapy for multiple myeloma were analyzed.Results:For infection site,digestive system,respiratory system,urinary system,skin and mucous membranes accounted for 43.40%,26.42%,20.75%,and 9.43%,respectively.For pathogenic bacteria,Gram-negative bacteria,Gram-positive bacteria and fungi accounted for 57.14%,26.98%,and 15.87%,respectively.The CC genotype frequency of STING gene rs587777609 locus in the infection group was lower than that in the non-infection group,while the TT genotype frequency was higher than that in the non-infection group(P<0.05).The proportions of patients with diabetes,chronic obstructive pulmonary disease,renal insufficiency,serum albumin level<35 g/L,ISS stage Ⅲ,mechanical ventilation,and indwelling catheter in the infection group were higher than those in the non-infection group(P<0.05).Multivariate logistic regression analysis showed that diabetes(OR=1.992),serum albumin level<35 g/L(OR=2.782),ISS stage Ⅲ(OR=2.707),mechanical ventilation(OR=3.031),and TT genotype(OR=2.401)were risk factors of infection after chemotherapy for multiple myeloma(P<0.05).Conclusion:There is a correlation between STING promoter polymorphism and the susceptibility to infection after chemotherapy for multiple myeloma,and patients with TT genotype have a higher risk of infection.
9.Expression of P33ING1 in stomach cancer and its clinical significance
Hou-Zhong DING ; Hai-Ren YANG ; Xiao-Feng CAI ; Liang-Bo LI ; Cai-Hua LI ; Xiao-Yang WU ; Dong YANG ; Xin LENG ; Can-Rong NI ; Ming-Hua ZHU ; Hai LI
Academic Journal of Second Military Medical University 2001;22(1):57-60
Objective:To discuss the pathological relationship between P33ING1 and stomach cancer and its clinical significance. Methods: In 71 cases of stomach cancer specimen, twelve cases of gas tric mu cous membrane atypical hyperplasia tissues and 18 cases of normal gastric mucous membrane tissue(as control),the expression of P33ING1 were detected b y EnVision immunohistochemical method,while the expression of P53 and Bcl -2 in stomach cancer were also detected. Results: P33IN G1 expression in mucous membrane atypical hyperplasia group and control group was positive, the expression in stomach cancer group was extremely low(62.0%,44 /71), significantly different from the other 2 groups(P<0.01).P33ING1 expression in stomach cancer was related to the tumor growth, lymph node meta s tasis and tumor polarization (P<0.01), P53 expression was related to tumor s ize, growth and lymph node metastasis (P<0.01). Bcl-2 expression was relate d to lymph node metatasis and tumor polarization.The expression of P33ING1 was related to that of P53 in stomach cancer(P<0.05),while had no relation with that of Bcl-2.Conclusion:P33ING1 may play an importa nt role in the occurrance and development of stomach cancer.It's very important to detect the expression of P33ING1 and P53 simultaneously.
10.One-step multiplex RT-PCR for rapid screening of type A, B and novel A (H1N1) influenza viruses.
Qiu-hua MO ; Cui-lan YANG ; Ji-can LIN ; Hua TAN ; Cheng-ning TU ; Li-qing YE ; Zhi-ming LIU ; Jian DU ; Hong SUN ; Ze YANG
Journal of Southern Medical University 2009;29(8):1545-1547
OBJECTIVETo developed a multiplex RT-PCR assay for simultaneous screening of type A, B and novel A (H1N1) influenza viruses.
METHODSTwo pairs of universal primers in were designed for amplifying the M gene and NS gene of type A and B influenza viruses, respectively. A pair of specific primers of HA gene was designed to detect novel A (H1N1) influenza virus. A one-step method was used to establish the multiplex RT-PCR system. A blinded experiment was carried out to validate the accuracy of this assay in comparison with the results of real-time fluorescence RT-PCR. The clinical practicability and efficacy of this assay was also evaluated.
RESULTSThe RT-PCR products were analyzed using agarose gel electrophoresis, which yielded distinct bands of the target fragments without non-specific reactions, suggesting the high efficiency and specificity of the multiplex RT-PCR. Blinded study of 50 samples demonstrated a concordance rate of 100%.
CONCLUSIONThis multiplex RT-PCR assay allows one-step simultaneous detection of type A, B and novel A (H1N1) influenza viruses rapidly and accurately, and provides a valuable low-cost screening technique for influenza epidemic monitoring and early diagnosis.
Humans ; Influenza A Virus, H1N1 Subtype ; genetics ; isolation & purification ; Influenza B virus ; genetics ; isolation & purification ; Reverse Transcriptase Polymerase Chain Reaction ; methods ; Time Factors ; Viral Matrix Proteins ; genetics ; Viral Nonstructural Proteins ; genetics