2016, 37(1).
Abstract:1
LI Ting , WANG Chen , CHENG Da-sheng , XIAO Shi-chu , WANG Guang-yi , MA Bing , BEN Dao-feng , XIA Zhao-fan
2016, 37(1):1-4. DOI: 10.16781/j.0258-879x.2016.01.0001
Abstract:Objective To investigate the clinical efficacy of artificial dermis scaffold combined with autologous split-thickness skin graft in repairing deep wounds on hands and feet after extensive burn by comparing with the traditional ways. Methods The patients with deep wounds on hands and feet, who were treated in Department of Burn Surgery, Changhai Hospital, Second Military Medical University from March 2012 to March 2015, were selected as participants. A total of 28 patients meeting the inclusion criteria were allocated into two groups according to the operations. The observation group (14 cases) received artificial dermis scaffold after crust resectional therapy at 4-7 days after burns, and they also received autologous split-thickness skin graft following crust resectional therapy at 21-28 days after burns. The control group (14 cases) received changing medicine to maintain the scab following crust resectional therapy at 4-7 days after burns, and they also received autologous split-thickness skin graft following crust resectional therapy at 28-35 days after burns. The following data were recorded: the operation time, survival rate of skin graft, the cause of the flap necrosis, healing time of donor site and whether it could donor more flap or not, and the hyperplastic scars on hands and feet. Results The observation group needed similar operation time when compared with the control group for the first operation ([4.50±0.76] h vs[4.14±0.86] h,P>0.05), while the second operation time of the observation group was significantly shorter than that of the control group ([2.11±0.35] h vs [3.39±0.49] h, P<0.001). When changing the medicine at the 8th day after skin grafting, the survival rate of skin graft in the observation group was 97.37%(37/38) and the infection rate was 2.63%(1/38); the survival rate of the whole skin graft in control group was 73.68%(28/38), and that of partial skin graft was 23.68%(9/38), with an infection rate of 2.63%(1/38). The healing time of donor site in the observation group was significantly shorter than that of the control group([6.07±0.83] d vs [14.64±0.93] d, P<0.001). And it was estimated that 78.57%(11/14) of the patients in the observation group and 14.29%(2/14) of patients in the control group could donor more graft(P<0.05). One year follow-up showed that hyperplastic scars on hands and feet in the observation group was significantly better than those in the control group according to the Vancouver Scar Scale (VSS, [5.07±1.21] vs [8.07±1.14], P<0.001). Conclusion Artificial dermis scaffold can be used at early time in repairing deep wounds on hands and feet after extensive burn, with no need for additional operation time; and both the survival rate of skin graft and long-term function are good, with less damage to the donor site.
TANG Liang , GAO Xu , XU Chuan-liang , CHEN Guo-qiang , WANG Yan , WANG Hai-feng , SUN Ying-hao
2016, 37(1):5-9. DOI: 10.16781/j.0258-879x.2016.01.0005
Abstract:Objective To indentify the high risk factors of bone metastasis in Chinese patients at the initial stage of prostate cancer (PCa) diagnosis, so as to elucidate the characteristics of patients with very low risk of bone metastasis at the initial stage of prostate cancer. Methods A consecutive series of 496 patients with newly diagnosed PCa between 2010 and 2015 were enrolled in the present study. All the patients were subjected to ECT scan for presence of bone metastasis (BM) using total-body 99mTc MDP scintigraphy regardless of baseline PCa characteristics. Factors including the age of diagnosis, prostate specific antigen (PSA) level at diagnosis, Gleason score, clinical T stage, bone scan and CT/MRI results were analyzed. Univariate and multivariate logistic regression analyses were performed to identify the predictors of bone metastases. Results Of the 496 patients, 81 patients (16.3%) had bone metastases. The PSA levels of patients with BM were significantly higher than those without BM (P<0.001). The mean age of the patients with BM was not significantly older than that of the patients without BM. Patients with higher PSA level, clinical T stage or Gleason score showed a significantly higher risk of BM (P<0.001). Univariate logistic regression analysis showed that PSA>20 ng/mL at diagnosis, clinical stage at T3-T4 and Gleason score≥8 were the risk factors of bone metastasis in PCa patients. The multivariate analysis showed that the PSA level>50 ng/mL and the Gleason score≥8 were the independent predictors of bone metastases. No bone metastasis was found in 79 patients with PSA≤20 ng/mL and at the same time with Gleason score≤6. Conclusion The bone metastases rate is very low in Chinese patients with a PSA level ≤20 ng/mL and at the same time with Gleason score≤6, so a bone scan is not necessary as a routine for these patients with newly diagnosed prostate cancer.
NING Zhou-yu , WANG Peng , CHEN Hao , XIE Jing , LIN Jun-hua , ZHU Xiao-yan , CHEN Qi-wen , XU Li-tao , SONG Li-bin , GAO Song , JIANG Feng , MENG Zhi-qiang
2016, 37(1):10-16. DOI: 10.16781/j.0258-879x.2016.01.0010
Abstract:Objective To investigate the apoptosis, immunity response and angiogenesis factor changes in rabbits with pancreatic cancer xenografts after treatment with irreversible electroporation (IRE,commonly known as nanoknife), cryoablation, or radiofrequency ablation (RFA), and to observe the antitumor effects of the above minimally invasive techniques for pancreatic cancer xenografts. Methods Eight pancreatic cancer xenograft model rabbits were randomly divided into the control, IRE, cryoablation, and RFA groups, with each group containing 2 rabbits. The vital signs of the animals were observed during the treatment and all the rabbits were executed on the next day after treatment. The serum samples were collected to examine the liver, kidney function and creatine kinase levels; and ELISA method was used to detect the cardiac troponin I(CTnI), Caspase-3, tumor necrosis factor-α (TNF-α) and vascular endothelial growth factor(VEGF) levels in the plasma. Morphological changes of the tumor tissues were subjected to H-E staining, and Tunnel assay was used to detect the apoptosis of tumor cells. Immunohistochemistry method was applied to detect Bcl-2, HSP70 and VEGF expression in pancreatic cancer xenograft tissues. Results All the rabbits survived after treatment. The tumors had a clear border and were hard in texture. Obvious coagulative necrosis areas were seen in the treatment areas in each treatment group. H-E staining showed a clear borderline between the necrotic and normal areas, which was especially true in the IRE group. A large number of red blood cells and inflammatory cell infiltration were seen around the border of the necrosis in each group, with some live cells seen in the cryoablation and RFA groups. Tunnel assay showed that RFA significantly increased the apoptosis in pancreatic cancer cells compared with the other two treatment groups. The plasma Caspase-3,TNF-α and VEGF levels were increased in each treatment group. Bcl-2 and VEGF expression was decreased and HSP70 expression was increased in the treatment areas. Post-treatment serological test showed that serum amylase, liver, kidney functions and CTnI were all within the normal range, except for a significantly higher level of creatine kinase in the IRE group. Conclusion IRE, cryoablation, and RFA can inhibit pancreatic cancer xenograft through inducing apoptosis, producing specific antitumor immune response and inhibiting angiogenesis; they are safe and effective. IRE has certain advantages in producing specific antitumor immune response and protecting important peripheral organs.
CHEN Jing , ZHANG Jing-qing , HE Dan , WANG Hong , LEI Ting-ting , JIANG Xin-hui
2016, 37(1):17-21. DOI: 10.16781/j.0258-879x.2016.01.0017
Abstract:Objective To develop a pre-column derivatization HPLC/FLD method for determining the content of cyclovirobuxine D (CB) in rat plasma, and to evaluate the pharmacokinetics of cyclovirobuxine D phospholipid complex (CBPC) and CB in SD rats by oral administration. Methods The solvent evaporation method was used to prepare CBPC. The preparation protocol was optimized by central composite design, with the ratio of phospholipid and CB, concentration of principal agent as the independent variables, and with the compound rate as the response variable. Twelve male rats were evenly randomized into two groups with each containing 6 animals. Rats were orally given CBPC and CB (60 mg/kg, with CB count). Blood samples were collected from the retinal venous plexus of SD rats after oral administration of CBPC and CB at 15 min, 30 min, 1, 2, 3, 4, 5, 6, 8, 12 and 24 h time points, and the blood concentrations of CB was determined by HPLC/FLD. The HPLC method employed the C18 column (250 mm × 4.6 mm,5 μm) with a mobile phase of methanol-water (85∶15) at a flow rate of 1.0 mL·min-1. The excitation wavelength was set at 231 nm, emission at wavelength 385 nm, and the column temperature was 25℃. Results The pharmacokinetic parameters of CBPC and CB were calculated as follows: AUC0-t(1 703.81±549.38) μg·h·L-1 and (619.93±75.67) μg·h·L-1, Tmax (6.00±0) h and (4.33±0) h, Cmax(82.32±9.55) μg·L-1 and (69.27±8.66) μg·L-1. The relative bioavailability of CBPC was 274.84%. Conclusion Phospholipid complex can improve the oral bioavailability of CB in rats.
SU Jie , LU Jian , HUANG Gao-xiang , CAO Dong-mei
2016, 37(1):22-26. DOI: 10.16781/j.0258-879x.2016.01.0022
Abstract:Objective To study the expression of Bin1b in primary cultured epididymal epithelial cells treated with different steroid hormones at various concentrations. Methods Expression of Bin1b mRNA was examined by agarose gel electrophoresis and PCR in primary cultured epididymal epithelial cells, which were treated with dihydrotestosterone (DHT, 10-9,10-8 and 10-7mol/L), estradiol (E2, 10-9 and 10-8mol/L)) or dexamethasone (Dex, 10-8 and 10-7mol/L) at different concentrations. Results The expression of Bin1b mRNA in primary cultured epididymal epithelial cells was decreased in a time-dependent manner. The mRNA level of Bin1b was decreased by 40% at day 2 and 70% at day 3; and it was hardly detectable at day 5. DHT up-regulated the expression of Bin1b mRNA in a dosage-dependent manner compared with corresponding vehicle control. 10-9mol/L DHT up-regulated Bin1b mRNA level by 37% compared with corresponding vehicle control(P<0.05), and it was further up-regulated after the treatment with 10-8mol/L and 10-7mol/L DHT. E2 and Dex at various concentrations showed no significant effects on the expression of Bin1b mRNA in primary cultured epididymal epithelial cells. Conclusion Dihydrotestosterone can up-regulate the expression of Bin1b mRNA in primary cultured epididymal epithelial cells, while estradio and dexamethasone can not.
CHEN Xu-jiao , TUO Su-xin , TAO Yu , BIAN Rong-rong , XING Xiao-hong , PAN Xiao-hong , CHEN Juan-juan , MAO Zhi-guo
2016, 37(1):27-33. DOI: 10.16781/j.0258-879x.2016.01.0027
Abstract:Objective To analyze the baseline detection indicator and clinical data of peritoneal dialysis (PD) patients with end-stage kidney disease (ESKD) and to identify the risk factors for PD drop-out in ESKD patients, so as to provide reference for selecting dialysis modes. Methods The baseline data of 99 ESKD patients starting to receive PD in Changzheng Hospital, Second Military University from July 2011 to July 2012, were analyzed retrospectively. The patients were divided into drop-out group (including patients who were dead and turned to hemodialysis ) and continuous PD group according to whether they were dropped out during a follow-up of 3 years. Correlation analysis was done for preoperative examination indices and clinical data to identify the risk factors of PD drop-out. Results Ten renal transplant patients and 6 who were lost in follow-up were excluded and finally there were 83 patients included. Fifty patients were in the continous PD group and 33 patients were dropped out during a 3-year follow-up period, with 19 died and 14 transferred to hemodialysis. Multivariate Cox regression analysis showed that presence of diabetes (P=0.003, HR:3.61, 95% CI:1.57-8.30), hyperphosphatemia (P<0.001, HR:1.65, 95% CI:1.26-2.13), and high serum total bilirubin (P=0.006, HR:1.11, 95% CI:1.03-1.19) were the independent risk factors of PD drop-out. In addition, age (P=0.035, HR:1.05, 95% CI:1.00-1.07) and anemia (P=0.016, HR:0.96, 95% CI:0.94-0.99) were the independent risk factors for all-caused mortality. Conclusion Presence of diabetes, hyperphosphatemia, and high serum total bilirubin are possible independent risk factors of PD drop-out.
CHEN Ting , LIU Jie , YU Yun-hua , BAO Li-zhi , KANG Bo , ZHENG Xing
2016, 37(1):34-39. DOI: 10.16781/j.0258-879x.2016.01.0034
Abstract:Objective To establish a cardiomyocyte model over-expressing mutant human PRKAG2 by infecting neonatal SD rat myocardial cells with constructed recombinant adenovirus vector Ad-PRKAG2 (R302Q)-IRES2-EGFP. Methods PRKAG2 (R302Q)-IRES2-EGFP was directly cloned into entry vector pDONR221 by using Invitrogen GatewayTM technology. Then BP and LR recombination reactions yielded the recombinant adenovirus vector containing human PRKAG2 (R302Q) gene. The pAd-PRKAG2 (R302Q)-IRES2-EGFP was digested by Pac Ⅰ, and transfected into 293 cells. After packaging, amplification and purification, the virus was used to infect neonatal rat cardiomyocytes. Then the expression of PRKAG2 protein was assayed by Western blotting analysis in the infected neonatal SD rat cardiomyocytes. Results Restriction enzyme digestion analysis and the sequence analysis confirmed that PRKAG2(R302Q) gene was successfully inserted into the adenovirus vector. The myocardial cells infected with Ad-PRKAG2(R302Q)-IRES2-EGFP gave off strikingly bright green fluorescence and PRKAG2 protein was proven significantly over-expressed by Western blotting analysis (P<0.05). Conclusion The recombinant adenovirus containing human PRKAG2(R302Q) gene has been successfully constructed and expressed in neonatal rat cardiomyocytes, which paves a way for further study of PRKAG2 (R302Q) gene mutation.
LI Rong , SHENG Dan-dan , ZHAO Xue , JING Ying-ying , ZHANG Li , HAN Zhi-peng
2016, 37(1):40-45. DOI: 10.16781/j.0258-879x.2016.01.0040
Abstract:Objective To observe the influence of interferon-γ(IFN-γ)and tumor necrosis factor-α(TNF-α)treated mesenchymal stem cells (MSCs) on the chemotherapy resistance of colon cancer cells(CRCs) and to discuss the related mechanism. Methods The supernatants of MSCs treated with IFN-γ and TNF-α were collected and used, together with chemotherapy drug cisplatin and 5-fluorouracil, to treat HCT116 and HT29 CRCs. Then the cellular morphology was observed under microscope, and the cell proliferation and apoptosis were examined by MTT and PI/Annexin Ⅴ-FITC assay. Furthermore, the mRNA levels of Bax and Bcl-2 were detected by RT-PCR. Results The CRCs treated with the supernatant of MSCs exposed to inflammatory factors, compared to CRCs treated with the supernatant of MSCs not exposed to inflammatory factors, had a slighter morphology changes, a significantly higher proliferation rate (P<0.05), and a significantly lower apoptosis rate following chemotherapy(P<0.05). Moreover, Bcl-2 mRNA level was higher and Bax mRNA level was lower in CRCs treated with the supernatant of MSCs exposed to inflammatory factors. Conclusion MSCs stimulated with inflammation factors IFN-γ and TNF-α can promote the chemotherapy resistance of human CRCs.
LONG Fei , LI Xue-zhi , GONG Biao , WANG Ying , DAI En-ze , GUO Quan-hu
2016, 37(1):46-51. DOI: 10.16781/j.0258-879x.2016.01.0046
Abstract:Objective To observe the effect of electro-acupuncture (EA) intervention on expression of Slit2 and SrGAP1 in rats with focal cerebral infarction and to study the underlying mechanism of EA intervention on neuronal plasticity after cerebral ischemia. Methods Sixty male Sprague Dawley rats were randomly divided into Model group(n=30) and EA group (n=30); and according to elctro-apunture treatment duration, both 2 groups were further randomized into 3 subgroups:0 d(n=10),7 d(n=10), and 14 d (n=10).The middle cerebral arteries of the model group and EA group were embolized for 1.5 hours by suture. Nissl staining, immunofluorescence method and Western blotting analysis were sued to observe the histology and morphology change around the cerebral infarction and to assay the expression of Slit2 and SrGAP1 in the cerebral cortex on the ischemic side on day 0, 7, and 14. Results In comparison with the model group, the neurological score of EA group had no obvious difference on day 0 (P>0.05) and was significantly lower on day 7 and day 14 (P<0.01). Nissl staining results showed that in comparison with the model group, EA group had no obvious difference and both groups had reduced nissl body number, disordered array and brain edema on day 0; even on day 7 the nissl bodies were still disordered in the EA group, but the nissl body number increased obviously; while on day 14 the EA group had increased and well arrayed nissl bodies. Immunofluorescence method and Western blotting analysis showed that the fluorescence intensities and grey levels of rat Slit2 and SrGAP1 had no significant differences between model group and EA group on day 1(P>0.05); but on day 7 and day 14, the fluorescence intensities and grey levels of EA group were significantly higher than those of the model group(P<0.05). In the model group the above values on day 0 were significantly lower than those on day 7 (P<0.05), and those on day 7 were significantly higher than those on day 14 (P<0.05). In the EA group the fluorescence intensities and grey levels on day 0 were significantly lower than those on day 7 (P<0.05), and those on day 7 were significantly higher than those on day 14 (P<0.05). Conclusion Slit2 and SrGAp1 are lowly expressed following focal cerebral infarction on day 0, and EA intervention for one and two weeks can promote their expression and prolong the duration of high expression, subsequently accelerating axonal regeneration and repair, which may be a mechanism of EA therapy for neurological function recovery following cerebral infarction.
XU Qian , LIU Gui-min , GU Lei , LIANG Wen-tong , CHENG Zhi-yong
2016, 37(1):52-58. DOI: 10.16781/j.0258-879x.2016.01.0052
Abstract:Objective To investigate the mechanism by which JAK2 inhibitor Ruxolitinib affecting the proliferation and apoptosis of human erythroleukemia leukemia(HEL) cells. Methods The HEL cells were treated with Ruxolitinib at different concentrations (1, 5, 10, 50, 100, and 500 nmol/L). Then the cell viability was detected by CCK-8 assay; the cell apoptosis was detected by Hochest staining method, the cell cycle was detected by flow cytometry, the mitochondrial membrane potential was assessed by rhodamine 123 with flow cytometry, and the Cysteine aspartic acid specific protease (Caspase)-3/7 protein activities were tested by kits. Moreover, the expression of JAK2 mRNA was measured by RT-PCR and the protein expressions of p-JAK2,p-ERK,Bcl-2 and Bim were observed by Western blotting analysis. Results After treated with different concentrations of Ruxolitinib at 1 nmol/L, 5 nmol/L,10 nmol/L, 50 nmol/L,100 nmol/L, and 500 nmol/L for 48 h, the HEL cell viabilities were (97.0±4.4)%,(92.0±3.9)%,(88.0±3.7)%,(81.0±3.1)%,(64.0±2.9)%,and (38.0±2.2)%, respectively. The ratio of high blue cells was significantly increased after treatment with 100 nmol/L Ruxolitinib for 48 h compared with the control group ([49.21±1.80]% vs [10.02±1.40]%, P<0.05). Flow cytometry showed G0/G1 phase cell ratio was higher after HEL cells exposed to 100nmol/L Ruxolitinib for 48 h compared with the control group ([73.1±3.6]% vs [45.2±3.0]%). The mitochondrial membrane potential was significantly decreased and Caspase-3/7 activity was significantly enhanced by treatment with Ruxolitinib at different concentrations (1-500 nmol/L) for 12 h and 24 h. RT-PCR showed that Ruxolitinib decreased JAK2 mRNA expression in a concentration-dependent manner in HEL cells after 48 h treatment.Western blotting analysis showed that the protein expressions of p-JAK2,p-ERK and Bcl-2 were significantly lower and Bim protein was significantly higher than those of control group(P<0.01). Conclusion Ruxolitinib may induce HEL cell apoptosis via JAK2 and ERK 1/2 pathways.
REN Han-xiao , GAO Qian , JIA Yin , ZHANG Jian-rong , ZHANG Jun-jie , LI Wen-jie
2016, 37(1):59-64. DOI: 10.16781/j.0258-879x.2016.01.0059
Abstract:Objective To explore the expression profile of lncRNAs in the testis tissue of CRYBB2 gene knockout (KO) mice and its possible role in the testis development. Methods Testis tissues(n=3)from wild-type (WT) and CRYBB2 KO mice were subjected to lncRNA and mRNA microarray profiling. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed to group the differentially expressed lncRNAs into regulated gene pathways and functions. The correlation matrix method was used to establish a network of lncRNA and mRNA co-expression. Quantitative (q)RT-PCR was used to verify expression of some differentially expressed lncRNAs and mRNAs. Results There were 140 differentially expressed lncRNAs and 477 differentially expressed mRNAs between testis tissues from WT and KO mice. There were 12 differentially expressed lncRNAs through the analyses of the GO, with 7 up-regulated and 5 down-regulated. The KEGG analysis showed that these differentially expressed mRNAs played important roles in Ca2+ signaling, ligand and receptor interactions, and so on. The correlation matrix method established an lncRNA and mRNA co-expression network, consisting of 9 lncRNAs and 8 mRNAs, with 17 nodes and 12 connections. Furthermore, expression of gene Rsl1 was regulated by three lncRNAs, expression of gene Lpo and gene Mpo was regulated by two lncRNAs, and expression of gene Hdac1 and gene Ephb4 was regulated by one lncRNA. qRT-PCR confirmed the significant down-regulation of lncRNA A-30-P01019163 expression, which significantly down-regulated its downstream gene P2rx7 in testis tissues of CRYBB2 KO mice(P<0.05). Conclusion LncRNA is closely related to the non-crystalline lens function of CRYBB2. LncRNA A-30-P01019163 may affect testicular cell cycle and signaling pathway by regulating P2rx7 expression in the testis tissues.
ZHANG Yin-ling , XUE Geng , SUN Shu-han , ZHANG Yi
2016, 37(1):65-71. DOI: 10.16781/j.0258-879x.2016.01.0065
Abstract:Folic acid, also know as pteroymonoglutamic acid and vitamin M, is one of the important constituents of vegetables and fruits. 5-methyltetrahydrofolate is the biologically active form of folate, and acts as carriers of one-carbon moieties for many biological processes, such as synthesis of nucleotide and proteins and epigenetic modification. Epigenetic modification plays an important role in the tumorigenesis. Recent epidemiological studies indicate that folic acid deficiency in vivo has a close correlation with tumorigenesis. Folate deficiency may induce tumorigenesis via global DNA hypomethylation and internal specific nucleotide site hypermethylation, finally leading to tumorigenesis. This review mainly focused on the correlation of folic acid deficiency with tumorigenesis.
HUANG Xiang-qin , CAO Xian , HUANG Qin
2016, 37(1):72-76. DOI: 10.16781/j.0258-879x.2016.01.0072
Abstract:Irisin is a newly discovered myogenic glycosylation of peptide which can promote expression of uncoupling protein in white fat cells, facilitate lipid droplet formation, increase mitochondrial density and oxygen consumption of fat cells, and results in the shift from white fat cells to brown fat cells and promotion of β cells regeneration, thus inhibiting the occurrence of obesity and insulin resistance. Meanwhile, Irisin can also increase brain-derived neurotrophic factor, activate genes involved in learning and memorizing, so as to improve cognition function. Furthermore, Irisin is also reported to mitigate aging by extending the length of telomeres. This paper reviewed the relationship between Irisin and type 2 diabetes in the elderly, hoping to provide reference for prevention and treatment of type 2 diabetes in the elderly.
ZHU Peng-yin , JIANG Zhong-wei , CHE Hao-yue , PAN Yong-hua , GAO Shen , WANG Zhong-zhuang , FU Peng
2016, 37(1):77-82. DOI: 10.16781/j.0258-879x.2016.01.0077
Abstract:Objective Alzheimer's disease(AD)is a brain neural degenerative disease characterized by progressive cognitive and memory impairment. The pathogenesis of Alzheimer's disease remains unclear and there has been no effective treatment up to now. Autophagy plays an important role in clearing abnormally accumulated proteins and damaged organelles and in maintaining intracellular homeostasis and cell metabolism. This paper reviewed the role of autophagy in treatment of Alzheimer's disease, hoping to provide reference for discovering new treatment target for Alzheimer's disease.
YANG Bo , GAO Xiao-feng , WANG Hui-qing , ZHANG Chao , LI Ling , PENG Yong-han , GUO Fei , SUN Ying-hao
2016, 37(1):83-86. DOI: 10.16781/j.0258-879x.2016.01.0083
Abstract:Objective To evaluate the safety and efficacy of laparoscopic partial nephrectomy via a combined "trans-retro-peritoneal three-step" approach. Methods The clinical data of 32 patients who received laparoscopic partial nephrectomy between Jul. 2015 and Nov. 2015 were retrospectively analyzed. Twenty cases were via the traditional transperitoneal approach and the other 12 cases via a novel combined "trans-retro-peritoneal three-step" approach. The 3 steps in this novel approach included: (1) Through transperitoneal approach, Gerota's fascia and perirenal fat were incised to expose the tumor; (2) The peritoneum and Gerota's fascia were incised along the Told's line, and the renal artery was then separated on the surface of the psoas muscle; and (3) The renal artery was clamped, the edge of the tumor was marked, and finally the tumor was resected and the kidney was reconstructed. The perioperative data of the two groups were compared. Results The surgeries were successfully performed in all the 32 patients. Compared to traditional transperitoneal approach, our novel approach significantly shortened the operation time (P=0.014). The other perioperative parameters, such as estimated blood loss, were comparable in the two groups. Conclusion This combined "trans-retro-peritoneal three-step" approach has the combined the advantage of traditional transperitoneal (enough room for manipulation) and retroperitoneal (convenience to separate the renal arteries) approaches, especially when the renal artery is abnormal. Further studies are needed to compare the present approach with the traditional surgeries.
CHEN Pin-zhong , CHEN Dan-lei , LIU An-an , TANG Liang , SHI Li-gang , SHAO Cheng-hao
2016, 37(1):87-90. DOI: 10.16781/j.0258-879x.2016.01.0087
Abstract:Objective To assess the effects of applying pancreaticogastrostomy and pancreaticojejunostomy in central pancreatectomy on postoperative outcome and short-term complications. Methods The clinical data of 25 patients who received central pancreatectomy from May 2013 to May 2015 were retrospectively analyzed. The reconstruction methods were pancreaticogastrostomy or pancreaticojejunostomy, and the pancreatic duct were anastomosed with stomach or intestinal mucosa lips openings by magnetic induction line suture. Then the postoperative pancreatic fistula and hospital stay were compared between the two groups. Results The baseline data of two groups were comparable, and there were no significant differences in postoperative pancreatic fistula rates or hospital stay between the two groups. The 25 patients did not have anastomotic bleeding. Two cases with proximal pancreatic stump fistula were observed and were cured by adequate drainage, octreotide acetate injection, parenteral nutrition and so on. Conclusion Central pancreatectomy can better maintain the pancreas function. pancreaticogastrostomy and pancreaticojejunostomy are both safe.
CHEN Guo-liang , LIU Xiao-rong , XU Fei
2016, 37(1):91-93. DOI: 10.16781/j.0258-879x.2016.01.0091
Abstract:Understanding the characteristics of medical support in naval warfare is the premise to determine the principles, requirements and measures of medical support and it is the foundation for organizing and implementing medical support in naval warfare. In this paper, using literature survey and research analysis we summarized the characteristics of medical support in modern naval warfare according to the types of naval warfare, input of army forces, weapons and equipment, war environment and so on. Finally we put forward six characteristics of modern naval warfare from the following perspectives: target, scope, wounding, rescue of the wounded, organizing and commanding, drug supply, and safety of medical support, hoping to provide reference for decision-making for military, logistics and health department.