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Objective To study predicting results of the back propagation (BP)neural network model for hematoma enlargement (HE)in patients with intracerebral hemorrhage. Methods The clinical data of 128 patients with cerebral hemorrhage admitted to the 309th hospital of People′s Liberation Army from January 2011 to December 2014 were analyzed retrospectively. The Matlab 7. 14 software was used to achieve BP neural network model for predicting hematoma enlargement within 24 hours in patients with intracerebral hemorrhage (HE ≥6. 0 ml and HE ≥12. 5 ml). The mean square error (MSE)of the model and the accuracy of the overall prediction were calculated. The receiver operation characteristic (ROC) curve was drawn for predicting HE. Results When the BP neural network predicted HE ≥6. 0 ml and HE ≥12. 5 ml,the mean square deviations of the training set,validation set,and test set were 0. 061, 0. 143,0. 052 and 0. 023,0. 057,and 0. 065,respectively. The best fitting performance verification of hematoma enlargement was as follows:≥ 6. 0 ml for network training 11 times and the error value 0. 224;≥12. 5 ml for network training 20 times,and the error value 0. 057. The overall accuracies of predicting HE ≥6. 0 ml and HE ≥12. 5 ml were 92. 2% (118/ 128)and 96. 9% (124/ 128)respectively. Conclusion The BP neural network model have no special limitation for data. It can accurately fit the hematoma expansion model of cerebral hemorrhage.
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Objective To examine the tegmental structure of Schistosoma nanjingi using scanning electron microscopy. Methods Adult schistosomes were obtained from infected rabbits with cercariae shedding from Oncomelania snails, which were infected with miracidia of Schistosoma nanjingi. The adult schistosomes were fixed with 4% glutaradehyde, and then, the samples were prepared with the conventional procedures and the schistosomes were examined with a scanning electron microscope (SX-40). Results There were two types of male and female adult worms. For the big male worm, there were big spines and deep cavity on the surface of middle back and some small spines on the surface of middle abdomen; for the small male worm, there were many small spines on the surface of whole back and abdomen. As the big female worm, there were some small spines on the whole tegumental surface. As the small female worm, there were some small spines on the surface of back and abdomen, but the shape of spines was different between the spines of back and abdomen. On the tail surface of the small female worm, there were two types of spines. The spoke-like acetabulum was found. The sensory organelle papillae with or without cilia were found on the tegmental surface of both male and female woems. Conclusion The tegmental structure of Schistosoma nanjingi is much different from that of Schistosoma japonicum.
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Objective To observe and count the number of schistosome eggs and miracidia hatched from bladder urine of a Schistosoma nanjingi-infected rabbit. Methods After the rabbit was infected with 1 000 5. nanjingi cercariae and dissected on day 75, the bladder was removed and the arlult worms in venous plexus of the bladder were counted, and schistosome eggs in the bladder urine were observed and counted. After washing the eggs with water, the eggs were incubated at 26 C , and then miracidia hatched were counted. Results The number of adult worms in bladder venous plexus was 14 pairs (28 worms) and 18 840 eggs were found in the bladder urine. The surface of eggs adhered to a lot of small granular substance. Some degenerated and black eggs were seen in the urine. The number of miracidia hatched was 874, covering 4. 6% of the total number of the eggs. Conclusion S. nanjingi is different from 5. japonicum. After the rabbit was infected with S. nanjingi a lot of schistosome eggs were shown in the urine and miracidia can be hatched out.
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Objective To observe the development of Schistosoma japonicum in Oncomelania hupensis. MethodsOncomelania snails were infected heavily with miracidia of S.japonicum and the snails were dissected in different time. The mothersporocysts, daughtersporocysts and cercariae were collected, fixed with Bouin's fluid, dyed with carminic stain, enveloped with neutral gum and examined. ResultsThe neural rings were found in 1-24 hours old mothersporocysts and disappeared in 2 days. In the mothersporocysts, germinal cells increased and developed to germ balls. One germ ball developed to one daughtersporocyst. In daughtersporocysts, there were germ balls of different development stages and at last they developed into cercariae. ConclusionThe development process from the miracidium to mothersporocyst, to daughtersporocyst, to cercaria is observed.
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Objective To delineate the m orp hology and ecology of a new human schistosome species. Methods (1)Adult schistosomes were obtained from infected mice and rabbi ts with cercariae shedding from snails which were infected with miracidia devel oping from the eggs in feces of acute schistosomiasis patients. (2)T he rabbits were dissected during 60-100 d infection period of cecariae, and thei r bladders were taken out for detecting eggs in the urine. (3)Schistosome eggs i n the feces of patients were examined with microscopy. Results (1)There were two types of male worms: one was with an average o f size 8.76 mm long and 0 43 mm wide while the other with an average size of 2 41 mm long and 0 091 mm wide and with undeveloped gynecophoral canal which ap peared in front of ventral sucker (2)There were two types of female worms: one was with an average of size 10 73 mm long and 0 74 mm wide while the other wi th an average of size 3 43 mm long and 0 12 mm wide and was fine, semitranspar ent and tape like with undeveloped ovary and vitellaria. Less than 10 eggs or none were found in t he uterus. (3)There were a lot of degenerated and black eggs in the feces of 2 p atients. (4) Schistosome eggs were detected in the urine and miracidia were hatc hed out from 8 out of 16 infected rabbits.(5) Others: 8 worms were detected in 1 mouse out of 12 dissected mice for evaluation of infectious water with sentry m ice in spite of that no Oncomelania snails were found in the area. Cercariae stayed on water surface in lying position like a c omma. The eggs returned forwardly a fter growing behind the ovary in female worm. ConclusionAccording to the primary investigation in morphology an d ecology, the new schistosome obtained is distinct from the 6 well defined ty p es of human schistosome. It is considered that a new schistosome species should be foun d and temporarily nominated as Schistosoma nanjingi( S.n.)
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Objective To identify genomic DNA of Schistosoma ?. Methods Amplification of genomic DNA by the random-amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) with 10-base pair was used. The 50 worms were collected from rabbits infected with cercariae of S.? and Schistosoma japonicum(S.j.) respectively. RAPD-PCR were performed on PCR-2400 according to the manufature's instruction. And 29 primers were adopted from Operon Company. The samples were run on 1.4% sepharose. Results RAPD fragments produced were various in quantity(4-12 bands)and size(0.5-5.2Kb) in S.? and S.j. , most of about 224 bands produced with 27 different primers were common, but 6 differential bands produced with 2 primers (J 01 CCCGGCATAA and L 12 GGGCGGTACT) of the 29 primers were found, 4 and 2 of the 6 differential bands seen in the S.? and S.j. respectively. Conclusion These specific fragments found in S.? and S.j. may be used as molecular markers for the identification of S.? and S.j.