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Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;48(6): 577-582, 06/2015. tab, graf
Article de Anglais | LILACS | ID: lil-748221

RÉSUMÉ

Male circumcision is the most frequently performed procedure by urologists. Safety and efficacy of the circumcision procedure requires continual improvement. In the present study, we investigated the safety and efficacy of a new male circumcision technique involving the use of a circular stapler. In total, 879 consecutive adult male patients were randomly divided into 2 groups: 441 underwent stapler circumcision, and 438 underwent conventional circumcision. The operative time, pain score, blood loss volume, healing time, treatment costs, and postoperative complications were compared between the two groups. The operative time and blood loss volume were significantly lower in the stapler group than in the conventional group (6.8 ± 3.1 vs 24.2 ± 3.2 min and 1.8 ± 1.8 vs 9.4 ± 1.5 mL, respectively; P<0.01 for both). The intraoperative and postoperative pain scores were significantly lower in the stapler group than in the conventional group (0.8 ± 0.5 vs 2.4 ± 0.8 and 4.0 ±0.9 vs 5.8 ± 1.0, respectively; P<0.01 for both). Additionally, the stapler group had significantly fewer complications than the conventional group (2.7% vs 7.8%, respectively; P<0.01). However, the treatment costs in the stapler group were much higher than those in the conventional group (US$356.60 ± 8.20 vs US$126.50 ± 7.00, respectively; P<0.01). Most patients (388/441, 88.0%) who underwent stapler circumcision required removal of residual staple nails. Overall, the present study has shown that stapler circumcision is a time-efficient and safe male circumcision technique, although it requires further improvement.


Sujet(s)
Adolescent , Adulte , Sujet âgé , Humains , Mâle , Adulte d'âge moyen , Jeune adulte , Circoncision masculine/instrumentation , Circoncision masculine/méthodes , Agrafeuses chirurgicales , Circoncision masculine/effets indésirables , Conception d'appareillage , Études de suivi , Illustration médicale , Durée opératoire , Satisfaction des patients , Complications postopératoires , Études prospectives , Statistique non paramétrique , Résultat thérapeutique , Cicatrisation de plaie
2.
Article de Anglais | IMSEAR | ID: sea-31407

RÉSUMÉ

The paper reports the result of identifying cirumsporozoite (CS) genotype of Plasmodium vivax by using PCR/DNA probe labeled with biotin. The sensitivity of this method to detect patient blood samples was 0.2 parasite/microl and also with high specific to P. vivax. CS genes from 52 blood samples collected from patients with P. vivax in Hainan and Yunnan Provinces were amplified by PCR and 49 were positive by gel-e electrophoresis analysis, positive rate was 94%. Then the amplified CS genes further were probed with special oligoprobes (PV210 and PV247) that hybridized with the predominant CS repeat region and the variant CS repeat region. The results showed 46 (88.5%) PV210 positive and 6 (11.5%) PV247 positive; 2 hybridized with both probes. The variant genotype was present only in samples from Yunnan Province. The above results showed that the PCR/DNA probe labeled with biotin was highly sensitive and specific to P. vivax and found a CS variant genotype of P. vivax in Yunnan Province of China.


Sujet(s)
Animaux , Études cas-témoins , Chine , Sondes d'ADN/diagnostic , ADN des protozoaires/analyse , Électrophorèse sur gel d'agar , Variation génétique/génétique , Génotype , Humains , Paludisme à Plasmodium vivax/sang , Plasmodium vivax/génétique , Réaction de polymérisation en chaîne/méthodes , Reproductibilité des résultats , Sensibilité et spécificité
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