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1.
Aust N Z J Obstet Gynaecol ; 48(3): 348-52, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18532970

RESUMO

OBJECTIVE: To assess whether immediate removal of an indwelling catheter after anterior colporrhaphy influences the rate of re-catheterisation and symptomatic urinary tract infections. METHODS: A prospective randomised study conducted on 90 women divided into two groups who underwent anterior repair. The indwelling catheter was removed immediately (early catheter removal), and at least 24 h after the operation in case and control groups, respectively. The association between clinical variables and the duration of catheterisation and continuous data were analysed by chi(2) test and two-tailed t-test, respectively. Excel and SPSS 15.0 software were used, and a P-value of 0.05 or less was considered to indicate statistically significant differences. RESULT: Symptomatic urinary tract infection was significantly lower in early catheter-removal group; also patients in this group reported significantly less pain and voiding disturbances. Only a few of women required re-catheterisation after failing to void and all were able to resume normal voiding, also had shorter ambulation time and hospital stay. CONCLUSION: Early removal of an indwelling catheter immediately after anterior colporrhaphy was not associated with adverse events and increased rate of re-catheterisation. In this group, symptomatic urinary tract infection was significantly lower. Moreover, early removal of indwelling catheters immediately after operation seemed to decrease the ambulation time and hospital stay.


Assuntos
Cateteres de Demora/efeitos adversos , Remoção de Dispositivo , Procedimentos Cirúrgicos em Ginecologia/efeitos adversos , Cateterismo Urinário/efeitos adversos , Infecções Urinárias/prevenção & controle , Feminino , Humanos , Estudos Prospectivos , Fatores de Tempo , Infecções Urinárias/etiologia
2.
J Matern Fetal Neonatal Med ; 22(1): 72-5, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19165682

RESUMO

AIM: To assess the efficacy and safety of tranexamic acid in reducing blood loss at caesarian section (CS). METHOD: A prospective randomised study conducted on 90 primiparas divided into two groups who underwent CS. The study group, 45 women, received tranexamic acid immediately before CS, whereas the control group, 45 women received placebo. Blood loss volume was measured from the end of CS to 2 h postpartum and compared between the two groups. Hemoglobin (Hb) and hematocrit (Hct) were tested 24 h after CS and compared between the two groups. RESULTS: Tranexamic acid significantly reduced the blood loss from the end of CS to 2 h postpartum; 28.02 +/- 5.53 mL in the tranexamic group versus 37.12 +/- 8.97 mL in the control group (p = 0.000). Hb 24 h after CS was significantly greater in tranexamic group than control group (12.57 +/- 1.33 in the tranexamic group and 11.74 +/- 1.14 in the control group, p = 0.002). No complications or side effects were reported in either group. CONCLUSIONS: Tranexamic acid statistically reduces blood loss from end to 2 h after CS and its use was not associated with any side effects or complications. Consequently, tranexamic acid can be used safely and effectively to reduce bleeding resulting from CS.


Assuntos
Cesárea , Hemorragia Pós-Operatória/prevenção & controle , Ácido Tranexâmico/uso terapêutico , Hemorragia Uterina/prevenção & controle , Adulto , Antifibrinolíticos/efeitos adversos , Antifibrinolíticos/uso terapêutico , Cesárea/reabilitação , Feminino , Humanos , Monitorização Fisiológica , Placebos , Gravidez , Cuidados Pré-Operatórios/efeitos adversos , Cuidados Pré-Operatórios/métodos , Transtornos Puerperais/prevenção & controle , Ácido Tranexâmico/efeitos adversos , Resultado do Tratamento , Adulto Jovem
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