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1.
Inflamm Bowel Dis ; 28(8): 1298-1299, 2022 08 01.
Artigo em Inglês | MEDLINE | ID: mdl-35700275

RESUMO

The infliximab biosimilar CT-P13 is used for the treatment of ulcerative colitis. We report for the first time the serum drug levels and long-term health status of the child of a patient treated with CT-P13 throughout her pregnancy.


Assuntos
Medicamentos Biossimilares , Colite Ulcerativa , Doenças Inflamatórias Intestinais , Medicamentos Biossimilares/uso terapêutico , Criança , Colite Ulcerativa/tratamento farmacológico , Feminino , Fármacos Gastrointestinais/uso terapêutico , Humanos , Doenças Inflamatórias Intestinais/tratamento farmacológico , Infliximab/uso terapêutico , Mães , Resultado do Tratamento
2.
Reprod Med Biol ; 11(2): 105-108, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29699115

RESUMO

A 27-year-old woman had massive genital bleeding after an artificial abortion. Color Doppler ultrasonography showed a hypervascular mass. Hysteroscopy revealed a placental polyp. Serum hemoglobin level was decreased to 7.7 g/dl. Although uterine artery embolization (UAE) followed by hysteroscopic resection has been used for treatment of a placental polyp, UAE may not be an ideal option for patients with intent for future pregnancy because of the risk of ovarian function failure. This report presents a case of a placental polyp managed successfully with intracervical injection of prostaglandin F2α, as an alternative UAE, followed by hysteroscopic resection.

3.
Bone ; 40(4): 1088-94, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17229597

RESUMO

OBJECTIVE: The aims of our study were to evaluate the changes in bone turnover markers during pregnancy and puerperium as a longitudinal study and to elucidate the effect of bed rest during pregnancy on bone turnover markers in pregnant and postpartum women. METHODS: The study population comprised 27 Japanese pregnant women aged 23-40 years. All women were recruited for the longitudinal study from the outpatients clinic of the Department of Obstetrics and Gynecology, Tokushima University Hospital. Concentrations of serum bone-specific alkaline phosphatase (BAP), urinary cross-linked type I collagen N-telopeptides (NTx), serum NTx and urinary C-terminal telopeptide of type I collagen (CTx) were measured at 10, 26, 30 and 36 weeks of pregnancy and at 4 days and 1 month postpartum. In addition, we recruited 15 pregnant women (aged 25-35 years) who were treated by bed rest before 30 weeks of pregnancy for threatened premature delivery and compared bone turnover markers in these women with those in 22 normal pregnant women (aged 22-39 years). Concentrations of serum BAP, serum NTx, urinary NTx and urinary CTx were measured at 30 and 34 weeks of pregnancy and at 4 days and 1 month postpartum. RESULTS: In the longitudinal study, serum BAP concentration at 1 month postpartum was significantly higher than that at any stage of pregnancy and that at 4 days postpartum. Urinary concentration of NTx increased gradually during pregnancy and showed a peak at 36 weeks of pregnancy, followed by a decrease in the postpartum period. Serum NTx concentration and urinary CTx concentration showed the same patterns of change as that of urinary NTx concentration. In the comparison study, urinary concentrations of NTx and CTx at 30 and 34 weeks of pregnancy in women with bed rest were significantly (p<0.0001 and p<0.001, respectively) higher than those in normal pregnant women. Serum NTx concentration at 34 weeks of pregnancy in women with bed rest was also significantly (p=0.0029) higher than that in normal pregnant women. Serum BAP concentration at 34 weeks of pregnancy in women with bed rest was significantly (p=0.0038) higher than that in normal pregnant women, and these high levels were maintained during puerperium. Serum BAP concentration at 34 weeks of pregnancy was significantly correlated with duration of bed rest (r=0.767, p=0.0041). CONCLUSION: Immobilization due to bed rest during pregnancy is associated with increases in bone turnover markers in pregnant and postpartum women. Concentrations of bone resorption markers increased rapidly at the start of bed rest, while the concentration of a bone formation marker gradually increased toward puerperium.


Assuntos
Repouso em Cama/efeitos adversos , Remodelação Óssea/fisiologia , Período Pós-Parto/metabolismo , Complicações na Gravidez/metabolismo , Complicações na Gravidez/terapia , Adulto , Fosfatase Alcalina/sangue , Biomarcadores/metabolismo , Cálcio/sangue , Estudos de Casos e Controles , Colágeno Tipo I/sangue , Colágeno Tipo I/urina , Feminino , Humanos , Estudos Longitudinais , Peptídeos/sangue , Peptídeos/urina , Gravidez , Estudos Prospectivos
4.
Eur J Obstet Gynecol Reprod Biol ; 101(2): 155-60, 2002 Mar 10.
Artigo em Inglês | MEDLINE | ID: mdl-11858891

RESUMO

OBJECTIVE: To investigate whether the human mast cell chymase-endothelin-1(1-31) system was present in human myometrium, chorion and umbilical cord in normal pregnancy. METHODS: Myometrium, placenta and umbilical cord were obtained from five normal pregnant women and 10 with preeclampsia. Each tissue was stained with antibodies against hMC and ET-1(1-31). RESULTS: Routine cells were located mainly around vessels. The number of hMC-positive cells and production of ET-1(1-31) were significantly higher in myometrium from patients with severe preeclampsia compared to those from normal pregnant women. In contrast, their numbers were significantly lower in placenta and umbilical cord in patients with severe preeclampsia. CONCLUSIONS: These results suggest that the hMC-ET-1(1-31) system is active in normal pregnancy. Overproduction of hMC and ET-1(1-31) in the myometrium may be involved in the pathogenesis of severe preeclampsia, and in such cases some defense mechanism may operate in the fetus to cope with the pathological effect of the hMC-ET-1(1-31) system.


Assuntos
Miométrio/enzimologia , Placenta/enzimologia , Pré-Eclâmpsia/enzimologia , Serina Endopeptidases/metabolismo , Quimases , Endotelina-1/metabolismo , Feminino , Humanos , Mastócitos/enzimologia , Gravidez , Valores de Referência , Cordão Umbilical/metabolismo
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