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1.
Arch Gynecol Obstet ; 288(5): 1149-52, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23666603

ABSTRACT

PURPOSE: The purpose of this study was to evaluate the initial and day 4 beta-human chorionic gonadotropin (ß-hCG) levels as a predictor of methotrexate (MTX) therapy success for ectopic pregnancy. METHODS: Retrospective study of 87 patients with tubal ectopic pregnancy treated with a single dose of 50 mg/m(2) MTX at Bursa Sevket Yilmaz Research and Education Hospital between January 2011 and July 2012 was performed. RESULTS: The overall success rate is measured as 72.4 %. The two groups of patients, successfully treated patients (n = 63) and unsuccessfully treated patients (n = 24), were compared. The mean initial ß-hCG level was significantly lower in the treatment success group than in the treatment failure group (1,417 mIU/mL versus 5,995 mIU/mL, p < 0.001). The number of cases with decreasing ß-hCG level on day 4 was significantly more in the success group compared to the failure group (61.9 and 37.5 %, respectively, p = 0.04). The success rate was 90 % when ß-hCG levels were <1,000 mIU/mL, 85.7 % when the levels were between 1,000 and 1,999 mIU/mL, and 76.5 % when the levels were between 2,000 and 2,999 mIU/mL, 54.5 % when the levels were between 3,000 and 3,999 mIU/mL. CONCLUSION: Single-dose MTX therapy is a safe and effective treatment modality for tubal ectopic pregnancies with the ß-hCG serum concentration below 3,000 mIU/mL, and ß-hCG level changes between days 0 and 4 after MTX therapy are important in predicting the outcome of treatment.


Subject(s)
Abortifacient Agents, Nonsteroidal/therapeutic use , Chorionic Gonadotropin, beta Subunit, Human/blood , Methotrexate/therapeutic use , Pregnancy, Tubal/blood , Pregnancy, Tubal/drug therapy , Adult , Female , Humans , Predictive Value of Tests , Pregnancy , Retrospective Studies , Time Factors , Treatment Failure , Young Adult
2.
Arch Gynecol Obstet ; 277(2): 151-4, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17710427

ABSTRACT

INTRODUCTION: The aim of this study was to evaluate the criteria of endometrial thickness to detect retained products of conception following first trimester spontaneous abortion or elective pregnancy termination. METHODS: This was a retrospective study on 116 patients who underwent uterine re-evacuation with a diagnosis of retained products of conception based on clinical and sonographic findings. Pathologic reports of samples obtained during re-evacuation were reviewed for the presence of gestational tissue. Endometrial thickness determined by transvaginal sonography and certain clinical features (gestational age and interval between initial curettage and re-evacuation, which may affect presence or absence of gestational tissue, parity, indication for initial curettage) were noted. The sensitivity and specificity of sonographic measurement of endometrial thickness for detecting retained products of conception were assessed. RESULTS: Histopathologic reports confirmed the diagnosis of retained products of conception in 66 of 116 patients (56.9%). Percentage of nulliparity and the time elapsed between initial curettage and re-evacuation were significantly high in patients with retained products of conception. The sensitivity and specificity of endometrial thickness greater than 13 mm for detecting retained products of conception were 85 and 64%, respectively. CONCLUSION: An endometrial thickness of 13 mm or more, detected by transvaginal sonography, has the best diagnostic efficiency for detection of retained products of conception following first trimester spontaneous abortion or elective pregnancy termination.


Subject(s)
Abortion, Incomplete/diagnosis , Abortion, Induced , Abortion, Spontaneous , Endometrium/diagnostic imaging , Adult , Dilatation and Curettage , Female , Humans , Parity , Predictive Value of Tests , Pregnancy , Pregnancy Trimester, First , Reoperation , Retrospective Studies , Sensitivity and Specificity , Time Factors , Ultrasonography
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