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1.
JBMS-Journal of the Bahrain Medical Society. 2008; 20 (3): 135-141
in English | IMEMR | ID: emr-87502

ABSTRACT

Infertility is distressing life crises for many couples. Of the 15% of childless couples around the world approximately 15-25% is due to ovulating disturbances. Ovulation induction [01] therefore strives to redress ovulation problems by replicating the natural physiology of the cyclic ovarian function, with the goal of achieving ovulation of single or more mature follicles. Since the first ever successful induction of ovulation using extract of human cadaver pituitary glands in 1958, there have been substantial advances in the management of anovulatory infertility and an improved insight into the physiology of the micro environments of ovulation. Progressively, the need for new and effective methods for ovulation induction became more intense particularly with the introduction of In Vitro Fertilization procedures in clinical practice. During the last five decades, a large inventory of hormonal therapies for 01 and many management protocols have been presented, but more importantly was the new understanding of the varieties of ovarian dysfunctions and the pathophysiology of ovulation failure. The objective of this mini review article is to inform the readers about the current practical approaches in management of ovulation induction addressing the costs, risks, and critical evaluation of their effectiveness


Subject(s)
Humans , Female , Anovulation , Infertility, Female , Clomiphene , Tamoxifen , Gonadotropins , Receptors, LHRH , Follicle Stimulating Hormone , Luteinizing Hormone , Gonadotropin-Releasing Hormone
2.
Journal of the Arab Board of Medical Specializations. 2002; 4 (4): 30-38
in English | IMEMR | ID: emr-59788

ABSTRACT

HELLP syndrome [hemolysis, elevated liver enzymes, low platelets] is associated with poor maternal and fetal outcomes. Maternal mortality has been estimated as high as 24%. These patients are also at greater risks from pulmonary edema, adult respiratory distress syndrome [ARDS], abruption placentae, disseminated intravascular coagulopathy [DIC], ruptured liver hematomas, and acute renal failure [ARF]. Perinatal mortality is equally high ranging from 79 to 367 per 1000 live births, and neonatal complications correlate with the severity of maternal disease. Many clinicians view HELLP syndrome as an entity of preeclampsia, and with the varied symptomatology, the initial diagnosis may be obscured. Prodromal signs include: 1] right upper quadrant and/or epigastric pain, 2] nausea and vomiting, 3] headache, 4] visual changes, 5] increased tendency to bleed from minor trauma, 6] jaundice, 7] diarrhea and 8] shoulder or neck pain. Prior to delivery, aggressive obstetric management is directed toward stabilization of the affected organ systems and timely interruption of the pregnancy in the early phase of accelerated disease progression. Definitive therapy is delivery. Parturients with HELLP syndrome are often critically ill; their infants are frequently premature and compromised. Management criteria should include a multidisciplinary approach in a tertiary care centre. The obstetric anesthesia personnel should petform a thorough preanaesthetic evaluation and have considerable knowledge of the pathophysiology of this syndrome. Unless significant coagulopathy is diagnosed, epidural anesthesia is preferred over general anesthesia, and spinal anesthesia is perhaps contraindicated


Subject(s)
Humans , HELLP Syndrome/diagnosis , HELLP Syndrome/therapy , Anesthesia, Epidural , Pregnancy Complications , Plasmapheresis , HELLP Syndrome/classification
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