The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2017
Effect of two high dose vitamin D by parenteral route in treating vitamin D deficiency a prospective interventional study.
Клиническое исследованиеСтатьяНазвание и аннотация: Перевод в очереди
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Gokhale Sanjay G, Gokhale Sankalp
Аннотация
BACKGROUND: Vitamin D deficiency is recognized as a global public health problem. Despite ample sunshine, vitamin D deficiency is very common in the Middle East (15°-36°N) and African (35°S-37°N) countries; and in South Asian countries.
AIM: To find a simple, affordable and practical plan to treat vitamin-d deficiency.
TYPE OF STUDY: This was a prospective interventional study.
OUTCOME VARIABLE: The primary outcome was typed as vitamin-D level more than 50 nanograms/ml as 'yes' and poor response or 'no' when it was less than 50 ng/ml.
PARTICIPANTS: 80 Women participated in study. Laboratory tests: Vitamin D [25-OHD]-estimations were performed with LCMSMS-liquid chromatography tandem mass spectrometry. Corrective vitamin-D doses: All participants received TWO doses of Vitamin-D injections one ml at a time [600K IU/ml or 600,000 IU/ml]. All participants received their first dose; after collecting blood samples for Vitamin-D estimations. Second dose was given about a month after the first one [range 30-37 days]. These doses were given to correct the deficiency.
RESULTS: Even with this high dose treatment 60% woman had unsatisfactory Vitamin-D levels.
AIM: To find a simple, affordable and practical plan to treat vitamin-d deficiency.
TYPE OF STUDY: This was a prospective interventional study.
OUTCOME VARIABLE: The primary outcome was typed as vitamin-D level more than 50 nanograms/ml as 'yes' and poor response or 'no' when it was less than 50 ng/ml.
PARTICIPANTS: 80 Women participated in study. Laboratory tests: Vitamin D [25-OHD]-estimations were performed with LCMSMS-liquid chromatography tandem mass spectrometry. Corrective vitamin-D doses: All participants received TWO doses of Vitamin-D injections one ml at a time [600K IU/ml or 600,000 IU/ml]. All participants received their first dose; after collecting blood samples for Vitamin-D estimations. Second dose was given about a month after the first one [range 30-37 days]. These doses were given to correct the deficiency.
RESULTS: Even with this high dose treatment 60% woman had unsatisfactory Vitamin-D levels.