000 03517nam a22005057a 4500
008 170731s20172017 xxu||||| |||| 00| 0 eng d
022 _a0002-9343
040 _aOvid MEDLINE(R)
099 _a28739199
245 _aResults of the First American Prospective Study of Intravenous Iron in Oral Iron Intolerant Iron Deficient Gravidas.
251 _aAmerican Journal of Medicine. 130(12):1402-1407, 2017 Dec
252 _aAm J Med. 130(12):1402-1407, 2017 Dec
253 _aThe American journal of medicine
260 _c2017
260 _fFY2018
266 _d2017-07-31
501 _aAvailable online from MWHC library: 1995 - present, Available in print through MWHC library: 1999 - present
520 _aBACKGROUND: Anemia affects up to 42% of gravidas. Neonatal iron deficiency is associated with low birth weight, delayed growth and development, and increased cognitive and behavioral abnormalities. While oral iron is convenient, up to 70% report significant gastrointestinal toxicity. Intravenous iron formulations allowing replacement in one visit with favorable side-effect profiles decrease rates of anemia with improved hemoglobin responses and maternal fetal outcomes.
520 _aCONCLUSION: Intravenous iron has less toxicity and is more effective supporting moving it closer to front line therapy.
520 _aCopyright (c) 2017. Published by Elsevier Inc.
520 _aMETHODS: 74 oral iron intolerant, 2<sup>nd</sup> and 3<sup>rd</sup> trimester iron deficient gravidas were questioned for oral iron intolerance and treated with intravenous iron. All received 1,000 mg of low molecular weight iron dextran in 250 ml normal saline. Fifteen minutes after a test dose, the remainder was infused over balance of 1 hour. Subjects were called at 1, 2 and 7 days to assess delayed reactions. Four weeks post-infusion or postpartum, hemoglobin levels and iron parameters were measured. Paired T-test was used for hemoglobin and iron. 58/73 women were questioned about interval growth and development of their babies.
520 _aRESULTS: 73 of 74 enrolled subjects completed treatment. Sixty had paired pre- and post-treatment data. The mean pre- and post-hemoglobin concentrations were 9.7 and 10.8 g/dl (P<0.00001), TSATs 11.7% and 22.6% (P=0.0003) and ferritins 14.5 and 126.3 ng/mL respectively (P<0.000001). Six experienced minor infusion reactions. All resolved. Data for 58 infants was available; one was low on its growth charts for 11 months. The remaining 57 were normal. None were diagnosed with iron deficiency anemia.
546 _aEnglish
650 _a*Iron Compounds/ad [Administration & Dosage]
650 _a*Iron/df [Deficiency]
650 _a*Pregnancy Complications/dt [Drug Therapy]
650 _aAdministration, Intravenous
650 _aAdministration, Oral
650 _aFemale
650 _aHumans
650 _aIron Compounds/ae [Adverse Effects]
650 _aPregnancy
650 _aProspective Studies
651 _aMedStar Franklin Square Medical Center
656 _aFamily Medicine
656 _aObstetrics and Gynecology
657 _aJournal Article
700 _aLenowitz, Steven
700 _aLondon, Nicola
700 _aNicoletti, Melissa
700 _aSmith, Samuel
790 _aAuerbach M, Bahrain HF, Derman R, James SE, Lenowitz S, London N, Nicoletti M, Smith S
856 _uhttps://dx.doi.org/10.1016/j.amjmed.2017.06.025
_zhttps://dx.doi.org/10.1016/j.amjmed.2017.06.025
942 _cART
_dArticle
999 _c2953
_d2953