1994
DOI: 10.1002/jmri.1880040611
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Effect on fetal mouse development of exposure to MR imaging and gadopentetate dimeglumine

Abstract: Pregnant mice were exposed to one of five regimens at 9.5 days of gestation: no treatment (group 1), intraperitoneal injection of normal saline (group 2), intraperitoneal injection of gadopentetate dimeglumine (group 3), intraperitoneal injection of gadopentetate dimeglumine and magnetic resonance (MR) exposure (group 4), and MR exposure alone (group 5). At 18 days of gestation, the mice were sacrificed and fetuses were removed and examined for the following end points: litter size, number alive or dead, fetal… Show more

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Cited by 52 publications
(21 citation statements)
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“…Neither intraperitoneal gadopentetate dimeglumine plus magnetic resonance nor intraperitoneal gadopentetate dimeglumine alone had any detectable effect on the development of mice [18]. No teratogenic effects or effects on postnatal development were seen following gadopentate dimeglumine, gadoteridol, gadobenate dimeglumine, or gadoversetamide use in animals [18][19][20][21].…”
Section: Mutagenicity and Teratogenicity Of Contrast Mediamentioning
confidence: 57%
“…Neither intraperitoneal gadopentetate dimeglumine plus magnetic resonance nor intraperitoneal gadopentetate dimeglumine alone had any detectable effect on the development of mice [18]. No teratogenic effects or effects on postnatal development were seen following gadopentate dimeglumine, gadoteridol, gadobenate dimeglumine, or gadoversetamide use in animals [18][19][20][21].…”
Section: Mutagenicity and Teratogenicity Of Contrast Mediamentioning
confidence: 57%
“…Animal studies have not documented teratogenicity or postnatal development effects after the administration of gadopentetate dimeglumine, gadoteridol, gadobenate dimeglumine or gadoversetamide [76][77][78][79]. There is, however, a reservation arising from the scientific observation that once excreted by foetal kidneys, the chelate of gadolinium remains in the amniotic fluid and is ingested through the gastrointestinal tube and re-excreted numerous times: the persistence of the molecule in a "closed" compartment such as the fetoplacental system could lead to the dissociation of the gadolinium ion (which is toxic per se) from the chelate, thus giving rise to a risk of toxicity that is still not fully known.…”
Section: Noise-induced Damagementioning
confidence: 97%
“…In customary dosages of 0.1-0.3 mmol/kg body weight, the likelihood of fetal injury has been estimated to be low [63]. In animal studies where gadolinium was administrated to pregnant animals in different dosages, no adverse effects on the fetuses were observed [64]. Only rabbits receiving 1×-12.5× human dosages for 5-12 days of Gd-DTPA compounds were reported to have retarded development, increased locomotor activity, and skeletal and visceral abnormalities [65].…”
Section: Normal Contrast-enhancementmentioning
confidence: 99%