Marius Meintjes
Presbyterian Hospital of Dallas
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Featured researches published by Marius Meintjes.
Human Reproduction | 2009
Marius Meintjes; S.J. Chantilis; J. Douglas; Alfred Rodriguez; A. Guerami; D.M. Bookout; B.D. Barnett; J.D. Madden
BACKGROUND The potentially damaging effect of free O(2) radicals to cultured embryos may be reduced by adding scavengers to the culture media or by reducing the incubator O(2) levels. However, lowering the O(2) in the culture environment can be expensive, troublesome and may not be justifiable. The objective of this study was to evaluate the effect of lowered incubator O(2) tension on live birth rates in a predominately Day 5 embryo transfer program. METHODS Two hundred and thirty first-cycle women undergoing routine IVF or ICSI with ejaculated sperm were randomized in a prospective clinical trial and stratified for patient age and physician. Embryos of patients were randomly assigned for culture in either a 21% O(2) (atmospheric) or 5% O(2) (reduced) environment. Clinical endpoints monitored were rates of implantation, clinical pregnancy, live birth and blastocyst cryopreservation. RESULTS Embryos cultured in a 5% O(2) environment consistently resulted in higher rates of live birth implantation (106/247, 42.9% versus 82/267, 30.7%; difference of 12.2% with 95% confidence interval (CI) of 3.9-20.3, P = 0.005) and live births (66/115, 57.4% versus 49/115, 42.6%; difference of 14.8% with 95% CI of 1.9-27.0, P = 0.043) when compared with rates among women whose embryos were cultured in an atmospheric O(2) environment. CONCLUSIONS The overall increase in live births demonstrated by this study indicates that the effort and expense to culture embryos in a low-O(2) environment is justified. The study was registered at clinicaltrials.gov. NCT00708487.
Human Reproduction | 2008
Marius Meintjes; S.J. Chantilis; D. Ward; J. Douglas; Alfred Rodriguez; A. Guerami; D.M. Bookout; B.D. Barnett; J.D. Madden
BACKGROUND It has been speculated that the addition of proteins more complex than human serum albumin (HSA) to culture media may improve IVF outcomes. Whether the expense, labor and risk of adding additional human-derived protein to IVF media are warranted is a question unanswered. METHODS In a randomized controlled trial with couples undergoing routine IVF or ICSI, 528 patients were assigned to one of two treatment groups. Embryos were cultured in either media supplemented with HSA as a solitary protein supplement or in media supplemented with HSA+serum substitute supplement (SSS) from the 2PN stage until the time of embryo transfer. Clinical end-points monitored included implantation (total 1151 embryos) and live birth rates (total 528 patients). RESULTS The transfer of embryos cultured in HSA+SSS resulted in higher embryo implantation (289/571, 50.6% versus 254/580, 43.8%; difference 6.8% with 95% CI 1.0-12.7, P = 0.042) and live birth rates (167/266, 62.8% versus 142/262, 54.2%; difference 8.6% with 95% CI 0.1-17.3, P = 0.043) when compared with those of women whose embryos were cultured with HSA as the sole protein supplement. CONCLUSIONS SSS added to commercial HSA-supplemented embryo culture media resulted in an overall increase in implantation and live birth rates. It remains uncertain whether the use of human-derived blood products in culture media and the requirement for ultra-rigorous quality control measures make these findings applicable to the average IVF laboratory. Protein enrichment of media may significantly improve the blastocyst implantation rate, creating opportunities to transfer single blastocysts without compromising the live birth rate. The study was registered at clinicaltrials.gov. NCT00708383.
Fertility and Sterility | 2015
Thorir Hardarson; Mona Bungum; Joe Conaghan; Marius Meintjes; Samuel J. Chantilis; Laszlo Molnar; Kristina Gunnarsson; Matts Wikland
OBJECTIVE To study whether a culture medium that allows undisturbed culture supports human embryo development to the blastocyst stage equivalently to a well-established sequential media. DESIGN Randomized, double-blinded sibling trial. SETTING Independent in vitro fertilization (IVF) clinics. PATIENT(S) One hundred twenty-eight patients, with 1,356 zygotes randomized into two study arms. INTERVENTION(S) Embryos randomly allocated into two study arms to compare embryo development on a time-lapse system using a single-step medium or sequential media. MAIN OUTCOME MEASURE(S) Percentage of good-quality blastocysts on day 5. RESULT(S) Percentage of day 5 good-quality blastocysts was 21.1% (standard deviation [SD] ± 21.6%) and 22.2% (SD ± 22.1%) in the single-step time-lapse medium (G-TL) and the sequential media (G-1/G-2) groups, respectively. The mean difference (-1.2; 95% CI, -6.0; 3.6) between the two media systems for the primary end point was less than the noninferiority margin of -8%. There was a statistically significantly lower number of good-quality embryos on day 3 in the G-TL group [50.7% (SD ± 30.6%) vs. 60.8% (SD ± 30.7%)]. Four out of the 11 measured morphokinetic parameters were statistically significantly different for the two media used. The mean levels of ammonium concentration in the media at the end of the culture period was statistically significantly lower in the G-TL group as compared with the G-2 group. CONCLUSION(S) We have shown that a single-step culture medium supports blastocyst development equivalently to established sequential media. The ammonium concentrations were lower in the single-step media, and the measured morphokinetic parameters were modified somewhat. CLINICAL TRIAL REGISTRATION NUMBER NCT01939626.
Archives Animal Breeding | 2002
Joel A. Carter; Shane Bellow; Marius Meintjes; Oscar Perez; Edward Ferguson; R. A. Godke
Theriogenology | 1994
N.J. Vitale; D.M. Barry; Marius Meintjes; R. A. Godke
Fertility and Sterility | 2003
Oscar Perez; Samuel J. Chantilis; James W. Douglas; Alfred Rodriguez; J.D. Madden; Marius Meintjes
Fertility and Sterility | 2003
Kristin Sieren; B.D. Barnett; James W. Douglas; Alfred Rodriguez; J.D. Madden; Marius Meintjes
Fertility and Sterility | 2007
S.J. Chantilis; D. Ward; T. Davidson; L. Blankenship; Marius Meintjes
Fertility and Sterility | 2003
Henry Werland; J.D. Madden; A. Guerami; Alfred Rodriguez; B.D. Barnett; Marius Meintjes
Fertility and Sterility | 2003
Keith Hill; B.D. Barnett; James W. Douglas; Alfred Rodriguez; Samuel J. Chantilis; Marius Meintjes