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<journal>
<language>en</language>
<journal_id_issn>1726-7536</journal_id_issn>
<journal_id_issn_online>1735-8507</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi></journal_id_doi>
<journal_id_isnet></journal_id_isnet>
<journal_id_iranmedex>69</journal_id_iranmedex>
<journal_id_magiran>2139</journal_id_magiran>
<journal_id_sid>288</journal_id_sid>
<pubdate PubStatus="epublish">
	<type>gregorian</type>
	<year>2020</year>
	<month>3</month>
	<day>17</day>
</pubdate>
<volume>21</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>32500013</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Outcomes of Preimplantation Genetic Testing for Single Gene Defects in a Privately Funded Period and Publicly Funded Period: A North-American Single Center Experience</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background: The purpose of this study was to assess whether the outcomes from IVF-preimplantation genetic testing (IVF-PGT) cycles for single gene defects (SGD) (PGT-M) differ between a privately funded period (PRP) and publicly funded period (PUP).&amp;nbsp;&amp;nbsp;&lt;br /&gt;
Methods: A retrospective cohort study was conducted in a North-American single tertiary center. The PRP (March 1998 to July 2010) comprised 56 PGT-M cycles from 58 IVF cycles in 38 couples, and the PUP (August 2010 to May 2015) comprised 59 PGT-M cycles from 87 IVF cycles in 38 couples. One PGT-M cycle is defined as one biopsy procedure from one or serial IVF cycles. A p-value of 0.05 was considered statistically significant.&amp;nbsp;&lt;br /&gt;
Results: The clinical pregnancy rates (CPR) per PGT-M cycle were 30.4% and 52.5% in each period, respectively (p=0.021). The live birth rates (LBR) per PGT-M cycle were 21.5% versus 40.9% in each period, respectively (p=0.037). A sub-analysis within the PUP comparing 39 PGT-M cycles from 39 IVF cycles with 20 PGT-M cycles from 49 IVF cycles yielded CPRs per PGT-M cycle of 64.1% and 30.0% and LBRs per PGT-M cycle of 53.8% and 15.0%, in each group, respectively (p&amp;lt;0.05 for both).&lt;br /&gt;
Conclusion: The transition from private to public funding and a single embryo transfer (ET) guideline has little impact on embryological and clinical outcomes of PGT-M cycles, and results in lower rates of multiple pregnancies. However, these two systems may serve different populations.&amp;nbsp;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>In Vitro, Preimplantation genetic testing, Public funding, Single embryo transfer, Single embryo transfer</keyword>
	<start_page>107</start_page>
	<end_page>116</end_page>
	<web_url>https://www.jri.ir/article/60079</web_url>
	<pdf_url>https://www.jri.ir/documents/fullpaper/en/60079.pdf</pdf_url>
	<author_list><author><first_name>Talya</first_name><middle_name></middle_name><last_name>Shaulov</last_name><suffix></suffix><affiliation>MUHC Reproductive Centre, Department of Obstetrics and Gynecology, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>62044</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Li</first_name><middle_name></middle_name><last_name>Zhang</last_name><suffix></suffix><affiliation>MUHC Reproductive Centre, Department of Obstetrics and Gynecology, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>62045</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Jin-Tae</first_name><middle_name></middle_name><last_name>Chung</last_name><suffix></suffix><affiliation>MUHC Reproductive Centre, Department of Obstetrics and Gynecology, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>62046</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Weon-Young</first_name><middle_name></middle_name><last_name>Son</last_name><suffix></suffix><affiliation>MUHC Reproductive Centre, Department of Obstetrics and Gynecology, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>62047</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>William</first_name><middle_name></middle_name><last_name>Buckett</last_name><suffix></suffix><affiliation>MUHC Reproductive Centre, Department of Obstetrics and Gynecology, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>62048</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Asangla</first_name><middle_name></middle_name><last_name>Ao</last_name><suffix></suffix><affiliation>McGill University Health Centre Research Institute, Montreal, Quebec, Canada</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email>asangla.ao@muhc.mcgill.ca</email><code>62049</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

