Hyperbaric oxygen therapy: a possible choice for patients with resistant thin endometrium during frozen embryo transfer treatments

Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, th...

Full description

Saved in:
Bibliographic Details
Published inReproductive biology and endocrinology Vol. 21; no. 1; pp. 1 - 10
Main Authors Chen, Jingjing, Huang, Fangling, Fu, Jing, Zhao, Jianjuan, Li, Jinsheng, Peng, Zhengrong, Zhao, Jing, Xu, Bin, Li, Shuyi, Zhang, Qiong, Liang, Shaolin, Li, Yanping
Format Journal Article
LanguageEnglish
Published London BioMed Central Ltd 01.09.2023
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments. Methods This prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others. Results Patients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 [+ or -] 1.66 vs. 6.57 [+ or -] 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017). Conclusions A period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments. Trial registration The trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered). Keywords: Resistant thin endometrium, Hyperbaric oxygen therapy, Frozen embryo transfer, Asherman syndrome
AbstractList Abstract Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments. Methods This prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others. Results Patients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 ± 1.66 vs. 6.57 ± 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017). Conclusions A period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments. Trial registration The trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered).
Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments. This prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others. A period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments.
Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments.BACKGROUNDThin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments.This prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others.METHODSThis prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others.Patients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 ± 1.66 vs. 6.57 ± 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017).RESULTSPatients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 ± 1.66 vs. 6.57 ± 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017).A period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments.CONCLUSIONSA period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments.The trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered).TRIAL REGISTRATIONThe trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered).
BackgroundThin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments.MethodsThis prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others.ResultsPatients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 ± 1.66 vs. 6.57 ± 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017).ConclusionsA period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments.Trial registrationThe trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered).
Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have reported promoted endometrial growth after a period of hyperbaric oxygen therapy (HBOT) in patients with intrauterine adhesion, there have been no reports in patients with resistant thin endometrium. The purpose of this study was to investigate the impact of HBOT on endometrium growth and pregnancy outcomes in patients with resistant thin endometrium during frozen embryo transfer (FET) treatments. Methods This prospective pre-post cohort study was conducted at a university-affiliated assisted reproductive medical center between October 2021 and December 2022. Patients who had experienced at least one canceled transfer cycle due to a thin endometrium(< 7 mm) on the endometrium transformation day, despite the use of standard therapies as well as adjuvant therapies, were enrolled in the study. Patients were assigned voluntarily to either the HBOT group or the concurrent control group. The HBOT group received daily HBOT for at least 10 days during the proliferative phase, in addition to the routine endometrium preparation methods and the concurrent control group underwent cycles without HBOT. Propensity score matching (PSM) was used to ensure comparability between the groups. Both self-control and case-control comparisons were conducted. The primary outcome measured was endometrial thickness (ET) on the day of endometrium transformation. Secondary outcomes included intrauterine pregnancy rate (IPR), embryo implantation rate (IR), miscarriage rate, and others. Results Patients in the HBOT group demonstrated a significantly thicker endometrial thickness on the day of endometrium transformation after undergoing therapy (5.76 [+ or -] 1.66 vs. 6.57 [+ or -] 1.23, P = 0.002). This improvement was accompanied by a decreased rate of cycle cancellations. Baseline parameters and endometrial thickness were comparable between the HBOT group and the concurrent control group during the cycle. The IPR was similar in patients who received cleavage-stage embryos (0.0% vs. 6.7%, P = 1.00), but significantly higher in patients in the HBOT group who received blastocysts (53.8% vs. 18.2%, P = 0.017). Conclusions A period of HBOT prior to endometrium transformation contributes to increased endometrial thickness and facilitates blastocyst implantation in patients with resistant thin endometrium during FET treatments. Trial registration The trial was registered on the Chinese Clinical Trial Registry (registration no. ChiCTR2300072831, retrospectively registered). Keywords: Resistant thin endometrium, Hyperbaric oxygen therapy, Frozen embryo transfer, Asherman syndrome
ArticleNumber 80
Audience Academic
Author Xu, Bin
Zhao, Jianjuan
Li, Shuyi
Chen, Jingjing
Zhang, Qiong
Zhao, Jing
Li, Yanping
Liang, Shaolin
Huang, Fangling
Li, Jinsheng
Fu, Jing
Peng, Zhengrong
Author_xml – sequence: 1
  givenname: Jingjing
  surname: Chen
  fullname: Chen, Jingjing
– sequence: 2
  givenname: Fangling
  surname: Huang
  fullname: Huang, Fangling
– sequence: 3
  givenname: Jing
  surname: Fu
  fullname: Fu, Jing
– sequence: 4
  givenname: Jianjuan
  surname: Zhao
  fullname: Zhao, Jianjuan
– sequence: 5
  givenname: Jinsheng
  surname: Li
  fullname: Li, Jinsheng
– sequence: 6
  givenname: Zhengrong
  surname: Peng
  fullname: Peng, Zhengrong
– sequence: 7
  givenname: Jing
  surname: Zhao
  fullname: Zhao, Jing
– sequence: 8
  givenname: Bin
  surname: Xu
  fullname: Xu, Bin
– sequence: 9
  givenname: Shuyi
  surname: Li
  fullname: Li, Shuyi
– sequence: 10
  givenname: Qiong
  surname: Zhang
  fullname: Zhang, Qiong
– sequence: 11
  givenname: Shaolin
  surname: Liang
  fullname: Liang, Shaolin
– sequence: 12
  givenname: Yanping
  surname: Li
  fullname: Li, Yanping
BookMark eNptkk1v1DAQhiNUJNrCH-BkiQuXFH8ltrmgqgJaqRKX3i3HHu96ldjBToDtkV-Ot1sBRciSPRq_84zGfs-ak5giNM1rgi8Ikf27QqjqZIspazEhdefPmlPChWiFpOLkr_hFc1bKDmOKsexPm5_X-xnyYHKwKP3YbyCiZQvZzPv3yKA5lRKGEZDdpmAB-ZTRbJYAcSnoe1i2KEMJZTFxqWUhIoguTbDksE7IrTnEDfI53VcqTEPeJ7RkE4uHXAMwy3QAvWyeezMWePV4njd3nz7eXV23t18-31xd3raWK7q0XCjqsXNOqp4YNQx-YF0HoCSjUnrFOsI9EaIbvBdAXW9dLzuHJWGOK8HOm5sj1iWz03MOk8l7nUzQD4mUN9rkJdgRNDNUSS6IEhRzJrlSnQUKDAYKHEBW1ocja16HCZytY2QzPoE-vYlhqzfpmyaYCyoYr4S3j4Scvq5QFj2FYmEcTYS0Fk1ljznmvCNV-uYf6S6tOdanOqg63mHM5R_VxtQJQvSpNrYHqL4UPav_3QlWVRf_UdXlYAq2esqHmn9SQI8FNlcvZPC_hyRYH6ynj9bT1Xr6wXqas1-P9c9a
Cites_doi 10.1001/archsurg.135.11.1293
10.1186/1477-7827-8-30
10.1007/s11357-022-00707-z
10.2147/DDDT.S281451
10.1136/bmjopen-2022-062322
10.1093/humrep/des370
10.1016/j.rbmo.2014.05.011
10.3390/biomedicines10123145
10.1002/advs.202100233
10.1016/j.fertnstert.2008.01.029
10.1186/s13287-021-02499-z
10.1016/j.rbmo.2017.12.016
10.3390/jcm12010308
10.1016/j.fertnstert.2013.07.1966
10.1186/s13287-019-1165-5
10.17305/bjbms.2006.3168
10.1016/j.fertnstert.2008.12.062
10.1016/j.fertnstert.2004.05.101
10.1093/humrep/der037
10.2147/DDDT.S297236
10.1016/j.fertnstert.2007.04.031
10.1007/s12576-019-00678-5
10.1093/humrep/15.suppl_2.199
10.1159/000516749
10.1093/humrep/13.6.1550
10.1093/humrep/deaa248
10.1136/jitc-2021-004006
10.1016/j.fertnstert.2011.07.1096
10.1016/j.rbmo.2019.09.005
10.1016/j.rbmo.2014.12.006
10.4103/0974-1208.178632
10.1111/j.1479-828X.2006.00634.x
10.1093/humupd/dmu011
10.1007/s00520-022-06994-8
10.1016/j.jri.2023.103796
10.1016/j.fertnstert.2019.08.077
10.1016/j.bbabio.2009.03.009
10.1016/S0015-0282(16)58082-0
10.1016/j.placenta.2018.03.003
10.1089/ars.2014.5940
10.1097/MD.0000000000009689
10.1007/978-3-319-47140-2_2
10.1007/s10815-006-9053-1
10.4103/2045-9912.310057
ContentType Journal Article
Copyright COPYRIGHT 2023 BioMed Central Ltd.
2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2023. BioMed Central Ltd., part of Springer Nature.
BioMed Central Ltd., part of Springer Nature 2023
Copyright_xml – notice: COPYRIGHT 2023 BioMed Central Ltd.
– notice: 2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2023. BioMed Central Ltd., part of Springer Nature.
– notice: BioMed Central Ltd., part of Springer Nature 2023
DBID AAYXX
CITATION
3V.
7QG
7X7
7XB
88E
8FI
8FJ
8FK
ABUWG
AFKRA
AN0
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
K9.
M0S
M1P
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
7X8
5PM
DOA
DOI 10.1186/s12958-023-01123-4
DatabaseName CrossRef
ProQuest Central (Corporate)
Animal Behavior Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest British Nursing Database
ProQuest Central Essentials - QC
ProQuest Central
ProQuest One
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni)
Medical Database
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ: Directory of Open Access Journal (DOAJ)
DatabaseTitle CrossRef
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest One Academic Eastern Edition
British Nursing Index with Full Text
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Animal Behavior Abstracts
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList

MEDLINE - Academic
Publicly Available Content Database

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1477-7827
EndPage 10
ExternalDocumentID oai_doaj_org_article_3a29847197204384995ce2e3eb2e4ee8
PMC10472734
A763020573
10_1186_s12958_023_01123_4
GeographicLocations China
United States--US
GeographicLocations_xml – name: China
– name: United States--US
GrantInformation_xml – fundername: ;
  grantid: 202203104548
– fundername: ;
  grantid: 2021YFC2700404; 2021YFC2700404; 2021YFC2700404; 2021YFC2700404; 2021YFC2700404; 2021YFC2700404; 2021YFC2700404
– fundername: ;
  grantid: 2021SK2028; 2021SK2028; 2021SK2028; 2021SK2028; 2021SK2028; 2021SK2028; 2021SK2028
GroupedDBID ---
0R~
29P
2WC
53G
5VS
7X7
88E
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AENEX
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AN0
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BNQBC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
DU5
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
ICW
IHR
INH
INR
ITC
KQ8
M1P
M48
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
PMFND
3V.
7QG
7XB
8FK
AZQEC
DWQXO
K9.
PJZUB
PKEHL
PPXIY
PQEST
PQUKI
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c492t-4792f0ddd8961a9bbfb355ee983288f93514f1775bff7e2d6cd685d0813d4973
IEDL.DBID M48
ISSN 1477-7827
IngestDate Wed Aug 27 01:32:03 EDT 2025
Thu Aug 21 18:36:16 EDT 2025
Fri Jul 11 16:11:35 EDT 2025
Fri Jul 25 22:02:52 EDT 2025
Tue Jun 17 22:22:03 EDT 2025
Tue Jun 10 21:16:51 EDT 2025
Tue Jul 01 03:45:10 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c492t-4792f0ddd8961a9bbfb355ee983288f93514f1775bff7e2d6cd685d0813d4973
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://doaj.org/article/3a29847197204384995ce2e3eb2e4ee8
PQID 2865450048
PQPubID 42860
PageCount 10
ParticipantIDs doaj_primary_oai_doaj_org_article_3a29847197204384995ce2e3eb2e4ee8
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10472734
proquest_miscellaneous_2860404451
proquest_journals_2865450048
gale_infotracmisc_A763020573
gale_infotracacademiconefile_A763020573
crossref_primary_10_1186_s12958_023_01123_4
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-09-01
PublicationDateYYYYMMDD 2023-09-01
PublicationDate_xml – month: 09
  year: 2023
  text: 2023-09-01
  day: 01
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
PublicationTitle Reproductive biology and endocrinology
PublicationYear 2023
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References SL Chen (1123_CR5) 2010; 8
BJ Van Voorhis (1123_CR20) 2005; 83
XX Chen (1123_CR45) 2023; 13
A Ishihara (1123_CR19) 2019; 69
X Liu (1123_CR43) 2021; 8
GK Velure (1123_CR47) 2022; 30
DK Gardner (1123_CR27) 2019; 112
K Ben (1123_CR48) 2020; 35
Y Zhang (1123_CR14) 2021; 12
T Zhang (1123_CR3) 2018; 97
AY Sheikh (1123_CR42) 2000; 135
K Li (1123_CR44) 2022; 10
N Gleicher (1123_CR12) 2013; 28
J Lindenmann (1123_CR39) 2022; 10
T El-Toukhy (1123_CR34) 2008; 89
MH Schoots (1123_CR37) 2018; 69
J Yuan (1123_CR41) 2009; 1787
JW Catt (1123_CR36) 2000; 15
1123_CR25
A Takasaki (1123_CR26) 2010; 93
D Glujovsky (1123_CR35) 2020; 10
Y Chang (1123_CR13) 2023; 156
R Israel (1123_CR4) 1996; 65
MJ Chen (1123_CR7) 2006; 23
A Mitrović (1123_CR22) 2006; 6
A Kasius (1123_CR29) 2014; 20
P Sundström (1123_CR33) 1998; 13
JH Check (1123_CR1) 2003; 30
D Kitala (1123_CR46) 2022; 12
KM Fosen (1123_CR40) 2014; 21
A Mitrović (1123_CR21) 2006; 46
J Leverment (1123_CR23) 2004; 31
W Feng (1123_CR8) 2021; 15
Y Tao (1123_CR10) 2020; 14
P Mensah-Kane (1123_CR18) 2023; 45
W Zakrzewski (1123_CR15) 2019; 10
J Zhao (1123_CR6) 2014; 29
B Xu (1123_CR11) 2015; 30
I Miwa (1123_CR32) 2009; 91
1123_CR16
D Zhou (1123_CR17) 2023; 59
1123_CR38
G Gao (1123_CR2) 2020; 40
RF Casper (1123_CR24) 2021; 96
X Li (1123_CR9) 2021; 86
L Dain (1123_CR31) 2013; 100
VC Ribeiro (1123_CR30) 2018; 36
N Mahajan (1123_CR28) 2016; 9
References_xml – volume: 135
  start-page: 1293
  issue: 11
  year: 2000
  ident: 1123_CR42
  publication-title: Arch Surg
  doi: 10.1001/archsurg.135.11.1293
– volume: 8
  start-page: 30
  year: 2010
  ident: 1123_CR5
  publication-title: Reprod Biol Endocrinol
  doi: 10.1186/1477-7827-8-30
– volume: 45
  start-page: 747
  issue: 2
  year: 2023
  ident: 1123_CR18
  publication-title: Geroscience
  doi: 10.1007/s11357-022-00707-z
– volume: 14
  start-page: 5289
  year: 2020
  ident: 1123_CR10
  publication-title: Drug Des Devel Ther
  doi: 10.2147/DDDT.S281451
– volume: 13
  start-page: e062322
  issue: 1
  year: 2023
  ident: 1123_CR45
  publication-title: BMJ Open
  doi: 10.1136/bmjopen-2022-062322
– volume: 28
  start-page: 172
  issue: 1
  year: 2013
  ident: 1123_CR12
  publication-title: Hum Reprod
  doi: 10.1093/humrep/des370
– volume: 29
  start-page: 291
  issue: 3
  year: 2014
  ident: 1123_CR6
  publication-title: Reprod Biomed Online
  doi: 10.1016/j.rbmo.2014.05.011
– volume: 10
  start-page: 3145
  issue: 12
  year: 2022
  ident: 1123_CR39
  publication-title: Biomedicines
  doi: 10.3390/biomedicines10123145
– volume: 8
  start-page: e2100233
  issue: 15
  year: 2021
  ident: 1123_CR43
  publication-title: Adv Sci (Weinh)
  doi: 10.1002/advs.202100233
– volume: 91
  start-page: 998
  issue: 4
  year: 2009
  ident: 1123_CR32
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2008.01.029
– volume: 12
  start-page: 420
  issue: 1
  year: 2021
  ident: 1123_CR14
  publication-title: Stem Cell Res Ther
  doi: 10.1186/s13287-021-02499-z
– volume: 36
  start-page: 416
  issue: 4
  year: 2018
  ident: 1123_CR30
  publication-title: Reprod Biomed Online
  doi: 10.1016/j.rbmo.2017.12.016
– volume: 12
  start-page: 308
  issue: 1
  year: 2022
  ident: 1123_CR46
  publication-title: J Clin Med
  doi: 10.3390/jcm12010308
– volume: 30
  start-page: 93
  issue: 2–3
  year: 2003
  ident: 1123_CR1
  publication-title: Clin Exp Obstet Gynecol
– volume: 100
  start-page: 1289
  issue: 5
  year: 2013
  ident: 1123_CR31
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2013.07.1966
– volume: 31
  start-page: 245
  issue: 2
  year: 2004
  ident: 1123_CR23
  publication-title: Undersea Hyperb Med
– volume: 10
  start-page: CD006359
  issue: 10
  year: 2020
  ident: 1123_CR35
  publication-title: Cochrane Database Syst Rev
– volume: 10
  start-page: 68
  issue: 1
  year: 2019
  ident: 1123_CR15
  publication-title: Stem Cell Res Ther
  doi: 10.1186/s13287-019-1165-5
– volume: 6
  start-page: 21
  issue: 2
  year: 2006
  ident: 1123_CR22
  publication-title: Bosn J Basic Med Sci
  doi: 10.17305/bjbms.2006.3168
– volume: 93
  start-page: 1851
  issue: 6
  year: 2010
  ident: 1123_CR26
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2008.12.062
– volume: 83
  start-page: 226
  issue: 1
  year: 2005
  ident: 1123_CR20
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2004.05.101
– ident: 1123_CR25
  doi: 10.1093/humrep/der037
– volume: 15
  start-page: 1521
  year: 2021
  ident: 1123_CR8
  publication-title: Drug Des Devel Ther
  doi: 10.2147/DDDT.S297236
– volume: 89
  start-page: 832
  issue: 4
  year: 2008
  ident: 1123_CR34
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2007.04.031
– volume: 69
  start-page: 573
  issue: 4
  year: 2019
  ident: 1123_CR19
  publication-title: J Physiol Sci
  doi: 10.1007/s12576-019-00678-5
– volume: 15
  start-page: 199
  issue: suppl 2
  year: 2000
  ident: 1123_CR36
  publication-title: Hum Reprod
  doi: 10.1093/humrep/15.suppl_2.199
– volume: 86
  start-page: 307
  issue: 3
  year: 2021
  ident: 1123_CR9
  publication-title: Gynecol Obstet Invest
  doi: 10.1159/000516749
– volume: 13
  start-page: 1550
  issue: 6
  year: 1998
  ident: 1123_CR33
  publication-title: Hum Reprod
  doi: 10.1093/humrep/13.6.1550
– volume: 35
  start-page: 2774
  issue: 12
  year: 2020
  ident: 1123_CR48
  publication-title: Hum Reprod
  doi: 10.1093/humrep/deaa248
– volume: 10
  start-page: e004006
  issue: 8
  year: 2022
  ident: 1123_CR44
  publication-title: J Immunother Cancer
  doi: 10.1136/jitc-2021-004006
– volume: 96
  start-page: 519
  issue: 3
  year: 2021
  ident: 1123_CR24
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2011.07.1096
– volume: 40
  start-page: 124
  issue: 1
  year: 2020
  ident: 1123_CR2
  publication-title: Reprod Biomed Online
  doi: 10.1016/j.rbmo.2019.09.005
– volume: 30
  start-page: 349
  issue: 4
  year: 2015
  ident: 1123_CR11
  publication-title: Reprod Biomed Online
  doi: 10.1016/j.rbmo.2014.12.006
– volume: 9
  start-page: 3
  issue: 1
  year: 2016
  ident: 1123_CR28
  publication-title: J Hum Reprod Sci
  doi: 10.4103/0974-1208.178632
– volume: 46
  start-page: 456
  issue: 5
  year: 2006
  ident: 1123_CR21
  publication-title: Aust N Z J Obstet Gynaecol
  doi: 10.1111/j.1479-828X.2006.00634.x
– volume: 20
  start-page: 530
  issue: 4
  year: 2014
  ident: 1123_CR29
  publication-title: Hum Reprod Update
  doi: 10.1093/humupd/dmu011
– volume: 30
  start-page: 5703
  issue: 7
  year: 2022
  ident: 1123_CR47
  publication-title: Support Care Cancer
  doi: 10.1007/s00520-022-06994-8
– volume: 59
  start-page: 762
  issue: 4
  year: 2023
  ident: 1123_CR17
  publication-title: Med (Kaunas)
– volume: 156
  start-page: 103796
  issue: March
  year: 2023
  ident: 1123_CR13
  publication-title: J Reprod Immunol
  doi: 10.1016/j.jri.2023.103796
– volume: 112
  start-page: e81
  issue: 4 Suppl1
  year: 2019
  ident: 1123_CR27
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2019.08.077
– volume: 1787
  start-page: 828
  issue: 7
  year: 2009
  ident: 1123_CR41
  publication-title: Biochim Biophys Acta
  doi: 10.1016/j.bbabio.2009.03.009
– volume: 65
  start-page: 262
  issue: 2
  year: 1996
  ident: 1123_CR4
  publication-title: Fertil Steril
  doi: 10.1016/S0015-0282(16)58082-0
– volume: 69
  start-page: 153
  year: 2018
  ident: 1123_CR37
  publication-title: Placenta
  doi: 10.1016/j.placenta.2018.03.003
– volume: 21
  start-page: 1634
  issue: 11
  year: 2014
  ident: 1123_CR40
  publication-title: Antioxid Redox Signal
  doi: 10.1089/ars.2014.5940
– volume: 97
  start-page: e9689
  issue: 4
  year: 2018
  ident: 1123_CR3
  publication-title: Med (Baltim)
  doi: 10.1097/MD.0000000000009689
– ident: 1123_CR38
  doi: 10.1007/978-3-319-47140-2_2
– volume: 23
  start-page: 337
  issue: 7–8
  year: 2006
  ident: 1123_CR7
  publication-title: J Assist Reprod Genet
  doi: 10.1007/s10815-006-9053-1
– ident: 1123_CR16
  doi: 10.4103/2045-9912.310057
SSID ssj0020086
Score 2.3693733
Snippet Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some...
Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some studies have...
BackgroundThin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies. While some...
Abstract Background Thin endometrium is considered suboptimal for embryo implantation, leading to compromised pregnancy rates without effective therapies....
SourceID doaj
pubmedcentral
proquest
gale
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 1
SubjectTerms Asherman syndrome
Blastocysts
Care and treatment
Complications and side effects
Embryo transfer
Embryo transplantation
Embryos
Endometriosis
Endometrium
Estrogens
Frozen embryo transfer
Hormone replacement therapy
Hospitals
Hyperbaric oxygen therapy
Hyperbaric oxygenation
Implantation
Infertility
Ovulation
Oxygen therapy
Patient outcomes
Patients
Platelet-rich plasma therapy
Pregnancy
Reproductive health
Resistant thin endometrium
Thoracic surgery
Ultrasonic imaging
Uterus
SummonAdditionalLinks – databaseName: DOAJ: Directory of Open Access Journal (DOAJ)
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9NAEF5VPXGpgFJhKNUgofZQWU28a3u3t4CoIiR6aqXeVt6XiETWVeJIhCO_nJm1E9Vw4MI1u46cndc3m5lvGPsgg6DxNy5vMLjnwiqRK2t5Hiw3zcQHq9I4n6-31fxefHkoH56M-qKasJ4euD-4K94UijyoomkqXCJAL60vPMeM0AvvU5svxrxdMjWkWoTUdy0ysrpaY1QrZY7xCVNn9NW5GIWhxNb_t0_-s07ySeC5ec6OBsQIs_5NX7ADH1-y41nEbHm5hXNINZzpcvyY_ZpjWkl_ICwstD-2qBzQN1htr6GBx5YM4LsHdHnoHwDxKgy8qmugC1nA3JvwZOzwsUUEH127pJFbmyX0_YwQVu1P_Fa_NKttC12CvX4F-3r19St2d_P57tM8H6Ys5FaooqOrtSJMnHNSVdNGGRMMYhDvFdq6lEFRqX-Y1nVpQqh94SrrKlk6hBLcCVXzE3YY2-hfM2hsMTW1MlYRqpHWEBsgN5UrJ84GZTN2uTtz_dhzaeiUg8hK9xLSKCGdJKRFxj6SWPY7iQc7fYDaoQft0P_SjoxdkFA1WSseiW2GpgN8YeK90jN0r6gtZc0zdjraiVZmx8s7tdCDla81dfWKkpxgxt7vl-lJqlyLvt2kPegniQYuY3KkTqNfNl6Ji2-J6Zt4NIh_6M3_OIu37FmRLIAK5E7ZYbfa-HeIqDpzloznN_DmID8
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lj9MwELZguXBBwILIsiAjITgga9vYSWwuqCBWFRKcFqk3K35BJZqUJJUoR345M47bJSBxjZ3nvCcz3xDyXAaB428cq8G4M2GVYMpazoLlpp75YFUc5_PxU7n8LD6silVKuPWprPKgE6Oidq3FHPkFdlCKAhnuzfY7w6lR-Hc1jdC4SW4hdBmWdFWr64AL_fVDo4wsL3qwbYVkYKUggAaNzcTEGEXM_n8189_Vkn-Yn8u75E7yG-liJPQ9csM398npooGYebOnL2is5Iwp8lPyawnBJf5GWFva_tgDi9CxzWr_mtZ026IYfPMUFB9oCQpeK03oqj3FtCyFCBy9ymaA09YN9Y1rNzh4a7ehY1cjDV37E67qN6bbt3SIzq_v6LFqvX9Ari7fX71bsjRrgVmh8gETbHmYOeekKue1MiYY8ES8VyDxUgaFBf9hXlWFCaHyuSutK2XhwKHgTqiKPyQnTdv4R4TWNp-bShmr0LeR1iAmIDelK2bOBmUz8urwzfV2RNTQMRKRpR4ppIFCOlJIi4y8RbIcdyIadjzQdl90Ei7N61yhlVU4cYdLCOIK63PPvcm98F5m5CUSVaPMwiexdWo9gAdG9Cu9ACUL3FJUPCPnk50ga3a6fGALnWS919ecmZFnx2U8E-vXGt_u4h7QlggGlxE5YafJm01XmvXXiPeNaBqIQnT2_7s_JrfzyNtYAHdOToZu55-AxzSYp1EsfgMLyBik
  priority: 102
  providerName: ProQuest
Title Hyperbaric oxygen therapy: a possible choice for patients with resistant thin endometrium during frozen embryo transfer treatments
URI https://www.proquest.com/docview/2865450048
https://www.proquest.com/docview/2860404451
https://pubmed.ncbi.nlm.nih.gov/PMC10472734
https://doaj.org/article/3a29847197204384995ce2e3eb2e4ee8
Volume 21
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3Na9RAFB_6cfEiahWj7TKC6EGiu8kkMyOI7ErLIrRIaWHxMmS-6kI3abNZ6Hr0L_e9SXYx2oOXHDKTkMz7nnnv9wh5LTzD9jc2LsC4x8xIFktj0tibVBdD540M7XxOz_LpJfs6y2Y7ZNPuqFvA5b2hHfaTuqyv39_drj-DwH8KAi_yD0uwWZmIwfpAYAyaOGa7ZB8sE0dBPWXbUwU86m-rjTiPwTLyTRHNve_oGaqA5_-v1v47k_IP03TyiDzsfEo6bpngMdlx5RNyMC4hnl6s6RsasjzD9vkB-TWFwBOPGOaGVndrYB_almCtP9KC3lQoIteOwrqABqHg0dIOeXVJccuWQnSOHmfZwGPzkrrSVgtsyrVa0Lbikfq6-glvdQtdryvaBMfY1XSb0b58Si5Oji--TOOuD0NsmEwa3HxL_NBaK2Q-KqTWXoOX4pwEbSCEl1gM4EecZ9p77hKbG5uLzIKzkVomefqM7JVV6Z4TWphkpLnURqLfI4xGvMBU5zYbWuOlici7zZqrmxZtQ4UoReSqpZACCqlAIcUiMkGybGciUna4UdVXqhM8lRaJRAsssRtPKiDAy4xLXOp04phzIiJvkagKOQyWxBRdWQJ8MCJjqTEoYOCcjKcROezNBDk0_eENW6gNGyus-2UZqsmIvNoO45OY21a6ahXmgCZFoLiIiB479f6sP1LOfwQscETaQISiF__9Gy_JgySwOebJHZK9pl65I3CsGj0gu3zGB2R_cnz27XwQticGQYLgej75_hu52SZN
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB6V9AAXBBSEocAi8Tggq4m9tneREEqhVUrbCKEi9bbyPlwiETvkIQhH_g__kZm1HTBI3HrNrp3E8_jmW88D4IkoOI2_sWGO4B5yI3kojYnDwsQ677vCSD_O53Scjj7yd-fJ-Rb8bGthKK2y9YneUdvK0Bn5HlVQ8oQU7vXsS0hTo-jtajtCo1aLY7f-ipRt8eroLcr3aRQdHpy9GYXNVIHQcBkt6SgpKvrWWiHTQS61LjRirnMSdVuIQlJqezHIskQXReYimxqbisQidMaWyyzG216BbR4jk-nB9v7B-P2HDcMjgtBW5oh0b4FgmogQYREZO0JEyDvo54cE_AsFf6dn_oF3hzfgehOosmGtWTdhy5W3YGdYIkmfrtkz5lNH_Zn8DvwYIZul9xYTw6pva9RJVtd1rV-ynM0qsrvPjqGnRbfEMExmTTvXBaNzYIaUn8LYcomXTUrmSltNadLXasrqMkpWzKvveFc31fN1xZY-2nZztkmTX9yGs8sQwx3olVXp7gLLTTTQmdRGUjAljKYmhLFObdK3ppAmgBftM1ezuoWH8tRHpKqWkEIJKS8hxQPYJ7FsdlL7bf9BNb9QjTWrOI8kwbqkET-xQNaYGBe52OnIcedEAM9JqIqcBD4Skze1DviDqd2WGqJXR21JsjiA3c5ONG7TXW7VQjXOZaF-m0IAjzfLdCUlzJWuWvk96J6p-1wAoqNOnX_WXSknn3yDcWrfQW2P7v3_2x_B1dHZ6Yk6ORof34drkddzyr7bhd5yvnIPMFxb6oeNkTBQl2yWvwDZwVXl
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Hyperbaric+oxygen+therapy%3A+a+possible+choice+for+patients+with+resistant+thin+endometrium+during+frozen+embryo+transfer+treatments&rft.jtitle=Reproductive+biology+and+endocrinology&rft.au=Chen%2C+Jingjing&rft.au=Huang%2C+Fangling&rft.au=Fu%2C+Jing&rft.au=Zhao%2C+Jianjuan&rft.date=2023-09-01&rft.pub=BioMed+Central+Ltd&rft.issn=1477-7827&rft.eissn=1477-7827&rft.volume=21&rft.issue=1&rft_id=info:doi/10.1186%2Fs12958-023-01123-4&rft.externalDocID=A763020573
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1477-7827&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1477-7827&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1477-7827&client=summon