27 results on '"de Coppi P"'
Search Results
2. Neuroprotection is improved by watertightness of fetal spina bifida repair in the sheep model
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Joyeux, L., primary, van der Merwe, J., additional, Aertsen, M., additional, Patel, P. A., additional, Khatoun, A., additional, Mori da Cunha, M. G. M. C., additional, De Vleeschauwer, S., additional, Parra, J., additional, Danzer, E., additional, McLaughlin, M., additional, Stoyanov, D., additional, Vercauteren, T., additional, Ourselin, S., additional, Radaelli, E., additional, de Coppi, P., additional, Van Calenbergh, F., additional, and Deprest, J., additional
- Published
- 2023
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3. Complex gastroschisis: a new indication for fetal surgery?
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Joyeux, L., primary, Belfort, M. A., additional, De Coppi, P., additional, Basurto, D., additional, Valenzuela, I., additional, King, A., additional, De Catte, L., additional, Shamshirsaz, A. A., additional, Deprest, J., additional, and Keswani, S. G., additional
- Published
- 2021
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4. COVID‐19 and vertical transmission: assessing the expression of ACE2/TMPRSS2 in the human fetus and placenta to assess the risk of SARS‐CoV‐2 infection
- Author
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Beesley, MA, primary, Davidson, JR, additional, Panariello, F, additional, Shibuya, S, additional, Scaglioni, D, additional, Jones, BC, additional, Maksym, K, additional, Ogunbiyi, O, additional, Sebire, NJ, additional, Cacchiarelli, D, additional, David, AL, additional, De Coppi, P, additional, and Gerli, MFM, additional
- Published
- 2021
- Full Text
- View/download PDF
5. Cranial findings detected by second‐trimester ultrasound in fetuses with myelomeningocele: a systematic review
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Kunpalin, Y, primary, Richter, J, additional, Mufti, N, additional, Bosteels, J, additional, Ourselin, S, additional, De Coppi, P, additional, Thompson, D, additional, David, AL, additional, and Deprest, J, additional
- Published
- 2021
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6. VP27.02: Incidence and patterns of abnormal corpus callosum in fetuses with spina bifida: a cross‐sectional study in two fetal surgery centres
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Kunpalin, Y., primary, Deprest, J., additional, Papastefanou, I., additional, Bredaki, E., additional, Sacco, A., additional, Russo, F., additional, Richter, J., additional, Jansen, K., additional, De Coppi, P., additional, David, A.L., additional, Ushakov, F., additional, and De Catte, L., additional
- Published
- 2020
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7. Reply
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Joyeux, L., primary, Danzer, E., additional, De Bie, F., additional, Russo, F. M., additional, Javaux, A., additional, Peralta, C. F. A., additional, De Salles, A. A. F., additional, Pastuszka, A., additional, Olejek, A., additional, Van Mieghem, T., additional, De Coppi, P., additional, Moldenhauer, J., additional, Whitehead, W. E., additional, Belfort, M. A., additional, Lapa, D. A., additional, Acacio, G. L., additional, Devlieger, R., additional, Hirose, S., additional, Farmer, D. L., additional, Van Calenbergh, F., additional, Adzick, N. S., additional, Johnson, M. P., additional, and Deprest, J., additional
- Published
- 2020
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8. VP28.07: Cranial findings detected by second trimester ultrasound in fetuses with spina bifida aperta: a systematic review
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Kunpalin, Y., primary, Richter, J., additional, Mufti, N., additional, Bosteels, J., additional, Ourselin, S., additional, De Coppi, P., additional, David, A.L., additional, and Deprest, J., additional
- Published
- 2020
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9. OC10.01: A novel training program for fetoscopic spina bifida repair
- Author
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Joyeux, L., primary, Basurto, D., additional, Eastwood, M., additional, Javaux, A., additional, De Bie, F., additional, Vergote, S., additional, Devlieger, R., additional, De Catte, L., additional, Van Calenbergh, F., additional, Belfort, M.A., additional, De Coppi, P., additional, and Deprest, J., additional
- Published
- 2020
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10. Learning curves of open and endoscopic fetal spina bifida closure: systematic review and meta‐analysis
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Joyeux, L., primary, De Bie, F., additional, Danzer, E., additional, Russo, F. M., additional, Javaux, A., additional, Peralta, C. F. A., additional, De Salles, A. A. F., additional, Pastuszka, A., additional, Olejek, A., additional, Van Mieghem, T., additional, De Coppi, P., additional, Moldenhauer, J., additional, Whitehead, W. E., additional, Belfort, M. A., additional, Lapa, D. A., additional, Acacio, G. L., additional, Devlieger, R., additional, Hirose, S., additional, Farmer, D. L., additional, Van Calenbergh, F., additional, Adzick, N. S., additional, Johnson, M. P., additional, and Deprest, J., additional
- Published
- 2020
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11. Experimental Induction of Complex Gastroschisis in the Fetal Lamb: Systematic Review.
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Arai T, Tianthong W, Russo FM, Basurto D, Joyeux L, De Coppi P, and Deprest J
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- Animals, Female, Pregnancy, Sheep, Disease Models, Animal, Gastroschisis etiology, Gastroschisis surgery
- Abstract
We systematically reviewed experiments in the fetal lamb model of gastroschisis using PubMed, Embase, Web of Science, and Scopus, seeking for standardized surgical techniques to obtain complex gastroschisis. Eligible were studies where an abdominal wall defect was surgically induced and gross anatomical findings at birth were available. The primary outcome was complex gastroschisis, defined by the presence of bowel stenosis, atresia, volvulus, perforation, and/or necrosis. Secondary outcomes were fetal death and additional readouts reported. Of ten eligible studies, six included lambs that had no additional prenatal manipulations and were assessed at term (35 lambs). Gastroschisis was induced at day 70-80 (term = 140-145), typically (n = 4/6 studies) in the left lower abdomen with defect size ranging from 0.5 to 4.0 cm. Only one study, in which a 1.5 cm diameter silicone ring was utilized, resulted in complex gastroschisis in 100% of term survivors. Fetal loss was more frequent in studies where a silicone ring and/or a right-sided defect were used. No changes unique to complex gastroschisis were identified in additional readouts, including bowel histology. When gastroschisis becomes "complex" following induction is uncertain. This knowledge is essential in studying potential prenatal interventions that may change the natural course., (© 2024 John Wiley & Sons Ltd.)
- Published
- 2024
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12. Exteriorization of the uterus reduces fetoscopic cannula-induced stress and strain: A finite element model analysis.
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Ahmad MA, Vergote S, Vander Poorten E, Devlieger R, De Coppi P, Mazza E, and Deprest J
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- Pregnancy, Female, Humans, Finite Element Analysis, Uterus surgery, Fetoscopy methods, Cannula, Urogenital Abnormalities
- Abstract
Objective: To estimate stresses and strains in the uterine wall and fetal membranes with single/multi-port fetoscopy, simulating either a percutaneous access or via exteriorized uterus., Study Design: Finite element models based on anatomical dimensions, material properties and boundary conditions were created to simulate stresses, strains and displacements on the uterine wall and fetal membranes during simulated fetal surgery either via exteriorized uterus or percutaneous approach, and with one or three cannulas. Clinically, we measured the anatomical layer thickness and cannula entry point displacement in patients undergoing single port percutaneous fetoscopy., Results: Simulations demonstrate that single port percutaneous fetoscopy increases stress on the fetal membranes (+105%, 128 to 262 kPa) and uterine wall (+115%, 0.89 to 1.9 kPa) compared to exteriorized uterine access. Using three ports increases stress by 110% (148 to 312 kPa) on membranes and 113% (1.08 to 2.3 kPa) on uterine wall. Finite Element Method showed 0.75 cm uterine entry point displacement from the cutaneous entry, while clinical measurements demonstrated displacement of more than double (1.69 ± 0.58 cm), suggesting modeled measurements may be underestimations., Conclusion: The stresses and strains on the fetal membranes and uterus are double as high when entering percutaneously than via an exteriorized uterus. Based on what can be clinically measured, this may be an underestimation., (© 2024 John Wiley & Sons Ltd.)
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- 2024
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13. Local host response of commercially available dural patches for fetal repair of spina bifida aperta in rabbit model.
- Author
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Kunpalin Y, Vergote S, Joyeux L, Telli O, David AL, Belfort M, De Coppi P, and Deprest J
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- Pregnancy, Female, Humans, Animals, Rabbits, Fetus surgery, Prenatal Care, Fetoscopy, Spinal Cord surgery, Spina Bifida Cystica surgery
- Abstract
Objective: Fetal surgery for spina bifida aperta (SBA) by open hysterotomy typically repairs anatomical native tissue in layers. Increasingly, fetoscopic repair is performed using a dural patch followed by skin closure. We studied the host response to selected commercially available patches currently being used in a fetal rabbit model for spina bifida repair., Methods: SBA was surgically induced at 23-24 days of gestation (term = 31 days). Fetal rabbits were assigned to unrepaired (SBA group), or immediate repair with Duragen™ or Durepair™. Non-operated littermates served as normal controls. At term, spinal cords underwent immunohistochemical staining including Nissl and glial fibrillary acidic protein. We hypothesized that spinal cord coverage with a dural patch and skin closure would preserve motor neuron density within the non-inferiority limit of 201.65 cells/mm
2 and reduce inflammation compared to unrepaired SBA fetuses., Results: Motor neuron density assessed by Nissl staining was conserved both by Duragen (n = 6, 89.5; 95% CI -158.3 to -20.6) and Durepair (n = 6, 37.0; 95% CI -132.6 to -58.5), whereas density of GFAP-positive cells to quantify inflammation was lower than in unrepaired SBA-fetuses (SBA 2366.0 ± 669.7 cells/mm2 vs. Duragen 1274.0 ± 157.2 cells/mm2 ; p = 0.0002, Durepair 1069.0 ± 270.7 cells/mm2 ; p < 0.0001)., Conclusions: Covering the rabbit spinal cord with either Duragen or Durepair followed by skin closure preserves motor neuron density and reduces the inflammatory response., (© 2023 John Wiley & Sons Ltd.)- Published
- 2023
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14. Pulmonary hypertension in congenital diaphragmatic hernia: Antenatal prediction and impact on neonatal mortality.
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Basurto D, Russo FM, Papastefanou I, Bredaki E, Allegaert K, Pertierra A, Debeer A, De Catte L, Lewi L, Devlieger R, De Coppi P, Gratacos E, Gomez O, and Deprest J
- Subjects
- Female, Fetoscopy, Gestational Age, Humans, Infant Mortality, Infant, Newborn, Lung diagnostic imaging, Pregnancy, Retrospective Studies, Ultrasonography, Prenatal, Hernias, Diaphragmatic, Congenital surgery, Hypertension, Pulmonary epidemiology
- Abstract
Objective: To determine the prevalence of pulmonary hypertension (PAH) in left-sided congenital diaphragmatic hernia (CDH); how we could predict it; and how PAH contributed to the model for mortality prediction., Study Design: Retrospective analysis in three European centers. The primary outcome was the presence of PAH on postnatal day (d) 1, 7, and at discharge. Studied predictors of PAH were: observed/expected-lung/head-ratio (o/e LHR), liver-herniation, fetoscopic endoluminal tracheal occlusion (FETO), and gestational age (GA) at delivery. The combined effect of pre- and postnatal variables on mortality was modeled by Cox regression., Results: Of the 197 neonates, 56 (28.4%) died. At d1, 67.5% (133/197) had PAH and 61.9% (101/163) by d7. Overall, 6.4% (9/141) had PAH at discharge. At d1, o/e LHR (odds ratio (OR) 0.96) and FETO (OR 2.99) independently correlated to PAH (areas under the curve [AUC]: 0.74). At d7, PAH significantly correlated only with the use of FETO (OR 3.9; AUC: 0.65). None were significant for PAH at discharge. Combining the occurrence of PAH with antenatal biomarkers improved mortality prediction (p = 0.02), in a model including o/e LHR (HR: 0.94), FETO (HR: 0.35), liver herniation (HR: 16.78), and PAH (HR: 15.95)., Conclusions: Antenatal prediction of PAH was only moderate. The postnatal occurrence of PAH further increases the risk of death. Whereas this may be used to counsel parents in the postnatal period, our study demonstrates there is a need to find more accurate antenatal predictors for PAH., (© 2022 John Wiley & Sons Ltd.)
- Published
- 2022
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15. Antenatal management of congenital diaphragmatic hernia: What's next ?
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Russo F, Benachi A, Gratacos E, Zani A, Keijzer R, Partridge E, Sananes N, De Coppi P, Aertsen M, Nicolaides KH, and Deprest J
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- Child, Female, Fetoscopy methods, Humans, Infant, Newborn, Pregnancy, Trachea diagnostic imaging, Trachea surgery, Balloon Occlusion, Fetal Therapies, Hernias, Diaphragmatic, Congenital diagnostic imaging, Hernias, Diaphragmatic, Congenital surgery
- Abstract
Congenital diaphragmatic hernia can be diagnosed in the prenatal period and its severity can be measured by fetal imaging. There is now level I evidence that, in selected cases, Fetoscopic Endoluminal Tracheal Occlusion with a balloon increases survival to discharge from the neonatal unit as well as the risk for prematurity. Both effects are dependent on the time point of tracheal occlusion. Fetoscopic Endoluminal Tracheal Occlusion may also lead to iatrogenic death when the balloon cannot be timely retrieved. The implementation of the findings from our clinical studies, may also vary based on local conditions. These may be different in terms of available skill set, access to fetal therapy, as well as outcome based on local neonatal management. We encourage prior benchmarking of local outcomes with optimal postnatal management, based on large enough numbers and using identical criteria as in the recent trials. We propose to work further on prenatal prediction methods, and the improvement of fetal intervention. In this manuscript, we describe a research agenda from a fetal medicine perspective. This research should be in parallel with innovation in neonatal and pediatric (surgical) management of this condition., (© 2022 John Wiley & Sons Ltd.)
- Published
- 2022
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16. What should we tell parents? Congenital diaphragmatic hernia.
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Russo FM, Debeer A, De Coppi P, Devriendt K, Crombag N, Hubble T, Power B, Benachi A, and Deprest J
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- Female, Humans, Parents, Pregnancy, Prenatal Diagnosis, Prognosis, Ultrasonography, Prenatal, Hernias, Diaphragmatic, Congenital diagnostic imaging
- Abstract
Congenital diaphragmatic hernia (CDH) is characterized by a defect in the muscle dividing the thoracic and abdominal cavities. This leads to herniation of the abdominal organs into the thorax and a disturbance of lung development. Two-thirds of cases are identified by prenatal ultrasound in the second trimester, which should prompt referral to a tertiary center for prognosis assessment and counseling by a multidisciplinary team familiar with this condition. In this review, we summarize evidence on prenatal diagnosis and postnatal management of CDH. There is a focus on information that should be provided to expecting parents during prenatal counseling., (© 2020 John Wiley & Sons Ltd.)
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- 2022
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17. Fetoscopic insufflation of heated-humidified carbon dioxide during simulated spina bifida repair is safe under controlled anesthesia in the fetal lamb.
- Author
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Joyeux L, Basurto D, Bleeser T, Van der Veeken L, Vergote S, Kunpalin Y, Trigo L, Corno E, De Bie FR, De Coppi P, Ourselin S, Van Calenbergh F, Hooper SB, Rex S, and Deprest J
- Subjects
- Animals, Female, Hot Temperature, Humidity, Pregnancy, Sheep, Anesthesia methods, Carbon Dioxide administration & dosage, Fetoscopy methods, Insufflation methods, Spinal Dysraphism surgery
- Abstract
Objective: To assess the safety of Partial-Amniotic-Insufflation-of-heated-humidified-CO
2 (hPACI) during fetoscopic spina bifida repair (fSB-repair)., Method: A simulated fSB-repair through an exteriorized uterus under hPACI was performed in 100-day fetal lambs (term = 145 days) under a laboratory anesthesia protocol (n = 5; group 1) which is known to induce maternal-fetal acidosis and hypercapnia. Since these may not occur clinically, we applied a clinical anesthesia protocol (n = 5; group 2), keeping maternal parameters within physiological conditions, that is, controlled maternal arterial carbon dioxide (CO2) pressure (pCO2 = 30 mmHg), blood pressure (≥67 mmHg), and temperature (37.1-39.8°C). Our superiority study used fetal pH as the primary outcome., Results: Compared to group 1, controlled anesthesia normalized fetal pH (7.23 ± 0.02 vs. 7.36 ± 0.02, p < 0.001), pCO2 (70.0 ± 9.1 vs. 43.0 ± 1.0 mmHg, p = 0.011) and bicarbonate (27.8 ± 1.1 vs. 24.0 ± 0.9 mmol/L, p = 0.071) at baseline. It kept them within clinically acceptable limits (pH ≥ 7.23, pCO2 ≤ 70 mmHg, bicarbonate ≤ 30 mm/L) for ≥120 min of hPACI as opposed to ≤30 min in group one. Fetal pO2 and lactate were comparable between groups and generally within normal range. Fetal brain histology demonstrated fewer apoptotic cells and higher neuronal density in the prefrontal cortex in group two. There was no difference in fetal membrane inflammation, which was mild., Conclusion: Fetoscopic insufflation of heated-humidified CO2 during simulated fSB-repair through an exteriorized uterus can be done safely under controlled anesthesia., (© 2022 John Wiley & Sons Ltd.)- Published
- 2022
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18. Incidence and patterns of abnormal corpus callosum in fetuses with isolated spina bifida aperta.
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Kunpalin Y, Deprest J, Papastefanou I, Bredaki E, Sacco A, Russo F, Richter J, Jansen K, Ourselin S, De Coppi P, David AL, Ushakov F, and De Catte L
- Subjects
- Adult, Agenesis of Corpus Callosum diagnosis, Agenesis of Corpus Callosum epidemiology, Cohort Studies, Female, Fetus surgery, Gestational Age, Humans, Incidence, Pregnancy, Retrospective Studies, Spina Bifida Cystica epidemiology, Agenesis of Corpus Callosum classification, Spina Bifida Cystica diagnosis
- Abstract
Objective: To determine the incidence and characterise corpus callosum (CC) abnormalities in fetuses with spina bifida aperta (SBA) between 18 and 26 weeks of gestation., Methods: This was a retrospective study on fetuses with isolated SBA and who were assessed for fetal surgery. Digitally stored ultrasound images of the brain were reviewed for the presence/absence of the CC, and the length and diameter of its constituent parts (rostrum, genu, body and splenium). We used regression analysis to determine the relationship between CC abnormalities and gestational age, head circumference, ventricle size, lesion level and lesion type., Results: Nearly three-quarters of fetuses with isolated SBA had an abnormal CC (71.7%, 76/106). Partial agenesis was most common in the splenium (18.9%, 20/106) and the rostrum (13.2%, 14/106). The most common abnormal pattern was of a short CC with normal diameter throughout. Of note, 20.8% (22/106) had a hypoplastic genu and 28.3% (30/106) had a thick body part. Larger lateral ventricle size was associated with partial agenesis of the CC (odds ratio [OR]: 0.14, p < 0.001) and inversely associated with a shorter CC (OR: 2.60, p < 0.01)., Conclusion: An abnormal CC is common in fetuses with isolated SBA who are referred for fetal surgery., (© 2021 John Wiley & Sons Ltd.)
- Published
- 2021
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19. Getting earlier, smaller and regenerative: The next 10 years of in utero spina bifida repair.
- Author
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Thompson D and De Coppi P
- Subjects
- Humans, Neurosurgical Procedures, Meningomyelocele surgery, Spinal Dysraphism surgery
- Published
- 2021
- Full Text
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20. Preclinical stem cell therapy in fetuses with myelomeningocele: A systematic review and meta-analysis.
- Author
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Kunpalin Y, Subramaniam S, Perin S, Gerli MFM, Bosteels J, Ourselin S, Deprest J, De Coppi P, and David AL
- Subjects
- Animals, Chi-Square Distribution, Female, Meningomyelocele metabolism, Pregnancy, Rats, Sheep, Fetus surgery, Meningomyelocele therapy, Stem Cell Transplantation methods
- Abstract
Objective: We performed a systematic review to summarize the efficacy and safety of in utero stem cells application in preclinical models with myelomeningocele (MMC)., Methods: The study was registered with PROSPERO (CRD42019160399). We searched MEDLINE, Embase, Web of Science, Scopus and CENTRAL for publications articles on stem cell therapy in animal fetuses with MMC until May 2020. Publication quality was assessed by the SYRCLE's tool. Meta-analyses were pooled if studies were done in the same animal model providing similar type of stem cell used and outcome measurements. Narrative synthesis was performed for studies that could not be pooled., Results: Nineteen and seven studies were included in narrative and quantitative syntheses, respectively. Most used mesenchymal stem cells (MSCs) and primarily involved ovine and rodent models. Both intra-amniotic injection of allogeneic amniotic fluid (AF)-MSCs in rat MMC model and the application of human placental (P)-MSCs to the spinal cord during fetal surgery in MMC ovine model did not compromise fetal survival rates at term (rat model, relative risk [RR] 1.03, 95% CI 0.92-1.16; ovine model, RR 0.94, 95% CI 0.78-1.13). A single intra-amniotic injection of allogeneic AF-MSCs into rat MMC model was associated with a higher rate of complete defect coverage compared to saline injection (RR 16.35, 95% CI 3.27-81.79). The incorporation of human P-MSCs as a therapeutic adjunct to fetal surgery in the ovine MMC model significantly improved sheep locomotor rating scale after birth (mean difference 5.18, 95% CI 3.36-6.99)., Conclusions: Stem cell application during prenatal period in preclinical animal models is safe and effective., (© 2021 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd.)
- Published
- 2021
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21. Antenatal corticosteroids and outcomes in gastroschisis: A multicenter retrospective cohort study.
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Carnaghan H, James CP, Charlesworth PB, Ghionzoli M, Pereira S, Elkhouli M, Baud D, De Coppi P, Ryan G, Shah PS, Davenport M, David AL, Pierro A, and Eaton S
- Subjects
- Adult, Cohort Studies, Delivery, Obstetric methods, Delivery, Obstetric statistics & numerical data, Enteral Nutrition, Female, Gastroschisis diagnosis, Gastroschisis epidemiology, Gestational Age, Humans, Infant, Newborn, Length of Stay statistics & numerical data, Male, Pregnancy, Pregnancy Outcome epidemiology, Prenatal Care statistics & numerical data, Prognosis, Retrospective Studies, Time Factors, Treatment Outcome, Adrenal Cortex Hormones administration & dosage, Gastroschisis drug therapy, Prenatal Care methods
- Abstract
Objective: In gastroschisis, there is evidence to suggest that gut dysfunction develops secondary to bowel inflammation; we aimed to evaluate the effect of maternal antenatal corticosteroids administered for obstetric reasons on time to full enteral feeds in a multicenter cohort study of gastroschisis infants., Methods: A three center, retrospective cohort study (1992-2013) with linked fetal/neonatal gastroschisis data was conducted. The primary outcome measure was time to full enteral feeds (a surrogate measure for bowel function) and secondary outcome measure was length of hospital stay. Analysis included Mann-Whitney and Cox regression., Results: Of 500 patients included in the study, 69 (GA at birth 34 [25-38] weeks) received antenatal corticosteroids and 431 (GA at birth 37 [31-41] weeks) did not. Antenatal corticosteroids had no effect on the rate of reaching full feeds (Hazard ratio HR 1.0 [95% CI: 0.8-1.4]). However, complex gastroschisis (HR 0.3 [95% CI: 0.2-0.4]) was associated with an increased time to reach full feeds and later GA at birth (HR 1.1 per week increase in GA [95% CI: 1.1-1.2]) was associated with a decreased time to reach full feeds., Conclusion: Maternal antenatal corticosteroids use, under current antenatal steroid protocols, in gastroschisis is not associated with an improvement in neonatal outcomes such as time to full enteral feeds or length of hospital stay., (© 2020 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd.)
- Published
- 2020
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22. The Effect of Glutamine Supplementation on Microbial Invasion in Surgical Infants Requiring Parenteral Nutrition: Results of a Randomized Controlled Trial.
- Author
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Bishay M, Simchowitz V, Harris K, Macdonald S, De Coppi P, Klein N, Eaton S, and Pierro A
- Subjects
- Dietary Supplements, Double-Blind Method, Enteral Nutrition, Humans, Infant, Infant, Newborn, Prospective Studies, Bacteremia prevention & control, Digestive System Surgical Procedures, Glutamine administration & dosage, Parenteral Nutrition
- Abstract
Background: To determine whether parenteral plus enteral glutamine supplementation influences microbial invasion in surgical infants who require parenteral nutrition (PN)., Methods: An prospective double-blind randomized controlled trial studying surgical infants receiving PN for at least 5 days for congenital or acquired intestinal anomalies (2009-2012) was used. Infants were randomized to receive either glutamine supplementation (parenteral plus enteral; total 400 mg/kg/d) or isonitrogenous control. The primary end point was microbial invasion evaluated after 5 days of supplementation and defined as: (i) positive conventional blood culture, (ii) evidence of microbial DNA in blood (polymerase chain reaction), (iii) plasma endotoxin level ≥50 pg/mL, or (iv) plasma level of lipopolysaccharide binding protein ≥50 ng/mL. Data are given as median (range) and compared by logistic regression., Results: Sixty infants were randomized and reached the primary end point. Twenty-five patients had intestinal obstruction, 19 had abdominal wall defects, and 13 had necrotizing enterocolitis. Thirty-six infants showed evidence of microbial invasion during the study, and 17 of these were not detected by conventional blood culture. There was no significant difference between the 2 groups in the primary outcome; evidence of microbial invasion after 5 days was found in 9/31 (control group) and 8/29 (glutamine group) (odds ratio 0.83 [0.24-2.86; P = 0.77])., Conclusion: More than half of surgical infants requiring PN showed evidence of microbial invasion. Approximately half of this was not detectable by conventional blood cultures. Parenteral plus enteral glutamine supplementation had no effect on incidence of microbial invasion., (© 2019 American Society for Parenteral and Enteral Nutrition.)
- Published
- 2020
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23. Super-resolution for upper abdominal MRI: Acquisition and post-processing protocol optimization using brain MRI control data and expert reader validation.
- Author
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Ebner M, Patel PA, Atkinson D, Caselton L, Firmin L, Amin Z, Bainbridge A, De Coppi P, Taylor SA, Ourselin S, Chouhan MD, and Vercauteren T
- Subjects
- Adult, Brain diagnostic imaging, Female, Healthy Volunteers, Humans, Image Enhancement methods, Imaging, Three-Dimensional methods, Male, Pilot Projects, Abdomen diagnostic imaging, Cholangiopancreatography, Magnetic Resonance methods, Image Interpretation, Computer-Assisted methods
- Abstract
Purpose: Magnetic resonance (MR) cholangiopancreatography (MRCP) is an established specialist method for imaging the upper abdomen and biliary/pancreatic ducts. Due to limitations of either MR image contrast or low through-plane resolution, patients may require further evaluation with contrast-enhanced computed tomography (CT) images. However, CT fails to offer the high tissue-ductal-vessel contrast-to-noise ratio available on T2-weighted MR imaging., Methods: MR super-resolution reconstruction (SRR) frameworks have the potential to provide high-resolution visualizations from multiple low through-plane resolution single-shot T2-weighted (SST2W) images as currently used during MRCP studies. Here, we (i) optimize the source image acquisition protocols by establishing the ideal number and orientation of SST2W series for MRCP SRR generation, (ii) optimize post-processing protocols for two motion correction candidate frameworks for MRCP SRR, and (iii) perform an extensive validation of the overall potential of upper abdominal SRR, using four expert readers with subspeciality interest in hepato-pancreatico-biliary imaging., Results: Obtained SRRs show demonstrable advantages over traditional SST2W MRCP data in terms of anatomical clarity and subjective radiologists' preference scores for a range of anatomical regions that are especially critical for the management of cancer patients., Conclusions: Our results underline the potential of using SRR alongside traditional MRCP data for improved clinical diagnosis., (© 2019 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine.)
- Published
- 2019
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24. A systematic review and meta-analysis on fetal ovarian cysts: impact of size, appearance and prenatal aspiration.
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Tyraskis A, Bakalis S, David AL, Eaton S, and De Coppi P
- Subjects
- Female, Humans, MEDLINE, Ovarian Cysts pathology, Ovarian Cysts surgery, Ovarian Diseases embryology, Ovarian Diseases epidemiology, Pregnancy, Risk Factors, Torsion Abnormality diagnosis, Torsion Abnormality embryology, Torsion Abnormality epidemiology, Treatment Outcome, Ultrasonography, Prenatal, Fetal Diseases surgery, Ovarian Cysts embryology, Suction adverse effects
- Abstract
Objective: The objective of the study is to compare outcomes of ultrasound-guided aspiration of fetal ovarian cysts with conservative management., Method: A systematic review of MEDLINE and Web of Science included studies reporting outcomes (prenatal and postnatal torsion, spontaneous resolution and surgery) of fetuses with ovarian cysts. Subgroup analysis was performed according to cyst diameter at diagnosis and cysts ≥40 mm., Results: Ninety-two non-randomised studies reported on 380 cysts (324 observed and 56 aspirated in utero) in 365 fetuses. All studies were case reports or series with high heterogeneity and risk of bias. The overall spontaneous resolution rate of conservatively managed cysts was 46%, yet decreased with increasing cyst size. Risk of prenatal ovarian torsion in conservatively managed cases depended on cyst size and was particularly important in the range 30 to 59 mm (15-34%). The rate of prenatal torsion in simple cysts ≥40 mm was lower in aspirated than conservatively managed cysts (0% vs 10%, p = 0.03). Aspirated cysts had lower rates of postnatal surgery (7%) compared with conservatively managed cysts (49%, p < 0.001)., Conclusion: Cysts 30 to 59 mm were at highest risk of torsion. Simple cysts >40 mm had lower rates of torsion when aspirated prenatally. Randomised studies and safety data are needed prior to routine prenatal ovarian cyst aspiration. © 2017 John Wiley & Sons, Ltd., (© 2017 John Wiley & Sons, Ltd.)
- Published
- 2017
- Full Text
- View/download PDF
25. The use of human amniotic fluid stem cells as an adjunct to promote pulmonary development in a rabbit model for congenital diaphragmatic hernia.
- Author
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DeKoninck P, Toelen J, Roubliova X, Carter S, Pozzobon M, Russo FM, Richter J, Vandersloten PJ, Verbeken E, De Coppi P, and Deprest J
- Subjects
- Abnormalities, Multiple embryology, Abnormalities, Multiple etiology, Animals, Combined Modality Therapy, Hernias, Diaphragmatic, Congenital complications, Humans, Lung Diseases embryology, Lung Diseases etiology, Rabbits, Abnormalities, Multiple prevention & control, Amniotic Fluid cytology, Fetal Organ Maturity, Fetal Stem Cells transplantation, Fetal Therapies methods, Hernias, Diaphragmatic, Congenital therapy, Lung abnormalities, Lung embryology, Lung Diseases prevention & control
- Abstract
Objective: This study aimed to evaluate the potential benefit of intra-tracheal injection of human amniotic fluid stem cells (hAFSC) on pulmonary development combined with TO in a rabbit model for CDH., Methods: In time-mated pregnant does a left diaphragmatic defect was created at d23 (term = 31). At d28, previously operated fetuses were assigned to either TO and injection with 70 μL of phosphate buffered saline (PBS) or 1.0 × 10(6) c-Kit positive hAFSC expressing LacZ or were left untouched (CDH). Harvesting was done at d31 to obtain their lung-to-body weight ratio (LBWR), airway and vascular lung morphometry, X-gal staining and immunohistochemistry for Ki67 and surfactant protein-B (SP-B)., Results: CDH-induced pulmonary hypoplasia is countered by TO + PBS, this reverses LBWR, mean terminal bronchiole density (MTBD) and medial thickness to normal. The additional injection of hAFSC decreases MTBD and results in a non-significant decrease in muscularization of intra-acinary vessels. There were no inflammatory changes and LacZ positive hAFSC were dispersed throughout the lung parenchyma 4 days after injection., Conclusion: HAFSC exert an additional effect on TO leading to a decrease in MTBD, a measure of alveolar number surrounding the terminal bronchioles, without signs of toxicity. © 2015 John Wiley & Sons, Ltd., (© 2015 John Wiley & Sons, Ltd.)
- Published
- 2015
- Full Text
- View/download PDF
26. Routine clonal expansion of mesenchymal stem cells derived from amniotic fluid for perinatal applications.
- Author
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Zia S, Toelen J, Mori da Cunha M, Dekoninck P, de Coppi P, and Deprest J
- Subjects
- Animals, Animals, Newborn, Cells, Cultured, Clone Cells cytology, Clone Cells physiology, Female, Humans, Mesenchymal Stem Cell Transplantation, Mesenchymal Stem Cells cytology, Mice, Mice, SCID, Pluripotent Stem Cells cytology, Pluripotent Stem Cells physiology, Pluripotent Stem Cells transplantation, Pregnancy, Amniotic Fluid cytology, Cell Culture Techniques methods, Cell Proliferation, Mesenchymal Stem Cells physiology, Prenatal Diagnosis methods
- Abstract
Introduction: Stem cells (SCs) isolated from amniotic fluid (AF) are a promising source for autologous perinatal cell therapy. The aim of this study was to develop a routine isolation, selection, and expansion protocol of clonal SC lines from redundant clinical amniocentesis samples., Materials and Methods: Amniotic fluids were collected between 15 and 22 weeks of gestation, and SCs were isolated by CD117-based and mechanical selection protocols. SCs were characterized by mesenchymal SC marker expression and differentiation protocols. Cells were manipulated with a lentiviral vector system expressing the β-galactosidase reporter gene and were injected into immunodeficient newborn mouse pups. Qualitative assessment was performed to detect the infused cells after 1 week., Results: A total of 78 clonal AF SC populations were successfully isolated by mechanical selection from 21 consecutive amniocentesis samples. They were positive for mesenchymal SC cluster of differentiation markers and could be differentiated into the different lineages. SCs were stably labeled using β-galactosidase and were detected in the lungs and hearts of the neonatal mice., Conclusion: We demonstrate that mesenchymal SCs can be routinely isolated and clonally expanded from mid-gestation human AF using mechanical isolation. They can easily be transduced and be tested for perinatal treatment in animal models., (© 2013 John Wiley & Sons, Ltd.)
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- 2013
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- View/download PDF
27. What can regenerative medicine offer for infants with laryngotracheal agenesis?
- Author
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Lange P, Fishman JM, Elliott MJ, De Coppi P, and Birchall MA
- Subjects
- Humans, Infant, Infant, Newborn, Regenerative Medicine, Respiration, Artificial, Stem Cell Transplantation, Tissue Scaffolds, Trachea abnormalities, Trachea surgery, Tracheostomy, Constriction, Pathologic surgery, Larynx abnormalities, Tissue Engineering methods
- Abstract
Background: Laryngotracheal agenesis is a rare congenital disorder but has devastating consequences. Recent achievements in regenerative medicine have opened up new vistas in therapeutic strategies for these infants., Objective: To provide a state-of-the-art review concerning recent achievements in tissue engineering as applied to fetal airway reconstruction and to discuss the use of autologous human amniotic stem cells to prepare organs in advance for babies with laryngotracheal agenesis., Data Sources and Review Methods: A structured search of the current literature (up to and including June 2011). The authors searched PubMed, EMBASE, CINAHL, Web of Science, BIOSIS Previews, Cambridge Scientific Abstracts, ICTRP, and additional sources for published and unpublished trials., Results: Over the past 15 years, progress has been made in advancing the boundaries of regenerative medicine from the laboratory to the clinical setting through translational research. Most experience has been gained with adult stem cells and synthetic materials or decellularized scaffolds. The optimal cell source for fetal tissue engineering remains to be determined, but a combination of decellularized scaffolds and amniotic fluid stem cells holds great promise for fetal tissue engineering., Conclusions and Implications for Practice: Current treatment strategies for laryngotracheal agenesis are suboptimal, and fetal tissue engineering offers an alternative to conventional treatments. Use of human amniotic fluid stem cells for preparing autologous tissue-engineered organ constructs prenatally is an attractive concept. Although this approach is still in its experimental stages, further preclinical and clinical studies are encouraged to define its exact role in the pediatric laryngological setting.
- Published
- 2011
- Full Text
- View/download PDF
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