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Dive into the research topics where Kristen Gosnell is active.

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Featured researches published by Kristen Gosnell.


Ultrasound in Obstetrics & Gynecology | 2011

Effect of selective fetoscopic laser photocoagulation therapy for twin–twin transfusion syndrome on pulmonary valve pathology in recipient twins

Anita J. Moon-Grady; Larry Rand; Breniel Lemley; Kristen Gosnell; Lisa K. Hornberger; Hanmin Lee

To investigate the impact of selective fetoscopic laser photocoagulation (SFLP) on pre‐existing pulmonary valve pathology in the recipient twin in twin–twin transfusion syndrome (TTTS).


Prenatal Diagnosis | 2011

Monochorionic twins discordant for congenital heart disease: a referral center's experience and possible pathophysiologic mechanisms

F. AlRais; Vickie A. Feldstein; Deepak Srivastava; Kristen Gosnell; Anita J. Moon-Grady

To describe the spectrum of cardiac defects in monochorionic (MC) twins discordant for congenital heart disease (CHD) in a referral center population.


Prenatal Diagnosis | 2018

Utility of chromosomal microarray in anomalous fetuses

Jacqueline Parchem; Teresa N. Sparks; Kristen Gosnell; Mary E. Norton

The objective of this study was to determine the association of copy number variants (CNV) with perinatal outcomes among fetuses with sonographic abnormalities.


Journal of Ultrasound in Medicine | 2018

Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter?: Hydrops With Polyhydramnios and Placentomegaly

Victoria Berger; Teresa N. Sparks; Angie C. Jelin; Chris Derderian; Cerine Jeanty; Kristen Gosnell; Tippi C. MacKenzie; Juan M. Gonzalez

Polyhydramnios and placentomegaly are commonly observed in nonimmune hydrops fetalis (NIHF); however, whether their ultrasonographic identification is relevant for prognosis is controversial. We evaluated outcomes of fetal or neonatal death and preterm birth (PTB) in cases of NIHF alone and in those with polyhydramnios and/or placentomegaly (P/PM).


American Journal of Perinatology | 2018

Fetal Congenital Pulmonary Airway Malformation: The Role of an Objective Measurement of Cardiomediastinal Shift

Teresa N. Sparks; Kristen Gosnell; Cinthia Blat; Mary E. Norton; Hanmin Lee; Juan M. Gonzalez-Velez; Ruth B. Goldstein; Rachel Shulman

Objective To examine the relationship between cardiomediastinal shift angle (CMSA) and adverse perinatal outcomes and hydrops in cases of congenital pulmonary airway malformation (CPAM). Study Design This retrospective study evaluated CPAM cases referred to our institution from 2008 to 2015. The primary outcome was a composite score for adverse perinatal outcome. CMSA was measured for each case and evaluated for its association with the primary outcome. The prediction accuracy of CMSA for adverse perinatal outcome was assessed using receiver operator characteristic (ROC) curves. Results Eighteen (21.2%) of the 85 cases experienced an adverse perinatal outcome. Increases in CMSA were associated with adverse perinatal outcomes and hydrops in bivariate analyses. Adjusted analyses found each 10‐degree increase in CMSA to be associated with increased odds of an adverse perinatal outcome (adjusted odds ratio [aOR] 2.2, 95% confidence interval [CI]: 1.4‐3.3) and hydrops (aOR 3.0, 95% CI: 1.5‐6.1). CMSA performed well and was comparable to CPAM volume ratio in predicting adverse perinatal outcomes (area under the curve 0.81 and 0.84, respectively). Conclusion We describe a novel measurement of mediastinal shift in cases of CPAM and its relationship with adverse perinatal outcomes and hydrops. These findings may shape the evaluation and management of CPAMs, improve our understanding of their prognosis, and influence patient counseling.


American Journal of Perinatology | 2018

Stage I Twin–Twin Transfusion Syndrome: Outcomes of Expectant Management and Prognostic Features

Erin E. Washburn; Teresa N. Sparks; Kristen Gosnell; Larry Rand; Juan M. Gonzalez; Vickie A. Feldstein

Objective This article describes the natural history of stage I twin‐twin transfusion syndrome (TTTS) including risk of progression to higher stage TTTS and pregnancy outcomes, and to identify risk factors for progression. Study Design Retrospective cohort study of monochorionic diamniotic (MCDA) twin pregnancies from 2006 to 2016 with expectantly managed Quintero stage I TTTS. Results A total of 30 MCDA twin pregnancies with expectantly managed stage I TTTS were identified. Of these, eight (26.7%) progressed to higher stage TTTS. Median gestational age (GA) at diagnosis for those that progressed was 18.9 ± 2.9 weeks versus 21.4 ± 3.4 weeks in those that remained stable (p = 0.06). Presence of an arterioarterial (A‐A) anastomosis was assessed for 20/30 patients, and eight A‐A were identified. Of those, 7/8 (87.5%) remained stable. In the complete cohort, a tiny or transiently visible bladder was noted in seven donor twins. Of these, 4/7 (57.1%) progressed. Excluding one termination, 47/58 (81.0%) fetuses survived. Conclusion With expectant management of stage I TTTS, nearly three‐fourths of pregnancies remain stable and most have survival of ≥ 1 twin. A‐A anastomoses were not associated with progression to higher stage TTTS, whereas earlier GA at diagnosis or a small or intermittently visible donor bladder may herald greater risk of progression.


American Journal of Perinatology | 2018

Prenatal Diagnosis of Congenital Diaphragmatic Hernia: Does Laterality Predict Perinatal Outcomes?

Jeffrey D. Sperling; Teresa N. Sparks; Victoria Berger; Jody A. Farrell; Kristen Gosnell; Roberta L. Keller; Mary E. Norton; Juan M. Gonzalez

Objective The objective of this study was to examine laterality as a predictor of outcomes among fetuses with prenatally diagnosed congenital diaphragmatic hernia (CDH). Methods This is a retrospective cohort study of pregnancies with CDH evaluated at our center from 2008 to 2016 compared cases with right‐sided CDH (RCDH) versus left‐sided CDH (LCDH). The primary outcome was survival to discharge. Secondary outcomes included ultrasound predictors of poor prognosis (liver herniation, stomach herniation, lung area‐to‐head circumference ratio [LHR]), concurrent anomalies, hydrops, stillbirth, preterm birth, mode of delivery, small for gestational age, use of extracorporeal membrane oxygenation, and length of stay. Terminations and stillbirths were excluded from analyses of neonatal outcomes. Results In this study, 157 (83%) LCDH and 32 (17%) RCDH cases were identified. Survival to discharge was similar (64 vs. 66.4%, p = 0.49) with regard to laterality. RCDH had higher rates of liver herniation (90.6 vs. 72%, p = 0.03), hydrops fetalis (15.6 vs. 1.3%, p < 0.01), and lower LHR (0.87 vs. 0.99, p = 0.04). LCDH had higher rates of stomach herniation (69.4 vs. 12.5%, p < 0.01). Rates of other outcomes were similar in univariate analyses. Adjusting for microarray abnormalities, the odds for survival to discharge for RCDH compared with LCDH was 0.93 (0.38‐2.30, p = 0.88). Conclusion Compared with LCDH, fetuses with RCDH had higher rates of adverse ultrasound predictors, but equivalent survival.


American Journal of Perinatology | 2017

Polyhydramnios Affecting a Recipient-like Twin: Risk of Progression to Twin–Twin Transfusion Syndrome and Outcomes

Erin E. Washburn; Teresa N. Sparks; Kristen Gosnell; Larry Rand; Juan M. Gonzalez; Vickie A. Feldstein

Objective The significance of polyhydramnios of one twin in the absence of oligohydramnios of the cotwin in monochorionic diamniotic (MCDA) twin pregnancies (polyhydramnios affecting a recipient‐like twin [PART]) is unknown. Our aim is to assess the risk of progression to twin‐twin transfusion syndrome (TTTS) with PART, progression to ≥ stage II TTTS, and neonatal survival. Study Design This study was a retrospective cohort study of MCDA twin pregnancies with PART evaluated at a referral center from 2008 to 2015. Results Sixty‐four MCDA twin pregnancies with PART were identified. Fifteen (23.4%) progressed to TTTS, including 10 (15.6%) who progressed to ≥ stage II TTTS. Three pregnancies were terminated and one underwent selective reduction by radiofrequency ablation. Overall survival was 113 out of 128 (88.3%). Of those who remained stable, 91.8% (N = 45) had survival of both neonates. In multivariate analysis, the presence of arterioarterial (A‐A) anastomosis by in utero Doppler ultrasound was associated with decreased risk of progression to TTTS (odds ratio: 0.12, p = 0.03, 95% confidence interval: 0.02‐0.78). Conclusion Most MCDA twin pregnancies with PART do not progress to TTTS and have a favorable prognosis. Progression rates are higher than observed in uncomplicated MCDA twins; however, so close surveillance is warranted. The presence of an A‐A anastomosis appears to confer decreased risk of progression to TTTS.


American Journal of Obstetrics and Gynecology | 2011

Diastolic cardiac pathology and clinical twin-twin transfusion syndrome in monochorionic/diamniotic twins

Anita J. Moon-Grady; Larry Rand; Salvador Gallardo; Kristen Gosnell; Hanmin Lee; Vickie A. Feldstein


American Journal of Obstetrics and Gynecology | 2018

253: Concurrent anomalies in fetuses with congenital diaphragmatic hernia and the association with copy number variants

Anne H. Mardy; Teresa N. Sparks; Victoria Berger; Jody A. Farrell; Kristen Gosnell; Rachael T. Overcash; Stephen B. Shew; Véronique Taché; Deborah A. Wing; Erica Wu; Mary E. Norton

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Larry Rand

University of California

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Mary E. Norton

University of California

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Hanmin Lee

University of California

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