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Dive into the research topics where Guillermo Hidalgo is active.

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Featured researches published by Guillermo Hidalgo.


Transplantation | 1999

Outcome of twin pregnancy in a renal transplant recipient treated with tacrolimus.

Shefali Vyas; Steven Piecuch; Guillermo Hidalgo; Anup Singh; Virginia Anderson; Mariana S. Markell; Noosha Baqi

Our report describes the outcome of a twin pregnancy in a woman who was maintained on tacrolimus after a living related renal transplant. Both babies born at 32 weeks of gestation developed severe respiratory distress requiring ventilator assistance and went on to develop congestive heart failure. Echocardiograms on both babies showed dilated heart chambers. Twin A succumbed to complications, but twin B, who was treated more aggressively with vasopressors, recovered. Autopsy findings on twin A revealed a thrombotic cardiomyopathy with degeneration of cardiac muscle. We believe that the unusual outcome in this set of twins may have been a result of cardiomyopathy secondary to tacrolimus used by the mother during her pregnancy.


American Journal of Kidney Diseases | 2013

Association of Income Level With Kidney Disease Severity and Progression Among Children and Adolescents With CKD: A Report From the Chronic Kidney Disease in Children (CKiD) Study

Guillermo Hidalgo; Derek K. Ng; Marva Moxey-Mims; Maria Lourdes Minnick; Tom Blydt-Hansen; Bradley A. Warady; Susan L. Furth

BACKGROUND Among adults, lower socioeconomic status (SES) is a risk factor for chronic kidney disease (CKD), progression to end-stage renal disease, and poor health outcomes; but its impact on young people with CKD is not established. STUDY DESIGN Prospective cohort study. SETTINGS & PARTICIPANTS 572 children and adolescents aged 1-16 years with mild to moderate CKD residing in the United States and Canada who were enrolled in the Chronic Kidney Disease in Children (CKiD) Study. PREDICTOR Self-reported annual household income category as a proxy measure for SES: ≥


Pediatric Nephrology | 2008

Obstacles to the prescribing of growth hormone in children with chronic kidney disease

Larry A. Greenbaum; Guillermo Hidalgo; Deepa H. Chand; Myra Chiang; Katherine M. Dell; Theresa Kump; Lena Peschansky; Holly K. Smith; Mary Boyle; Michelle Kopf; Lisa C. Metz; Margaret Kamel; John D. Mahan

75,000 (high income),


Kidney International | 2016

Implementation of standardized follow-up care significantly reduces peritonitis in children on chronic peritoneal dialysis.

Alicia M. Neu; Troy Richardson; John Lawlor; Jayne Stuart; Jason G. Newland; Nancy McAfee; Bradley A. Warady; Joshua Zaristky; Susan Kieffner; Allison Redpath Mahon; Dawn Foster; Mahima Keswani; Nancy Majkowski; Richard Blaszak; Christine Blaszak; Michael J. Somers; Theresa Pak; Diego H. Aviles; Evie Jenkins; Rachel Lestz; Alice Sanchez; Cynthia G. Pan; Jackie Dake; Raymond Quigley; Jo Lyn Grimes; Kirtida Mistry; Jennifer Carver; Rene Van De Voorde; Ellen Irvin; Samhar I. Al-Akash

30,000 to <


Pediatric Research | 2017

Developing a neonatal acute kidney injury research definition: a report from the NIDDK neonatal AKI workshop

Michael Zappitelli; Namasivayam Ambalavanan; David J. Askenazi; Marva Moxey-Mims; Paul L. Kimmel; Robert A. Star; Carolyn L. Abitbol; Patrick D. Brophy; Guillermo Hidalgo; Mina H. Hanna; Catherine M Morgan; Tonse N.K. Raju; Patricio E. Ray; Zayhara Reyes-Bou; Amani Roushdi; Stuart L. Goldstein

75,000 (middle income) and <


The Journal of Pediatrics | 2015

Renin Angiotensin System Blocker Fetopathy: A Midwest Pediatric Nephrology Consortium Report

Shahid Nadeem; Shireen Hashmat; Marissa DeFreitas; Katherine D. Westreich; Ibrahim F. Shatat; David T. Selewski; Ali Mirza Onder; Myra Chiang; Donald J. Weaver; Julia Steinke; John Barcia; Joel Hernandez; Guillermo Hidalgo; Susan E. Ingraham; Carolyn L. Abitbol; Cynthia G. Pan; Larry A. Greenbaum

30,000 (low income). OUTCOMES & MEASUREMENTS Clinical characteristics and CKD severity at baseline (glomerular filtration rate [GFR] and comorbid conditions related to disease severity and management) and longitudinally (GFR decline and changes in blood pressure z scores and height z scores per year). RESULTS At baseline, low and middle household incomes, compared to high income, were associated with minority race (39% and 20% vs. 7%), lower maternal education (28% and 5% vs. 1%), abnormal birth history (34% and 32% vs. 21%), and having at least one clinical comorbid condition (66% and 64% vs. 55%). Baseline median GFRs were similar across income categories (43-45 mL/min/1.73 m2). After adjusting for baseline differences, average GFR declines per year for the low-, middle-, and high-income categories were -2.3%, -2.7%, and -1.9%, respectively, and were not statistically significantly different among groups. Blood pressure control tended to improve in all groups (z score, -0.10 to -0.04) but higher income was associated with a faster improvement. Each group showed similar deficits in height at baseline. Height deficits diminished over time for participants from high-income families, but not among those from low-income families (z scores for height per year, 0.05 and -0.004, respectively; P = 0.03 for comparison of high and low income). LIMITATIONS Income is an imperfect measure for SES; CKiD participants are not representative of children and adolescents with CKD who are uninsured or not receiving care; statistical power to detect associations by income level is limited. CONCLUSIONS GFR decline was similar across income groups but better improvement in BP was observed among those with high income. Children and adolescents with CKD from lower income households are at higher risk of impaired growth.


Scientific Reports | 2016

Pioglitazone Enhances the Beneficial Effects of Glucocorticoids in Experimental Nephrotic Syndrome

S. Agrawal; M. A. Chanley; D. Westbrook; X. Nie; T. Kitao; A. J. Guess; Rainer Benndorf; Guillermo Hidalgo; William E. Smoyer

Despite its effectiveness, recombinant human growth hormone (rhGH) is under-utilized in short children with chronic kidney disease (CKD). We conducted a multicenter study to explore the obstacles preventing children with CKD from receiving rhGH. We investigated the use of rhGH in 307 children with CKD from seven pediatric nephrology centers. Among the 110 patients who fell below the 5th percentile, 56 (51%) had not received rhGH. The most common reasons given for these children not receiving rhGH were family refusal, secondary hyperparathyroidism, and non-compliance. However, no explanation was apparent for 25% of the short children with CKD. Boys were more likely than girls to receive rhGH (65% vs 31%; P = 0.002). Use of rhGH was similar in African Americans and non-Hispanic Whites. Children who had received rhGH achieved a 0.5 increase in height z-score in the first year after the initiation of rhGH therapy. Children who had not received rhGH achieved a 0.03 increase in height z-score during the first year after falling below the 5th percentile (P = 0.005 vs the children who had received rhGH). Waiting for insurance company approval led to a significant delay in the initiation of rhGH treatment in 18% of patients. The fact that more than 50% of short children with CKD did not receive rhGH is secondary to multiple factors, many of which may be amenable to intervention efforts.


The Journal of Pediatrics | 2016

Depressive Symptoms in Children with Chronic Kidney Disease

Amy Kogon; Matthew Matheson; Joseph T. Flynn; Arlene C. Gerson; Bradley A. Warady; Susan L. Furth; Stephen R. Hooper; Allison Dart; Larry A. Greenbaum; Jens Goebel; Mark Mitsnefes; Craig S. Wong; Sahar Fathallah; Isidro B. Salusky; Ora Yadin; Katherine M. Dell; Bruce Z. Morgenstern; Tom Blydt-Hansen; Cynthia G. Pan; Keefe Davis; Amira Al-Uzri; Randall Jenkins; Anthony A. Portale; Mouin G. Seikaly; Martin A. Turman; Cynthia Wong; Steven R. Alexander; Colleen Hastings; Nancy Rodig; William E. Harmon

The Standardizing Care to improve Outcomes in Pediatric End stage renal disease (SCOPE) Collaborative aims to reduce peritonitis rates in pediatric chronic peritoneal dialysis patients by increasing implementation of standardized care practices. To assess this, monthly care bundle compliance and annualized monthly peritonitis rates were evaluated from 24 SCOPE centers that were participating at collaborative launch and that provided peritonitis rates for the 13 months prior to launch. Changes in bundle compliance were assessed using either a logistic regression model or a generalized linear mixed model. Changes in average annualized peritonitis rates over time were illustrated using the latter model. In the first 36 months of the collaborative, 644 patients with 7977 follow-up encounters were included. The likelihood of compliance with follow-up care practices increased significantly (odds ratio 1.15, 95% confidence interval 1.10, 1.19). Mean monthly peritonitis rates significantly decreased from 0.63 episodes per patient year (95% confidence interval 0.43, 0.92) prelaunch to 0.42 (95% confidence interval 0.31, 0.57) at 36 months postlaunch. A sensitivity analysis confirmed that as mean follow-up compliance increased, peritonitis rates decreased, reaching statistical significance at 80% at which point the prelaunch rate was 42% higher than the rate in the months following achievement of 80% compliance. In its first 3 years, the SCOPE Collaborative has increased the implementation of standardized follow-up care and demonstrated a significant reduction in average monthly peritonitis rates.


The Journal of Pediatrics | 2016

Kidney Disease Progression in Autosomal Recessive Polycystic Kidney Disease.

Katherine M. Dell; Matthew Matheson; Erum A. Hartung; Bradley A. Warady; Susan L. Furth; Alvaro Muñoz; Allison Dart; Larry A. Greenbaum; Jens Goebel; Mark Mitsnefes; Joseph T. Flynn; Craig S. Wong; Sahar Fathallah; Isidro B. Salusky; Ora Yadin; Bruce Z. Morgenstern; Tom Blydt-Hansen; Keefe Davis; Cynthia G. Pan; Amira Al-Uzri; Randall Jenkins; Anthony A. Portale; Mouin G. Seikaly; Martin A. Turman; Cynthia Wong; Steven R. Alexander; Colleen Hastings; Nancy Rodig; William E. Harmon; Sharon M. Bartosh

Developing a neonatal acute kidney injury research definition: a report from the NIDDK neonatal AKI workshop


Pediatric Nephrology | 2008

Vitamin D insufficiency and hyperparathyroidism in children with chronic kidney disease

Shina Menon; Rudolph P. Valentini; Guillermo Hidalgo; Lena Peschansky; Tej K. Mattoo

OBJECTIVES Fetuses continue to be exposed to renin angiotensin system (RAS) blockers despite their known teratogenicity and a black box warning. We hypothesized that fetopathy from in utero exposure to RAS blockers has a broader spectrum of clinical manifestations than described previously and that there are a variety of clinical scenarios leading to such exposures. STUDY DESIGN This was a retrospective study performed through the Midwest Pediatric Nephrology Consortium. Cases of RAS blocker fetopathy were identified, with determination of renal and extrarenal manifestations, timing of exposure, and the explanation for the fetal exposure. RESULTS Twenty-four cases were identified. RAS blocker exposure after the first trimester was associated with more severe renal manifestations. Chronic dialysis or kidney transplantation was required in 8 of 17 (47%) patients with RAS blocker exposure after the first trimester and 0 of 7 patients with exposure restricted to the first trimester (P = .05). Extrarenal manifestations, some not previously noted in the literature, included central nervous system anomalies (cystic encephalomalacia, cortical blindness, sensorineural hearing loss, arachnoid cysts) and pulmonary complications (pneumothorax, pneumomediastinum). RAS blocker exposure usually was secondary to absent or poor prenatal care or undiagnosed pregnancy. CONCLUSION RAS blocker fetopathy continues to be a cause of considerable morbidity, with more severe renal manifestations associated with exposure after the first trimester. A variety of significant extrarenal manifestations occur in these patients. Clinicians should emphasize the risk of fetopathy when prescribing RAS blockers to women of childbearing age.

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Cynthia G. Pan

Children's Hospital of Wisconsin

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Jens Goebel

Cincinnati Children's Hospital Medical Center

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Susan L. Furth

Children's Hospital of Philadelphia

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Tom Blydt-Hansen

University of British Columbia

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Deepa H. Chand

Boston Children's Hospital

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John D. Mahan

Nationwide Children's Hospital

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Katherine M. Dell

Case Western Reserve University

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