A. Alonso Melgar
Hospital Universitario La Paz
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Featured researches published by A. Alonso Melgar.
Clinical Nephrology | 2004
M. Melgosa Hijosa; C. García Meseguer; P. Pena Garcia; A. Alonso Melgar; L. Espinosa Román; A. Peña Carrión; M. Navarro Torres
This prospective study examines 42 children in the first year after renal transplantation. They all received intravenous ganciclovir prophylaxis for cytomegalovirus in the immediate post-transplant period. Quantitative antigenemia (pp68) determinations and blood, urine and throat cultures were done on a scheduled basis to detect cytomegalovirus. Infection was detected in 22 children (52.4%) within an average 44.31 +/- 27.38 days; 5/22 were symptomatic. The antigenemia was positive (+) in all the infected patients, and so were blood culture in 68.2%, urine culture in 59.1% and throat culture in 31.8%. A positive antigenemia was the earliest finding in all cases but 1. The 5 children with clinical symptoms received intravenous ganciclovir. Asymptomatic infected children received oral ganciclovir at an average dose of 47.64 +/- 8.10 mg/kg/day (median 46.58 (range 33-58.7) mg/kg/day) for an average of 58.47 +/- 27.76 days (median 58 (range 26-211) days). No patient developed disease or ganciclovir resistance during the treatment. No patient presented acute graft rejection or renal dysfunction and their glomerular filtrate rate at 1 year was similar to that of noninfected children (90.38 +/- 26.51 vs. 93.93 +/- 36.24 ml/min/1.73 m2). We conclude that preemptive treatment with oral ganciclovir is useful and safe in children with renal transplantation and that monitoring blood antigenemia is a sensitive and early method to detect and control CMV infection.
Anales De Pediatria | 2014
R. Montañés Bermúdez; S. Gràcia García; G.M. Fraga Rodríguez; J. Escribano Subias; M.J. Diez de los Ríos Carrasco; A. Alonso Melgar; V. García Nieto
The appearance of the K/DOQI guidelines in 2002 on the definition, evaluation and staging of chronic kidney disease (CKD) have led to a major change in how to assess renal function in adults and children. These guidelines, recently updated, recommended that the study of renal function is based, not only on measuring the serum creatinine concentration, but this must be accompanied by the estimation of glomerular filtration rate (GFR) obtained by an equation. However, the implementation of this recommendation in the clinical laboratory reports in the paediatric population has been negligible. Numerous studies have appeared in recent years on the importance of screening and monitoring of patients with CKD, the emergence of new equations for estimating GFR, and advances in clinical laboratories regarding the methods for measuring plasma creatinine and cystatin C, determined by the collaboration between the departments of paediatrics and clinical laboratories to establish recommendations based on the best scientific evidence on the use of equations to estimate GFR in this population. The purpose of this document is to provide recommendations on the evaluation of renal function and the use of equations to estimate GFR in children from birth to 18 years of age. The recipients of these recommendations are paediatricians, nephrologists, clinical biochemistry, clinical analysts, and all health professionals involved in the study and evaluation of renal function in this group of patients.
Pediatric Transplantation | 2007
M.J. Martínez Urrutia; P. Olivares Arnal; P. López Pereira; R. Lobato Romera; A. Alonso Melgar; E. Jaureguizar Monereo
Abstract: Bilateral nephrectomy prior to transplantation is indicated in some patients with end‐stage renal disease. The indications for bilateral nephrectomy include persistent heavy proteinuria, refractory hypertension, and urinary tract infections. We report an eight‐month‐old baby with male pseudohermaphroditism and renal failure secondary to diffuse mesangial sclerosis. While awaiting renal transplantation, dialysis became necessary and the child presented standard drug therapy‐resistant hypertension. A bilateral nephrectomy was performed simultaneously to peritoneal dialysis catheter implantation by using laparoscopy. At the present time, the patient is doing well with ambulatory dialysis and all antihypertensive medication has been discontinued. We recommend this technique in children who require bilateral nephrectomy and peritoneal dialyisis. Not only is it somewhat less aggressive than traditional open surgery, but it also reduces post‐operative pain, allows earlier initiation of peritoneal dialysis, and improves cosmetic appearance.
Transplantation Proceedings | 2015
A. Zarauza Santoveña; C. García Meseguer; S. Martínez Mejía; A. Alonso Melgar; C. Fernández Camblor; M. Melgosa Hijosa; A. Peña Carrión; L. Espinosa Román
BACKGROUND Polyomavirus BK (BKV) is a common complication after renal transplantation and an important cause of graft loss. The purpose of this study was to determine the incidence of BKV infection (viremia) in our population and to describe clinical features, global outcomes, and potential correlations with clinical or epidemiologic factors. METHODS This retrospective single-center study included 84 pediatric recipients of kidney transplantation from January 2006 to September 2012. BKV infection screening consisted of periodic determination of decoy cells in urine samples, confirmed by means of quantitative polymerase chain reaction test in blood. RESULTS Twenty-two patients (26%) developed BKV viremia. BKV replication appeared early after renal transplantation (median, 2 months). One-third of patients remained asymptomatic, and 27% presented elevated serum creatinine. Immunosuppression was reduced in 90% of patients, and 83% achieved clearance of viremia within 6 months. There was only 1 case of histologically confirmed BKV nephropathy, which evolved to graft loss despite leflunomide, intravenous immunoglobulins, and mycophenolate discontinuation. Risk of BKV viremia was associated with younger age at transplantation (5.9 y vs 10.9 years; P = .001) and cadaveric donor (relative risk, 3.2; P < .05). BKV infection did not affect short-term renal function and graft survival. CONCLUSIONS BKV viremia is very common in the pediatric renal transplant population, especially in younger children and in those receiving a kidney from cadaveric donors. It develops in the 1st months after transplantation. Reduction of immunosuppression seems to be a good therapeutic option, with high rates of clearance of the infection, although the only patient with confirmed BKV nephropathy had poor outcome.
Nefrologia | 2014
S. Gràcia García; J. Escribano Subias; Ríos Carrasco; A. Alonso Melgar
The appearance of the K/DOQI guidelines in 2002 on the definition, evaluation and staging of chronic kidney disease (CKD) have led to a major change in how to assess renal function in adults and children. These guidelines, recently updated, recommended that the study of renal function is based, not only on measuring the serum creatinine concentration, but this must be accompanied by the estimation of glomerular filtration rate (GFR) obtained by an equation. However, the implementation of this recommendation in the clinical laboratory reports in the paediatric population has been negligible. Numerous studies have appeared in recent years on the importance of screening and monitoring of patients with CKD, the emergence of new equations for estimating GFR, and advances in clinical laboratories regarding the methods for measuring plasma creatinine and cystatin C, determined by the collaboration between the departments of paediatrics and clinical laboratories to establish recommendations based on the best scientific evidence on the use of equations to estimate GFR in this population. The purpose of this document is to provide recommendations on the evaluation of renal function and the use of equations to estimate GFR in children from birth to 18 years of age. The recipients of these recommendations are paediatricians, nephrologists, clinical biochemistry, clinical analysts, and all health professionals involved in the study and evaluation of renal function in this group of patients.
Anales De Pediatria | 2004
A. Peña Carrión; L. Espinosa Román; Ma Fernandez Maseda; C. García Meseguer; A. Alonso Melgar; M. Melgosa Hijosa; R. Rodríguez Lemos; M. Navarro Torres
Anales De Pediatria | 2007
F.J. Alados Arboledas; P de la Oliva Senovilla; MªJ García Muñoz; A. Alonso Melgar; F. J. Ruza Tarrio
Transplantation proceedings | 2015
S. Martínez Mejía; A. Alonso Melgar; M. Melgosa Hijosa; C. Fernández Camblor; A. Peña Carrión; C. García Meseguer; L. Espinosa Román
Archive | 2016
A. Peña Carrión; L. Espinosa Román; C. García Meseguer; A. Alonso Melgar; M. Melgosa Hijosa; R. Rodríguez Lemos; M. Navarro Torres
Revista española de pediatría | 2013
Laura Espinosa Román; A. Alonso Melgar; C. Fernández Camblor; M. C. García Meseguer; M. Melgosa Hijosa; A. Peña Carrión; Pilar Aparicio; Mercedes Navarro Torres