Skip to main content
Erschienen in: Journal of Nephrology 6/2022

15.02.2022 | original Article

Nephrotoxic medications and associated acute kidney injury in hospitalized neonates

verfasst von: Tahagod H. Mohamed, Hibo H. Abdi, Jacqueline Magers, Pavel Prusakov, Jonathan L. Slaughter

Erschienen in: Journal of Nephrology | Ausgabe 6/2022

Einloggen, um Zugang zu erhalten

Abstract

Objectives

Hospitalized neonates are often treated with nephrotoxic medications, a known risk factor for acute kidney injury (AKI). Nephrotoxic medications and AKI, especially in periviable neonates, could be detrimental to nephrogenesis. Our objectives were to evaluate the prevalence of neonatal treatment with nephrotoxic medications and its relationship with AKI in in the first 28 days of life, and to delineate the associated demographics and diagnoses.

Study design

Multicenter retrospective analysis using the national Pediatric Hospital Information System database, including 49 pediatric hospitals. Neonates admitted within the first two postnatal days were included. Treatment with 37 nephrotoxic medications across demographics and clinical variables, and relationship with AKI were evaluated. AKI was determined by using the International Classification of Diseases codes.

Results

Of 192,229 neonates, 74% were treated with at least one nephrotoxic medication. Incidence of AKI was significantly higher in the treated group (aRR 3.68 [95% CI: 2.85, 4.75]). The aRRs of treatment were increased in infants born < 32-week, and < 2000 g. Nephrotoxic medications were prescribed to 90–95% of  neonates born ≤ 28-week gestational age. Most treatments (95–98%) occurred in the first 3 days. Intravascular aminoglycosides were the most frequent type; 28% of neonates were treated for ≥ 4 calendar days. Most common diagnoses were infections (25%) and patent ductus arteriosus (20%).

Conclusions

Neonatal treatment with nephrotoxic medications is common, especially among the smallest, most immature preterm neonates and demonstrates a need for initiatives to reduce neonatal exposure to these agents, when feasible. Across all gestational age categories, the prevalence of AKI is higher in the neonates treated with nephrotoxic drugs. The long-term effects of treatment with nephrotoxic medications and subsequent AKI on nephrogenesis and nephron endowment will need to be evaluated.

Graphical abstract

Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Rhone ET, Carmody JB, Swanson JR, Charlton JR (2014) Nephrotoxic medication exposure in very low birth weight infants. J Matern Fetal Neonatal Med 27(14):1485–1490CrossRef Rhone ET, Carmody JB, Swanson JR, Charlton JR (2014) Nephrotoxic medication exposure in very low birth weight infants. J Matern Fetal Neonatal Med 27(14):1485–1490CrossRef
2.
Zurück zum Zitat Stoops C, Stone S, Evans E et al (2019) Baby NINJA (nephrotoxic injury negated by just-in-time action): reduction of nephrotoxic medication-associated acute kidney injury in the neonatal intensive care unit. J Pediatr 215:223-228.e226CrossRef Stoops C, Stone S, Evans E et al (2019) Baby NINJA (nephrotoxic injury negated by just-in-time action): reduction of nephrotoxic medication-associated acute kidney injury in the neonatal intensive care unit. J Pediatr 215:223-228.e226CrossRef
3.
Zurück zum Zitat Charlton JR, Boohaker L, Askenazi D et al (2019) Incidence and risk factors of early onset neonatal AKI. Clin J Am Soc Nephrol 14(2):184–195CrossRef Charlton JR, Boohaker L, Askenazi D et al (2019) Incidence and risk factors of early onset neonatal AKI. Clin J Am Soc Nephrol 14(2):184–195CrossRef
4.
Zurück zum Zitat Brenner BM, Garcia DL, Anderson S (1988) Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens 1(4 Pt 1):335–347CrossRef Brenner BM, Garcia DL, Anderson S (1988) Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens 1(4 Pt 1):335–347CrossRef
5.
Zurück zum Zitat Salerno SN, Liao Y, Jackson W et al (2021) Association between nephrotoxic drug combinations and acute kidney injury in the neonatal intensive care unit. J Pediatr 228:213–219CrossRef Salerno SN, Liao Y, Jackson W et al (2021) Association between nephrotoxic drug combinations and acute kidney injury in the neonatal intensive care unit. J Pediatr 228:213–219CrossRef
6.
Zurück zum Zitat Jetton JG, Boohaker LJ, Sethi SK et al (2017) Incidence and outcomes of neonatal acute kidney injury (AWAKEN): a multicentre, multinational, observational cohort study. Lancet Child Adolesc Health 1(3):184–194CrossRef Jetton JG, Boohaker LJ, Sethi SK et al (2017) Incidence and outcomes of neonatal acute kidney injury (AWAKEN): a multicentre, multinational, observational cohort study. Lancet Child Adolesc Health 1(3):184–194CrossRef
7.
Zurück zum Zitat Harer MW, Pope CF, Conaway MR, Charlton JR (2017) Follow-up of Acute kidney injury in Neonates during Childhood Years (FANCY): a prospective cohort study. Pediatr Nephrol 32(6):1067–1076CrossRef Harer MW, Pope CF, Conaway MR, Charlton JR (2017) Follow-up of Acute kidney injury in Neonates during Childhood Years (FANCY): a prospective cohort study. Pediatr Nephrol 32(6):1067–1076CrossRef
8.
Zurück zum Zitat Mammen C, Al Abbas A, Skippen P et al (2012) Long-term risk of CKD in children surviving episodes of acute kidney injury in the intensive care unit: a prospective cohort study. Am J Kidney Dis 59(4):523–530CrossRef Mammen C, Al Abbas A, Skippen P et al (2012) Long-term risk of CKD in children surviving episodes of acute kidney injury in the intensive care unit: a prospective cohort study. Am J Kidney Dis 59(4):523–530CrossRef
9.
Zurück zum Zitat Maqsood S, Fung N, Chowdhary V, Raina R, Mhanna MJ (2017) Outcome of extremely low birth weight infants with a history of neonatal acute kidney injury. Pediatr Nephrol 32(6):1035–1043CrossRef Maqsood S, Fung N, Chowdhary V, Raina R, Mhanna MJ (2017) Outcome of extremely low birth weight infants with a history of neonatal acute kidney injury. Pediatr Nephrol 32(6):1035–1043CrossRef
10.
Zurück zum Zitat Carmody JB, Charlton JR (2013) Short-term gestation, long-term risk: prematurity and chronic kidney disease. Pediatrics 131(6):1168–1179CrossRef Carmody JB, Charlton JR (2013) Short-term gestation, long-term risk: prematurity and chronic kidney disease. Pediatrics 131(6):1168–1179CrossRef
12.
Zurück zum Zitat Janevic T, Zeitlin J, Auger N et al (2018) Association of race/ethnicity with very preterm neonatal morbidities. JAMA Pediatr 172(11):1061–1069CrossRef Janevic T, Zeitlin J, Auger N et al (2018) Association of race/ethnicity with very preterm neonatal morbidities. JAMA Pediatr 172(11):1061–1069CrossRef
13.
Zurück zum Zitat Ryan RM, Feng R, Bazacliu C et al (2019) Black race is associated with a lower risk of bronchopulmonary dysplasia. J Pediatr 207:130-135.e132CrossRef Ryan RM, Feng R, Bazacliu C et al (2019) Black race is associated with a lower risk of bronchopulmonary dysplasia. J Pediatr 207:130-135.e132CrossRef
14.
Zurück zum Zitat Flidel-Rimon O, Galstyan S, Juster-Reicher A, Rozin I, Shinwell ES (2012) Limitations of the risk factor-based approach in early neonatal sepsis evaluations. Acta Paediatr 101(12):e540-544CrossRef Flidel-Rimon O, Galstyan S, Juster-Reicher A, Rozin I, Shinwell ES (2012) Limitations of the risk factor-based approach in early neonatal sepsis evaluations. Acta Paediatr 101(12):e540-544CrossRef
15.
Zurück zum Zitat Kuzniewicz MW, Puopolo KM, Fischer A et al (2017) A quantitative, risk-based approach to the management of neonatal early-onset sepsis. JAMA Pediatr 171(4):365–371CrossRef Kuzniewicz MW, Puopolo KM, Fischer A et al (2017) A quantitative, risk-based approach to the management of neonatal early-onset sepsis. JAMA Pediatr 171(4):365–371CrossRef
16.
Zurück zum Zitat Downes KJ, Boge CLK, Baro E et al (2020) Acute kidney injury during treatment with intravenous acyclovir for suspected or confirmed neonatal herpes simplex virus infection. J Pediatr 219:126-132.e122CrossRef Downes KJ, Boge CLK, Baro E et al (2020) Acute kidney injury during treatment with intravenous acyclovir for suspected or confirmed neonatal herpes simplex virus infection. J Pediatr 219:126-132.e122CrossRef
17.
Zurück zum Zitat Barhight M, Altaye M, Gist KM, Isemann B, Goldstein SL, Akinbi H (2017) Nephrotoxic medications and associated acute kidney injury in very low birth weight infants. J Clin Nephrol Res 4(4):1070PubMedPubMedCentral Barhight M, Altaye M, Gist KM, Isemann B, Goldstein SL, Akinbi H (2017) Nephrotoxic medications and associated acute kidney injury in very low birth weight infants. J Clin Nephrol Res 4(4):1070PubMedPubMedCentral
18.
Zurück zum Zitat Travers CP, Carlo WA, McDonald SA et al (2020) Racial/ethnic disparities among extremely preterm infants in the United States from 2002 to 2016. JAMA Netw Open 3(6):e206757CrossRef Travers CP, Carlo WA, McDonald SA et al (2020) Racial/ethnic disparities among extremely preterm infants in the United States from 2002 to 2016. JAMA Netw Open 3(6):e206757CrossRef
19.
Zurück zum Zitat David RJ, Collins JW (1991) Bad outcomes in black babies: race or racism? Ethn Dis 1(3):236–244PubMed David RJ, Collins JW (1991) Bad outcomes in black babies: race or racism? Ethn Dis 1(3):236–244PubMed
20.
Zurück zum Zitat Beck AF, Edwards EM, Horbar JD, Howell EA, McCormick MC, Pursley DM (2020) The color of health: how racism, segregation, and inequality affect the health and well-being of preterm infants and their families. Pediatr Res 87(2):227–234CrossRef Beck AF, Edwards EM, Horbar JD, Howell EA, McCormick MC, Pursley DM (2020) The color of health: how racism, segregation, and inequality affect the health and well-being of preterm infants and their families. Pediatr Res 87(2):227–234CrossRef
23.
Zurück zum Zitat Carmody JB, Swanson JR, Rhone ET, Charlton JR (2014) Recognition and reporting of AKI in very low birth weight infants. Clin J Am Soc Nephrol 9(12):2036–2043CrossRef Carmody JB, Swanson JR, Rhone ET, Charlton JR (2014) Recognition and reporting of AKI in very low birth weight infants. Clin J Am Soc Nephrol 9(12):2036–2043CrossRef
24.
Zurück zum Zitat Norris AH, Shrestha NK, Allison GM et al (2019) 2018 Infectious Diseases Society of America clinical practice guideline for the management of outpatient parenteral antimicrobial therapy. Clin Infect Dis 68(1):1–4CrossRef Norris AH, Shrestha NK, Allison GM et al (2019) 2018 Infectious Diseases Society of America clinical practice guideline for the management of outpatient parenteral antimicrobial therapy. Clin Infect Dis 68(1):1–4CrossRef
25.
Zurück zum Zitat Stark A, Childers J, England M et al (2020) Dosing of antimicrobials in the neonatal intensive care unit: does clinical practice reflect pharmacokinetics-based recommendations? Pediatr Infect Dis J 39(8):713–717CrossRef Stark A, Childers J, England M et al (2020) Dosing of antimicrobials in the neonatal intensive care unit: does clinical practice reflect pharmacokinetics-based recommendations? Pediatr Infect Dis J 39(8):713–717CrossRef
26.
Zurück zum Zitat Metsvaht T, Nellis G, Varendi H et al (2015) High variability in the dosing of commonly used antibiotics revealed by a Europe-wide point prevalence study: implications for research and dissemination. BMC Pediatr 15:41CrossRef Metsvaht T, Nellis G, Varendi H et al (2015) High variability in the dosing of commonly used antibiotics revealed by a Europe-wide point prevalence study: implications for research and dissemination. BMC Pediatr 15:41CrossRef
27.
Zurück zum Zitat Liem TB, Krediet TG, Fleer A, Egberts TC, Rademaker CM (2010) Variation in antibiotic use in neonatal intensive care units in the Netherlands. J Antimicrob Chemother 65(6):1270–1275CrossRef Liem TB, Krediet TG, Fleer A, Egberts TC, Rademaker CM (2010) Variation in antibiotic use in neonatal intensive care units in the Netherlands. J Antimicrob Chemother 65(6):1270–1275CrossRef
28.
Zurück zum Zitat Bradley JS, Nelson JD (eds) (2019) Nelson’s pediatric antimicrobial therapy, 25th edn. American Academy of Pediatrics, Itasca Bradley JS, Nelson JD (eds) (2019) Nelson’s pediatric antimicrobial therapy, 25th edn. American Academy of Pediatrics, Itasca
29.
Zurück zum Zitat American Academy of Pediatrics (AAP) (2018) In: Kimberlin DW, Brady MT, Jackson MA, Long SA (eds) Red Book: 2018 Report of the Committee on Infectious Diseases, 31st edn. American Academy of Pediatrics, Itasca American Academy of Pediatrics (AAP) (2018) In: Kimberlin DW, Brady MT, Jackson MA, Long SA (eds) Red Book: 2018 Report of the Committee on Infectious Diseases, 31st edn. American Academy of Pediatrics, Itasca
30.
Zurück zum Zitat Micromedex® (electronic version). IBM Watson Health, Greenwood Village, Colorado Micromedex® (electronic version). IBM Watson Health, Greenwood Village, Colorado
34.
Zurück zum Zitat Schmidt B, Davis P, Moddemann D et al (2001) Long-term effects of indomethacin prophylaxis in extremely-low-birth-weight infants. N Engl J Med 344(26):1966–1972CrossRef Schmidt B, Davis P, Moddemann D et al (2001) Long-term effects of indomethacin prophylaxis in extremely-low-birth-weight infants. N Engl J Med 344(26):1966–1972CrossRef
35.
Zurück zum Zitat Ohlsson A, Walia R, Shah SS (2020) Ibuprofen for the treatment of patent ductus arteriosus in preterm or low birth weight (or both) infants. Cochrane Database Syst Rev 2:CD003481PubMed Ohlsson A, Walia R, Shah SS (2020) Ibuprofen for the treatment of patent ductus arteriosus in preterm or low birth weight (or both) infants. Cochrane Database Syst Rev 2:CD003481PubMed
36.
Zurück zum Zitat Ohlsson A, Shah SS (2020) Ibuprofen for the prevention of patent ductus arteriosus in preterm and/or low birth weight infants. Cochrane Database Syst Rev 1:CD004213PubMed Ohlsson A, Shah SS (2020) Ibuprofen for the prevention of patent ductus arteriosus in preterm and/or low birth weight infants. Cochrane Database Syst Rev 1:CD004213PubMed
37.
Zurück zum Zitat Ment LR, Oh W, Ehrenkranz RA et al (1994) Low-dose indomethacin and prevention of intraventricular hemorrhage: a multicenter randomized trial. Pediatrics 93(4):543–550CrossRef Ment LR, Oh W, Ehrenkranz RA et al (1994) Low-dose indomethacin and prevention of intraventricular hemorrhage: a multicenter randomized trial. Pediatrics 93(4):543–550CrossRef
38.
Zurück zum Zitat Evans P, O’Reilly D, Flyer JN, Soll R, Mitra S (2021) Indomethacin for symptomatic patent ductus arteriosus in preterm infants. Cochrane Database Syst Rev 1:CD013133PubMed Evans P, O’Reilly D, Flyer JN, Soll R, Mitra S (2021) Indomethacin for symptomatic patent ductus arteriosus in preterm infants. Cochrane Database Syst Rev 1:CD013133PubMed
Metadaten
Titel
Nephrotoxic medications and associated acute kidney injury in hospitalized neonates
verfasst von
Tahagod H. Mohamed
Hibo H. Abdi
Jacqueline Magers
Pavel Prusakov
Jonathan L. Slaughter
Publikationsdatum
15.02.2022
Verlag
Springer International Publishing
Erschienen in
Journal of Nephrology / Ausgabe 6/2022
Print ISSN: 1121-8428
Elektronische ISSN: 1724-6059
DOI
https://doi.org/10.1007/s40620-022-01264-6

Weitere Artikel der Ausgabe 6/2022

Journal of Nephrology 6/2022 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Nach Herzinfarkt mit Typ-1-Diabetes schlechtere Karten als mit Typ 2?

29.05.2024 Herzinfarkt Nachrichten

Bei Menschen mit Typ-2-Diabetes sind die Chancen, einen Myokardinfarkt zu überleben, in den letzten 15 Jahren deutlich gestiegen – nicht jedoch bei Betroffenen mit Typ 1.

15% bedauern gewählte Blasenkrebs-Therapie

29.05.2024 Urothelkarzinom Nachrichten

Ob Patienten und Patientinnen mit neu diagnostiziertem Blasenkrebs ein Jahr später Bedauern über die Therapieentscheidung empfinden, wird einer Studie aus England zufolge von der Radikalität und dem Erfolg des Eingriffs beeinflusst.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.