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  1. Article ; Online: The Nephrologist Has Great Potential to Have an Important Role in the Intensive Care Unit: Reply to the Letter to the Editor of David J.R. Morgan.

    Askenazi, David J / Faubel, Sarah

    Blood purification

    2017  Volume 44, Issue 4, Page(s) 269–270

    MeSH term(s) Intensive Care Units ; Nephrologists
    Language English
    Publishing date 2017-10-12
    Publishing country Switzerland
    Document type Letter ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, P.H.S. ; Comment
    ZDB-ID 605548-5
    ISSN 1421-9735 ; 0253-5068
    ISSN (online) 1421-9735
    ISSN 0253-5068
    DOI 10.1159/000478974
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: The Nephrologist Has Great Potential to Have an Important Role in the Intensive Care Unit: Reply to the Letter to the Editor of David J.R. Morgan

    Askenazi, David J. / Faubel, Sarah

    Blood Purification

    2017  Volume 44, Issue 4, Page(s) 269–270

    Institution Department of Pediatrics, Division of Pediatric Nephrology, University of Alabama at Birmingham, Birmingham, AL, and Department of Medicine, University of Colorado, and Denver VA Medical Center, Denver, CO, USA
    Language English
    Publishing date 2017-10-12
    Publisher S. Karger AG
    Publishing place Basel, Switzerland
    Document type Article
    Note Letter to the Editor
    ZDB-ID 605548-5
    ISSN 1421-9735 ; 0253-5068
    ISSN (online) 1421-9735
    ISSN 0253-5068
    DOI 10.1159/000478974
    Database Karger publisher's database

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  3. Article ; Online: No matter the hemisphere or language, neonatal acute kidney injury is common and is associated with poor outcomes.

    Askenazi, David J

    Jornal de pediatria

    2022  Volume 99, Issue 3, Page(s) 203–204

    MeSH term(s) Infant, Newborn ; Humans ; Language ; Acute Kidney Injury
    Language English
    Publishing date 2022-12-26
    Publishing country Brazil
    Document type Editorial ; Comment
    ZDB-ID 731324-x
    ISSN 1678-4782 ; 0021-7557
    ISSN (online) 1678-4782
    ISSN 0021-7557
    DOI 10.1016/j.jped.2022.12.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Risk of chronic kidney disease in children who developed acute kidney injury secondary to nephrotoxic medication exposure in infancy.

    Ameta, Priyanka / Stoops, Christine / Askenazi, David J

    Renal failure

    2023  Volume 45, Issue 1, Page(s) 2218486

    Abstract: Introduction: Nephrotoxic medication (NTM) is one of the common causes of acute kidney injury (AKI) in critically ill infants. Current knowledge about the long-term effects of NTM exposure and associated AKI during the neonatal period and early infancy ... ...

    Abstract Introduction: Nephrotoxic medication (NTM) is one of the common causes of acute kidney injury (AKI) in critically ill infants. Current knowledge about the long-term effects of NTM exposure and associated AKI during the neonatal period and early infancy is limited. Hence, we aimed to explore the risk of chronic kidney disease (CKD) after NTM-AKI in this age group.
    Methods: We performed a cross-sectional study including children 2-7 years of age, who had a history of high NTM exposure during NICU hospitalization. Cases and controls were defined as children who developed AKI and who did not develop AKI after NTM exposure, respectively. The primary outcome of interest was to explore the prevalence of composite CKD. In addition, we explored differences in urinary biomarker kidney injury molecule-1 (KIM-1) between the groups.
    Results: We enrolled 48 children, 18 cases and 30 controls in which 25/48 (52%) had at least one finding of CKD. The composite CKD outcome tended to be higher in cases vs controls (61.1% vs. 46.6%, odds ratio = 1.79 (95% confidence interval 0.54-5.8)); however, this was not statistically significant. Median urinary KIM-1 value trended higher in controls, 0.367(0.23-0.59) vs. 0.20 (IQR 0.11-0.47), which was not statistically significant.
    Conclusion: In this study, 52% of children exposed to NTM had at least one marker of CKD at a median age of 5 years. Multicenter, large prospective studies are needed to improve our understanding of the natural course of NTM-AKI and to determine risk factors and strategies to reduce CKD in this high-risk population.
    MeSH term(s) Infant, Newborn ; Humans ; Infant ; Child ; Child, Preschool ; Cross-Sectional Studies ; Acute Kidney Injury/chemically induced ; Acute Kidney Injury/epidemiology ; Acute Kidney Injury/complications ; Renal Insufficiency, Chronic/epidemiology ; Renal Insufficiency, Chronic/complications ; Kidney ; Prospective Studies ; Risk Factors ; Drug-Related Side Effects and Adverse Reactions/complications ; Retrospective Studies
    Language English
    Publishing date 2023-04-25
    Publishing country England
    Document type Multicenter Study ; Journal Article
    ZDB-ID 632949-4
    ISSN 1525-6049 ; 0886-022X
    ISSN (online) 1525-6049
    ISSN 0886-022X
    DOI 10.1080/0886022X.2023.2218486
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Selective Cytopheretic Device Use in Continuous Kidney Replacement Therapy in Children: A Cohort Study With a Historical Comparator.

    Goldstein, Stuart L / Ollberding, Nicholas J / Askenazi, David J / Basu, Rajit K / Selewski, David T / Krallman, Kelli A / Yessayan, Lenar / Humes, Harvey David

    Kidney medicine

    2024  Volume 6, Issue 4, Page(s) 100792

    Abstract: Rationale and objective: Critically ill children with acute kidney injury (AKI) requiring continuous renal replacement therapy (CRRT) are at increased risk of death. The selective cytopheretic device (SCD) promotes an immunomodulatory effect at circuit- ... ...

    Abstract Rationale and objective: Critically ill children with acute kidney injury (AKI) requiring continuous renal replacement therapy (CRRT) are at increased risk of death. The selective cytopheretic device (SCD) promotes an immunomodulatory effect at circuit-ionized calcium of <0.40 mmol/L. In an adult CRRT patient study, SCD-treated patients reported improved survival or dialysis independence. We reported safety data from children who received CRRT-SCD therapy and compared outcomes with a historic pediatric CRRT cohort.
    Study design: We performed 2 prospective multicenter studies to evaluate the safety and feasibility of SCD in critically ill children.
    Setting and participants: Four pediatric institutions enrolled children weighing 10 kg or more with AKI and multi-organ dysfunction receiving CRRT as the standard of care with the SCD-integrated post-CRRT membrane.
    Exposure: Patients received CRRT-SCD with regional citrate anticoagulation for up to 7-10 days, or CRRT discontinuation, whichever came first.
    Analytical approach: We reported serious adverse events among patients and CRRT-SCD-related process and outcome variables. We compared survival to intensive care unit (ICU) discharge rates between the CRRT-SCD cohort and a matched cohort from the prospective pediatric CRRT registry, using odds ratios in multivariable analysis for factors associated with prospective pediatric CRRT patient ICU mortality. To validate these crude analyses, Bayesian logistic regression was performed to assess for attributable benefit-risk assessment of the SCD.
    Results: Twenty-two patients received CRRT-SCD treatments. Fifteen serious adverse events were recorded; none were SCD-related. Seventeen patients survived till ICU discharge or day 60. Both multivariable and Bayesian analyses revealed a probable benefit of the addition of SCD. Fourteen of the 16 patients surviving ICU discharge reported a normal estimated glomerular filtration rate and no patient was dialysis dependent at 60 days.
    Limitations: The study had a few limitations, such as (1) a small sample size in the SCD-PED cohort group; (2) unchanging historic control group; and (3) adverse events were not recorded in the control group.
    Conclusions: The SCD therapy is feasible, safe, and demonstrates probable benefit for critically ill children who require CRRT for AKI.
    Language English
    Publishing date 2024-02-15
    Publishing country United States
    Document type Journal Article
    ISSN 2590-0595
    ISSN (online) 2590-0595
    DOI 10.1016/j.xkme.2024.100792
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Receipt of high-frequency ventilation is associated with acute kidney injury in very preterm neonates.

    Haynes, Nicholas / Bell, Jeremiah / Griffin, Russel / Askenazi, David J / Jetton, Jennifer / Kent, Alison L

    Pediatric nephrology (Berlin, Germany)

    2023  Volume 39, Issue 2, Page(s) 579–587

    Abstract: Background: High-frequency ventilation (HFV) is frequently used in critically ill preterm neonates. We aimed to determine the incidence of acute kidney injury (AKI) in neonates less than 29 weeks gestation who received HFV in the first week of life and ... ...

    Abstract Background: High-frequency ventilation (HFV) is frequently used in critically ill preterm neonates. We aimed to determine the incidence of acute kidney injury (AKI) in neonates less than 29 weeks gestation who received HFV in the first week of life and to determine if the rates of AKI differed in those who received other forms of respiratory support.
    Methods: This retrospective cohort study of 24 international, level III/IV neonatal intensive care units (NICUs) included neonates less than 29 weeks gestation from the AWAKEN study database. Exclusion criteria included the following: no intravenous fluids ≥ 48 h, admission ≥ 14 days of life, congenital heart disease requiring surgical repair at < 7 days of life, lethal chromosomal anomaly, death within 48 h, severe congenital kidney abnormalities, inability to determine AKI status, insufficient data on ventilation, and when the diagnosis of early AKI was unable to be made. Subjects were grouped into three groups based on ventilation modes (CPAP/no ventilation, conventional ventilation, and HFV).
    Results: The incidence of AKI was highest in the CPAP/no ventilation group, followed by HFV, followed by conventional ventilation (CPAP/no ventilation 48.5% vs. HFV 42.6% vs. conventional ventilation 28.4% (p = 0.009). An increased risk for AKI was found for those on HFV compared to CPAP/no ventilation (HR = 2.65; 95% CI:1.22-5.73).
    Conclusions: HFV is associated with AKI in the first week of life. Neonates on HFV should be screened for AKI. The reasons for this association are not clear. Further studies should evaluate the relationship between ventilator strategies and AKI in premature neonates. A higher resolution version of the Graphical abstract is available as Supplementary information.
    MeSH term(s) Infant, Newborn ; Humans ; Retrospective Studies ; Infant, Extremely Premature ; High-Frequency Ventilation/adverse effects ; Infant, Newborn, Diseases/epidemiology ; Acute Kidney Injury/epidemiology ; Acute Kidney Injury/etiology ; Acute Kidney Injury/therapy
    Language English
    Publishing date 2023-08-18
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 631932-4
    ISSN 1432-198X ; 0931-041X
    ISSN (online) 1432-198X
    ISSN 0931-041X
    DOI 10.1007/s00467-023-06077-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Neonatal fluid overload-ignorance is no longer bliss.

    Weaver, Lucinda J / Travers, Colm P / Ambalavanan, Namasivayam / Askenazi, David

    Pediatric nephrology (Berlin, Germany)

    2022  Volume 38, Issue 1, Page(s) 47–60

    Abstract: Excessive accumulation of fluid may result in interstitial edema and multiorgan dysfunction. Over the past few decades, the detrimental impact of fluid overload has been further defined in adult and pediatric populations. Growing evidence highlights the ... ...

    Abstract Excessive accumulation of fluid may result in interstitial edema and multiorgan dysfunction. Over the past few decades, the detrimental impact of fluid overload has been further defined in adult and pediatric populations. Growing evidence highlights the importance of monitoring, preventing, managing, and treating fluid overload appropriately. Translating this knowledge to neonates is difficult as they have different disease pathophysiologies, and because neonatal physiology changes rapidly postnatally in many of the organ systems (i.e., skin, kidneys, and cardiovascular, pulmonary, and gastrointestinal). Thus, evaluations of the optimal targets for fluid balance need to consider the disease state as well as the gestational and postmenstrual age of the infant. Integration of what is known about neonatal fluid overload with individual alterations in physiology is imperative in clinical management. This comprehensive review will address what is known about the epidemiology and pathophysiology of neonatal fluid overload and highlight the known knowledge gaps. Finally, we provide clinical recommendations for monitoring, prevention, and treatment of fluid overload.
    MeSH term(s) Infant ; Infant, Newborn ; Child ; Adult ; Humans ; Acute Kidney Injury/etiology ; Risk Factors ; Water-Electrolyte Imbalance/etiology ; Water-Electrolyte Imbalance/therapy ; Water-Electrolyte Balance ; Kidney ; Heart Failure
    Language English
    Publishing date 2022-03-29
    Publishing country Germany
    Document type Journal Article ; Review ; Research Support, N.I.H., Extramural
    ZDB-ID 631932-4
    ISSN 1432-198X ; 0931-041X
    ISSN (online) 1432-198X
    ISSN 0931-041X
    DOI 10.1007/s00467-022-05514-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Neonatal nephrotoxic medication exposure and early acute kidney injury: results from the AWAKEN study.

    Steflik, Heidi J / Charlton, Jennifer R / Briley, Meagan / Selewski, David T / Gist, Katja M / Hanna, Mina H / Askenazi, David / Griffin, Russell

    Journal of perinatology : official journal of the California Perinatal Association

    2023  Volume 43, Issue 8, Page(s) 1029–1037

    Abstract: Background: We aimed to describe nephrotoxic medication exposure and investigate associations between exposure and acute kidney injury (AKI) in the neonatal intensive care unit during the first postnatal week.: Design/methods: Secondary analysis of ... ...

    Abstract Background: We aimed to describe nephrotoxic medication exposure and investigate associations between exposure and acute kidney injury (AKI) in the neonatal intensive care unit during the first postnatal week.
    Design/methods: Secondary analysis of the AWAKEN cohort. We evaluated nephrotoxic medication exposure during the first postnatal week and associations with AKI using time-varying Cox proportional hazard regressions models. Nephrotoxic medication exposure categories were defined as: no nephrotoxic medication, nephrotoxic medications excluding aminoglycosides, aminoglycoside alone, and aminoglycoside and another nephrotoxic medication.
    Results: Of 2162 neonates, 1616 (74.7%) received ≥1 nephrotoxic medication. Aminoglycoside receipt was most common (72%). AKI developed in 211(9.8%) neonates and was associated with a nephrotoxic medication exposure (p < 0.01). Nephrotoxic medication exposures including a nephrotoxic medication excluding aminoglycoside (aHR 3.14, 95% CI 1.31-7.55) and aminoglycoside and  another nephrotoxic medication (aHR 4.79, 95% CI 2.19-10.50) were independently associated with AKI and severe AKI (stage 2/3), respectively.
    Conclusions: Nephrotoxic medication exposure in critically ill infants is common during the first postnatal week. Specific nephrotoxic medication exposure, principally aminoglycosides with another nephrotoxic medication, are independently associated with early AKI.
    MeSH term(s) Infant ; Infant, Newborn ; Humans ; Retrospective Studies ; Acute Kidney Injury/chemically induced ; Acute Kidney Injury/epidemiology ; Anti-Bacterial Agents/adverse effects ; Aminoglycosides/adverse effects ; Intensive Care Units, Neonatal ; Risk Factors
    Chemical Substances Anti-Bacterial Agents ; Aminoglycosides
    Language English
    Publishing date 2023-04-26
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 645021-0
    ISSN 1476-5543 ; 0743-8346
    ISSN (online) 1476-5543
    ISSN 0743-8346
    DOI 10.1038/s41372-023-01684-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Incidence, Risk Factors, and Outcomes Associated With Recurrent Neonatal Acute Kidney Injury in the AWAKEN Study.

    Rutledge, Austin D / Griffin, Russell L / Vincent, Katherine / Askenazi, David J / Segar, Jeffrey L / Kupferman, Juan C / Rastogi, Shantanu / Selewski, David T / Steflik, Heidi J

    JAMA network open

    2024  Volume 7, Issue 2, Page(s) e2355307

    Abstract: Importance: The incidence and associated outcomes of recurrent acute kidney injury (rAKI) in neonates remain largely unknown.: Objective: To determine the incidence, risk factors, and clinical outcomes associated with rAKI in critically ill neonates.! ...

    Abstract Importance: The incidence and associated outcomes of recurrent acute kidney injury (rAKI) in neonates remain largely unknown.
    Objective: To determine the incidence, risk factors, and clinical outcomes associated with rAKI in critically ill neonates.
    Design, setting, and participants: This cohort study was a secondary analysis of the multicenter, international Assessment of Worldwide Acute Kidney Injury Epidemiology in Neonates retrospective study. Comparisons were made among neonates with no AKI, a single AKI episode (sAKI), and rAKI. All neonates younger than 14 days who were admitted between January 1 and March 31, 2014, to 24 participating level II to IV neonatal intensive care units and received intravenous fluids for at least 48 hours were considered for inclusion. Neonates with congenital heart disease requiring surgery within the first week of life, lethal chromosomal anomalies, death within 48 hours of admission, or severe congenital kidney abnormalities were excluded. Data were analyzed from May 23, 2022, to December 8, 2023.
    Exposure: Recurrent AKI using the neonatal Kidney Disease: Improving Global Outcomes criteria. Determination of each rAKI required a complete return to the baseline serum creatinine level that defined the prior AKI episode.
    Main outcomes and measures: Incidence and risk factors of rAKI and associations of rAKI with length of stay (LOS; ie, birth to hospital discharge) and mortality.
    Results: The study cohort (n = 2162) included 1233 male neonates (57.0%). Gestational age distribution was less than 29 weeks for 276 neonates (12.8%), 29 to less than 36 weeks for 958 (44.3%), and 36 weeks or older for 928 (42.9%). Of 605 neonates with AKI, 133 (22.0%) developed rAKI with risk factors including younger gestational age, lower birthweight, and higher stage of initial AKI. Infants with rAKI experienced longer median LOS (no AKI, 17 [IQR, 8-34] days; sAKI, 18 [IQR, 9-45] days; rAKI, 60 [IQR, 25-109] days; P < .001). Time-varying Cox proportional hazards regression models suggest rAKI is independently associated with a lower hazard of discharge (adjusted hazard ratio, 0.7 [95% CI, 0.6-0.9]; P = .01) when compared with sAKI, but mortality did not differ between groups (adjusted hazard ratio, 1.4 [95% CI, 0.6-3.0]; P = .44).
    Conclusions and relevance: In this cohort study, neonatal rAKI was independently associated with longer LOS when compared with sAKI, suggesting that rAKI in neonates may be an important clinical distinction warranting further study and careful monitoring after an initial AKI episode.
    MeSH term(s) Humans ; Infant, Newborn ; Male ; Acute Kidney Injury/epidemiology ; Cohort Studies ; Incidence ; Retrospective Studies ; Risk Factors ; Multicenter Studies as Topic
    Language English
    Publishing date 2024-02-05
    Publishing country United States
    Document type Journal Article
    ISSN 2574-3805
    ISSN (online) 2574-3805
    DOI 10.1001/jamanetworkopen.2023.55307
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Perinatal risk factors associated with acute kidney injury severity and duration among infants born extremely preterm.

    Sanderson, Keia / Griffin, Russell / Anderson, Nekayla / South, Andrew M / Swanson, Jonathan R / Zappitelli, Michael / Steflik, Heidi J / DeFreitas, Marissa J / Charlton, Jennifer / Askenazi, David

    Pediatric research

    2024  

    Abstract: Background: We evaluated time-varying perinatal risk factors associated with early (≤7 post-natal days) and late (>7 post-natal days) severe acute kidney injury (AKI) occurrence and duration.: Methods: A secondary analysis of Preterm Erythropoietin ... ...

    Abstract Background: We evaluated time-varying perinatal risk factors associated with early (≤7 post-natal days) and late (>7 post-natal days) severe acute kidney injury (AKI) occurrence and duration.
    Methods: A secondary analysis of Preterm Erythropoietin Neuroprotection Trial data. We defined severe AKI (stage 2 or 3) per neonatal modified Kidney Disease: Improving Global Outcomes criteria. Adjusted Cox proportional hazards models were conducted with exposures occurring at least 72 h before severe AKI. Adjusted negative binomial regression models were completed to evaluate risk factors for severe AKI duration.
    Results: Of 923 participants, 2% had early severe AKI. In the adjusted model, gestational diabetes (adjusted HR (aHR) 5.4, 95% CI 1.1-25.8), non-steroidal anti-inflammatory drugs (NSAIDs) (aHR 3.2, 95% CI 1.0-9.8), and vancomycin (aHR 13.9, 95% CI 2.3-45.1) were associated with early severe AKI. Late severe AKI occurred in 22% of participants. Early severe AKI (aHR 2.5, 95% CI 1.1-5.4), sepsis (aHR 2.5, 95% CI 1.4-4.4), vasopressors (aHR 2.9, 95% CI 1.8-4.6), and diuretics (aHR 2.6, 95% CI 1.9-3.6) were associated with late severe AKI. Participants who had necrotizing enterocolitis or received NSAIDs had longer severe AKI duration.
    Conclusion: We identified major risk factors for severe AKI that can be the focus of future research.
    Impact statement: Time-dependent risk factors for severe acute kidney injury (AKI) and its duration are not well defined among infants born <28 weeks' gestation. Over 1 in 5 infants born <28 weeks' gestation experienced severe AKI, and this study identified several major time-dependent perinatal risk factors occurring within 72 h prior to severe AKI. This study can support efforts to develop risk stratification and clinical decision support to help mitigate modifiable risk factors to reduce severe AKI occurrence and duration.
    Language English
    Publishing date 2024-03-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 4411-8
    ISSN 1530-0447 ; 0031-3998
    ISSN (online) 1530-0447
    ISSN 0031-3998
    DOI 10.1038/s41390-024-03102-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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