Robert Nee
Walter Reed National Military Medical Center
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Featured researches published by Robert Nee.
American Journal of Kidney Diseases | 2015
Robert Nee; Christina M. Yuan; Dustin J. Little; Maura A. Watson; Lawrence Y. Agodoa; Kevin C. Abbott
BACKGROUNDnA recent study showed an increased risk of death in African Americans compared with whites with end-stage renal disease (ESRD) due to lupus nephritis (LN). We assessed the impact of age stratification, socioeconomic factors, and kidney transplantation on the disparity in patient survival among African American versus non-African American patients with LN-caused ESRD, compared with other causes.nnnSTUDY DESIGNnRetrospective cohort study.nnnSETTING & PARTICIPANTSnUsing the US Renal Data System database, we identified 12,352 patients with LN-caused ESRD among 1,132,202 patients who initiated maintenance dialysis therapy from January 1, 1995, through December 31, 2006, and were followed up until December 31,xa02010.nnnPREDICTORSnBaseline demographics and comorbid conditions, Hispanic ethnicity, socioeconomic factors (employment status, Medicare/Medicaid insurance, and area-level median household income based on zip code as obtained from the 2000 US census), and kidney transplantation as a time-dependent variable.nnnOUTCOMEnAll-cause mortality.nnnMEASUREMENTSnMultivariable Cox and competing-risk regressions.nnnRESULTSnMean duration of follow-up in the LN-caused ESRD and other-cause ESRD cohorts were 6.24±4.20 (SD) and 4.06±3.61 years, respectively. 6,106 patients with LN-caused ESRD (49.43%) and 853,762 patients with other-cause ESRD (76.24%) died during the study period (P<0.001). Patients with LN-caused ESRD were significantly younger (mean age, 39.92 years) and more likely women (81.65%) and African American (48.13%) than those with other-cause ESRD. In the fully adjusted multivariable Cox regression model, African American (vs non-African American) patients with LN-caused ESRD had significantly increased risk of death at age 18 to 30 years (adjusted HR, 1.43; 95% CI, 1.24-1.65) and at age 31 to 40 years (adjusted HR, 1.17; 95% CI, 1.02-1.34). Among patients with other-cause ESRD, African Americans were at significantly increased risk at age 18 to 30 years (adjusted HR, 1.17; 95% CI, 1.11-1.22).nnnLIMITATIONSnWe used zip code-based median household income as a surrogate for patient income. Residual socioeconomic confounders may exist.nnnCONCLUSIONSnAfrican Americans are at significantly increased risk of death compared with non-African Americans with LN-caused ESRD at age 18 to 40 years, a racial disparity risk that is 10 years longer than that in the general ESRD population. Accounting for area-level median household income and transplantation significantly attenuated the disparity in mortality of African American versus non-African American patients with LN-caused ESRD.
BMC Nephrology | 2014
David J Yoo; Lawrence Y. Agodoa; Christina M. Yuan; Kevin C. Abbott; Robert Nee
BackgroundAn analysis of intracranial hemorrhage (ICH) in a national sample of autosomal dominant polycystic kidney disease (ADPKD) patients receiving long-term dialysis has not been reported. It is often assumed that patients with ADPKD are not at increased risk of ICH after starting dialysis. We hypothesized that patients with ADPKD would have a higher subsequent risk of ICH even after the start of chronic dialysis.MethodsRetrospective cohort study of Medicare primary patients with and without ADPKD in the United States Renal Data System (USRDS), initiated on chronic dialysis or transplanted between 1 January 1999 and 3 July 2009, and followed until 31 December 2009. Covariates included age, gender, race, prior stroke, diabetes mellitus, dialysis modality, body mass index, serum albumin and other co-morbid conditions from the Medical Evidence Form. Primary outcome was ICH, based on inpatient and outpatient Medicare claims, and all-cause mortality. Kaplan-Meier analysis was used for unadjusted assessment of time to events. Cox regression was used for assessment of factors associated with ICH and mortality. We performed competing risk regression using kidney transplant and death as competing risks. Kidney transplant was also modeled as a time-dependent covariate in Cox regression.ResultsCompeting risk regression demonstrated that ADPKD had a subhazard ratio 2.97 for ICH (95% CI 2.27-3.89). Adjusted Cox analysis showed that ADPKD patients had an AHR for death of 0.59 vs. non-ADPKD patients (95% CI 0.57-0.61).ConclusionsADPKD is a significant risk factor for ICH among patients on maintenance dialysis. Our Medicare primary cohort was older than in previous studies of intracranial aneurysm rupture among ADPKD patients. There are also limitations inherent to using the USRDS database.
American Journal of Kidney Diseases | 2015
Christina M. Yuan; Lisa K. Prince; James D. Oliver; Kevin C. Abbott; Robert Nee
Beginning in the 2014-2015 training year, the US Accreditation Council for Graduate Medical Education (ACGME) required that nephrology Clinical Competency Committees assess fellows progress toward 23 subcompetency context nonspecific internal medicine subspecialty milestones. Fellows advancement toward the ready for unsupervised practice target milestone now is tracked in each of the 6 competencies: Patient Care, Medical Knowledge, Professionalism, Interpersonal Communication Skills, Practice-Based Learning and Improvement, and Systems-Based Practice. Nephrology program directors and subspecialty societies must define nephrology-specific curricular milestones, mapped to the nonspecific ACGME milestones. Although the ACGME goal is to produce data that can discriminate between successful and underperforming training programs, the approach is at risk to produce biased, inaccurate, and unhelpful information. We map the ACGME internal medicine subspecialty milestones to our previously published nephrology-specific milestone schema and describe entrustable professional activities and other objective assessment tools that inform milestone decisions. Mapping our schema onto the ACGME subspecialty milestone reporting form allows comparison with the ACGME subspecialty milestones and the curricular milestones developed by the American Society of Nephrology Program Directors. Clinical Competency Committees may easily adapt and directly translate milestone decisions reached using our schema onto the ACGME internal medicine subspecialty competency milestone-reporting format.
Ndt Plus | 2016
Robert Nee; Christina M. Yuan; Frank P. Hurst; Rahul M. Jindal; Lawrence Y. Agodoa; Kevin C. Abbott
Background Access to nephrology care prior to end-stage renal disease (ESRD) is significantly associated with lower rates of morbidity and mortality. We assessed the association of area-level and individual-level indicators of poverty and race/ethnicity on pre-ESRD care provided by nephrologists. Methods In this retrospective cohort study using the US Renal Data System database, we identified 739 537 patients initiated on maintenance dialysis from 1 January 2007 through 31 December 2012. We assessed the Medicare–Medicaid dual eligibility status as an indicator of individual-level poverty and ZIP code–level median household income (MHI) data obtained from the 2010 US census. We conducted multivariable logistic regression of pre-ESRD nephrology care as the outcome variable. Results Among patients in the lowest area-level MHI quintile, 61.28% received pre-ESRD nephrology care versus 67.68% among those in higher quintiles (P < 0.001). Similarly, the proportions of dual-eligible and nondual-eligible patients who had pre-ESRD nephrology care were 61.49 and 69.84%, respectively (P < 0.001). Patients in the lowest area-level MHI quintile were associated with significantly lower likelihood of pre-ESRD nephrology care (adjusted odds ratio [aOR] 0.86 [95% confidence interval (CI) 0.85–0.87]) compared with those in higher quintiles. Both African American (AA) and Hispanic patients were significantly less likely to have received pre-ESRD nephrology care [aOR 0.85 (95% CI 0.84–0.86) and aOR 0.72 (95% CI 0.71–0.74), respectively]. Conclusions Individual- and area-level measures of poverty, AA race and Hispanic ethnicity were independently associated with a lower likelihood of pre-ESRD nephrology care. Efforts to improve pre-ESRD nephrology care may require focusing on the poor and minority groups.
American Journal of Kidney Diseases | 2014
Lisa K. Prince; Kevin C. Abbott; Felicidad Green; Dustin J. Little; Robert Nee; James D. Oliver; Erin M. Bohen; Christina M. Yuan
Objectively structured clinical examinations (OSCEs) are widely used in medical education, but we know of none described that are specifically for nephrology fellowship training. OSCEs use simulation to educate and evaluate. We describe a technically simple, multidisciplinary, low-cost OSCE developed by our program that contains both examination and training features and focuses on management and clinical knowledge of rare hemodialysis emergencies. The emergencies tested are venous air embolism, blood leak, dialysis membrane reaction, and hemolysis. Fifteen fellows have participated in the OSCE as examinees and/or preceptors since June 2010. All have passed the exercise. Thirteen responded to an anonymous survey in July 2013 that inquired about their confidence in managing each of the 4 tested emergencies pre- and post-OSCE. Fellows were significantly more confident in their ability to respond to the emergencies after the OSCE. Those who subsequently saw such an emergency reported that the OSCE experience was somewhat or very helpful in managing the event. The OSCE tested and trained fellows in the recognition and management of rare hemodialysis emergencies. OSCEs and simulation generally deserve greater use in nephrology subspecialty training; however, collaboration between training programs would be necessary to validate such exercises.
American Journal of Kidney Diseases | 2014
Christina M. Yuan; Lisa K. Prince; Amy J. Zwettler; Robert Nee; James D. Oliver; Kevin C. Abbott
BACKGROUNDnEntrustable professional activities (EPAs) are complex tasks representing vital physician functions in multiple competencies, used to demonstrate trainee development along milestones. Managing a nephrology outpatient clinic has been proposed as an EPA for nephrology fellowship training.nnnSTUDY DESIGNnRetrospective cohort study of nephrology fellow outpatient clinic performance using a previously validated chart audit tool.nnnSETTING & PARTICIPANTSnOutpatient encounter chart audits for training years 2008-2009 through 2012-2013, corresponding to participation in the Nephrology In-Training Examination (ITE). A median of 7 auditors (attending nephrologists) audited a mean of 1,686±408 (SD) charts per year. 18 fellows were audited; 12, in both of their training years.nnnPREDICTORSnProportion of chart audit and quality indicator deficiencies.nnnOUTCOMESnLongitudinal deficiency and ITE performance.nnnMEASUREMENTS & RESULTSnAmong fellows audited in both their training years, chart audit deficiencies were fewer in the second versus the first year (5.4%±2.0% vs 17.3%±7.0%; P<0.001) and declined between the first and second halves of the first year (22.2%±6.4% vs 12.3%±9.5%; P=0.002). Most deficiencies were omission errors, regardless of training year. Quality indicator deficiencies for hypertension and chronic kidney disease-associated anemia recognition and management were fewer during the second year (P<0.001). Yearly audit deficienciesxa0≥5% were associated with an ITE score less than the 25th percentile for second-year fellows (P=0.03), with no significant association for first-year fellows. Auditor-reported deficiencies declined between the first and second halves of the year (17.0% vs 11.1%; P<0.001), with a stable positive/neutral comment rate (17.3% vs 17.8%; P=0.6), suggesting that the decline was not due to auditor fatigue.nnnLIMITATIONSnRetrospective design and small trainee numbers.nnnCONCLUSIONSnManaging a nephrology outpatient clinic is an EPA. The chart audit tool was used to assess longitudinal fellow performance in managing a nephrology outpatient clinic. Failure to progress may be quantitatively identified and remediated. The tool identifies deficiencies in all 6 competencies, not just medical knowledge, the primary focus of the ITE and the nephrology subspecialty board examination.
Ndt Plus | 2017
Christina M. Yuan; Robert Nee; Kevin A. Ceckowski; Kendral R. Knight; Kevin C. Abbott
Abstract Background: End-stage renal disease (ESRD) incidence due to Type 2 diabetic nephropathy (DN) is 35–50%, according to the United States Renal Data System. Methods: A single-center, retrospective cohort study to determine incidence and diagnostic accuracy for Type 2 DN as the primary cause of ESRD (Code 250.40) on the Center for Medicare & Medicaid (CMS) Medical Evidence Report form (CMS2728) submitted at renal replacement therapy initiation. All patients u2009≥18 years of age with a CMS2728 submitted between 1 March 2006 and 31 March 2015 at a single academic military medical center (ESRD Network 5) were included. Medical records of those with a Code 250.40 diagnosis were reviewed to determine whether they met the Kidney Disease Outcomes Quality Initiative (KDOQI) 2007 criteria for DN. Results: ESRD incidence secondary to Type 2 DN was 18.7% (56/299 individual CMS2728 submissions over 9.09 years). In all, 12/56 (21.4%) did not meet KDOQI criteria for Type 2 DN. Although all had diabetes, those not meeting criteria had shorter disease duration (P u2009= u20090.007), were more likely to have active urine sediment (P u2009= u20090.006), and were less likely to have macroalbuminuria (P u2009= u20090.037) or retinopathy (P u2009= u20090.002) prior to ESRD. On exact logistic regression, retinopathy was significantly associated with KDOQI-predicted DN [odds ratio u2009=u2009 19.16 (confidence interval 2.76–223.7), P u2009= u20090.0009]. Conclusions: In this single-center cohort, 21.4% identified as having Type 2 DN as the primary cause of ESRD were incorrectly assigned per KDOQI 2007 clinical criteria. If replicated in larger populations, this could have substantial implications regarding the epidemiology of ESRD in the USA.
Kidney International Reports | 2017
Dustin J. Little; Matthew Ward; Robert Nee; Christina M. Yuan; David K. Oliver; Kevin C. Abbott; Rahul M. Jindal
To the Editor: Kidney transplantation improves survival and quality of life for patients with end-stage renal disease. Lifelong immunosuppressive therapy (IST) is required for kidney transplant (graft) survival, at an average cost of >
Ndt Plus | 2018
Lisa K. Prince; Ruth C. Campbell; Sam W Gao; Jessica Kendrick; Christopher J. LeBrun; Dustin J. Little; David L Mahoney; Laura A Maursetter; Robert Nee; Mark Saddler; Maura A. Watson; Christina M. Yuan
20,000 per year. More than 10% of graft failure cases are attributed to IST nonadherence. Under current US policy, Medicare IST coverage is limited to 3 years after transplantation for nondisabled recipients <65 years of age. Transplant survival rates in the United States are lower than those in developed nations that provide lifelong governmentfunded IST. Patients with lifelong Medicare coverage have substantially better >3-year outcomes than those whose Medicare is limited to 3 years after transplantation, and 51% of surveyed adult US transplant centers reported deaths or graft failures due to costrelated IST nonadherence. Advocates for legislation to increase the duration of Medicare IST coverage contend that this would likely improve IST adherence. However, IST adherence has not been reported in a cohort of US transplant recipients who receive lifelong IST at no out-of-pocket cost. We studied IST adherence rates in adult US Military Healthcare System beneficiaries, who receive free lifelong IST after transplantation. This study was approved by Walter Reed National Military Medical Center’s institutional review board. Informed consent was obtained from adult (
Kidney International Reports | 2018
Amarpali Brar; Dimitre G. Stefanov; Rahul M. Jindal; Moro O. Salifu; Madhu Joshi; Bair Cadet; Robert Nee
18 years of age) kidney transplant recipients seen in the Walter Reed National Military Medical Center nephrology or organ transplant clinics. Demographic and clinical characteristics were ascertained by an electronic medical record review. Patients were recruited consecutively and were administered the Immunosuppressive Therapy Adherence Scale (ITAS) and Beck Depression Inventory-II (BDI-II). The ITAS is a questionnaire that consists of 4 questions measuring IST nonadherence, each scored by percentage of nonadherence (0 points for >50% of the time, 1 point for 21%–50% of the