Jarrod Dalton

Dr. Jarrod Dalton

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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2016 in Anesthesia & Analgesia
Verified
Journal Article
Closed access
JDJarrod Dalton
Jarrod Dalton
SBShari D. Bolen
Shari D. Bolen
EMEdward J. Mascha
Edward J. Mascha

3 October 2017 in Annals of Internal Medicine
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Journal Article
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JDJarrod Dalton
Jarrod Dalton
APAdam T. Perzynski
Adam T. Perzynski
DZDavid A. Zidar
David A. Zidar
MRMichael B. Rothberg
Michael B. Rothberg
CCClaudia J. Coulton
Claudia J. Coulton
NDNeal V. Dawson
Neal V. Dawson
Using an observational cohort analysis, the authors studied the predictive accuracy of the Pooled Cohort Equations Risk Model of the American College of Cardiology and American Heart Association in... Background: Inequality in health outcomes in relation to Americans' socioeconomic position is rising. Objective: First, to evaluate the spatial relationship between neighborhood disadvantage and ma...

3 February 2009 in BMC Anesthesiology
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Journal Article
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EFEdith Fleischmann
Edith Fleischmann
CMCorinna Marschalek
Corinna Marschalek
KSKatja Schlemitz
Katja Schlemitz
JDJarrod Dalton
Jarrod Dalton
TGThomas Gruenberger
Thomas Gruenberger
Daniel SesslerDaniel Sessler
Daniel Sessler
Even the best cancer surgery is usually associated with minimal residual disease. Whether these remaining malignant cells develop into clinical recurrence is at least partially determined by adequacy of host defense, especially natural killer cell function. Anesthetics impair immune defenses to varying degrees, but nitrous oxide appears to be especially problematic. We therefore tested the hypothesis that colorectal-cancer recurrence risk is augmented by nitrous oxide administration during colorectal surgery.

20 January 2020 in Journal of the American Geriatrics Society
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Journal Article
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JDJarrod Dalton
Jarrod Dalton
MRMichael B. Rothberg
Michael B. Rothberg
NDNeal V. Dawson
Neal V. Dawson
NKNikolas I. Krieger
Nikolas I. Krieger
DZDavid A. Zidar
David A. Zidar
APAdam T. Perzynski
Adam T. Perzynski

16 March 2023 in Journal of the American Geriatrics Society
Verified
Journal Article
Open access
ABAlissa Becerril
Alissa Becerril
EPElizabeth R. Pfoh
Elizabeth R. Pfoh
AHArdeshir Z. Hashmi
Ardeshir Z. Hashmi
LMLyla Mourany
Lyla Mourany
DGDouglas D. Gunzler
Douglas D. Gunzler
JDJarrod Dalton
Jarrod Dalton
Background: Evidence on the effects of neighborhood socioeconomic disadvantage on dementia risk in racially and ethically diverse populations is limited. Our objective was to evaluate the relative extent to which neighborhood disadvantage accounts for racial/ethnic variation in dementia incidence rates. Secondarily, we evaluated the spatial relationship between neighborhood disadvantage and dementia risk. Methods: In this retrospective study using electronic health records (EHR) at two regional health systems in Northeast Ohio, participants included 253,421 patients aged >60 years who had an outpatient primary care visit between January 1, 2005 and December 31, 2015. The date of the first qualifying visit served as the study baseline. Cumulative incidence of composite dementia outcome, defined as EHR‐documented dementia diagnosis or dementia‐related death, stratified by neighborhood socioeconomic deprivation (as measured by Area Deprivation Index) was determined by competing‐risk regression analysis, with non‐dementia‐related death as the competing risk. Fine‐Gray sub‐distribution hazard ratios were determined for neighborhood socioeconomic deprivation, race/ethnicity, and clinical risk factors. The degree to which neighborhood socioeconomic position accounted for racial/ethnic disparities in the incidence of composite dementia outcome was evaluated via mediation analysis with Poisson rate models. Results: Increasing neighborhood disadvantage was associated with increased risk of EHR‐documented dementia diagnosis or dementia‐related death (most vs. least disadvantaged ADI quintile HR = 1.76, 95% confidence interval = 1.69–1.84) after adjusting for age and sex. The effect of neighborhood disadvantage on this composite dementia outcome remained after accounting for known medical risk factors of dementia. Mediation analysis indicated that neighborhood disadvantage accounted for 34% and 29% of the elevated risk for composite dementia outcome in Hispanic and Black patients compared to White patients, respectively. Conclusion: Neighborhood disadvantage is related to the risk of EHR‐documented dementia diagnosis or dementia‐related death and accounts for a portion of racial/ethnic differences in dementia burden, even after adjustment for clinically important confounders.

8 April 2021 in Journal of Bone and Joint Surgery
Verified
Journal Article
Closed access
EREric T. Ricchetti
Eric T. Ricchetti
BJBong-Jae Jun
Bong-Jae Jun
YJYuxuan Jin
Yuxuan Jin
JHJason C. Ho
Jason C. Ho
TPThomas E. Patterson
Thomas E. Patterson
JIJoseph P. Iannotti
Joseph P. Iannotti
Background: The purpose of this study was to evaluate glenoid component position and radiolucency following anatomic total shoulder arthroplasty (TSA) using sequential 3-dimensional computed tomography (3D CT) analysis. Methods: In a series of 152 patients (42 Walch A1, 16 A2, 7 B1, 49 B2, 29 B3, 3 C1, 3 C2, and 3 D glenoids) undergoing anatomic TSA with a polyethylene glenoid component, sequential 3D CT analysis was performed preoperatively (CT1), early postoperatively (CT2), and at a minimum 2-year follow-up (CT3). Glenoid component shift was defined as a change in component version or inclination of ≥3° from CT2 to CT3. Glenoid component central anchor peg osteolysis (CPO) was assessed at CT3. Factors associated with glenoid component shift and CPO were evaluated. Results: Glenoid component shift occurred from CT2 to CT3 in 78 (51%) of the 152 patients. CPO was seen at CT3 in 19 (13%) of the 152 patients, including 15 (19%) of the 78 with component shift. Walch B2 glenoids with a standard component and glenoids with higher preoperative retroversion were associated with a higher rate of shift, but not of CPO. B3 glenoids with an augmented component and glenoids with greater preoperative joint-line medialization were associated with CPO, but not with shift. More glenoid component joint-line medialization from CT2 to CT3 was associated with higher rates of shift and CPO. A greater absolute change in glenoid component inclination from CT2 to CT3 and a combined absolute glenoid component version and inclination change from CT2 to CT3 were associated with CPO. Neither glenoid component shift nor CPO was associated with worse clinical outcomes. Conclusions: Postoperative 3D CT analysis demonstrated that glenoid component shift commonly occurs following anatomic TSA, with increased inclination the most common direction. Most (81%) of the patients with glenoid component shift did not develop CPO. Longer follow-up is needed to determine the relationships of glenoid component shift and CPO with loosening over time. Level of Evidence: Therapeutic Level IV. See Instructions for Authors for a complete description of levels of evidence.