The Incidence, Risk Factors and Impact of 30-Day Readmission Among Patients With Variceal Gastrointestinal Hemorrhage on Mortality, Morbidity and Healthcare Resource Utilization: A Nationwide Analysis

2018 ◽  
Vol 113 (Supplement) ◽  
pp. S471-S472
Author(s):  
Obada Tayyem ◽  
Mohammad Bilal ◽  
Marwan S. Abougergi ◽  
Sreeram Parupudi ◽  
Don C. Rockey
Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 29-29
Author(s):  
Archana Ramgopal ◽  
James Zullo ◽  
Jignesh Dalal ◽  
Meghan McCormick ◽  
Ram Kalpatthi

Background: Sinusoidal obstructive syndrome (SOS) is a life-threatening complication of hematopoietic stem cell transplant (HSCT) characterized by hepatomegaly, jaundice, weight gain, and hyperbilirubinemia. SOS can be associated with prolonged hospitalizations and significantly increased health care costs in HSCT patients. However, studies evaluating the healthcare burden associated with SOS are limited. In this study we used a large inpatient Pediatric Health Information System database (PHIS) to complete a comprehensive review of pediatric patients undergoing HSCT to identify risk factors for SOS development and morbidity, mortality and healthcare resource utilization associated with this complication. Methods: PHIS is an administrative database containing data from 49 US children's hospitals. We identified patients under 21 years admitted between 01/01/2016 - 12/30/2019 with a primary or secondary ICD-10 diagnosis of SOS and procedure code for HSCT. We collected the following: 1) Demographics: age, sex, race, geographic location; 2) Length of stay (LOS); 3) ICU admission; 4) Infections; 5) Graft-versus-host disease (GVHD); 6) Mortality; 7) Hospitalization costs; 8) Hospital resource utilization; and 9) Medications including defibrotide use. Differences in outcomes between patients with and without SOS were assessed by Chi-square tests or Wilcoxon nonparametric test for categorical and continuous variables respectively. Univariate and multivariate regression models were used to identify risk factors associated with SOS and the association of SOS on outcomes. P-values <0.05 were considered significant. Results: In 6,153 patients undergoing HSCT 263 patients (4.3%) experienced SOS. Median age at diagnosis was 5 years and males represented 60.8% of patients with SOS. The majority of patients experiencing SOS identified as white, though patients identifying as Asian or American Indian disproportionately experienced SOS. Allogeneic HSCT represented 81.75% of patients with SOS. Patient age, gender and race were not associated with significantly increased odds of SOS, the odds of SOS were 3 times greater in patients undergoing allogeneic transplantation (OR 3.0, 95% CI 2.2-4.1). Average LOS was significantly higher in patients diagnosed with SOS (71 days vs 43 days, p<0.001). ICU admission was more common in patients with SOS (68% vs 22%) with significantly longer ICU LOS as well (16.6 days vs 4.3 days, p<0.001). Mean hospitalization costs were greater in patients diagnosed with SOS ($803,956 vs $326,853, p < 0.001). Patients who experienced SOS had increased odds of developing GVHD (OR 2.7, 95%CI 1.9-3.8) and infection (OR 4.4, 95% CI 3.4-5.7). Mortality was greater in patients who developed SOS (17.5% vs 3.7%, p<0.001). However, SOS was not associated with a significant increase in mortality after adjusting for GVHD, infection and ICU admission (OR 1.4, 95% CI 0.9-2.1). In patients with medication data available (n=1956), defibrotide was administered to 67.1% of patients who experienced SOS and 5.8% of patients who did not. There was no significant difference in mortality between patients who received defibrotide and those who did not in patients with SOS (p=0.4). Conclusions: In this largest inpatient cohort of pediatric HSCT recipients to date, morbidity and healthcare resource utilization remain high among patients who experience SOS. This stresses the importance of early recognition and treatment of SOS, and the importance of novel therapeutic approaches to decrease the morbidity and improve quality of life in these patients. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 3048-3048
Author(s):  
Asher Chanan-Khan ◽  
Keri Yang ◽  
Sizhu Liu ◽  
Zhun Cao ◽  
Dorothy Baumer ◽  
...  

Abstract Introduction: Mantle cell lymphoma (MCL), Waldenström macroglobulinemia (WM), marginal zone lymphoma (MZL) and chronic lymphocytic leukemia (CLL) are subtypes of non-Hodgkin's lymphoma. Collectively, these subtypes constitute a large proportion of all B-cell malignancies; however, they are typically associated with survival spanning several years with multiple interspersed treatment periods due to frequent relapses. This can predispose patients to repeated hospitalization resulting in significant economic impact. The objectives of this study were to examine real-world treatment patterns, costs and healthcare resource utilization for patients with these lymphomas, as well as identify disparities and risk factors associated with costs incurred in US hospitals. Methods: A retrospective study was conducted using the Premier Healthcare Database, a geographically diverse all-payer, hospital administrative database containing more than one billion inpatient and hospital-based outpatient encounters. Patients aged ≥18 years with at least 1 inpatient or 2 hospital-based outpatient visits with a MCL, WM, CLL, or MZL diagnosis, and who received treatment for these conditions from 1/1/2014 to 10/31/2019 were included in the study. Descriptive analysis was conducted to examine patient sociodemographic and hospital characteristics, all-cause and lymphoma-related healthcare resource utilization and costs. Costs were obtained from patients' discharge files and hospital billing records. Multivariable analysis was performed using generalized linear models to examine risk factors associated with costs and LOS for each lymphoma type. Treatment evaluated including any use of supportive care (blood transfusion, granulocyte colony stimulating factors [GCSF]), and by regimen (steroids alone, chemotherapy alone, chemo-immunotherapy, rituximab alone, targeted therapy alone, targeted therapy in combination with chemotherapy, other). Statistical significance was determined as a p-value of <0.05. Results: The study population included 23,952 CLL, 3,387 MCL, 2,655 MZL, and 1,811 WM patients in the US hospital database. Patients with WM were statistically significantly older (77 ± 58.5 years) compared to patients with CLL (74.2 ± 30.2 years), MCL (70.7 ± 37.3 years) or MZL (69.3 ± 33.8 years). More male (71.7%) and white (87.8%) patients were identified in the MCL cohort compared to the general lymphoma cohorts (Males: 58.7%; whites: 86.3). The most common comorbidities included chronic pulmonary disease (27.1%), gastroesophageal reflux disease (17.6%), moderate-severe renal disease (16.6%), congestive heart failure (15.7%) and diabetes without chronic complications (15.2%). Overall, more than two-thirds of patients in each lymphoma group received treatment with steroids alone during hospitalizations. While the use of steroids alone was higher among whites compared to non-white patients (69.5% vs. 60.4%), the use of chemo-immunotherapy was lower in whites compared to non-whites (11.9% vs. 16.2%). The average LOS of inpatient hospitalization ranged from 6.3 days for CLL to 7.4 days for MCL, with the mean costs per hospitalization from $19,566 (CLL) to $24,439 (MCL). Non-white patients have significantly longer mean LOS days compared with white patients (CLL: 18.3 vs. 14.8; MCL: 21.7 vs. 18.3; MZL: 21.6 vs. 18.5; WM 19.0 vs. 14.5). Across the 4 lymphoma types, multivariable regression confirmed the descriptive results and demonstrated that higher hospitals costs were associated with patients who were non-white, Hispanic/Latino, treated in hospitals located in the Northeast or West, or had Medicaid; statistically significant increased cost of care was also noted for patients who received targeted therapy or supportive care, such as blood transfusion or GCSF (Table 1). Conclusions: Real-world data demonstrated the significantly high total hospital costs once patients with MCL, WM, MZL, and CLL patients were hospitalized, with significantly higher impact to minority populations. Given the increased availability of effective oral therapeutics, optimal and timely disease control in the outpatients setting can potentially prevent or decrease hospitalizations and reduce economic burden on healthcare. Future studies are needed to explore the reason for admission, clinical outcomes, and potential preventive interventions. Figure 1 Figure 1. Disclosures Chanan-Khan: Alpha2 Pharmaceuticals: Patents & Royalties: Tabi; Ascentage, Starton, Cellectar, NonoDev, Alpha2 Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees; BeiGene, Jansen, Ascentage: Honoraria; Cellectar: Current equity holder in publicly-traded company; Ascentage: Research Funding; Alpha2 Pharmaceuticals, NonoDev, Starton: Current holder of stock options in a privately-held company; BieGene, Jansen, Ascentage: Consultancy. Yang: BeiGene, Ltd.: Current Employment. Liu: BeiGene, Ltd.: Current Employment. Cao: Premier, Inc.: Current Employment; BeiGene, Ltd.: Consultancy. Baumer: BeiGene, Ltd.: Consultancy; Premier, Inc.: Current Employment. Krishnaswami: BeiGene, Ltd.: Consultancy; Premier, Inc.: Current Employment. Tang: BeiGene, Ltd.: Current Employment. Ailawadhi: Karyopharm: Consultancy; AbbVie: Consultancy; Genentech: Consultancy; Takeda: Consultancy; GSK: Consultancy, Research Funding; Xencor: Research Funding; Cellectar: Research Funding; Medimmune: Research Funding; Ascentage: Research Funding; Pharmacyclics: Consultancy, Research Funding; Amgen: Consultancy, Research Funding; Janssen: Consultancy, Research Funding; Bristol Myers Squibb: Consultancy, Research Funding; BeiGene, Ltd.: Consultancy; Sanofi: Consultancy; Oncopeptides: Consultancy.


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