LONGITUDINAL ASSESSMENT OF ECONOMIC BURDEN AND CLINICAL OUTCOMES IN ACROMEGALY

2001 ◽  
Vol 7 (3) ◽  
pp. 170-180 ◽  
Author(s):  
Leslie S. Wilson, PhD ◽  
Jennifer L. Shin ◽  
Shereen Ezzat, MD
Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4549-4549
Author(s):  
Gwilym J Thompson ◽  
Vincent Lévy ◽  
Krista Payne ◽  
Radek Wasiak ◽  
Yvonne Lis

Abstract Abstract 4549 Introduction Chronic lymphocytic leukemia (CLL) is the most common adult haematological malignancy in the Western world. It remains incurable and follows an extremely variable clinical course with survival ranging from months to decades. In those who become refractory to fludarabine based therapy, median survival is less than 1 year. Methods To identify data related to the clinical and economic sequelae of patients in routine clinical care diagnosed with refractory CLL, a systematic literature search of MEDLINE and EMBASE was conducted for the period January 1999-July 2009. The search terms used included incidence, prevalence, natural history, characteristics, clinical management, clinical outcomes, use of health care resources and was focused on patients with fludarabine refractory CLL also refractory to alemtuzumab (fludarabine and alemtuzumab refractory) or less suitable for alemtuzumab due to bulky lymph nodes (bulky fludarabine refractory). Supplementary checks were made of reference lists, particularly in review articles. Relevant conference proceedings for the period January 2006-July 2009 were also examined. Results The search of MEDLINE and EMBASE identified 102 articles of which 26 reported on the more general populations of patients with haematological malignancies, 61 on CLL and 15 on refractory CLL. Of those articles reporting data in relation to CLL (n=61), 49 described patient characteristics and outcomes, prognostic factors, diagnostic and treatment options, natural history of the disease, epidemiology, patient management and specific treatment outcomes and 12 review articles addressed areas such as prognostic factors and treatment options. Of those reporting on refractory CLL (n=15), one was a review article of novel agents and 14 were studies evaluating outcomes following salvage treatment with various pharmaceutical agents and other therapeutic interventions but mainly in patients refractory to fludarabine. Only one US study had evaluated patients who were refractory to both fludarabine and alemtuzumab or were bulky fludarabine refractory, examining response and survival following a variety of salvage treatments (Tam et al. Leukemia and Lymphoma 2007;48:1931-9). The search of conference proceedings identified 27 abstracts, 19 of which evaluated patients with CLL reporting on a range of topics including natural history and survival, prognostic factors and outcomes achieved with existing and experimental pharmaceutical interventions. Only two abstracts specifically reported on patients who were refractory to both fludarabine and alemtuzumab or were bulky fludarabine refractory, examining response rates following administration of a novel pharmaceutical agent (European Haematology Association Meeting 2009, abstracts 0494 and 0919). Conclusions There is very little data from clinical practice on clinical outcomes and none on economic sequelae for patients with double refractory or bulky nodal refractory disease. The lack of such data is likely to hinder the achievement of better outcomes for patients and the evaluation of cost effectiveness for newer agents. This lack of data to inform clinical practice and decision making has prompted the initiation of an observational study in five European countries with the objectives of characterising the current patterns of care, survival outcomes and resource utilization in double refractory and bulky nodal refractory CLL patients in Europe. The study, based on a retrospective chart review of approximately 250 patients, is currently underway in France, Germany, Italy, Spain and the UK. It is anticipated that the results, planned to be available by the end of 2009, will help to identify unmet clinical needs, quantify the clinical and economic burden in this particular population and contribute to the development of new treatment guidelines. Disclosures: Lévy: GlaxoSmithKline: Consultancy. Payne:GlaxoSmithKline: Consultancy. Wasiak:GlaxoSmithKline: Consultancy. Lis:GlaxoSmithKline: Consultancy.


2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
Ulysses Ribeiro Jr. ◽  
Daiane O. Tayar ◽  
Rodrigo A. Ribeiro ◽  
Priscila Andrade ◽  
Silvio M. Junqueira Jr.

Purpose. Anastomotic leaks (AL) present a significant source of clinical and economic burden on patients undergoing colorectal surgeries. This study was aimed at evaluating the clinical and economic consequences of AL and its risk factors. Methods. A retrospective cohort study was conducted between 2012 and 2013 based on the billing information of 337 patients who underwent low anterior resection (LAR). The outcomes evaluated were the development of AL, use of antibiotics, 30-day readmission and mortality, and total hospital costs, including readmissions and length of stay (LOS). The risk factors for AL, as well as the relationship between AL and clinical outcomes, were analyzed using multivariable Poisson regression. Generalized linear models (GLM) were employed to evaluate the association between AL and continuous outcomes (LOS and costs). Results. AL was detected in 6.8% of the patients. Emergency surgery (aRR 2.56; 95% CI: 1.15–5.71, p=0.021), blood transfusion (aRR 4.44; 95% CI: 1.86–10.64, p=0.001), and cancer diagnosis (aRR 2.51; 95% CI: 1.27–4.98, p=0.008) were found to be independent predictors of AL. Patients with AL showed higher antibiotic usage (aRR 1.69; 95% CI: 1.37–2.09, p<0.001), 30-day readmission (aRR 3.34; 95% CI: 1.53–7.32, p=0.003) and mortality (aRR 13.49; 95% CI: 4.10–44.35, p<0.001), and longer LOS (39.6 days, as opposed to 7.5 days for patients without AL, p<0.001). Total hospital costs amounted to R$210,105 for patients with AL in comparison with R$34,270 for patients without AL (p<0.001). In multivariable GLM, the total hospital costs for AL patients were 4.66 (95% CI: 3.38–6.23, p<0.001) times higher than those for patients without AL. Conclusions. AL leads to worse clinical outcomes and increases hospital costs by 4.66 times. The risk factors for AL were found to be emergency surgery, blood transfusion, and cancer diagnosis.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3350-3350
Author(s):  
Jennifer M. Stephens ◽  
Sarah Y. Liou ◽  
Kimbach T. Tran ◽  
Marc F. Botteman

Abstract OBJECTIVES: Hematologic adverse events such as neutropenia, thrombocytopenia, and anemia are commonly experienced by cancer patients receiving chemotherapy. These cytopenias are associated with increased morbidity and mortality, high healthcare costs, and decreases in quality of life. The objective of this study was to review the economic burden of these hematologic adverse events associated with chemotherapy in cancer patients. METHODS: A systematic search of the English-language medical literature published between 1990 and 2006 was conducted. Online conference proceedings and a review of article bibliographies were included in the review. Articles selected included prospective or retrospective studies specifically designed to examine burden of illness, direct medical costs, indirect costs, or cost drivers associated with neutropenia, thrombocytopenia, and anemia in adult cancer patients treated with chemotherapy. All original costs were reported, with adjusted figures (to 2006 US dollars) presented in parentheses using the medical care component of the consumer price index from the US Bureau of Labor Statistics. RESULTS: Of 160 studies initially identified, 64 met selection criteria and were reviewed in detail. The cost of neutropenia ranged from $1,893 (2006 US $2,632) per episode in the outpatient setting to $38,583 ($54,807) for a febrile neutropenia hospitalization. The cost of treating thrombocytopenia ranged from $1,037 ($1,395) to $7,550 ($9,336) per cycle or episode. Costs attributable to treating anemia ranged from $18,418 ($22,775) to $69,478 ($93,454) per year. Key cost drivers include hospitalization, drugs (e.g., granulocyte colony-stimulating factors and antibiotics), and diagnostic tests for neutropenia; hospitalization, major bleeding episodes, and platelet transfusions for thrombocytopenia; and inpatient and outpatient services, erythropoietic agents, and red blood cell transfusions for anemia. Another finding was that the costs of hematologic adverse events for patients with hematologic malignancies were up to twice that of patients with solid tumors. CONCLUSIONS: Chemotherapy-related cytopenias result in a substantial economic burden on patients, payers, caregivers, and society in general. This burden is particularly high for patients with hematologic malignancies due to the underlying malignancy. Furthermore, AEs affect the ability to deliver planned treatments, resulting in potentially suboptimal clinical outcomes. An evaluation of both clinical outcomes of chemotherapy and economic consequences as a result of chemotherapy-induced toxicities is recommended in determining optimal treatments for patients with cancer.


2018 ◽  
Vol 19 (6) ◽  
pp. 879-886 ◽  
Author(s):  
Sanminder Singh ◽  
Robert E. Kalb ◽  
Elke M. G. J. de Jong ◽  
Neil H. Shear ◽  
Mark Lebwohl ◽  
...  

Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 36-37
Author(s):  
Saaya Tsutsué ◽  
Takahiro Suzuki ◽  
Hyojin Kim ◽  
William YuanHao Kuan ◽  
Bruce Crawford

Introduction: Myelodysplastic syndromes (MDS) are a group of progressive clonal hematopoietic malignancies that primarily affect an elderly demographic. MDS is treated based on age, symptoms, disease severity, and prognostic scoring. There is limited evidence on the health economic burden and how transfusion dependency affects clinical outcomes of patients with MDS in Japan. This is the first retrospective database analysis study that was performed to elucidate the patient baseline characteristics, 1-year medical costs, and 3-year overall survival (OS) in patients treated for MDS using an administrative claims database of more than 150 hospitals in Japan. Methods: In this study, we used the Medical Data Vision (MDV) database to identify patients diagnosed with MDS (International Classification of Diseases, Tenth Revision, [ICD-10]: code D46.9) using a nationwide administrative database comprising anonymized data covering more than 25 million patients. Patients who received transfusions, erythropoiesis-stimulating agents (ESA) with or without transfusions, azacitidine (AZA) with or without transfusions, and other (e.g. chemotherapy such as doxorubicin, cytarabine) as the index treatment during the identification period from October 1, 2009 to June 30, 2018 were included if they had 1 year of lookback data before the index date and a follow-up period of ≥ 1 year. Results: Of the 5,981 patients with MDS who met the eligibility criteria for this study, 37.8% were female; the median age of patients was &gt; 70 years. Patients receiving transfusion in their index line of therapy was the largest regimen group (n = 2,844, 47.6%), followed by AZA + transfusion (n = 703, 11.8%), ESA (n = 294, 4.9%), and AZA (n = 288, 4.8%). The AZA regimen had the youngest mean age of 70.2 years while the ESA + transfusion group had the oldest (77.8 years). AZA and AZA + transfusion groups recorded a median Charlson Comorbidity Index score of 1.9 and 2.0, respectively, whereas ESA and ESA + transfusion groups had a mean score of 3.2 and 2.6, respectively. Medical costs varied widely for these groups (Figure 1). Mean overall costs were highest for the AZA + transfusion regimen group (USD 63,226) and lowest for the ESA group (USD 15,931). Mean overall costs for regimen groups without transfusion were highest for AZA (USD 47,475), followed by ESA (USD 15,931; P &lt; 0.0001), and the addition of the transfusion component was observed to incur higher overall costs, inpatient costs, and MDS-related treatment costs. Inpatient costs for the ESA groups ranged from USD 16,717 for ESA only to USD 30,347 for ESA + transfusion. The highest outpatient costs were observed for the AZA group (USD 20,011; P &lt; 0.0001). MDS-related treatment costs were highest for the AZA + transfusion group (USD 32,123) and lowest for the ESA group (USD 2,518; P &lt; 0.0001). Overall, there were 1,966 deaths (32.9%) recorded within 3 years of index treatment. The median OS for patients receiving AZA + transfusion was 957 days (Figure 2). Conclusions: In this study, mean overall costs, inpatient costs, and outpatient costs were highest for the AZA + transfusion regimen group. Consistent with the trend of MDS studies, the majority of patients with MDS received supportive transfusion-dependent therapy. Transfusion dependency led to considerable incremental cost and poorer clinical outcomes compared with other regimens. This study provides insights into the real-world disease burden for patients with MDS and the current treatment options available for MDS in Japan. Disclosures Tsutsué: Celgene KK, a Bristol-Myers Squibb Company: Current Employment. Suzuki:Bristol Myers Squibb: Honoraria; Nippon Shinyaku Co., Ltd: Honoraria; Kyowa Hakka Kirin Co., Ltd: Honoraria, Research Funding; Novartis Pharmaceuticals: Honoraria. Kim:Syneos Health: Current Employment. Kuan:Syneos Health Clinical K.K.: Current Employment. Crawford:Syneos Health: Current Employment.


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