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      Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease

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          Abstract

          <div class="section"> <a class="named-anchor" id="ab-zoi190587-1"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e337">Question</h5> <p id="d8815928e339">What is the association between sickle cell disease and life expectancy and lifetime income? </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-2"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e342">Findings</h5> <p id="d8815928e344">This cohort simulation modeling study showed that projected life expectancy (54 vs 76 years) and quality-adjusted life expectancy (33 vs 67 years) were lower in the sickle cell disease cohort relative to the non–sickle cell disease cohort. Projected lifetime income was also lower in individuals with sickle cell disease ($1 227 000 vs $1 922 000), reflecting lost income ($695 000) owing to reduced life expectancy. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-3"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e347">Meaning</h5> <p id="d8815928e349">Sickle cell disease appears to have important societal consequences in terms of reductions in life expectancy and lifetime income, underscoring the need for disease-modifying therapies to improve sickle cell disease–related morbidity and mortality. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-4"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e353">Importance</h5> <p id="d8815928e355">Individuals with sickle cell disease (SCD) have reduced life expectancy; however, there are limited data available on lifetime income in patients with SCD. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-5"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e358">Objective</h5> <p id="d8815928e360">To estimate life expectancy, quality-adjusted life expectancy, and income differences between a US cohort of patients with SCD and an age-, sex-, and race/ethnicity-matched cohort without SCD. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-6"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e363">Design, Setting, and Participants</h5> <p id="d8815928e365">Cohort simulation modeling was used to (1) build a prevalent SCD cohort and a matched non-SCD cohort, (2) identify utility weights for quality-adjusted life expectancy, (3) calculate average expected annual personal income, and (4) model life expectancy, quality-adjusted life expectancy, and lifetime incomes for SCD and matched non-SCD cohorts. Data sources included the Centers for Disease Control and Prevention, National Newborn Screening Information System, and published literature. The target population was individuals with SCD, the time horizon was lifetime, and the perspective was societal. Model data were collected from November 29, 2017, to March 21, 2018, and the analysis was performed from April 28 to December 3, 2018. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-7"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e368">Main Outcomes and Measures</h5> <p id="d8815928e370">Life expectancy, quality-adjusted life expectancy, and projected lifetime income.</p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-8"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e373">Results</h5> <p id="d8815928e375">The estimated prevalent population for the SCD cohort was 87 328 (95% uncertainty interval, 79 344-101 398); 998 were male and 952 were female. Projected life expectancy for the SCD cohort was 54 years vs 76 years for the matched non-SCD cohort; quality-adjusted life expectancy was 33 years vs 67 years, respectively. Projected lifetime income was $1 227 000 for an individual with SCD and $1 922 000 for a matched individual without SCD, reflecting a lost income of $695 000 owing to the 22-year difference in life expectancy. One study limitation is that the higher estimates of life expectancy yielded conservative estimates of lost life-years and income. The analysis only considered the value of lost personal income owing to premature mortality and did not consider direct medical costs or other societal costs associated with excess morbidity (eg, lost workdays for disability, time spent in the hospital). The model was most sensitive to changes in income levels and mortality rates. </p> </div><div class="section"> <a class="named-anchor" id="ab-zoi190587-9"> <!-- named anchor --> </a> <h5 class="section-title" id="d8815928e378">Conclusions and Relevance</h5> <p id="d8815928e380">In this simulated cohort modeling study, SCD had societal consequences beyond medical costs in terms of reduced life expectancy, quality-adjusted life expectancy, and lifetime earnings. These results underscore the need for disease-modifying therapies to improve the underlying morbidity and mortality associated with SCD. </p> </div><p class="first" id="d8815928e383">This simulated cohort modeling study compares life expectancy, quality-adjusted life expectancy, and projected lifetime income between individuals with and without sickle cell disease. </p>

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          Most cited references66

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          Mortality in sickle cell disease. Life expectancy and risk factors for early death.

          Information on life expectancy and risk factors for early death among patients with sickle cell disease (sickle cell anemia, sickle cell-hemoglobin C disease, and the sickle cell-beta-thalassemias) is needed to counsel patients, target therapy, and design clinical trials. We followed 3764 patients who ranged from birth to 66 years of age at enrollment to determine the life expectancy and calculate the median age at death. In addition, we investigated the circumstances of death for all 209 adult patients who died during the study, and used proportional-hazards regression analysis to identify risk factors for early death among 964 adults with sickle cell anemia who were followed for at least two years. Among children and adults with sickle cell anemia (homozygous for sickle hemoglobin), the median age at death was 42 years for males and 48 years for females. Among those with sickle cell-hemoglobin C disease, the median age at death was 60 years for males and 68 years for females. Among adults with sickle cell disease, 18 percent of the deaths occurred in patients with overt organ failure, predominantly renal. Thirty-three percent were clinically free of organ failure but died during an acute sickle crisis (78 percent had pain, the chest syndrome, or both; 22 percent had stroke). Modeling revealed that in patients with sickle cell anemia, the acute chest syndrome, renal failure, seizures, a base-line white-cell count above 15,000 cells per cubic millimeter, and a low level of fetal hemoglobin were associated with an increased risk of early death. Fifty percent of patients with sickle cell anemia survived beyond the fifth decade. A large proportion of those who died had no overt chronic organ failure but died during an acute episode of pain, chest syndrome, or stroke. Early mortality was highest among patients whose disease was symptomatic. A high level of fetal hemoglobin predicted improved survival and is probably a reliable childhood forecaster of adult life expectancy.
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            Sickle Cell Disease

            New England Journal of Medicine, 376(16), 1561-1573
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              Sickle cell disease

              Sickle cell disease is a common and life-threatening haematological disorder that affects millions of people worldwide. Abnormal sickle-shaped erythrocytes disrupt blood flow in small vessels, and this vaso-occlusion leads to distal tissue ischaemia and inflammation, with symptoms defining the acute painful sickle-cell crisis. Repeated sickling and ongoing haemolytic anaemia, even when subclinical, lead to parenchymal injury and chronic organ damage, causing substantial morbidity and early mortality. Currently available treatments are limited to transfusions and hydroxycarbamide, although stem cell transplantation might be a potentially curative therapy. Several new therapeutic options are in development, including gene therapy and gene editing. Recent advances include systematic universal screening for stroke risk, improved management of iron overload using oral chelators and non-invasive MRI measurements, and point-of-care diagnostic devices. Controversies include the role of haemolysis in sickle cell disease pathophysiology, optimal management of pregnancy, and strategies to prevent cerebrovascular disease.
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                Author and article information

                Journal
                JAMA Network Open
                JAMA Netw Open
                American Medical Association (AMA)
                2574-3805
                November 01 2019
                November 15 2019
                : 2
                : 11
                : e1915374
                Affiliations
                [1 ]Outcomes Insights Inc, Westlake Village, California
                [2 ]Global Blood Therapeutics Inc, South San Francisco, California
                [3 ]Global Pediatric Medicine, St. Jude Children’s Research Hospital, Memphis, Tennessee
                [4 ]Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland
                Article
                10.1001/jamanetworkopen.2019.15374
                7b4e4521-ec88-4c09-b1f1-e78fe4bebedd
                © 2019
                History

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