Increasing Rate of Hospital Admissions in Patients With Amyloidosis (from the National Inpatient Sample)

被引:25
作者
Sperry, Brett W. [1 ,2 ]
Saeed, Ibrahim M. [1 ,2 ]
Raza, Shahzad [2 ,3 ]
Kennedy, Kevin F. [1 ,2 ]
Hanna, Mazen [4 ]
Spertus, John A. [1 ,2 ]
机构
[1] St Lukes Mid Amer Heart Inst, Kansas City, MO 64111 USA
[2] Univ Missouri, Kansas City, MO 64110 USA
[3] St Lukes Hosp, Canc Inst, Kansas City, MO USA
[4] Cleveland Clin Fdn, 9500 Euclid Ave, Cleveland, OH 44195 USA
关键词
MONOCLONAL GAMMOPATHY; SYSTEMIC AMYLOIDOSIS; PREVALENCE;
D O I
10.1016/j.amjcard.2019.08.045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac amyloidosis is an increasingly recognized cause of heart failure with preserved or mildly reduced ejection fraction with emerging treatment options. We sought to analyze the temporal trends and impact of hospital admissions in patients with amyloidosis. The National Inpatient Sample was queried to identify patients from 2005 to 2014 who were hospitalized with a diagnosis of amyloidosis using ICD9 codes. Trends over time of prevalence, demographics, co-morbidities, and outcomes were described. Propensity-matching was used to assess the impact of amyloidosis on in-hospital outcomes, including mortality. A total of 156,914 admissions in patients with amyloidosis (age 69.86 +/- 12.33 years, 45.7% female, 68.5% Caucasian) were identified. Hospitalizations more than doubled with a peak of 21,740 per year and 62 per 100,000 admissions in 2014. Over time, patients admitted with amyloidosis were older and more likely to have co-morbid medical conditions. A diagnosis of heart failure was present in 34.7% of patients, increased over time (p = 0.001), and was associated with further morbidity and mortality. In a propensity-matched analysis, patients admitted with amyloidosis had a longer length of stay (7.5 vs 6.2 days), were less likely to be discharged home (43.6% vs 48.7%), and were more likely to die during the hospitalization (7.4% vs 4.9%, p <0.001 for all). In conclusion, inpatient hospitalizations in the United States in patients with amyloidosis have increased over time and are associated with high morbidity and mortality, particularly when there is concomitant heart failure. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:1765 / 1769
页数:5
相关论文
共 15 条
  • [1] Geographic Disparities in Reported US Amyloidosis Mortality From 1979 to 2015 Potential Underdetection of Cardiac Amyloidosis
    Alexander, Kevin M.
    Orav, John
    Singh, Avinainder
    Jacob, Sophia A.
    Menon, Adil
    Padera, Robert F.
    Kijewski, Marie F.
    Liao, Ronglih
    Di Carli, Marcelo F.
    Laubach, Jacob P.
    Falk, Rodney H.
    Dorbala, Sharmila
    [J]. JAMA CARDIOLOGY, 2018, 3 (09) : 865 - 870
  • [2] Comorbidity measures for use with administrative data
    Elixhauser, A
    Steiner, C
    Harris, DR
    Coffey, RN
    [J]. MEDICAL CARE, 1998, 36 (01) : 8 - 27
  • [3] A long-term study of prognosis in monoclonal gammopathy of undetermined significance
    Kyle, RA
    Therneau, TM
    Rajkumar, SV
    Offord, JR
    Larson, DR
    Plevak, MF
    Melton, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (08) : 564 - 569
  • [4] Prevalence of monoclonal gammopathy of undetermined significance
    Kyle, RA
    Therneau, TM
    Rajkumar, SV
    Larson, DR
    Plevak, MF
    Offord, JR
    Dispenzieri, A
    Katzmann, JA
    Melton, LJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (13) : 1362 - 1369
  • [5] KYLE RA, 1992, BLOOD, V79, P1817
  • [6] Incidence of AL Amyloidosis in Olmsted County, Minnesota, 1990 through 2015
    Kyle, Robert A.
    Larson, Dirk R.
    Kurtin, Paul J.
    Kumar, Shaji
    Cerhan, James R.
    Themeau, Terry M.
    Rajkumar, S. Vincent
    Vachon, Celine M.
    Dispenzieri, Angela
    [J]. MAYO CLINIC PROCEEDINGS, 2019, 94 (03) : 465 - 471
  • [7] Systemic immunoglobulin light chain amyloidosis
    Merlini, Giampaolo
    Dispenzieri, Angela
    Sanchorawala, Vaishali
    Schoenland, Stefan O.
    Palladini, Giovanni
    Hawkins, Philip N.
    Gertz, Morie A.
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2018, 4
  • [8] The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans
    Quarta, C. Cristina
    Buxbaum, Joel N.
    Shah, Amil M.
    Falk, Rodney H.
    Claggett, Brian
    Kitzman, Dalane W.
    Mosley, Thomas H.
    Butler, Kenneth R.
    Boerwinkle, Eric
    Solomon, Scott D.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (01) : 21 - 29
  • [9] Epidemiology of AL amyloidosis: a real-world study using US claims data
    Quock, Tiffany P.
    Yan, Tingjian
    Chang, Eunice
    Guthrie, Spencer
    Broder, Michael S.
    [J]. BLOOD ADVANCES, 2018, 2 (10) : 1046 - 1053
  • [10] Estimating the global prevalence of transthyretin familial amyloid polyneuropathy
    Schmidt, Hartmut H.
    Waddington-Cruz, Marcia
    Botteman, Marc F.
    Carter, John A.
    Chopra, Avijeet S.
    Hopps, Markay
    Stewart, Michelle
    Fallet, Shari
    Amass, Leslie
    [J]. MUSCLE & NERVE, 2018, 57 (05) : 829 - 837