Sepsis Among Medicare Beneficiaries: 2. The Trajectories of Sepsis, 2012-2018.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
03 2020
Historique:
entrez: 15 2 2020
pubmed: 15 2 2020
medline: 24 10 2020
Statut: ppublish

Résumé

To distinguish characteristics of Medicare beneficiaries who will have an acute inpatient admission for sepsis from those who have an inpatient admission without sepsis, and to describe their further trajectories during and subsequent to those inpatient admissions. Analysis of paid Medicare claims via the Centers for Medicare and Medicaid Services DataLink Project. All U.S. acute care hospitals, excepting federal hospitals (Veterans Administration and Defense Health Agency). Medicare beneficiaries, 2012-2018, with an inpatient hospital admission including one or more explicit sepsis codes. None. Prevalent diagnoses in the year prior to the inpatient admission; healthcare contacts in the week prior to the inpatient admission; discharges, transfers, readmissions, and deaths (trajectories) for 6 months following discharge from the inpatient admission. Beneficiaries with no sepsis inpatient hospital admission for a year prior to an index hospital admission for sepsis were nearly indistinguishable by accumulated diagnostic codes from beneficiaries who had an index hospital admission without sepsis. Although the timing of healthcare services in the week prior to inpatient hospital admission was similar among beneficiaries who would be admitted for sepsis versus those whose inpatient admission did not include a sepsis code, the setting differed: beneficiaries destined for a sepsis admission were more likely to have received skilled nursing or unskilled nursing (e.g., nursing aide for activities of daily living) care. In contrast, comparing beneficiaries who had been free of any inpatient admission for an entire year and then required an inpatient admission, acute inpatient stays that included a sepsis code led to more than three times as many deaths within 1 week of discharge, with more admissions to skilled nursing facilities and fewer discharges to home. Comparing all beneficiaries who were admitted to a skilled nursing facility after an inpatient hospital admission, those who had sepsis coded during the index admission were more likely to die in the skilled nursing facility; more likely to be readmitted to an acute inpatient hospital and subsequently die in that setting; or if they survive to discharge from the skilled nursing facility, they are more likely to go next to a custodial nursing home. Although Medicare beneficiaries destined for an inpatient hospital admission with a sepsis code are nearly indistinguishable by other diagnostic codes from those whose admissions will not have a sepsis code, their healthcare trajectories following the admission are worse. This suggests that an inpatient stay that included a sepsis code not only identifies beneficiaries who were less resilient to infection but also signals increased risk for worsening health, for mortality, and for increased use of advanced healthcare services during and postdischarge along with an increased likelihood of an inpatient hospital readmission.

Identifiants

pubmed: 32058367
doi: 10.1097/CCM.0000000000004226
pii: 00003246-202003000-00003
pmc: PMC7017944
doi:

Substances chimiques

Metalloproteins 0
Succinates 0
iron protein succinylate VBJ9L90P4L

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

289-301

Commentaires et corrections

Type : CommentIn

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Auteurs

Timothy G Buchman (TG)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.
Emory Critical Care Center, Emory University, Atlanta, GA.

Steven Q Simpson (SQ)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.
Division of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Kansas, Kansas City, KS.

Kimberly L Sciarretta (KL)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Kristen P Finne (KP)

Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Nicole Sowers (N)

Acumen, LLC, Burlingame, CA.

Michael Collier (M)

Acumen, LLC, Burlingame, CA.

Saurabh Chavan (S)

Acumen, LLC, Burlingame, CA.

Ibijoke Oke (I)

Acumen, LLC, Burlingame, CA.

Meghan E Pennini (ME)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Aathira Santhosh (A)

Acumen, LLC, Burlingame, CA.

Marie Wax (M)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Robyn Woodbury (R)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Steve Chu (S)

Center for Medicare and Medicaid Services, United States Department of Health and Human Services, Baltimore, MD.

Tyler G Merkeley (TG)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Gary L Disbrow (GL)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Rick A Bright (RA)

Biomedical Advanced Research and Development Authority, Office of the Assistant Secretary for Preparedness and Response, United States Department of Health and Human Services, Washington, DC.

Thomas E MaCurdy (TE)

Acumen, LLC, Burlingame, CA.
Department of Economics, Stanford University, Stanford, CA.
Hoover Institution, Stanford University, Stanford, CA.
Stanford Institute for Economic Policy Research, Stanford University, Stanford, CA.

Jeffrey A Kelman (JA)

Center for Medicare and Medicaid Services, United States Department of Health and Human Services, Baltimore, MD.

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