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A controlled trial to improve care for seriously ill hospitalized patients. The study to understand prognoses and preferences for outcomes and risks of treatments (SUPPORT). The SUPPORT Principal Investigators
Abstract
OBJECTIVES: To improve end-of-life decision making and reduce the frequency of a mechanically supported, painful, and prolonged process of dying. DESIGN: A 2-year prospective observational study (phase I) with 4301 patients followed by a 2-year controlled clinical trial (phase II) with 4804 patients and their physicians randomized by specialty group to the intervention group (n = 2652) or control group (n = 2152). SETTING: Five teaching hospitals in the United States. PATIENTS: A total of 9105 adults hospitalized with one or more of nine life-threatening diagnoses; an overall 6-month mortality rate of 47%. INTERVENTION: Physicians in the intervention group received estimates of the likelihood of 6-month survival for every day up to 6 months, outcomes of cardiopulmonary resuscitation (CPR), and functional disability at 2 months. A specifically trained nurse had multiple contacts with the patient, family, physician, and hospital staff to elicit preferences, improve understanding of outcomes, encourage attention to pain control, and facilitate advance care planning and patient-physician communication. RESULTS: The phase I observation documented shortcomings in communication, frequency of aggressive treatment, and the characteristics of hospital death: only 47% of physicians knew when their patients preferred to avoid CPR: 46% of do-not-resuscitate (DNR) orders were written within 2 days of death; 38% of patients who died spent at least 10 days in an intensive care unit (ICU); and for 50% of conscious patients who died in the hospital, family members reported moderate to severe pain at least half the time. During the phase II intervention, patients experienced no improvement in patient-physician communication (eg, 37% of control patients and 40% of intervention patients discussed CPR preferences) or in the five targeted outcomes, ie, incidence or timing of written DNR orders (adjusted ratio, 1.02; 95% confidence interval [CI], 0.90 to 1.15), physicians' knowledge of their patients' preferences not to be resuscitated (adjusted ratio, 1.22; 95% CI, 0.99 to 1.49), number of days spent in an ICU, receiving mechanical ventilation, or comatose before death (adjusted ratio, 0.97; 95% CI, 0.87 to 1.07), or level of reported pain (adjusted ratio, 1.15; 95% CI, 1.00 to 1.33). The intervention also did not reduce use of hospital resources (adjusted ratio, 1.05; 95% CI, 0.99 to 1.12). CONCLUSIONS: The phase I observation of SUPPORT confirmed substantial shortcomings in care for seriously ill hospitalized adults. The phase II intervention failed to improve care or patient outcomes. Enhancing opportunities for more patient-physician communication, although advocated as the major method for improving patient outcomes, may be inadequate to change established practices. To improve the experience of seriously ill and dying patients, greater individual and societal commitment and more proactive and forceful measured may be needed.
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Metadata
- Authors
- Connors, A. F., Dawson, N. V., Desbiens, N. A., Fulkerson, W. J., Goldman, L., Knaus, W. A., Lynn, J., Oye, R. K., Bergner, M., Damiano, A., Hakim, R. B., Murphy, D. J., Teno, J. M., Virnig, B. A., Wagner, D. P., Wu, A. W., Yasui, Y., Robinson, D. K., Kreling, B. A., Dulac, J., Baker, R., Holayel, S., Meeks, T., Mustafa, M., Vegarra, J., Alzola, C., Harrell, F. E., Cook, E. F., Hamel, M. B., Peterson, L., Phillips, R. S., Tsevat, J., Forrow, L., Lesky, L., Davis, R., Kressin, N. R., Solzan, J., Puopolo, A. L., Barrett, L. Q., Bucko, N., Brown, D., Burns, M., Foskett, C., Hozid, A., Keohane, C., Martinez, C., McWeeney, D., Melia, D., Otto, S., Sheehan, K., Smith, A., Tofias, L., Arthur, B., Collins, C., Cunnion, M., Dyer, D., Kulak, C., Michaels, M., O'Keefe, M., Parker, M., Tuchin, L., Wax, D., Weld, D., Hiltunen, L., Marks, G., Mazzapica, N., Medich, C., Soukup, J., Califf, R. M., Galanos, A. N., Kussin, P., Muhlbaier, L. H., Winchell, M., Mallatratt, L., Akin, E., Belcher, L., Buller, E., Clair, E., Drew, L., Fogelman, L., Frye, D., Fraulo, B., Gessner, D., Hamilton, J., Kruse, K., Landis, D., Nobles, L., Oliverio, R., Wheeler, C., Banks, N., Berry, S., Clayton, M., Hartwell, P., Hubbard, N., Kussin, I., Norman, B., Noveau, J., Read, H., Warren, B., Castle, J., Turner, K., Perdue, R., Coulton, C., Landefeld, C. S., Speroff, T., Youngner, S., Kennard, M. J., Naccaratto, M., Roach, M. J., Blinkhorn, M., Corrigan, C., Geric, E., Haas, L., Ham, J., Jerdonek, J., Landy, M., Marino, E., Olesen, P., Patzke, S., Repas, L., Schneeberger, K., Smith, C., Tyler, C., Zenczak, M., Anderson, H., Carolin, P., Johnson, C., Leonard, P., Leuenberger, J., Palotta, L., Warren, M., Finley, J., Ross, T., Solem, G., Zronek, S., Davis, S., Broste, S., Layde, P., Kryda, M., Reding, D. J., Vidaillet, H. J., Folien, M., Mowery, P., Backus, B. E., Kempf, D. L., Kupfer, J. M., Maassen, K. E., Rohde, J. M., Wilke, N. L., Wilke, S. M., Albee, E. A., Backus, B., Franz, A. M., Henseler, D. L., Herr, J. A., Leick, I., Lezotte, C. L., Meddaugh, L., Duffy, L., Johnson, D., Kronenwetter, S., Merkel, A., Bellamy, P. E., Hiatt, J., Wenger, N. S., Leal-Sotelo, M., Moranville-Hawkins, D., Sheehan, P., Watanabe, D., Yamamoto, M. C., Adema, A., Adkins, E., Beckson, A.-M., Carter, M., Duerr, E., El-Hadad, A., Farber, A., Jackson, A., Justice, J., O'Meara, A., Benson, L., Cheney, L., Medina, C., Moriarty, J., Baker, K., Marsden, C., Watne, K., Goya, D., Desbiens, N., Fulkerson, W. J., Carpenter, C. C. J., Carson, R. A., Detmer, D. E., Steinwachs, D. E., Mor, V., Harootyan, R. A., Leaf, A., Watts, R., Williams, S., & Ransohoff, D. F.
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 1995-11-22
- Volume
- 274
- Issue
- 20
- Pages
- 1591
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- OpenAlex
- W2137325786
- Cited by
- 2,764
- References
- 2
- FWCI
- 113.48
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.