Table 2.
Study first author | Total patient numbers | Total RRT reviews | NFR/LOMT before RRT review | NFR/LOMT during or after RRT review | Escalation to higher level care, e.g. ICU | In-hospital mortality | Formal advance care planning | Discussion with patient, family or proxy decision maker | Palliative care consultation |
---|---|---|---|---|---|---|---|---|---|
Austin24 | Ca centre: 135 Gen med: 422 Total: 557 |
NS | 9.6%* | 1.5% D*
13.3% A* |
34.8% | 21.5% | NS | NS | 1.5% B*
4.4% A* |
Boniatti25 | 901 | 1051 | 5.1% | 3.3% A | 55.4% | 46.9% at 30 days | NS | NS | NS |
Calzavacca26 | 1664 | 2237 | 22.7% | 8.5% A | 16% | 34.3% | NS | NS | NS |
Calzavacca27 | 200 | 200 | 15% | 9.5% | 17.5% | 27% | NS | NS | NS |
Calzavacca28 | 228 | 251 | 14.5% | 9.2% | 16.7% | 40% | NS | NS | NS |
Cardona-Morrell29 | 2353 | 328# | 12.5% | 32.5% D | NS | 7.8% of patients aged 60+ | 5% | NS | NS |
Casamento30 | NS | 195 | 20% | 15% | 28% | 34% | NS | NS | NS |
Chen20 | NS | 4161^ | 45.4% | 3.85% | 19.1% | 47.2% | NS | NS | NS |
Dargin31 | 998 | 1156 | 8.65% | 5% D | 39.7% | 17% | NS | 44%@ | 2.68% |
Downar32 | NS | 291 | 8.9% | NS | 33% | 24.7% | NS | 16.5% within 48 h | 0% B 13% within 48 h^^ 17% after 48 h^^ |
Gouda and Alqahtani33 | NS | 5904 | 6.66% D 1.27% A |
34.5% | NS | NS | NS | NS | |
Jäderling34 | 1818 | 2189 | 4.7% | 16.3% D 14.4% A |
31.5% | 25.6% | NS | NS | NS |
Jäderling35 | NS | 3063 | 34.2% Sweden 30.8% Australia |
14.4% Sweden 12.6% Australia |
18.7% Sweden 9.9% Australia |
27.7% Sweden 29.4% Australia |
NS | NS | NS |
Jones11 | 518 | 652 | 20.3% | 10.8% | NS | NS | NS | NS | |
Medical Emergency Team End-of-Life Care investigators14 | 518 | 652 | Early/late reviews 16.9%/26.3% |
Early/late reviews 25.4%/35.9% |
NS | Early/late review 12.8%/32.3% |
NS | NS | NS |
Knott17 | 71 | NS | 32% | 62% | NS | 42% | NS | NS | NS |
O’Horo36 | NS | Retrospective 4408 Prospective 135 |
Retrospective/prospective study 13.5%/16.3% |
Retrospective/prospective study 7.2% D /5.9% D |
Retrospective study: 58.6% Prospective study: 62.2% |
NS | NS | NS | NS |
Parr37 | 559 | 713 | 0% | 4.8% A | 45% | 6.9% D | NS | NS | NS |
Psirides38 | 313 | 351 | NS | 31.3% (22.5% NFR, 8.8% other LOMT) | 13.1% | 2.8% at time of RRT 19.8% at 30 days |
NS | NS | NS |
Schneider39 | 458 | 557 | 19.7% | 7% D | 11.4% | 20.1% | NS | NS | NS |
Silva40 | 389 | 389 | 7.7% B | 24.1% D | 39.3% | 18.7% D 52.8% overall |
NS | NS | NS |
Smith41 | 1117 | NS | 11.01% B | 5.55% D | 17.91% | 18.8%: deterioration group 62.64%: cardiac arrest group |
NS | NS | NS |
Smith42 | 2843 | 3860 | 15.2% | 5.7% D | 15.5% | 12.8% early RRT review 16.7% intermediate RRT review 30.6% for late RRT review 59.4% for patients who had cardiac arrest |
NS | NS | NS |
Smith13 | NS | 390 | 11.5% | 16.4% A | 54% | NS | NS | NS | NS |
Stelfox21 | 5103 | NS | 3.8% 4910/5103 | 8.05% D | 24.83% | 32.6% | NS | NS | NS |
Sulistio19 | 351 | 456 | 17.9% NFR 1.42% LOMT |
21.7% | 24.5% | NS | NS | 15.1% | |
Sundararajan43 | NS | 994 | Group 1 LOMT not associated with RRT team review 100% |
Group 2: Limitations of Medical Treatment at time of RRT review 5% | NS | NS | NS | Group 1 50% with patient 90% with next of kin Group 2: 18% with patient 58% with next of kin |
NS |
Tam44 | 5320 | NS | 58% | 17% D | 8.4% of ‘end-of-life’ group 17% of ‘non-end-of-life’ group |
25% of ‘end-of-life’ group 8% of ‘non-end-of-life’ group |
NS | NS | 34% of ‘end-of-life’ group 5.3% of ‘non-end-of-life’ group |
Tirkkonen45 | 640 | 774 | 0% | 9.22% | 26% (no LOMT) 3.4% (LOMT) |
14% (no LOMT) 44% (LOMT) |
NS | 76% for new LOMT (7% of total patients) | NS |
Tirkkonen46 | 458 | 569 | 6.3% | 7.4% D | 27.2% | 26% | NS | NS | NS |
Visser47 | 132 | 141 | 79.4% | 24.2% D | 10.6% | 28% | NS | NS | NS |
White48 | 800 | 1151 | 22.2% | 2% D 5% A |
17.2% | 12.6% | NS | NS | NS |
A, after; B, before; D, During; ICU, intensive care unit; LOMT, limitations of medical treatment; NFR, not for resuscitation; NS, not stated; RRT, Rapid Response Team.
Cancer centre patients.
Included 184 cases where patient died following RRT review; 144 controls who lived.
Hospitals with an RRT (control hospitals without RRT were excluded).
Resuscitation status at admission.
Subset of patients who had a change in NFR status following the RRT review.