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Tele-ICU rounds increased breathing trials and shortened weaning time without improving weaning success

Critical care (London, England) (PubMed)Aug 7, 2026

AI-summarized from the linked source. Educational brief, not medical advice.

Brief summary

A secondary analysis of a stepped-wedge cluster-randomized ICU trial found that daily telemedicine rounds by an intensivist and ICU nurse increased spontaneous breathing-trial use and shortened time from the first trial to successful weaning, but did not improve the overall weaning-success rate.

What NurseJet pulled from the source

Among 308 ventilated patients with at least one spontaneous breathing trial, trials occurred on 51% of intervention patient-days versus 27% of control patient-days. Adjusted analysis associated the intervention with shorter time to successful weaning, while weaning classification and success did not differ significantly.

Why this matters for nurses

ICU nurses identify readiness cues, coordinate spontaneous breathing trials, monitor tolerance, and communicate barriers during weaning. The study suggests structured remote interprofessional review can improve process reliability, while the absence of a clear success-rate benefit keeps attention on patient selection and local workflow.

Bedside takeaway

Make daily weaning readiness and breathing-trial plans visible, documented, reassessed, and easy for bedside and tele-ICU teams to coordinate.

How This Applies in Practice

Use this when: Participating in daily ventilator-weaning review for an ICU patient within an approved bedside or tele-ICU pathway.

On your shift

  • Confirm that readiness screening, sedation targets, mobility, secretion management, and the spontaneous breathing-trial plan are addressed during rounds.
  • Document trial timing, tolerance criteria, reasons for deferral or failure, and the next reassessment so remote and bedside teams share one plan.
  • Escalate respiratory, neurological, or hemodynamic instability immediately rather than waiting for the next scheduled telemedicine review.
Keep in mind: The study does not establish one weaning schedule or tele-ICU model for every patient or unit. Follow the critical-care protocol, facility policy, and provider orders.

Key takeaways

  • The analysis included 308 patients from ten ICU clusters who received invasive ventilation for at least two days and at least one spontaneous breathing trial.
  • Spontaneous breathing trials occurred on 51% of intervention patient-days and 27% of control patient-days.
  • Weaning success was 36% with the intervention and 28% under the control condition, a nonsignificant difference.
  • The adjusted model associated telemedicine support with a shorter interval from the first breathing trial to successful weaning.

Practice implications

  • During an approved weaning pathway, document daily readiness screening, the planned breathing trial, tolerance findings, sedation and mobility barriers, and the next reassessment. Use tele-ICU input to clarify the plan without delaying bedside escalation for instability.

Limitations & cautions

  • This was a secondary analysis of one metropolitan stepped-wedge trial, with 55 patients in the control condition and 253 in the intervention condition. It included only patients ventilated for at least two days who had at least one breathing trial, and the intervention bundled telemedicine rounding around several ICU quality indicators, limiting causal attribution and generalizability.
  • AI-summarized from the linked source. Review the original article before applying to practice.

Citations

Exact source links

Public citations are filtered to exact credible source pages. Homepage-only or invalid links stay in admin review and are not shown here.

Critical care (London, England) (PubMed)

Critical care (London, England) (PubMed). The impact of an intensive care telemedicine program on weaning from invasive ventilation: a secondary analysis of the ERIC trial.

Open original source

https://pubmed.ncbi.nlm.nih.gov/42568095/

Professional education only

This summary does not replace clinical judgment, facility policy, provider orders, or official guidelines. Verify practice changes against the original source and local protocol.

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