TMLA international digital scientific congresses Fifth edition

5th International Conference on Healthcare Quality and Patient Safety

Clinical Research into Safer Care: Evidence, Implementation and Patient Outcomes

Monday, 16 November 202608:00–18:00 GMT (London)Online · recorded-only

Recorded material with written discussion. There is no live session.

Congress focus

Research → safer care

Evidence, implementation and patient outcomes across the care pathway.

Structured abstracts are free

Submit research, a systematic review, clinical audit, quality-improvement project or case report. Submission does not imply acceptance.

Written scientific discussion

The congress uses recorded material and written discussion rather than live sessions.

Attendance is separate

Register to attend for £149. Abstract submission is independent of attendance registration.

Twelve routes from evidence to safer care

Congress topics

Each topic connects rigorous inquiry with preventable harm, implementation in real services and patient-centred outcomes.

01

Diagnostic uncertainty, test-result follow-up and missed diagnoses

Study how diagnostic evidence and follow-up systems can reduce preventable harm while preserving a patient’s understanding of uncertainty.

02

Deprescribing, polypharmacy and medication harm at discharge

Examine evidence on medication review at discharge, with attention to treatment burden, adverse effects and outcomes that matter to patients.

03

Clinical AI evaluation: calibration, bias and post-deployment monitoring

Evaluate clinical AI in real care settings: calibration, bias, monitoring and the safety consequences of decisions made with its support.

04

Sepsis pathways: time-critical decisions and treatment-related harm

Explore research on sepsis recognition and escalation that balances time-critical action with the potential for treatment-related harm.

05

Antimicrobial stewardship, resistance and infection prevention

Connect stewardship and infection-prevention evidence with safer prescribing, resistance reduction and person-centred care outcomes.

06

Surgical outcomes, shared decisions and patient-reported recovery

Consider surgical evidence, shared decisions and recovery measures that reflect both safety and patient-reported experience.

07

Maternal and newborn safety: escalation and continuity of care

Address escalation, communication and continuity across maternal and newborn care, focusing on preventable harm and family-centred outcomes.

08

Paediatric dosing, weight-based prescribing and safer handovers

Investigate dosing, prescribing and handover practices that make paediatric care safer for children and the people who care for them.

09

Frailty, delirium, falls and safer care for older adults

Examine evidence for safer care in frailty, delirium and falls, including outcomes valued by older adults and their supporters.

10

Device, infusion and transfusion safety across specialties

Study device, infusion and transfusion safety across specialties, linking systems learning with avoidable-harm reduction.

11

Patient partnership, health literacy and equity in safety research

Bring patient partnership, health literacy and equity into safety research so findings are meaningful across diverse communities.

12

Research into practice: pragmatic trials, audit and implementation science

Translate pragmatic trials, audit and implementation science into safer everyday care while testing whether improvements endure for patients.

Thematic programme · GMT

Scientific programme

A one-day thematic programme connecting clinical evidence, safer systems and patient-centred outcomes.

Opening orientation

Theme, recorded-only format and written discussion pathway.

Programme begins at 08:00 GMT

Evidence at the diagnostic edge

Diagnostic uncertainty, test-result follow-up and missed diagnoses.

Medicines, infection and safe transitions

Deprescribing, antimicrobial stewardship and medication harm at discharge.

Written discussion interval

A dedicated interval for participant reflection and written questions.

Technology under evaluation

Clinical AI evaluation, device safety and monitoring after implementation.

Time-critical pathways

Sepsis decisions, escalation and treatment-related harm.

Midday reading interval

Time to review recorded material and contribute to written discussion.

Safety across the life course

Maternal, newborn, paediatric, frailty and older-adult safety.

Care shaped with patients

Shared decisions, health literacy, equity and patient-reported recovery.

Audit to implementation

Pragmatic trials, clinical audit and quality-improvement learning.

Structured abstract focus

Research, systematic review, clinical audit, QIP and case-report methods.

Written discussion synthesis

Closing thematic reflection and next steps for safer care research.

Programme close

End of the scheduled congress day.

Scientific review

Scientific review panel

Scientific review considers methodological quality, relevance and the contribution of each abstract to safer patient care.

Dr.Frances Gay Pia-Acuńa

Scientific review panel

DR. RICARDO G. DRAGON

Scientific review panel

VANESSA MARIE O. DEMATA

Scientific review panel

Read the scientific review process Reviewer sign in

For researchers

Bring evidence into safer care

Submit free with clear field-by-field guidance and no patient identifiers. Follow dated updates in your private record, read review comments and respond with a revised scientific version when requested.

Submit a free abstract

For attendees

Join the congress day

Register to attend for £149. No payment is collected by the registration form; attendance access is activated only after payment is confirmed.

Register to attend · £149