Peter Falkenhagen
Qualitätsmanagementbeauftragter
Gustav-Adolf-Straße 15 a
04849 Bad Düben
Phone:
034243
-76-2052
Mail:
ed.nilcidem@negahneklaF.reteP
Beteiligung aller Mitglieder der Klinikleitung und des Qualitätsmanagementbeauftragten
Conference frequency: jährlich
Anlassbezoge Teilnehmerauswahl
Conference frequency: jährlich
No. | Explanation |
---|---|
RM01 |
Comprehensive quality and/or risk management documentation (QM/RM documentation) is available Qualitätsmanagement-Handbuch (08.12.2022) |
RM02 |
Regular further education and training measures |
RM03 |
Employee surveys |
RM04 |
Clinical emergency management Qualitätsmanagement-Handbuch (08.12.2022) |
RM05 |
Pain management Qualitätsmanagement-Handbuch (08.12.2022) |
RM06 |
Fall prophylaxis Qualitätsmanagement-Handbuch (08.12.2022) |
RM07 |
Use of a standardised concept for pressure ulcer prophylaxis (e.g. “Expert Standard for Pressure Ulcer Prophylaxis in Nursing”) Qualitätsmanagement-Handbuch (08.12.2022) |
RM08 |
Regulated handling of custodial measures Qualitätsmanagement-Handbuch (08.12.2022) |
RM09 |
Regulated handling of occurring malfunctions of devices Qualitätsmanagement-Handbuch (08.12.2022) |
RM10 |
Structured implementation of interdisciplinary case discussions/conferences Case review conference
|
RM12 |
Use of standardised information sheets |
RM13 |
Application of standardised surgical check lists |
RM14 |
Preoperative summary of predictable critical surgical steps, surgical time and expected blood loss Qualitätsmanagement-Handbuch (08.12.2022) |
RM15 |
Preoperative, complete presentation of necessary findings Qualitätsmanagement-Handbuch (08.12.2022) |
RM16 |
Procedure to avoid procedural and patient mix-ups Qualitätsmanagement-Handbuch (08.12.2022) |
RM17 |
Standards for recovery and postoperative care Qualitätsmanagement-Handbuch (08.12.2022) |
RM18 |
Discharge management Qualitätsmanagement-Handbuch (08.12.2022) |
Conference frequency: bei Bedarf
Verträglichkeits- und Therapieerfolgskontrolle bei Medikamenten (Berichterstattung bei Auftreten unerwünschter Arzneimittelwirkungen) Teilnahme am Endoprothesenregister Deutschland
No. | Explanation |
---|---|
IF01 |
Documentation and procedural instructions for handling the error reporting system are available As of: 03.03.2020 |
IF02 |
Internal evaluation of the received reports taken quartalsweise |
IF03 |
Training of employees in handling the error reporting system and in implementing the findings from the error reporting system taken jährlich |
Conference frequency: