Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03759652
Other study ID # PTZS Neurosurgery 2018
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2003
Est. completion date December 2017

Study information

Verified date November 2018
Source Polskie Towarzystwo Zakazen Szpitalnych
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Continuous surveillance in 2003-2017 allowed to detect HAIs in patients staying in a 42-bed neurosurgery unit with 6 intensive neurosurgical supervision beds. 10,332 surgical patients were qualified for the study. The study was carried out in the framework of a national surveillance of HAI programme following methodology recommended by Healthcare-Associated Infections Surveillance Network (HAI-Net), European Centre for Disease Prevention and Control. Intervention in this before-after study (2003-2017) comprised standardised surveillance of HAI with regular analysis and feedback.


Description:

Supervision of HAIs was carried out in the neurosurgery unit in 2003-2017 in St. Luke Provincial Hospital in Tarnów, Poland. The department offers 42 hospital beds (including 6 intensive supervision beds, where mechanical ventilation is also used). Patients in very poor clinical condition do not stay in this department as they are generally sent to a separate general intensive care unit. Active surveillance of infections was implemented in the hospital in 2001 and the experiences concerning the neurosurgery unit were already the subject of previous general analyses not including trend analysis or detailed analyses of various HAI clinical forms [Wałaszek NCH 2015]. The Infection Control Team consists of a doctor, who is employed on a 1/3 full-time equivalent basis and 4 full-time epidemiological nurses.

The data analysed involve the time when the unit in question began targeted, active surveillance of infections, initially: 2003-2012, using tools (definitions, protocols) in accordance with the National Healthcare Safety Network (NHSN) [Emori, NNIS], then from 2012, HAI recognition methodology and HAI record-keeping has followed the Surveillance Network (HAI-Net), European Centre for Disease Prevention and Control (ECDC) [ECDC 4.3, 2012; HAI-Net ICU 1.02. ECDC; 2015]. For the purposes of this analysis, HAI cases originally qualified in 2002-2012 according to the NHSN criteria were retrospectively subjected to reclassification according to the ECDC definitions from 2012 (they concerned BSI, PN and UTI), hence, all HAI cases were qualified into individual HAI categories according to the ECDC case definition keeping the division into: catheter-related BSI and BSI secondary to another infection, five subcategories of PN and three forms of SSI. The surgeries performed were stratified by type of operation conforming to the International Classification of Procedures in Medicine ICD 9-CM, according to the NHSN code (International Classification of Diseases) (Supplementarty Material, Table 1).

Beginning in 2003, changes were being implemented as regards supervision of infections by the Infection Control Team together with the staff of the departments (neurosurgery, operating block and infection control team), which encompassed, among others:

1. hospital admission rules for shortening of the pre-operative stay and optimal patient preparation for surgery to limit emergency surgery; preparation of the surgical team

2. work organization of the operating block: among others, preoperative checklist, surgical hand hygiene, preparation of the operating field and surgical drape, application of antiseptic to the edges of the wound before sewing it;

3. perioperative procedure: patient preparation for surgery, among others, bathing the patient immediately prior to surgery, hair removal, changing the bed linen and patient's clothing immediately before surgery, patient care during the postoperative period, and above all, the 5 moments for hand hygiene and post-operative dressing and wound control.

In addition: regular analysis and feedback have also been implemented.


Recruitment information / eligibility

Status Completed
Enrollment 10332
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- clinical diagnosis of neurosurgical disorders

- requiring surgery

Exclusion Criteria:

patients without surgery intervention

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
before-after study
The data analysed involve the time when the targeted, active surveillance of infections was establised, initially: 2003-2017, using tools (definitions, protocols) in accordance with the National Healthcare Safety Network (NHSN), then from 2012, HAI recognition methodology and HAI record-keeping has followed the Surveillance Network (HAI-Net), European Centre for Disease Prevention and Control (ECDC).

Locations

Country Name City State
Poland Jagiellonian University Medical School Kraków

Sponsors (1)

Lead Sponsor Collaborator
Polskie Towarzystwo Zakazen Szpitalnych

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary incidence of surgical site infection the cumulative incidence of surgical site infection (SSI) was calculated by dividing the number of SSI cases by the number of patients undergoing surgery and multiplying by 100 2003-2017
Primary incidence of pneumonia the cumulative incidence of post-procedure pneumonia was calculated by dividing the number of pneumonia cases by the number of patients undergoing surgery and multiplying by 100 2003-2017
Primary incidence of bloodstream infections the cumulative incidence of bloodstream infections (BSI) was calculated by dividing the number of BSI cases by the number of patients undergoing surgery and multiplying by 100 2003-2017
See also
  Status Clinical Trial Phase
Completed NCT03682198 - Neuro-Ox 2018: Assessment of Cerebral Oxygenation Under Three Clinically Relevant Conditions N/A
Withdrawn NCT00925093 - Study of Antibiotics in Cerebrospinal Fluid Following Intravenous Injection Phase 1
Completed NCT05264012 - Incidence, Risk Factors and Impact of Significant Pain in Patients Undergoing Neurosurgery
Recruiting NCT05397574 - Intraoperative Hyperspectral Imaging for Fluorescence Guided Surgery in Low Grade Gliomas
Completed NCT04153396 - Preemptive Infiltration With Betamethasone and Ropivacaine for Postoperative Pain in Laminoplasty or Laminectomy Phase 4
Recruiting NCT03087981 - Parameters Analysis in Neurosurgical Critical Patients Through Big Data Acquisition N/A
Completed NCT01513213 - Correlation of PaCO2 to the Inspired and Expired Oxygen Gradient N/A
Recruiting NCT04034836 - Parecoxib as an Adjuvant to Scalp Nerve Blocks for Relief of Post-craniotomy Pain Phase 4
Completed NCT03532256 - Post-op Crowd Sourcing Health Data Via Text-messaging
Completed NCT05108337 - Superficial Cervical Plexus Block for Postoperative Chronic Pain N/A
Completed NCT02987816 - Neurosurgical Skill Enhancement Using Transcranial Stimulation N/A
Completed NCT03193905 - Preventing Inadvertent Hypothermia in Patients Undergoing Major Spinal Surgery N/A
Completed NCT00122096 - Perioperative Inflammation and Cyclooxygenase 2 (COX-2) Phase 4
Recruiting NCT05874050 - Arterial Pressure and Surgical Hemostasis in Elective Neurosurgery.
Completed NCT01122537 - Characterization and Differential Diagnosis of Postneurosurgical Meningitis N/A
Recruiting NCT05294185 - Intra-operative Hyperspectral Imaging in Neurosurgery
Completed NCT04142203 - Implementation of 23 Hour Surgery Model in a Tertiary Hospital
Completed NCT05169281 - Distribution of Medication Disposal Packets - Acute Opioid Prescribing N/A
Recruiting NCT06264037 - The Experience in Neurorehabilitation Setting: a Qualitative Study
Recruiting NCT05860790 - Prospective Validation of Clinical Prediction Model for Venous Thromboembolism Following Neurosurgery