Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Evaluation of Bacterial Flora Among Operation Theatre Staff at a Tertiary Care Hospital

12 september 2019 uppdaterad av: Metta Jayachandra Reddy, Kamineni Academy of Medical Sciences and Research Centre

Evaluation of Bacterial Flora Among Operation Theatre Staff at a Tertiary Care Hospital - An Observational Prospective Study

Health care associated infection (HCAI) is a serious health hazard as it leads to increased morbidity and mortality of patients, length of hospital stay and costs associated with increased hospital stay.

A total of 361 subjects divided into four groups were included in this study. The first group comprised of 179 doctors, the second had 31 nurses, third group had 110 OT Technicians and the fourth group included 41 subjects which included housekeeping staff and cleaners. Swabs were collected from OT staff at the time of entry and at exit from the OT. Places of swabs taken were: A) Web space, B) OT dress and C) Anterior nares.

Studieöversikt

Status

Avslutad

Intervention / Behandling

Detaljerad beskrivning

Introduction:

Health care associated infection (HCAI) is a serious health hazard as it leads to increased morbidity and mortality of patients, length of hospital stay and costs associated with increased hospital stay. Infections from OT is well known and is well established which are often referred to as "hot zones" for emergence & spread of microbial resistance. Contamination in an operation theatre is an important cause of HCAIs and is the third leading cause of HCAIs.

This was a prospective observational study conducted in the operation theatre of a tertiary hospital once a month randomly from April 2014 - April 2016. All Operation theatre (OT) staff were included in the study. All the patients in OT and samples from the OT air & equipment were excluded from the study. A total of 361 subjects divided into four groups were included in this study. The first group comprised of 179 doctors, the second had 31 nurses, third group had 110 OT Technicians and the fourth group included 41 subjects which included housekeeping staff and cleaners. Swabs were collected from OT staff at the time of entry and at exit from the OT. Places of swabs taken were: A) Web space, B) OT dress and C) Anterior nares.

Studietyp

Observationell

Inskrivning (Faktisk)

361

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

All OT staff viz. Surgeons, Anesthetists, Residents, OT matron/Nurse, OT Technicians, Housekeeping and Cleaning staff were include in the study. All the patients in OT and samples from the OT air & equipment were excluded from the study. All subjects were screened as per inclusion and exclusion criteria and selected without any gender bias.

The study population contained 361 subjects among which were divided into four groups. Doctors, Nurses, OT technicians and others. Swabs were collected from OT staff at the time of entry in to OT and at the time of exit from OT. Places of swabs taken are: A) Web space, B) OT dress, C) Anterior nares (distal 1cm in a circular motion). Swabs were inoculated on 5% sheep blood agar/ Mueller-Hinton agar/ Mannitol salted agar/ MacConkey agar and were incubated at 35-37 degree centigrade under aerobic conditions for 48hrs with observation once in 24hrs. The age, gender and rank of the OT staff were collected as a part of demographic data.

Beskrivning

Inclusion Criteria: All Operation Theatre staff -

Exclusion Criteria: Patients in Operation Theatre, Operating room air & equipment

-

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Doctors
Swabs collected from Web space, Scrub, Anterior nares before entering Operation theatre and while exit from operation theatre
Swab sticks collected from Web Spaces, Scrub, Anterior Nares
Nurses
Swabs collected from Web space, Scrub, Anterior nares before entering Operation theatre and while exit from operation theatre
Swab sticks collected from Web Spaces, Scrub, Anterior Nares
OT Technicians
Swabs collected from Web space, Scrub, Anterior nares before entering Operation theatre and while exit from operation theatre
Swab sticks collected from Web Spaces, Scrub, Anterior Nares
House keeping staff and cleaners
Swabs collected from Web space, Scrub, Anterior nares before entering Operation theatre and while exit from operation theatre
Swab sticks collected from Web Spaces, Scrub, Anterior Nares

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Bacterial flora harboured at Web spaces among OT staff
Tidsram: 2 years
Swabs will be taken from web spaces before entering Operation Theatre and while going out of OT at the end of the day and cultured to look for growth of Bacteria
2 years
Bacterial load on OT dress among OT staff
Tidsram: 2 years
Swabs will be taken from OT dress while donning them and before going out of OT at the end of the day and cultured to look for growth
2 years
To identify the nasal carriers of organisms among OT staff
Tidsram: 2 years
Swabs will be taken from anterior nares while entering OT at the end of the day while leaving OT and cultured to look for growth
2 years

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 april 2014

Primärt slutförande (Faktisk)

1 april 2016

Avslutad studie (Faktisk)

1 april 2016

Studieregistreringsdatum

Först inskickad

6 september 2019

Först inskickad som uppfyllde QC-kriterierna

12 september 2019

Första postat (Faktisk)

13 september 2019

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 september 2019

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

12 september 2019

Senast verifierad

1 september 2019

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

OBESLUTSAM

IPD-planbeskrivning

Study Protocol

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera