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Risk Factors for Pressure Ulcers

14. oktober 2015 oppdatert av: latifa, Centre Hôpital Universitaire Farhat Hached

Case Control Study of the Risk Factors for Pressure Ulcers in Tunisian Patients

Development of pressure ulcer (PU) is complex and multifactorial. The association of a constituted PU and of clinical / biological major elements is demonstrated and justifies. Prevention of PU is an important health priority, one that requires clear identification of risk factors.

Studieoversikt

Status

Fullført

Forhold

Studietype

Observasjonsmessig

Registrering (Faktiske)

313

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Sousse, Tunisia, 4000
        • Latifa KHLIFI

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

19 år til 88 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

This prospective study consisted of 100 patients were having at least one wound of pressure ulcer that met the following inclusion criteria. Who followed in many departments (emergency, orthopedic, physical medicine) of three University Regional hospitals of Tunisia (Farhat Hached and Sahloul Sousse, Fattouma Bourguiba Monastir) were evaluated prospectively.

Beskrivelse

Inclusion Criteria:

  • presenting with at least of a wound and confirmed diagnosis of PU, age≥18 years old, bedridden, not feeds only and without trophic and mental disorders.

Exclusion Criteria:

  • paediatric study populations, age > 90 years old, allergy to wound products, malignant origin

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: Case-Control
  • Tidsperspektiver: Retrospektiv

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
100 patients suffering from pressure ulcer
100 subjects were having at least one wound of pressure ulcer (74 men and 26 women) middle-aged (55.5±20 years) and were recruited from many services of three University Regional hospitals of Tunisia.
213 healthy subjects
213 healthy subjects (125 men and 88 women) middle-aged (51.5±17 years). Although, healthy individuals, were included as controls, followed in the outpatient services of the University Hospital Farhat Hached and they considered clinically free of pressure ulcer and tissue necrosis.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Anthropometric characteristics
Tidsramme: one hour
Body Mass Index (BMI) is a simple index of weight-for-height. It is defined as the weight in kilograms divided by the square of the height in metres (kg/m2).
one hour
Diabetes mellitus
Tidsramme: one hour
- Plasma levels glucose in mmol/l was measured by standard enzymatic methods using reagents in a fully automated analyzer Cx5 Pro-Bechman Coulter-Fuller-Ton
one hour
Dyslipidemia
Tidsramme: one hour
  • Lipid markers: total serum cholesterol (CH), serum triglyceride, serum HDL- CH, in mmol/l, levels were measured by standard enzymatic methods using reagents in a fully automated analyzer (Randox Antrim, UK; CX9-BECKMANN).
  • Low density lipoprotein cholesterol (LDL-C) in mmol / l was determined by Friedewald formula.
  • non esterified fatty acids in serum was determined by colorimetric method at 550 nm (mmol/l)
one hour
Renal failure
Tidsramme: one hour
- renal profile: urea (mmol/l), creatinine and uric acid (μmol/l) levels were measured by standard enzymatic methods using reagents in a fully automated analyzer ( Cx9 Pro-Bechman Coulter-Fuller-Ton).
one hour
Inflammatory parameter
Tidsramme: one hour
- C-reactive protein (CRP), in mg/l, was measured using immunoturbidimetric methods (COBAS INTEGRA 400 Roche).
one hour
Endogenous inflammatory marker
Tidsramme: one hour
- α1-acid glycoprotein, in g/l, measured using the dry chemistry method (BN prospec, siemens)
one hour
Markers of nutritional status
Tidsramme: one hour
  • albumin (chronic marker) and prealbumin (early marker) were measured, in g/l, using the dry chemistry method (BN prospec, siemens).
  • Protide in g/l was measured by standard enzymatic methods using reagents in a fully automated analyzer (CX9-BECKMANN).
one hour
Marker of lipid peroxidation
Tidsramme: one day
  • Serum total homocysteine concentrations in μmol/l were measured by using an AxSYM (ABBOTT) homocysteine assay.
  • thiobarbituric acid reactive substances (TBARS) in serum was determined by the fluorimetric method of Yagi in μmol/l.
one day
Antioxidant parameters
Tidsramme: one day
- Serum catalase activity in KU/l was determined according to the spectrophotometric method of Goth .
one day
Total antioxidant status
Tidsramme: one hour
Serum total antioxidant status in mmol/l was measured with RANDOX kit (Cat. No. NZ 2332; Randox Labs Ltd., Crumlin, UK) by colorimetric method at 600 nm .
one hour
Determination of trace elements
Tidsramme: one hour

Serum copper in μmol/l was indicated spectrophotometrically with RANDOX kit (Cat. No. CU 2340; Randox Labs Ltd., Crumlin, UK) at 580 nm according.

Serum zinc was measured in μmol/l with RANDOX kit (Cat. No. ZN 2341; Randox Labs Ltd, Crumlin, UK) at 560 nm.

one hour
Nutritional status
Tidsramme: 3 hours
- Nutritional Risk Index (NRI) was originally derived from the serum albumin concentration and the ratio of present to usual weight [NRI = (1.489 x albumin, g/L) + (41.7 x present weight/ideal body weight)] and categorized as follows: severe risk (NRI < 83.5), moderate risk (83.5 < NRI < 97.5) and no risk (NRI > 97.5).
3 hours
Nutritional risk
Tidsramme: 3 hours

- Prognostic Inflammatory and Nutritional Index (PINI) is a simple clinical [PINI = AAG x CRP / albumine x prealbumin] and classificated as follows: normal (1<PINI score <10), mild malnutrition (11<PINI score<20), severe malnutrition (21<PINI score<30) and risk for death when PINI score >30.

These scores gained in popularity as it uses an objective rather than subjective measurements to determine nutritional risk in hospitalized patient populations.

3 hours
A microbiological diagnosis
Tidsramme: 3 days

The bacterial colonization of a wound is a recognized detrimental factor in the multifactorial process of wound healing.

wound per patient suffering from pressure ulcer was cultured by swab to determine the bacterial species of the infection and helps guide antibiotic therapy.

The representative sample is collected before topical or systemic antibiotics are initiated and pain assessment should be conducted prior to wound procedures such as dressing changes and debridement. Bacterial swabs provide information on the predominant flora.

3 days
Proteomics
Tidsramme: 2 days
- Serum gelatinase activities of MMP-9 by zymography (%)
2 days
DNA extraction
Tidsramme: 2 days
Genomic DNA was extracted from whole blood using the salting out method for the part of molecular biology.
2 days
Genotype for the MMP9-1562 C/T polymorphism
Tidsramme: 1 days
  • Genetic polymorphism in the MMP9 coding region 1562C>T was screened following the polymerase chain reaction and restriction fragment length polymorphism (RFLP-PCR).
  • The frequency distributions of different MMP9-1562 C/T genotypes and allele were investigated.
  • The relationship between the polymorphism of the MMP-9 gene and the severity of PU was analyzed.
1 days
Genotyping of TNF- α G238A
Tidsramme: 1 days
  • TNF-α G238A promoter polymorphism were determined by the RFLP-PCR method.
  • The genotypic and allelic frequencies of -238G/A were calculated
  • This study investigated the association between TNF-α-238G>A and Pressure ulcer in Tunisian population.
1 days
Genotyping of TNF- α G308A
Tidsramme: 1 days
  • The genotypic analysis of the TNF-α G308A polymorphism was performed using Allele-specific PCR (AS-PCR) amplification.
  • In this study, we have analyzed the TNF-α gene promoter -308G/A polymorphism in Tunisian patients with PU to evaluate the contribution of this SNP in genetic susceptibility to PU.
1 days

Samarbeidspartnere og etterforskere

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Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. januar 2013

Primær fullføring (Faktiske)

1. april 2014

Studiet fullført (Faktiske)

1. juni 2015

Datoer for studieregistrering

Først innsendt

9. oktober 2015

Først innsendt som oppfylte QC-kriteriene

14. oktober 2015

Først lagt ut (Anslag)

16. oktober 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

16. oktober 2015

Siste oppdatering sendt inn som oppfylte QC-kriteriene

14. oktober 2015

Sist bekreftet

1. oktober 2015

Mer informasjon

Begreper knyttet til denne studien

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