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Production of enteral feeds : manual vs mechanised vs 'ready to hang'Joubert, Polly Ann 12 1900 (has links)
Thesis (Mnutr)--Stellenbosch University, 2003. / ENGLISH ABSTRACT: INTRODUCTION
Many patients seen by dietitians in Tygerberg Academic Hospital require feeding
via the enteral route. Prior to this study all enteral feeds were mixed individually
by hand, and production was time consuming and very labour intensive. The purpose
of this study was, therefore, to compare the current method of production, with
mechanised bulk production (MP) and "Ready to hang" (RTH) products, taking time,
safety and cost effectiveness into consideration.
MATERIALS AND METHODS
A machine was designed and built to produce and decant bulk volumes of enteral
feed. Production methods were evaluated and data was obtained regarding the
time taken to produce a feed, and the true cost of the feeds produced.
Microbiological samples were collected and the safety of all the three systems was
determined and compared.
RESULTS
MP production time was significantly longer than hand production (HP), but MP
decanting was significantly more accurate. RTH feeds cost 152% more than HP
feeds, and MP feeds cost 95% of HP feeds. Seventy-one per cent of HP feeds,
74% of MP feeds and 34% of RTH feeds were contaminated just after
administration had began.
CONCLUSIONS
Mechanisation is less labour intensive than HP and helps to decrease total costs.
RTH feeds quickly become contaminated after administration decreasing their
other advantages. / AFRIKAANSE OPSOMMING: IN L E ID IN G
Baie van die pasiente wat deur dieetkundiges in Tygerberg hospitaal gesien word,
benodig buisvoedings. Vo or hierdie studie geloots was, was alle buisvoedings by
Tygerberg hospitaal met die hand gemaak. Hierdie metode is baie tydsaam en
arbeidsintensief. Die doel van hierdie studie was, om die voorlopige sisteem van
produksie te vergelyk met gemeganiseerde grootmaat produksie en "ready to hang"
(RTH). Die studie het die volgende in ag geneenv produksietyd, mikrobiologiese
veiligheid en koste effektieweteit.
METODE
'n Masjien was ontwerp en gebou om grootmaat buisvoedings aan te maak en
aftegiet. Produksie metodes was geevalueer en inligting bymekaar gemaak met
betrekking tot produksietyd, en die ware koste van die voedings. Mikrobiologiese
monsters was versamel en die mikrobiologiese veiligheid van al drie sisteme is
bepaal en vergelyk.
RESULTATE
Produksie met die masjien was betekenisvol longer as die voedings wat met die hand
gemaak was, maar die masjien het betekenisvol meer akkuraat afgemeet met afgiet.
RTH voedings se koste beloop 152% meer as voedings wat met die hand gemaak
word, en voedings wat deur die masjien gemaak word kos 95% van die wat met die
hand gemaak is. Een en sewentig persent van die voedings wat met die hand gemaak
was, 74% van die masjiengemaakte voedings en 34% van die RTH voedings was
besmet net na toediening begin was. GEVOLGTREKKINGS
Meganisasie is minder arbeidsintensief as voedings wat met die hand gemaak is en
help om die kostes af te bring. RTH voedings word vinnig besmet met organismes
na die begin van toediening en dit verminder hulle ander voordele.
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Micronutrient supplementation for critically ill adults : a systematic review of the evidenceVisser, Janicke 12 1900 (has links)
Thesis (MNutr (Human Nutrition))--Stellenbosch University, 2008. / Background
Critical illness is associated with increased production of reactive oxygen species
and oxidative stress, and low levels of most micronutrients with resultant diminished
endogenous antioxidant defences. Micronutrient supplementation is thought to be
beneficial to the critically ill patient by ameliorating oxidative stress and by improving
clinical outcome.
Objectives
This systematic review assessed the effects of micronutrient supplementation on
adults recovering from critical illness. Primary outcomes included clinical endpoints
[mortality, infectious complications, length of intensive care unit and hospital stay
(LICU and LOS)]. Secondary outcomes included descriptions of practice issues,
micronutrient status, morbidity, course of the acute phase response and oxidative
stress.
Search strategy
An electronic bibliographic database search was carried out, bibliographies of
retrieved articles were reviewed and personal files searched to obtain additional
citations. Databases were searched from inception until 29 February 2008.
Selection criteria
Randomized controlled trials (RCTs) of micronutrient supplementation (by any route)
in adult critically ill patients, given in addition to their routine care, were included.
Data collection and analysis
Two authors independently extracted data and assessed trial quality. For the primary
outcomes the random-effects model was used to estimate overall relative risk /
mean difference and effect size due to the presence of study heterogeneity.
Selected exploratory analyses were undertaken. Differences at the level of p<0.05
was considered to be statistically significant. The secondary outcomes were sparse
and variably recorded such that this data was not formally aggregated.
Main results
Fifteen RCTs involving 1714 participants and 18 RCTs involving 1849 participants were
included for the primary and secondary objectives respectively. The quality of the
RCTs, as reported, was disappointing, particularly for allocation concealment.
Fourteen trials (n=1468) of micronutrient supplementation showed a statistically significant reduction in overall mortality [relative risk (RR) 0.78, 95% confidence
interval (CI) 0.67-0.90, I2=0%, p=0.0009]. An asymmetrical funnel plot necessitates
caution when directly interpreting these results. Six RCTs (n=1194) indicated a
statistically significant reduction in 28 day mortality (RR 0.75, 95% CI 0.63-0.88, I2=0%,
p=0.0006) (symmetrical funnel plot). Micronutrient supplementation in this systematic
review was not associated with a reduction in infectious complications, LICU or LOS.
In sub-group analyses, single nutrients were associated with borderline statistical
significance (RR 0.82, 95% CI 0.66-1.01, I2=0%, p=0.06) in terms of mortality, whist a
sensitivity analysis of combined micronutrients indicated a significant reduction in
mortality (RR 0.69, 95% CI 0.54-0.90, I2=2%, p= 0.006). This review did not find clear
evidence that parenteral is superior to enteral administration in terms of clinical
outcomes. The secondary outcomes confirmed that timing, duration and dosing are
key factors to ensure optimal clinical benefit.
Conclusion
This review does suggest potential benefit of micronutrient supplementation in
critically ill adults for some clinical outcomes (especially mortality), but also highlights
that caution is warranted as nutrient interactions and risk of toxicity are not clearly
defined in critical illness. More large multi-centre randomized trials are necessary to
assess the effects of different types and doses of micronutrient supplementation in
selected groups of patients with different types of critical illness.
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