Table 36.4
Selected published surface hygiene swabbing protocols (adapted from
Davidson, 2001)
Sampling variableCollinset al.(1989)Robertset al.(1995)Harrigan (1998)Type of swabCotton wool or alginateCotton woolCotton wool or alginateArea of surface sampled5 cm5 cm5 cm5 cmNot specifiedSwabbing protocolSwab within 25 cm2card orcellophane template area usingone swabUsing aluminium template, swabentire area using two swabs, onemoist and one dry, rotating swabs.Return both swabs to one diluenttubeSwab predetermined area byrubbing firmly over the surface inparallel strokes, with slow rotationof the swabType of diluentNutrient brothMRD or ‹ St Ringers‹ St RingersRelease methodSoak and squeeze swabShake until cotton wool brokendown into fibresAgitate/shake swab in tube up anddown 10 timesType of culture mediaNot specifiedPlate count agarNutrient agar or trypticase soyaagarCultivation/plating methodNot specifiedSpread/pour plates1 mL pour plates for cotton swabs,0.1 mL and 1 mL plates foralginate swabsTime and temperature of samplestorage /incubationNot specifiedNot specifiedNot specifiedTime and temperature ofincubationNot specified30 ÎC, 48±72 hoursNot specifiedExpression of resultsCount/25 cm2Count/cm2Count/cm2Dacron is now the most widely used `bud' material. MRD= maximum recovery diluent