Презентация на тему THEATRE DESIGN AND VENTILATION

Презентация на тему Презентация на тему THEATRE DESIGN AND VENTILATION, предмет презентации: Красота и здоровье. Этот материал содержит 33 слайдов. Красочные слайды и илюстрации помогут Вам заинтересовать свою аудиторию. Для просмотра воспользуйтесь проигрывателем, если материал оказался полезным для Вас - поделитесь им с друзьями с помощью социальных кнопок и добавьте наш сайт презентаций ThePresentation.ru в закладки!

Слайды и текст этой презентации

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THEATRE DESIGN AND VENTILATION

DR.LOKESH SHAROFF Orthopaedic surgeon, Mumbai, India


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CONCEPT

It was first introduced by SIR JOHN CHARNLEY


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ZONES IN THEATRE

OUTER ZONE – rest of the hospital outside the theatre complex CLEAN ZONE – theatre complex outside the operating area ASEPTIC ZONE – Operating area DISPOSAL ZONE – Separate exit for contaminated / used linen and instruments


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REQUIREMENTS

AIR DELIVERY SYSTEM AIR FILTERATION SYSTEM TEMPERATURE CONTROL HUMIDITY CONTROL


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TEMPERATURE CONTROL

- Ideal working temperature is 19-20 * C – to minimize perspiration
- But causes pt. hypothermia - PT. body temp. should be 24-26 * C TO AVOID HYPOTHERMIA


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HUMIDITY CONTROL

- Should be around 40-60% - Fastest death of organisms occur at 50% humidity


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AIRBORNE PARTICLES

- Measured as BCP/MM3 – Bacteria carrying particles OR CFU/MM3 – Colony forming units - Each person emits 10k cfu/min at rest and 50k cfu/min with activity - This is reduced in SCRUBS to 140-830 cfu/min with fask mask and caps.


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AIRBORNE PARTICLES

- CONVENTIONAL AC (well maintained)- gives 50-500 cfu/mm3 - All particles are not viable – viable : non viable ratio is 1:1000 - Smallest particle in theatre seen in bright light is 12 microns - Smallest particle that can carry bacteria is 4-5 microns


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AIR FILTERS- 4 LEVELS

ROUGHING FILTERS removes Large particles and also protects sensitive final filters
PREFILTERS should be 95% efficient
FINAL FILTERS should be 95% efficient with a particle size of 3 microns
HEPA FILTERS should be 99.97% efficient with a particle size of 0.3 microns


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HEPA FILTERS

- Each hepa filter has a manometer attached to it to measure the amount of resistance to filteration for clogging purposes.


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TYPES OF VENTILATION

High velocity air flow - high speed jets towards operating table - high speed air at periphery Laminar air flow - horizontal - vertical


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CONVENTIONAL WALL DIFFUSER


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- Produces plenum - No control of air over operating area - Upto 500 bcp/mm3 – not acceptable for operation theatres


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HIGH VELOCITY AIR JET


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- Jets increase air turbulence - Flow at 0.6 m/s - Jets may not point at right place and may dessicate the wound


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Vertical laminar flow

- Room within a room principle - Air is passed through hepa filters from ceiling downwards - Flow at 0.3 m/s - entrainment can happen by moving personnel


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Horizontal laminar flow

- Forms part of a wall - Easy to install - Movement across it will cause uncontrollable turbulence - adequate clean zone is not possible


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PERIPHERAL LAMINAR


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CONVENTIONAL LAMINAR


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Vertical laminar with canopy and side panels

- Canopy – to overcome peripheral entrainment - side panels – extend down to floor to within 20cms from floor - very successful – 10 bcp/m3


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Without side panels


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- Peripheral entrainment air 0.6 m/s - Higher energy consumption - movement causes deflection of contaminants


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EXPONENTIAL AIR FLOW


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- Trumpet shaped air flow - Downward and radially outward flow of air - fliteration down to 1 micron - Trays can be positioned even upto ½ m outside the actual canopy


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STANDARDS IN AIR FLOW

- Direction of air flow shall be under positive control - max. viable organisms should be not more than 1 cfu/mm3 - ULTRA CLEAN ZONE – is less than 10 cfu/mm3


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AIR CHANGES

ATLEAST 20-40 AIR CHANGES PER HOUR
Pressure gradient should be 1.3-2.5mm h2O (more pressure causes rapid drying of the wound)


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AIR QUALITY CONTROL

- Done by CASTELLA SLIT SAMPLER


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WATER SUPPLY IN OT

- Tanks and pipes – regular inspection for leakages - Bore well water should be avoided as far as possible - tanks and containers should have covers/lids to protect from dust - water sterilised by ultraviolet radiation


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ANTIBIOTIC PROPHYLAXIS

- CHOICE OF AGENT Active against comon pathogens Take into account drug allergy and sensitivity cefazolin/cefotaxim preferred-long duration clinda/vanco in penicillin allergy pts. Modification for pre-existing cultures if already on abx – then continue same


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ANTIBIOTIC PROPHYLAXIS

TIMING Within 15-60 mins prior to incision Vanco should be given 2 hrs before

Infusion should complete before incision


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ANTIBIOTIC PROPHYLAXIS

- DURATION Further dose efficacy is doubtful Max 24 hrs if only prophylatic intra-op – repeat if length of sx more than half life of drug repeat dose if blood loss >1500ml not to continue abx till drain removal


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ANTIBIOTIC PROPHYLAXIS

- RISKS - PENICILLIN ALLERGY - ANAPHYLAXIS - ABX ASSOCIATED DIARRHOEA - CLOSTRIDIUM DIFFICLE INFECTION - ABX RESISTANCE - MULTI-RESISTANCE CARRIAGE – SCREENING SHOULD BE DONE IN HIGH RISK CASES


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THANK YOU

*Pictures taken from journal of orthopedics today


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