ASHRAE 170-2008 Ventilation of Health Care Facilities

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  • 8/19/2019 ASHRAE 170-2008 Ventilation of Health Care Facilities

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    ANSI/ASHRAE/ASHE Standard 170 2008

    ASH W SHE STANDARD

    Ventilation of

    Health Care

    Facilities

    Approved by the ASHRAE Standards Committee on June 21,2008; by the ASHRAE Board of Directors on

    June 25,2008; by the American Society for Healthcare Engineering of the American Hospital Association on

    July 18,2008; and by the American National Standards Institute on July 24, 2008.

    This standard is under conlnuous maintenance by a Standing Standard Project Committee (SSPC) for which

    the Standards Committee has established a documented program for regular publication of addenda or revi-

    sions, including procedures for timely, documented, consensus action on requests for change to any part of

    the standard. The change submittal form, instructions, and deadlines may be obtained in electronic form from

    the ASHRAE Web site, hHp:llwww.ashrae.org, or in paperform from the Manager of Standards. The latest edi-

    l o n of an ASHRAE Standard may be purchased from ASHRAE Customer Sewice, 1791 Tuiiie Circle, NE,

    Atlanta, GA 30329-2305. E-mail: [email protected]: 404-321-5478. Telephone: 404-636-8400 (world-

    wide), or toil free. 1-800-527-4723

    (for

    om effi in US and Canada).

    Copyright 2008 American Society of Healna, Refricleratina and Air-conditioning Engineers. Inc.

    American

    Society

    olHeating.

    Rerrigeracing

    ~Imerienn

    SodeiyrarHdth nglnee

    and

    Air conditioningEngineers. Inc.

    c~ll l~i.dmuiicul

    Iurl~iWi \rri~or~on

    179

    Tullie

    Circle NE, Atlanta.

    GA

    30329

    www ashrae org

  • 8/19/2019 ASHRAE 170-2008 Ventilation of Health Care Facilities

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    ASHRAE Standing Standard Project Commi ttee

    170

    Cognizant TC: TC 9.6 Healthcare Facilities

    SPLS Liaison: H. Michael Newman

    Richard D. Hermans, Chair' Peter Hogan Langowski'

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    CONTENTS

    ANSVASHRAUASHE Standard 170-2008

    Ventilation of Health Care Facilities

    SECTION PAGE

    ~

    Foreword

    ...................................................................................................................................................................

    2

    1 Purpose .................................................................................................................................. 2

    2 Scope .................................................................................................................................................... 2

    3

    Definitions

    ................................................................................................................................................

    2

    4 Compliance

    .................................................................................................................................................

    3

    5 Planning

    ..................................................................................................................................................

    4

    6

    Systems and Equipment...............................................................................................................................

    4

    7 Space Ventilation

    ........................................................................................................................................ 6

    Planning Construction and System Start Up

    .........................................................................................

    11

    9 Normative References

    ............................................................................................................................

    12

    lnformative Annex A ...................................................................................................................................... 12

    lnformative Annex B: Bibliography 13

    NOTE

    When addenda, interpretations, or errata to this standard have been approved, they can

    be

    downloaded free of

    charge from he

    SHR E

    Web sit at *wm.ashrae.org.

    O Copyright 2008 American Society of Heating,

    Refrigerating and Air-Conditioning Engineers,

    Inc.

    1791 Tullie Circle NE

    Atlanta. GA 30329

    www.ashrae.org

    All rights reserved.

  • 8/19/2019 ASHRAE 170-2008 Ventilation of Health Care Facilities

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    lriglr risk

    irrr~~~trnocorr~pror~risPdpatients

    atients who have

    the greatest risk of infection caused by airborne or waterborne

    microorganisms. T hese patients include but are not limited to

    allogeneic stem-cell transplant patients and intensive chemo-

    atients.

    rrrfectron c orth olri sk assessrrrent ICRA): a determination of

    the potential risk of transmission of various infectious agents

    in the facility, a classification of those risks, and a list of

    requiredp ractices fo r mitigating those risks during conshuc-

    tion or renovation.

    ir~r~r~trr~aconrpranrisedatients: patients whose immune

    mechanisms are deficient because of immunologic disorders

    (e.g., human immunodeficiency

    virus [HIV]

    infection or

    congenital immune deficiency syndrome), chronic diseases

    (e.g., diabetes, canc er, emp hysem a, or cardiac failure), or

    imm unosup pressive therapy (e.g., radiation, cytotoxic chemo-

    therapy, anti-rejection medication, or steroids) (see CDC

    [2003] in Informative

    nnex

    B: B ibliography).

    inpotierrt apatient whose stay at the health care facility is antic-

    ipated to require twenty-four hours or m ore of patient care.

    irrvasive if~ro ~~r rgpr oced rrreoom: a room in which radio-

    graphic im aging is used and in which instruments o r devices

    are insertedinto patients through the skin orbody o s c e under

    sterile conditions for diagnosis andlor treatment.

    non aspirating

    difftrser: a diffuser that has unidirectional

    downward airflow from the ceiling with minimum entrain-

    ment of room air. Classified as ASHRAE Group E, these

    diffusers generally have very low overage veloci@ For the

    purposes of this s tandard, the performance of these d i e r s s

    to b e measused i n terms o f average velocity.

    pro tect ive environrne~rt oorrr:

    a patient room that is designed

    according to this standard and intended to protect a high ~isli

    in~mtrnocompmmisedpatientrom human and environmental

    airborne pathogens.

    triage: the process of determining the severity of the illness of

    or injury to patients so that those who have the m ost emergent

    illnesses/iinjuries can be treated immediately and those less

    severely injured can be treated later or in another area.

    4 COMPLIANCE

    4 1 Com pliance Requirements

    4 1 1

    New Buildings. New buildings shall comply with

    the provisions of this standard.

    4 1 2

    Existing Buildings

    4 1 2 1

    Additions to Existing Buildings. Additions

    shall comply with the provisions of this

    stmdard.

    4 1 2 2

    Al terati ons t o Existing Buildings. Portions of

    a heating, ventilating, and air-conditioning system and other

    systems and equipment that re being altered shall comply

    with th e applicable requirements of this standard.

    4 1 2 2 1 Head.g Ven~ation ~ndiMonditioning

    System Alterations. Alterations to mechanical systems sewing

    the building heating, cooling, or ventilating needs shall comply

    with the requirements of Section 6, Systems an d Equipmenk

    applicab le to those specific poltions of the building an d its sys -

    tems that are being altered. Any new mechanical equipment

    installed

    in

    conjunction with the alteration as a direct replace-

    ment of existing mechanical equipment shall comply with the

    provisions of Sections 6.2,6.4,6.5, and 6.6.

    4 1 2 2 2

    Space Alterations. Alterations to spaces

    listed in Table 6-1 (see page 5) shall comply with the require-

    men ts of Section 6.7 and Section 7, Space Ventilation, appli-

    cable to those specific portions of the building and its systems

    that are being altered Any alteration to existing health care spa ce

    in a building that w ill continue to treat patients during conshu c-

    tion shall com ply with Sections 8.1, 8.3, 8.4, and 8.5.

    4 2 Adm inistrative Requirements. Administrative

    requirements relating to permit requirements, enforcem ent by

    the authority having jurisdiction, interpretations, claims of

    exemption, approved calculation methods, rights o f approve d

    calculation methods, and rights of appeal are spe cified by the

    authority having jurisdiction.

    4 3 Compliance D ocuments

    4 3 1

    GeneraL Compliance documents are those plans,

    specifications, engineering calculations, diagrams, reports,

    and other data that are approved as part of the perm it by the

    authority having jurisdiction. The compliance documents

    shall include all specific construction-relatedrequirements of

    the owner's infection contra1 risk assessm ent.

    4 3 2 Con struction Details. Compliance documents sh all

    contain ll pertinent data and features of the building, equip-

    ment, andsystems

    n

    sufficient detail to allow a d etermin ation

    of com pliance by the authorityhaving jurisdiction a nd to indi-

    cate compliance with the requirements of this s ta nd ar d

    4 3 3

    Supplemental Information. Supplemental infor-

    mation necessary to veriFy compliance with this standar4

    such a s calculations, worksheets, compliance forms, v end or

    literature, or other data, shall be made available when requ ired

    by the authority having jurisdiction.

    4 4 Alternate Materials, Methods of Construction , o r

    Design. The provisions of this standard are not intended to

    prevent the use of any material, method of construction,

    design, o r building system not specifically prescribed herein ,

    provided such construction, design, or building system has

    been approved by the authority having jurisdiction as meetin g

    the intent of this standa rd

    4 5

    Info rm ative Appendices. T he informative appendices

    to this standard andinformative notes located within th is stan-

    dard contain recommendations, explanations, and other non-

    mandatory information and are not part of this standard.

    4 6 Cr ite ria R anges. This standard often specifies a range

    of values that will comply with a speciiic requirem ent o f the

    stand ard Ifi t ispermittedby the authority havingjurisdiction,

    compliance with this requirementmay be achieved by the pre-

    sentation of compliance documents that demonstrate a sys-

    tem's ability to perform within the specified range.

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    TABLE

    6 1

    Minimu m Filter Efficiencies

    Fi te r Bank Number 1 Filter Bank Number

    2

    Space Designation (According to Bunction)

    (MERV) W R v ) '

    Classes

    B

    and C surgery; inpatient and ambulatory diagnostic and therapeutic

    radiolow; inpatient delivery and recovery spaces

    7 14

    Inpatient care, treatment, and diagnosis, and those spaces providing direct service or

    clean supplies and clean processing (except as noted below);

    7

    14

    An (rooms)

    Protective environment rooms (PE)

    7

    17

    (HEPA)

    Laboratories; Class A surgery and associated semi-reshicted spaces 1 3 ~ NIR*

    Administrative; bulk storage; soiled holding spaces; food preparation spaces;

    and

    laundries

    All other outpatient spaces

    Skilled nursine facilities

    NIR

    NIR

    NIR

    R not rqu ired

    N o t e s The

    minimum

    cficiency reportingvnlue MERV)r

    basedon

    Ule meUlad oitening dsmibibcd

    in..tNSI/A5fRdE Sior~dotd2.11-2007

    Metbod of Tertinp, Genem l l enriiotion

    Air-CleoningDwicer orRemo~01Ej7cIe8tq @P~?rticlcize

    i e e I n f o d v c

    h e n :Bihl iapphy) .

    Note b: Additional picfillen m y be usedtoroducc mnintmancc for fil le n w ith e f i c i e n d s h i g h m h MERV 7.

    Note

    c

    Fiitcr

    B d c

    No. may be

    n MERV

    14 if

    n

    MERV

    17

    t d q erminn1 fiitrri3 provided for t he e ipnces.

    TABLE

    6 2

    Supply Air Outlets

    Space Designation (According to Function) Supply

    Air

    Outlet ClassEcationn

    Primary

    supply diffusers Group E, non-aspirating

    All class A,

    B,

    and C surgeriesb

    additional supply difwesers, Group E

    Protective environment (PE) rooms

    Group E, non-aspirating

    Wound intensive care units (bum units) Group

    E,

    non-aspirating

    Trauma rooms (crisis or shock) Group

    E,

    non-aspirating

    A11 rooms

    Group A or Group E

    All other spaces Group A or Gmup E

    Note e f a to

    2 M 5 ~ H o n d b o o k - F u n d ~ m e n 1 ~ ,

    bppta35,

    for

    de hi tio m reinred to

    auua

    clasiifimtion n n d p e r f o m c e

    see

    Informotive

    Amen :

    Bib l iopphy) .

    Note

    b Swgeonr

    may require

    tonnte

    air-dir ibibudonsystem forromespe ciakc d m g n i s .

    Suchrystcmr

    r b l i

    be

    consideredocccptnblc iffltey meet

    or a c e d

    he requircrnents

    oilhi. s t m d d

    6.5.2

    Ra dian t Cooling Systems.

    If

    radiant coolmg panels

    are utilized, the chilled-water temperature shall always

    remain above the dew point temperature of the space.

    6.5.3

    Radiant Heating Systems.

    If

    radiant heating is pro-

    vided for an

    A11

    room, aprotective environment room, a wound

    intensive care unit

    @urn

    unit), or aroom for any class of sur-

    gery, either flat andsmooth radiant ceilingpanels with exposed

    cleanable surfaces or radiant floor heating shall be used.

    6.6

    Humidifiers. When outdoor hum~dityand internal

    moisture sources are not sufficient to meet the requirements

    of Table 7.1, humidification shall be provided by means of

    the health-care facility air-handling systems. Locate humid-

    ifiers within air-handling units or

    duchvork to avoid mois-

    ture accumulation in downstream components, including

    filters and insulation. Chemical additives used for steam

    humidifiers serving health care facilities shall comply with

    FDA requirements.' Reservoir-type water humidifiers or

    evaporative-pan-type humidifiers shall not he used i n duct-

    work or air-handling units in health care facilities. A humid-

    ity sensor shall be provided, located at a suitable distance

    downstream from the steam injection source. Controls shall

    he provided to limlt duct humidity to a maximum value of

    90

    R

    when the humidifier is operating. Humidifier steam

    control valves shall be designed so that they remain om

    whenever the air-handling unit is not in operation.

    6.7

    ir

    Distribution Systems

    6.7.1

    General. Maintain the pressure relationships

    requiredinTable 7-1

    in

    all modes ofHVAC system operation,

    except as noted

    in

    the table. Spaces listed

    in

    Table 7-1 that

    have required pressure relationships shall be served by fully

    ducted returns. The air-distribution design shall maintain the

    required space pressure relationships, taking into accountrec-

    ommeoded maximu& filter loading, heating-season lowered

    aimow operation, and cooling-season higher airflow opera-

    tion. Airstream surfaces of the air-distribution system down-

    stream of Filter Bank No. 2, shall comply with Section 5.5 of

    ANSVASHRAE Standard 62.1-2007. The air-distribution

    system shall be provided with access doors, panels, or other

    means to allow convenient access for inspection and cleaning.

    (For further information, see ANSIIASHRAE Standard 62.1.

    6.7.2

    Air-Distribution Devices. All air-distribution

    devices shall meet the following requirements:

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    a.

    Surfa ces of air-distribution devices shall be suitable fo r

    ture and humidity conditions based upon the

    cleaning. Supply air outlets in accordance with Table 6-2 spac e coo lin g or heating load.

    shall be used

    2. Air filtration for spaces shall comply with Table 6-1.

    b. Th e supply difFusers in Classes B and

    C

    surgeries shall be

    3

    Supply ir outlets for spaces shall comply with Table 6 2.

    designed and in stalled to allow for internal cleaning.

    4

    In

    A11 rooms, protective environm entroom s, wound inten-

    c.

    Psychiatric, seclusion, an d holding-patient rooms shall be

    sive -care units

    bum

    units), and rooms for all classes of

    designed with security ditfusers, grilles, and

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    r

    T BLE

    7 1

    Design Parameters

    Pressure

    LA

    I[), Dcsign Tem perat ure l),

    2

    Classes B and C operating rooms, m), n), 0) Positive 4 20 N R No 30-60 68-75120-24

    g

    Opemtinglsurgical cystoscopic rooms,

    m),

    n) 0) Positive 4 20 N R No 30-60 68-75120-24

    0

    Delivery room Caesarean) m), n), 0) Positive 4 20 NiR No 30-60 68-75120-24

    Substeri le service area N R 2 6 N R No NIR NIR

    Recovery room N R 2 6 NiR No 30-60 70-75/2 1-24

    Critical and intensive care

    Wound intensive a r e

    burn

    unit)

    Newbom intensive care

    Treahnent room p)

    Trauma room crisis or shock) c)

    Medicallanesthesia gas stomge r)

    Laser eye room

    ER waiting rooms q)

    Triage

    ER decontamination

    Positive

    Positive

    Positive

    N R

    Positive

    Negative

    Positive

    Negative

    Negntive

    Negative

    NiR

    N R

    NIR

    NIR

    N/R

    Yes

    N/R

    Yes

    Yes

    Yes

    No

    No

    No

    N R

    No

    NIR

    No

    N R

    N R

    No

    30-60

    40-60

    30-60

    30-60

    30-60

    NIR

    30-60

    mnx 65

    max 60

    NIR

    70-7512 1-24

    70-75/21-24

    70-75/21-24

    70-7512 1-24

    70-7512 1-24

    NIR

    70-7512 1-24

    70-75/2 1-24

    70-7512 1-24

    NIR

    Rndiology waiting rooms

    q)

    Neg ative 2 12 Yes NIR maw 60 70-7512 1-24

    Class A Opern tingPro cedur e room o), d) Positive 3 15 N R No 30-60 70-7512 1-24

    INPATIENT NURSING

    Patient room s) NIR 2 6 NiR NIR max 60 70-75/2 1-24

    Toilet room Negative NIR 10 Yes No NIR NIR

    Newbom nursery suite NIR 2 6 NIR No

    30-60 72-78/22-26

    Protective environment room 0, n), t) Positive

    2 I2 NIR No max 60

    70-7512 1-21

    A11 room e),

    n), u)

    Negative 2 12 Yes No mnx 60 70-7 97 1-24

    A11 isolntiol~ nterooln t)

    u)

    N R N R O Yes No N R NIR

    Labor/deliveryIrecovery/poslpartum LDRP)

    s) N R 2

    6 N IR N R m a x 6 0

    70-75/2 1-24

    Laboddeliverylrecove ry LDR) s) NIR 2

    6 N IR N R m a x 6 0

    70-7512 1-24

    Note NiR=

    no

    requirement

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      i

    T BLE

    7-1 Deslgn Parameters

    Pressure

    R

    I[), Design Temperature I),

    O DAPP

    F

    , -

    (n)

    t o

    Outdoors

    j)

    Exnmination room N R 2 6 N R NIR max 60 70-75D 1-24

    Medication room

    Endoscopy

    Endoscope cleaning

    Treahnent room

    Hydrotherapy

    Pllysical tl~em py

    STERILIZING

    Positive

    2

    4 NIR NIR

    Positive 15 NIR No

    mnx 60 70-7512 1-24

    30-60 68-7300-23

    Negative

    2

    I0 Yes No NIR NIR

    N R 2 6 N IR N R m ax 6 0

    70-7512 1-24

    Negative 2 6

    N R N R NIR 72-80122-27

    Negative 2 6 NIR NIR Max 65 72-80122-27

    Sterilizer equipm ent room Negative NIR 10 Yes No NIR NIR

    CENTRAL MEDICAL AND SURGICAL SUPPLY

    Soiled or deconhmination room Negative

    2 6 Yes No NIR 72-78122-26

    Clean worlcroom

    Positive 4

    NiR No lnax 60 72-78122-26

    Sterile stornge

    SERVICE

    Food preparntion center

    i)

    Warewashing

    Dietnry storage

    Posit ive 2 4 N R N R max 60 72-7802-26

    N R 2 10 NIR No NIR 72-78122-26

    Negative N R 10 Yes No NIR NIR

    N R N R 2 N R No NIR 72 -78122-26

    Laundry, general Negative 2 10 Yes No NIR NIR

    Soiled linen sorting and storage Negative N R 10 Yes No NIR NIR

    Clenn linen storage Positive N R 2 N R NIR NIR 72-78122-26

    Linen and trash chute room Negative N R 10 Yes No NIR NIR

    Bedpan room Negative NIR 10 Yes No NIR NIR

    Bathroom

    Janitor s closet

    SUPPORT SPACE

    Negative N R 10 Y es No NIR 72-78122-26

    Negative

    NIR 10

    Y es N o N R N IR

    Soiled workroom or soiled l~ ol d ig Negative

    2 10 Yes No NIR

    Clean worlctoom or clean holding Posit ive 2 4 N R N R N R

    Havlrdous material storage Negative 2 10 Yes No NIR NIR

    Noto

    m =

    no r quir m nt

    D

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    8.66 V ~ J N l ~aunploaae

    q

    pap noid a q l ~ e q s ~ o d e ~na maqa

    1

    sase8 sno xou j o lchomai aql 103 saa nap lsncqxa pun spooq a~ eu do ~d dcannba r uaqM

    'UO lLIUUOj~

    a l O U l l O J

    h l l d & ~ l q ~ aXaUU\r aAgCUlOJOl

    U

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    ~UB

    ptauluo nnua an ga alo ~d aa q aq Zu rpl msjo asod md aql lu j suo s nmd mow e alq u anal q n\ sur ooa 'sioomn a Lpaanp pa8ie1eqasp 8u aq

    01 loud s a~c dsIV-UOU sahlas le~l l

    C

    lsnoqxa I [ ~ M m Lour s w o o~ 1 ~oy no isnnqxa palally

    V ~ E H

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    -l aal aq Kem ap slno Lllaal p lsnollxa ol [ca lamdm s l qa qM mo y m o o l uaged plopm ls mo y pa uy oq u am leql smooi 1m .pann ba1 n )s ale sa8ueqa 1 e looplno all1 'lanamoq :saZueqaxa no moo1

    ~ua lcnln ba ll1 asoalau

    01

    mo oi ?ua lcd atn

    II

    pau uuad aq ll eqs =a lly v d m Z ~ s naa nap Z q o l n a n a x l q u a w a l d d n ~s uo ) ne au d u og cl os Z q n b a ~

    OU

    s po ua d 8 u y p u e a lua led lcuuou 103 uo s ~

    ~ ~

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    1

    nllaa len 'salseam so rpn s 'saseaskp snoga apn jo pca ~d s moq ne aql Zm,lelos ~ojpasnaq ll eqs p~ op uq s y l aquasap moo1

    IIV

    a l u

    . p a ~ p u a d q

    IOU

    lluqs suo laury 1 1 '~ ue Iuamuoqnua a~ ~a a lo ~da a q a q

    8u qal msjo asodmd all? o j suo s ~ o~dmop n a lq sl ana l qj m s m o o ~pap no~d aq plnoqs mo olque ue 'qua ged quamuonnua a~g oal old03 rClsssaaau s

    I I ~

    ell1 al eq pq nu alu3 uZ sap aq J1 .luau1

    -uonAua pal3aloid aql

    JOJ

    uo lel luaA ?uals suoa lo j pan nb a~ movn o aUIlllOA lu qs uo 3 .paI nbal 11 ~ sm saBmqa ne 1oop)no alp kanamoq :sa8ucqaxa no moo1 luapn nba alp ascalaq 01 pa ~ uu ad

    aq [lcq s slally vd zl-1 uo lo1"3~ 3a~ fsa lod s snll Zlads)I

    ' . a , )

    saqola m snogaapn amo qne 1 qua mo qA ua uommoa m oy lua led all1 loalmd suo )eay aads u8 sap

    MOWO

    ]uaumonAua an paqold a l u

    'pasn ale ( 'a~ aXugcaq plcoqascq '8u looa pue

    Zqleaq ?uo pru) smalsLs Zu 1ooa l op un Zq lcaq [quam alddns uaqm paukuuad aq [loqs 113s lq ol ln oj sm oo ~

    m ~ e ~ s o d l k a n o 3 a l l k a ~ ~ a p l l o q c ~

    m s m o o ~ a ~ o a a i/ k a n l a p / ~ o q e lswam lua lcd

    108

    8 . q u a w a ~ n b a ~ ~ a ~ ~ u n j ~ o j6 V ~ J N aS

    ,ascas p &olru dsa~jo sou5e p

    iql

    sKcr-xlsaqo Zq omo quagod ploq o] pamm&old smoo, 8ql em 01 Lluo sagddn ~u am an nb a~ l ~sa3ods Iaqlo Kuc qu paanpoilu

    s l a lo jaq u a l ly v d ~ ~ql 118nolln sassed l e

    um?u

    alp pap no~d uoop lno alp

    q

    s aaeds a saq) moy n o a q Z q s n o ~ p

    O

    p e a l sq p a q u u a d a q l ~ o q slal[y \r dm 'malsKs uo lepluaA Sq)e[n31 3al e ul

    .Sam8 alscM o laqlsauu Bu lsneqxa

    JOJ

    suo s ~wd qq u o a 1lells ap Fo SnOqN q] m sam paa o~d

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    c.

    Air distribution patterns within the protective environ-

    ment room shall conform to the fo llowing:

    Supply air diffusers shall be above the patient be&

    unless it can he dem onstrated that such a location is

    not practical. Diffuser design shall limit air velocity

    at the patient bed to reduce patient discomfort. (See

    ANSI/ASHR/IE Staildard 55-2004 Tlzerntal Einli

    rortntentol Coilditions for Htrnlail Ocnrpanqi in

    Informa tive Annex B: Bibliography.)

    Returdexhaust grilles or registers shall be located

    near the patient room door.

    d.

    Differential pressure between any dissimilar adjacent

    paces shall be a minimum of +0.01 in. wc (t2 .5 Pa).

    e.

    PE rooms retrofitted from standard patient rooms m ay be

    ventilated with recirculated air, provided that air lint

    passes through aH EP A filter and the roo m com plies with

    parts a through

    d

    of this section.

    7 3 Crit ical Care Un its

    7 3 1 Wound Intensive Care Units (Bur n Units). Bum

    unit patient rooms that require humidifiers to comply with

    Table 7-1 shall be prov ided with individual hum idity control.

    7 4 Surgery Rooms

    7 4 1 Class B an d C O pera ting Rooms. Operatingrooms

    shall be maintained at a positive pressure with respect to a ll

    adjoining spaces at all times. A pressu re differential shall be

    maintained at a value of at least +0.01 in. wc (2.5 Pa). Ope r-

    ating rooms sball be provided w ith prirnnry supply diffusers

    that are designed as follows:

    a

    The airflow shall be unidirectional, downwards, and the

    merage velocity of the diffusers shall he 25 to 35 ciW@

    (127 ~ l d m ' o 1 78 ~ s l m ' ) .Th e diffusers shall be concen-

    trated to provide an airflow pattem over the patient and

    surgical team. (see Memanadeh [2002] and Memarzadeh

    [2004] in Informative AunexB: Bibliography.)

    b.

    The area of the p h a r y supply

    diffuser

    array shall extend

    a minimum of 12 in. (305

    mm

    beyond the footprint of

    the surgical table on each side. No m ore than 30 of the

    primary supply d i e r rray area sbal l be used for non-

    d i i s e r uses such as lights, gas columns, etc. Additional

    supply d i e t s may be required to provide additional

    ventilation to the operating room to achieve the environ-

    mental requirements of Table 7-1 relating to temperature,

    humidity, etc.

    The rooms ball he provided with at least two low sidewall

    rehlrn or exhaust ,dies spaced at opposite corners o r as far

    apart as possible, with the bottom of these grilles installed

    approximately8 in. (203 mm bove the floor.

    7 4 2

    Sterilization Rooms. Steam that escapes from a

    steam sterilizer shall be exhausted using an exhaust hood or

    other suitable means. Ethylene oxide that escapes from a ga s

    sterilizer shall be exhausted using an exhaust hood or o ther

    suitable means.

    7 4 3 Imaging P roce dure Room s. If invasive procedures

    occur in this type of room, ventilation shall be provided in

    accordance wtth the vent~lation

    equirements

    for Class A sur-

    gexy. If anesthetic ga ses a re adm inistered, ventilation shall be

    provided in accordance with the ventilation requirements for

    Class B or C surgery.

    7 5 Sup port Spaces

    7 5 1 Morgue and Autopsy Rooms. Low sidewall

    exhaust grilles shall be providedunless exhaus t air is removed

    through an autopsy table designed for this purpose. All exhaust

    air from autopsy, nonrekigerated body-holding, and morgue

    rooms shall he discharged directly to the outdoors without

    mixing with air from any other room or exhaust system.

    8. PLANNING, CONSTRUCTION, AND

    SYSTEM STARTUP

    8 1

    Overv iew. F or HVAC systems serving surgery and crit-

    ical care spaces, compliance with this standard requires prep-

    aration of n acceptance testing plan.

    8 2

    Planning for the HVAC Services in New Facility.

    Design documents for new construction shall meet the follow-

    ing requirements:

    a General Mecl~anicalEquipment Rooms. The access to

    mechanical rooms shall be planned to avoid the intrusion

    of maintenance personnel into surgical and critical care

    patient spaces.

    b. Mechanical Room Layout. Mechanical room layout

    shall include sufficient space for access to equipment for

    operation, maintenance, and replacement. Floors in

    mechanical rooms shall be sealed, including sealmg

    around aU penetrations, when they are above surgical

    su ites and critical care.

    c.

    MaintenancdRepair Personnel Access. Safe andpractical

    means of accessing equipment shall be provided. Clear-

    ance is required at all senrice points to mechanical equip-

    ment to allow personnel access and working space. The

    access to mechanical equipment sball he planned to make

    it unnecessary for maintenance

    personnel to intrude into

    surgical o r critical care rooms.

    d.

    Cooling Towers

    Cooling towers shall be located so that

    drift is directed away from air-handlmg un it intakes. They

    sball meet the requirements of Sec tion 6.3.2.

    8 3

    Planning for tbeHVAC Services in an Existing Facility.

    If any existing air-handling equipment is reused, the designer

    shall evaluate the capacity of the equipment to determine

    whetber it will meet the requirements of this standard for the

    remodeled space.

    8 4 Planning for Infection Control During Rem odeling

    of a n Ex istin g Facility. Prior to beginning modifications or

    rem ode ling of HVAC systems in an existing facility, an owner

    sball conduct an infection control risk assessment (ICRA).

    The ICRA shall establish those procedures required to

    mini-

    mize the dismption of facility operation and the distribution

    of dust, odo rs and particulates.

    ANSUASH RAUASHE Standard

    110 2008

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    8.5 Docum entation of New o r Remodeled HVAC Sys-

    tems. O wners shall retain an acceptance testingreportfo r their

    files. In addition, the design shall include requirements for

    operations and maintenance staff training that is sufficient for

    the staff to keep all HVAC equipm ent in a condition that will

    maintain the original design intent fo r ventilation. Training of

    operating staff shall include an explanation of the design

    intent. The training materials shall include, at a m i n i m , he

    following:

    a. O M procedures

    b. Temp eratuse and pressure contro l opera tion in

    all modes

    c. Acceptable tolerances for system temperatures and

    pressures

    Procedures for operations under emergency power or

    other abnormal conditions that have been considered in

    the facility design.

    8.6

    Duct Cleanliness. The duct supply system shall meet

    the following requirements for cleanliness:

    The duct system shall be free of construction debris. New

    supply duct system installations shall comply with level

    WB: the Intermediate Level of SMACNA Duct Cleanli-

    ness for New Construction ~u ide lin es ?

    h.

    The supply diffusers in the Class B C operatin, rooms

    shall he opened and cleaned before the space is used.

    c. The permanent W A C systems shall not be operated

    unless protection from contamination of the air distribu-

    tion system is provided.

    9. NORMATIVE REF ERE NCE S

    Code of Federal Regulations: 21CFR 173.310 (April

    1999), US Dept. of Health and Human Services, Food

    and Drug Administration.

    DHHS

    (NIOSH) Publication No. 94-100 (NIOSH Alert)

    Controlling Exposures to Nitrotis Oxide During An--

    thetic Administration National Institute for Occupa-

    tional Safety and Hea lth (CDC), Atlanta, GA.

    3 ~ ~ ~

    1994]. Computerized information system. Wash-

    ington, DC: U.S. Department of Labor, Occupational

    Safety and Health Ad ministration.

    4 ~ ~ ~ ~ ~ ~ H R A Etandard 154-2003 Ventilation for Cont-

    rnercial Cook ing Operatio ns American Society of Heat-

    ing, Re£tigerating and Air-Conditioning Engineers,

    Atlanta, GA.

    'NFPA 90A. National F i e Protection Association 1 Battery-

    march Park, Quincy,

    MA

    02169.

    'NFPA 96. Nation al Fire Protec tion Associa tion 1 Battery -

    march Park, Q uincy, MA 02169.

    NIOSH

    Critical Documents. National Institute for Occupa-

    tional Safety and Health, available at the Centers for

    Disease Control and Prevention (CDC) web site: http://

    www.cdc.gov/nioshlpubs/

    criteria~date~desc~nopubnumhers hhnl

    'NFPA 99-2005: Standard for Healtl? Care Facilities.

    National Fire Protection Association 1 Batterymarch

    Park, Quincy, Massachusetts USA 02169

    'SMACNA Duct Cleanliness for

    Nenl

    Consshiction Guide-

    Imes (2000), Chantilly, VA 20151.

    (This annex is not par t of this s tandard. I t i s merely

    informative an d does not contain requirem ents necessary

    for conformance to the s tandard. I t has not been

    processed according to the ANSI requirements for a

    s tandard and may contain mater ial that has not been

    subjec t to public review o r a consensus process.

    Unresolved objectors on informative material are not

    offered th e ri gh t to appe al a t ASHRAI?. o r ANSI.)

    INFORMATIVE ANNEX A

    A l . O M IN HEALTH CA RE FACILITIES

    The following operations and maintenance procedures

    are recom mended for health care facilities.

    Al l Operating Rooms. Each operating room should be

    tested for positive pressure semi-annually o r on an e ffective

    preventative maintenance schedule. When HEPA filters are

    present with'm the diffuser of operating room s, the filter

    shou ld he replaced based on pressure drop.

    A1 2

    Protective Environment (PE) Rooms. PE rooms

    should remain under positive pressure with respect to all

    adjoiningrooms whenever an imrnunocomp~omisedpatients

    present. PE rooms sho uld be testedfor positive pressure daily

    when an immunocom promised patient is present. W hen

    HEPA filters are present within the diffuser of protective envi-

    ronment rooms, the filter should he replaced based on pres-

    sure drop.

    A1 3

    Airborne Infection Isolation

    AII)

    Rooms . U

    rooms shou ld remain u nder negative pressure relative to aU

    adjoining rooms whenever an infectious patient is present

    They shou ld he tested for negative pressure daily whe neve r an

    infectious patient is present.

    A1 4 Filte rs. Final filters and filter frames sh ould be v isu-

    ally inspected for pressure drop and for bypass monthly. Fil-

    ters shouldh e replacedbasedonpressure drop with filters that

    provide the efficiencies specified in Table 6-1.

    A2. SP EC IAL MAINTENANCE FOR HVAC UNITS

    The following special maintenance procedures are

    recomm ended for health care facilities.

    A2 1

    Pnn-Coil Unit and Heat Pumps. The fan-coil unit

    and heat pump filters serving patient rooms should be

    inspected monthly or on an effective preventative mainte-

    nance cycle forpressure drop andreplaced when that pressure

    drop causes a reduction in air flow. Fan-coil unit and heat

    pump drain pans under cooling coils should be cleaned

    monthly, or on a n effective preventative maintenance cycle.

    A2 2

    Pi -Tube Radia t ion Uni t s , Induct ion Uni t s and

    Convection Units. Fm-tube radiation

    units,

    induction units

    and co nvection units serving patient rooms shou ld be cle ane d

    quarterly, or on an effective preventative m aintenance cycle .

    A2 3

    Fan-Powered Terminal Units. Fan-powered te m i-

    nal unit filters serving patient rooms should be inspected @

    monthly or on an effective preventative maintenance cycle fo r

    pressure drop and replaced when the pressure drop causes a

    reduc tion in air flow.

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     This ann ex is not p ar t of this standard. I t is merely

    informative an d does not contain requirements necessary

    for conformance to the standard. It has not been

    processed according to the ANSI requirements for a

    standard and may contain material that has not been

    subject to public review or a consensus process.

    Unresolved objectors on informative material are not

    offered the right to appeal at SHR E o r ANSI.)

    INFORM TIVE NNEX B

    BIBLIOGR PHY

    ACS, 2000.

    Gu~ deliiies or Optiiital Ainbtrlato~y Si~r gica l

    Care aird Oflce-based Sirrgeiy.

    31d ed. American Col-

    lege of S urgeons, Chicago, IL 6061 1

    AIA

    2006. The American Institute of Architects and The

    Facilities Gu~d elines nstitute.

    G~rideliitesor Design

    and Conshrctioir of Hospital aiid Health Care Faci11-

    ties. American Institute of Architects Press, Washiig-

    ton, DC 2006.

    ASHRAE, 1999. hfethod of Testing General VentilationAir-

    Cleaning Devices for Removal Eficiency by Particle

    Size.

    ANSUASHRAE Standard 522-1999.

    ASHRAE, 2003. 2003 A S H M Handbaok-Applica tions ,

    Chapter 7, Health C are Facilities. American Society of

    Heating, Rehgerating, and Air-Conditioning Engi-

    neers, Inc., Atlanta GA.

    ASHRAE, 2003.

    W A C Desigrl 12faniinl for Hospita ls and

    Health Care Facilities,

    American Society of Heating,

    Refrigerating, and Air-Conditioning Engineers, Inc.,

    Atlanta GA.

    ASHRAE, 2004.

    77teimal Enviroi~mental Cai ~dit iom i r

    Hiiman O cciipai~cy,

    NSUASHRAE Standard 55-2004.

    ASHRAE, 2005. 2005

    A S H M Handbook-Frmdomentals ,

    Chap ter 35, Duct Desifg. American Society of Heating,

    Refrigerating, and Air-Conditioning Engineers, Inc.,

    Atlanta GA.

    ASHRAE, 2007.

    Ventilat ion for Acceptable Indoor

    Air

    Ouality,

    ANSUASHRA E Standard 62.1-2007. Am eri-

    Society of Heating, Refrigerating,

    and

    Air-

    Conditionin g Engineers, Inc. Atlanta, GA.

    CANICSA-2317.2-01 Special Requirements for Heating,

    Ventilation, and ii Conditioning Systems

    in

    Health

    Care Facilities Sep tember 2001.

    CDC, 2005.

    Gtiideliiles or Preoeiitiiig the Transntissioil of

    ~fj~cabocteri~ii i liberculosis br Healtli-Care Facilities.

    FederalRegistei;

    2005. Centers for Disease Control and

    Prevention, A tlanta, GA.

    CDC, 2003. Guideliires or Ein~iroirii~ei~tali$ectioit coiitrol

    in health-care facilities. Morbidity and klortality

    Weeldy Report MMWR), June

    6,

    2003. Centers for

    Disease Control and Prevention, Atlanta, GA.

    Charles S. Hayden 11, O.E. Jo hnston, RT . Hugh es, and P.A.

    Jensen, 1998.Air

    Volimieiz.figration

    i r

    Negative Pres-

    sure Isolatioir Ra onls Dririiig Eiib y/E xit.

    Applied Occu-

    pational and Enviranmeotal Hygiene, 13 7): 518-527;

    1998.

    Coogan, JJ, 1996.

    Effects of Sui~ olind iiig paces an Roonis

    Presstriized y Differential Flow Control.

    ASHRAE

    Transaction s 1996, 102, Pt 1.

    Hermans,

    RD.

    2000.

    Healtlz C are Facilify Design Ma nual-

    Room Design.

    ASHR AE Transactions Vol. 1 06, Pt. 2

    Lewis,

    J.R,

    1987.

    Operatiiig room air distributioil effective-

    ness.

    ASHR AE Transactions 93 2):1191-1198.

    Mem arzadeh F and Manning A, 2002.

    Comparison of oper-

    ating room ventilatioit ?stems in the protection of the

    surgical site. ,

    ASHRAE Transactions, V.108, Pt. 2,

    2002.

    Memarzadeh

    F and Jiang Z. 2004. Effects of Operoting

    Room Geom ehy and Vei~tilation ystem Parameter Vari

    ations oil the Protectioii of the S ~rrg icnl ite , LAQ 2004:

    Critical Operations: Supporting the Healing Environ-

    ment through IAQ Performance Stand ards.

    Ni iom ura , P. and Judene Bartley, 2001.

    Nav Veiztilatioii

    Guide lines for Healtlr-Care Facilities,

    ASHRAE Jour-

    nal, June 2001, Atlanta, GA

    NFPA, 2005. Standard for Health Care Facilities. NFPA-99-

    2005. National Fire Protection Association 1 Battery-

    march Park, Quincy, M assachusetts USA 02169

    SMACNA,

    Duct Cleaiiliness or Nav Canstnrction Guide-

    lines.

    USP-797, Guidebook to Pharmaceutical Compounding-

    Sterile Preparations, US Pha ma cop eial Convention.

    29 C FR Pa rt 1910.1047, Occupational Exposlue to Ethylene

    Oxide.

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    NOTICE

    INSTRUCTIONS FO R SUBM ITTING PROPOSED CH NGE TO

    THIS ST ND RD UN DE R CONT INUOUS M INTEN NCE

    Thi s stand ard is maintained under continuous maintenan ce procedures by a Standing Standard Project C ommittee (SSPC) for

    wh ich the Standards Comm ittee has established a docum ented progtam for regular publication of addenda or revisions, includ-

    ing procedures for timely, documented, consensus action on requests for change to any part of the standard. SSPC consider-

    ation w ill be given to proposed changes within 13 months of receipt by the ma nager of standards (MOS).

    Proposed changes must be submitted to the M OS in the latest published form at available fio m the MOS. However, the MOS

    m ay accept proposed changes in an earlier published format if the M O S conc ludes that the diEferences are imm aterial to the

    proposed change submittal.

    f

    the MOS concludes that a current form must he utilized, the proposer may he giv n up to

    20 additional days to resubmit the proposed changes in the current format.

    ELECTRONIC PREP R TIONISUBMISSION OF FORM

    FO R PROPOSING CH NGES

    n electtonic version of each change, which mu st com ply with the instructions in the Notice and the Form, is the prefe ned

    fo rm of submittal to ASHRAE H eadquarters at the address shown below. The electronic format facilitates both paper-based

    and computer-based processing. Submittal in pape r form is acceptable. The following instructions apply to chnnge proposals

    submitted in electronic form .

    U se the appropriate file format for your wo rd processor and save the file in either a recent version of Microsoft Word (pre-

    ferred ) or another commonly used word-processing program. Please save each change proposal file with a different nam e (for

    exam ple, propOl.doc, prop02.doc:' etc .).

    f

    supplemental background documents to support changes submitted are

    inclu ded, it is preferred that they also be in e lectro nic form as word-pro cessed or scanned documents.

    ASHRAE will accept the following as equivalent to the signature required on the change submittal form to convey non-

    exclusive copyright:

    Files attached to a n e-mail:

    Files on a CD:

    Eleclm nic signature on change submittal form

    (as apicture; *.tif, or *.wpg).

    Electronic signature on change submittal form

    (as a pictute; *.tif, or *.wpg) or a letter with submitter's

    signature accompanying the CD or sent by facsimile

    (single letter may covet all o f proponent's proposed cbanges).

    Submit an e-mail or

    a

    CD containing the change proposal files to:

    Manager of Standards

    ASHRAE

    1791 Tullie Circle, NE

    Atlanta, GA 30329-2305

    E-mail: change proposal@ashrae org

    (Alternatively, mail paper versions to ASHRAE address or fax to 404-321-5478.)

    T h e form and instructions for electronic submittal may b e obtained from the Standards section of ASHRAE's Home Page,

    www .ashrae.org, or by contacting a Standards Secretary, 1791 Tullie Circle, NE Atlanta, GA 30329-2305.

    Ph one : 404-636-8400. Fax: 404-321 -5478, E-mail: [email protected].

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    POLICY STATEMENT DEFINING ASHRA E S CONC ERN

    FOR THE ENVIRONMENTAL IMPACT OF ITS ACTIVITIES

    ASHR AE is concerned with the impact of its mem bers activities on both the indoor and outdoor environment. ASHRA E s

    members will strive to minimize any possible deleterious effect on the indoor and outdoor environment of the systems and

    components in their responsibility while m aximizing the b eneficial effects these systems provide, consistent with acce pted

    standard s an d the practical state of the art.

    ASHR AE s short-range goal is to ensure that the system s an d components within its scope do not impact the indoor and

    outdoor environment to a greater extent than specified by the standards and guidelines as established by itself and other

    responsible bodies.

    As an ongoing goal. ASHRAE will, through its Standards Committee and extensive technical committee structure,

    continue to generate up-to-date standards and guidelines where appropriate and adopt, recomm end, and promote those new

    an d revised standards developed by other responsible organizations.

    Through its Handbook, appropriate chapters w ill contain up-to-da te standards and design considerations as the material is

    systematically revised.

    ASHR AE will take the lead with respect to dissemination of environmental information of its prirnaty interest and will seek

    out and disseminate information from other responsible organizations that is pertinent, as guides to updating standards and

    guidelines.

    The e ffects of the design and selection of equipment and systems w ill be considered within the scope of the system s

    intended use and expected misuse. The disposal of hazardous m aterials, if any, will also be considered.

    ASHR AE s primary concern for environmental im pact will be at the site where equipment within ASHR AE s scope

    operates. However, energy source selection and the possible environmental impact due to the energy source and energy

    transportation will be considered where possible. Recommendations concerning energy source selection should be made by

    its m embers.