Nosocomial Infections: Dr. Tjatur Winarsanto SPPD RST Ciremai Cirebon

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Nosocomial

infections
Dr. Tjatur Winarsanto SpPD
RST Ciremai
Cirebon

NOSOCOMIAL INFECTIONS
Infection in a hospitalized patient
Not present or incubating on admission
Hospital acquired infection

Nosocomial Infections
5-10% of patients admitted to acute care

hospitals acquire infections


2 million patients/year
of nosocomial infections occur in ICUs
90,000 deaths/year
Attributable annual cost: $4.5 $5.7 billion
Cost is largely borne by the healthcare facility not
3rd party payors
Weinstein RA. Emerg Infect Dis 1998;4:416-420.
Jarvis WR. Emerg Infect Dis 2001;7:170-173.

NOSOCOMIAL INFECTIONS
Infections acquired in the hospital
infection was neither present nor incubating when admitted
2 million infections in 1995 in USA
90,000 deaths
may range from mild to serious (including death)
Although acquired in the hospital-may appear after discharge from
hospital
Some infections occur in outbreaks or clusters (10%)
but majority are endemic
Can result from diagnostic or therapeutic procedures
catheters in bladder or blood vessel, surgery
correlate with length of stay

PATHOGENESIS OF NOSOCOMIAL INFECTIONS

3 ingredients
Susceptible host
Virulent organism
Portal (mode) of entry

Where do the microbes come from?

patient's own flora


cross infection from medical personnel
cross infection from patient to patient
hospital environment- inanimate objects
- air
- dust
- IV fluids & catheters
- washbowls
- bedpans
- endoscopes
- ventilators & respiratory equipment
- water, disinfectants etc

The Inanimate Environment Can


Facilitate Transmission
X

represents VRE culture positive sites

~ Contaminated surfaces increase cross-transmission ~


Abstract: The Risk of Hand and Glove Contamination after Contact with
a VRE (+) Patient Environment. Hayden M, ICAAC, 2001, Chicago, IL.

SOURCES OF PATHOGENS IN NI
Reactivation of latent infection: TB, herpes

viruses

Less common

Endogenous: normal commensals of the skin,

respiratory, GI, GU tract


common

Exogenous
Inanimate environment: Aspergillus from hospital

construction, Legionella from contaminated water


Animate environment: hospital staff, visitors,
other patients

Cross transmission- common

MECHANISMS OF TRANSMISSION
Contact: direct (person-person), indirect

(transmission through an intermediate object-contaminated instruments


Cross transmission

Airborne: organisms that have a true airborne

phase as pattern of dissemination (TB, Varicella)


Common-vehicle: common animate vehicle as
agent of transmission (ingested food or water,
blood products, IV fluids)
Droplet: brief passage through the air when the
source and patient are in close proximity
Arthropod: not reported in US

SITES OF NOSOCOMIAL INFECTIONS


Urinary tract 40%
Pneumonia 20%
Surgical site 17%
Bloodstream (IV) 8%

Nosocomial Pneumonia

NOSOCOMIAL PNEUMONIA
Lower respiratory tract infection
Develops during hospitalization
Not present or incubating at time of

admission
Does not become manifest in the
first 48-72 hours of admission

EPIDEMIOLOGY
13-18% of nosocomial infections
6-10 episodes/1000 hospitalizations
Leading cause of death from NI
Economic consequences
prolongation of hospital stay 8-9 days
Costs $1 billion/year

Nosocomial Pneumonia
Cumulative incidence = 1-3% per day of intubation
Early onset (first 3-4 days of mechanical ventilation)
Antibiotic sensitive, community organisms

(S. pneumoniae, H. influenzae, S. aureus)

Late onset
Antibiotic resistant, nosocomial organisms (MRSA, Ps.

aeruginosa, Acinetobacter spp, Enterobacter spp)

PREDISPOSING FACTORS
Endotracheal intubation!!!!!!!!!!!!!!
ICU
Antibiotics
Surgery
Chronic lung disease
Advanced age
immunosuppression

PATHOGENESIS
Oropharyngeal colonization
- upper airway
colonization affected by
host factors, antibiotic use,
gram negative adherence
- hospitalized pts have
high rates of gram
negative colonization
Gastric colonization
-increased gram
negatives with high
gastric pH
- retrograde colonization
of the oropharynx

DIAGNOSIS AND TREATMENT


Clinical diagnosis

- fever, change in O2, change in sputum, CXR


Microbiologic Confirmation
Suctioned Sputum sample
Bronchoscopy with brochoalveolar lavage

Empiric antibiotic- clinical acumen

- Rx based on previous cultures, usual


hospital flora and susceptibilities
- sputum gram stain
- colonization vs. infection

PREVENTION
Pulmonary toilet
Change
Elevate

Deep

position q 2 hours
head to 30-45 degrees

breathing, incentive spirometry


Frequent suctioning
Bronchoscopy to remove mucous
plugging

Nosocomial Urinary Tract Infections

URINARY TRACT INFECTIONS


Most common site of NI (40%)
Affects 1/20 (5%) of admissions
80% related to urinary catheters
Associated with 2/3 of cases of nosocomial

gram negative bacteremias


Costs to health care system up to $1.8
billion

Nosocomial Urinary Tract


Infections
25% of hospitalized patients will have a urinary catheter for part of

their stay
20-25 million urinary catheters sold per year in the US
Incidence of nosocomial UTI is ~5% per catheterized day
Virtually all patients develop bacteriuria by 30 days of catheterization
Of patients who develop bacteriuria, 3% will develop bacteremia
Vast majority of catheter-associated UTIs are silent, but these
comprise the largest pool of antibiotic-resistant pathogens in the
hospital

Safdar N et al. Current Infect Dis Reports 2001;3:487-495.

PATHOGENESIS
Source of uropathogens
Endogenous- most common

- catheter insertion
- retrograde movement up the urethrea (7080%)
- patients own enteric flora (E.coli)
Exogenous

- cross contamination of drainage systems


- may cause clusters of UTIs

PATHOGENESIS
Major risk factors: 1)

pathogenic bacteria in
periurethral area 2)
indwelling urinary
catheter
Duration catheterization

Bacterial factors:
properties which favor

attachment to
uroepithelium, catheters

Growth in biofilm
Bladder trauma decreases

local host defenses

Urinary (Foley)
Catheter

ETIOLOGIC AGENTS: catheter associated


UTI
Bacteria
E. coli
Proteus spp
Enterococcus
Klebsiella
Pseudomonas
Enterobacter
Candida
Serratia
Other

% Distribution
32
14
12
9
9
4
4
1
15

TREATMENT
Is this a UTI vs asymptomatic bacteruria?
Use clinical judgement

- urine WBC- pyuria


- bacterial colony counts > 103
- clinical signs/symptoms
No antibiotic treatment for bacteruria
- resolves with catheter removal
7-10 days of therapy for UTI
Empiric therapy typically initiated pending
microbiologic results

Prevention of Nosocomial UTIs


Avoid catheter when possible & discontinue

ASAP- MOST IMPORTANT


Aseptic insertion by trained HCWs
Maintain closed system of drainage
Ensure dependent drainage
Minimize manipulation of the system
Silver coated catheters

Surgical Site Infections

SURGICAL SITE INFECTIONS


325,000/year (3rd most common)
Incisional infections
Infection at surgical site
Within 30 days of surgery
Involves skin, subcutaneous tissue, or muscle above

fascia
Accompanied by:

Purulent drainage
Dehiscence of wound
Organism isolated from drainage
Fever, erythema and tenderness at the surgical site

SSI: Superficial

SURGICAL SITE INFECTIONS


Deep surgical wound infection
Occurs beneath incision where operation took place
Within 30 days after surgery if no implant, 1 year if

implant
Infection appears to be related to surgery
Occurs at or beneath fascia with:

Purulent drainage
Wound dehiscence
Abscess or evidence of infection by direct exam
Clinical diagnosis

SSI: Deep

SURGICAL SITE INFECTIONS


Risk of infection dependent upon:
Contamination level of wound
Length of time tissues are exposed
Host resistance

SURGICAL SITE INFECTIONS


Clean wound

* elective, primarily closed, undrained


* nontraumatic, uninfected
Clean-Contaminated wound
* GI, resp, GU tracts entered in a controlled manner
* oropharynx, vagina, biliary tract entered
Contaminated wound
* open, fresh, traumatic wounds
* gross spillage from GI tract
* infected urine, bile

PATHOGENS ASSOCIATED WITH SWI


Pathogen
S. aureus
Enterococci
Coag - Staph
E. coli
P. aeruginosa
Enterobacter
P. mirabilis
K. pneumoniae
Streptococci

% of Isolates
17
13
12
10
8
8
4
3
3

RISK FACTORS
Age (extremes)
Sex

* post cardiac surgery


Underlying disease
* obesity (fat layer < 3 cm 6.2%; >3.5 cm 20%)
* malnutrition
* malignancy
* remote infection

RISK FACTORS
Duration of pre-op hospitalization

* increase in endogenous reservoir


Pre-op hair removal
* esp if time before surgery > 12 hours
* shaving>>clipping>depilatories
Duration of operation
*increased bacterial contamination
* tissue damage
* suppression of host defenses
* personnel fatigue

PREVENTION
Limit pre-op hospitalization
Stabilize underlying diseases
Avoid hair removal by shaving
Clipping of skin is preferred

Skin decolonization
Chlorhexidine
Intranasal Mupirocin for S.aureus carriers

Impermeable drapes
Maximum sterile barrier precautions

PROPHYLACTIC PREOPERATIVE
ANTIBIOTICS

Indicated for clean-contaminated,

contaminated operations
High risk or devastating effect of infection
Dirty wounds already infected (therapy)
Administer at appropriate time
(tissue levels)
30-60 minutes prior to skin incision

Nosocomial Bloodstream Infections

NOSOCOMIAL BACTEREMIA
4th most frequent site of NI
Attributable mortality 20%
Primary

* IV access devices
* gram positives (S. aureus, CNS)
Secondary
* dissemination from a distant site
* gram negatives

The risk factors


interact in a
dynamic fashion
The Host

The CVC is the


greatest risk
factor for
Nosocomial BSI
The CVC: Subclavian, Femoral and IJ sites

The intensity of the Catheter Manipulation

As the host cannot be altered, preventive measures are focused on risk factor
modification of catheter use, duration, placement and manipulation

The major risk factor is the Central Venous Catheter


(CVC)

The CVC- is one of the most


commonly used catheters in
medicine
The CVC is typically placed
through a central vein such as
the IJ, Subclavian or femoral

These serve as
direct line for
microbial
bloodstream
invasion

PATHOGENESIS
Direct innoculation

* during catheter insertion


Retrograde migration
* skinsubcutaneous tunnelfibrin sheath at
vein
Contamination
* hub-catheter junction
* infusate

Risk Factors for Nosocomial BSIs


Heavy skin colonization at the insertion site
Internal jugular or femoral vein sites
Duration of placement
Contamination of the catheter hub

Nosocomial Bloodstream
Infections
12-25% attributable mortality
Risk for bloodstream infection:
BSI per 1,000
catheter/days
Subclavian or internal jugular CVC

5-7

Hickman/Broviac (cuffed, tunneled)

PICC

0.2 - 2.2

Catheter type and expected duration of use should be


taken into consideration

Nosocomial Bloodstream Infections,


1995-2002
Rank

N= 20,978

Pathogen

Percent

Coagulase-negative Staph

31.3%

S. aureus

20.2%

Enterococci

9.4%

Candida spp

9.0%

E. coli

5.6%

Klebsiella spp

4.8%

Pseudomonas aeruginosa

4.3%

Enterobacter spp

3.9%

Serratia spp

1.7%

10

Acinetobacter spp

1.3%

Edmond M. SCOPE Project.

Risk Factors for Nosocomial BSIs


Heavy skin colonization at the insertion site
Internal jugular or femoral vein sites
Duration of placement
Contamination of the catheter hub

Prevention of Nosocomial BSIs


Limit duration of use of intravascular

catheters

No advantage to changing catheters routinely

Maximal barrier precautions for insertion


Sterile gloves, gown, mask, cap, full-size drape
Moderately strong supporting evidence

Chlorhexidine prep for catheter insertion


Significantly decreases catheter colonization; less

clear evidence for BSI


Disadvantages: possibility of skin sensitivity to
chlorhexidine, potential for chlorhexidine
resistance

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