key: cord-0006679-zxn4oqly authors: Lodha, Rakesh; Chandra, Uma; Natchu, Mouli; Nanda, Mrinal; Kabra, S. K. title: Nosocomial infections in pediatric intensive care units date: 2001 journal: Indian J Pediatr DOI: 10.1007/bf02722358 sha: a58fca85c424037e44ad6c976011fa5f98d4672e doc_id: 6679 cord_uid: zxn4oqly Nosocomial infections are a significant problem in pediatric intensive care units. While Indian estimates are not available, western PICUs report incidence of 6–8%. The common nosocomial infections in PICU are bloodstream infections (20–30% of all infections), lower respiratory tract infections (20–35%), and urinary tract infections (15–20%); there may be some differences in their incidence in different PICUs. The risk of nosocomial infections depends on the host characteristics, the number of interventions, invasive procedures, asepsis of techniques, the duration of stay in the PICU and inappropriate use of antimicrobials. Most often the child had endogenous flora, which may be altered because of hospitalization, are responsible for the infections. The common pathogens involved areStaphylococcus aureus, coagulase negativestaphylococci, E. coli Pseudomonas aeruginosa, Klebsiella, enterococci, andCandida. Nosocomial pneumonias predominantly occur in mechanically ventilated children. There is no consensus on the optimal approach for their diagnosis. Bloodstream infections are usually attributable to the use of central venous lines; use of TPN and use of femoral site for insertion increase the risk. Urinary tract infections occur mostly after catheterization and can lead to secondary bacteremia. The diagnostic criteria have been discussed in the review. With proper preventive strategies, the nosocomial infection rates can be reduced by up to 50%; handwashing, judicious use of interventions, and proper asepsis during procedures remain the most important practices. Nosocomial or hospital acquired infections are all infections that occur during a patient's hospitalization and not present or incubating at admission. Also any infection that appears to have been acquired in hospital but does not manifest until after discharge is judged to be a nosocornial infection. Therefore, all infections diagnosed 48 hours after admission till 72 hours after discharge should be considered as nosocomial. 1, 2 Nosocomial infections are a significant problem in pediatric intensive care units. The National Nosocomial Infection Surveillance System (NNIS) in the United States reports a rate of 14.1 nosocomial infections per 1000 patient days for pediatric ICUs. 3 The overall nosocomial infection rates in the PICUs in the west are reported to be 6-8%. 3.5 These rates are lower than those seen in adult intensive care units. 3, 6 The infections in pediatric intensive care units (PICU) are more widespread than in general pediatric wards. The infection rates depend on the type of PICU: multidisciplinary, medical, surgical, or cardiac. There are no data on the incidence of nosocomial infections in Indian PICUs. It is possible that infection rates here are higher than those reported in the west. According to NNIS, primary bloodstream infections are the commonest nosocomial infections (28%) in PICUs followed by the lower respiratory tract infections (21%) and urinary tract infection (UTI) (15%). 3 In another study, lower respiratory tract infections were the commonest Reprint requests : Dr. Rakesh Lodha, Assistant Professor, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi-110029. E-mail : skkabra@hotmail.com (35%), followed by bloodstream infections (21%) and UTI (16%). 4 These variations may arise from the differences in the proportion in the children ventilated in the PICUs. In adults, UTI is the commonest nosocomial infection followed by surgical infection and lower respiratory tract infections. 6 Staphylococcous aureus, coagulase negative staphylococci, E. coli, Pseudomonas aeruginosa, Klebseilla, enterococci and Candida are the significant pathogens in pediatric services in the various sites examined. 3, 4 The risk of nosocomial infections in a PICU is the direct consequence of the severity of illness, 4 the level of invasive monitoring, the indiscriminate use of antimicrobials and the nature of diagnostic procedures. The NNIS data emphasizes that the duration of stay in an ICU is an important determinant of nosocomial infection; therefore, the length of stay should be one of the denominators in calculation of nosocomial infection rates2 In addition, it highlight the importance of invasive devices (endotracheal tubes, intravascular catheters, urinary catheters) in development of nosocomial infections. 3 In order to control for device usage and duration the infection rates can be represented as ratios per thousand device days. According to the latest report, ventilator associated pneurnonia (VAP) occurrence is 5.7 episodes per thousand ventilator days, UTI 5.2 per thousand catheter days, and bloodstream infection is 8 per thousand central line days. 3 In the same study, it was observed that 91% of all nosocomial bloodstream infections occurred in children with central venous lines, 95% of nosocomial pneumonias occurred in those on mechanical ventilation and 77% of UTIs in children with urinary catheters. 3 These figures highlight the important role of various devices in nosocomial infections. Nosocomial infections may be caused by organisms that originate from exogenous sources in hospital or from endogenous sources such as child's own flora. Because of alteration of child's flora associated with the illness and hospitalization, such distinction may not be easy. A recent study has shown that the mean number of days after admission to PICU to abnormal colonization were as follows: gastric aspirate, 2 days; tracheal aspirate, 5 days; urine 10 days; and stool, 4 days. The altered flora mainly included gram-negative bacilli and Staphylococcus aureus, which were often antibiotic resistant/ The hospital environment contributes minimally to acquisition and spread of most endemic nosocomial infections directly. Even if environmental surfaces are contaminated with microbes, they can be spread to patients by hand contact only ~. Occasionally, environment may be responsible for life threatening nosocomial infections such as aspergillus in immunocompromised individuals. It is estimated that the overall mortality attributed to nosocomial infections is about 10%. 9 The mortality is associated with nosocomial infections is multifactorial; some of these factors are the type of patient, the number of altered organs, and the microbes responsible for the infection. Blood stream infections caused by Klebsiella pneumoniae or the fungi have mortality range of 18-20%2 ~ The nosocomial infections increase the duration of stay in hospital and also the cost of therapy. We restrict further discussion to nosocomial pneumonias, bloodstream infection and urinary tract infections. Pneumonias constitute a common but potentially life threatening complication of hospitalization. The mortality rates associated with nosocomial pneumonia ranges from 20-50%22,~3 Other studies have reported lower mortality rates. 14 While a few pneumonias represent hematogenous seeding of the lungs from a distant suppurative focus; in most patients, subclinical aspiration of oropharyngeal secretions containing bacteria that have colonized the upper airway of the patient is responsible for nosocomial pneu-monia~ This flora includes both gram-positive and gramnegative bacteria, which the patient acquires within 1-4 days after hospitalization. The risk factors for upper airway colonization includ(, acidosis, hypotension, endotracheal intubation, and broad-spectrum antimicrobial ther-apy25 Only a few patients will develop nosocomial pneumonia in absence of colonization of the upper airways. 13 Most nosocomial pneumonias are caused by gram-negative organisms. TM Bacteria of enterobacteriaceae family eg. E. coli, Klebsiella are usually isolated from the hypophar-ynx and rectum before they are isolated from the trachea. 12 However, non-Enterobacteriaceae e.g.P, aeruginosa, Acinetobacter are rarely demonstrated prior to their isolation from the trachea. 12 This suggests that colonization with enterobacteriaceae occurs from patient's endogenous flora and that non-Enterobacteriaceae bacteria have environrnental origin. Therefore, the hands of the health care workers and components of the respiratory therapy equipment may be important factors in the transmission of bacteria. The most important risk factor for nosocomial pneumonia in children is endotracheal intubation. Nosocomial pneumonias are nearly four times more common in intubated patients than in non-intubated patients2 TM The risk may be greater with tracheostomy tubes. The filtration system of upper airways and mucociliary system of the large airways is bypassed during intubation, predisposing the patient to colonization with potential pathogens. Children with asymptomatic or symptomatic aspiration are at risk22 Children with tracheoesophageal fistula, pharyngeal aspiration, gastroesophageal reflux, pulmonary disease, malnutrition or immunodeflciency are at greater risk. The etiologic microorganisms for nosocomial pneumonia vary from hospital to hospital. The pediatrician must be familiar with the common microbes and the antimicrobial susceptibility of these microbes at his/her hospital. Gram-negative bacilli are the most important cause; 3,~5 staphylococci are the most important gram-positive organisms. Viruses such as respiratory syncytial virus are also important pathogens responsible for nosocomial pneumonia in PICUs. 3 However, some authors have suggested that viruses are less frequent as nosocomial pathogens in PICUs than in other areas of pediatric hospitals. 16 The optimal approach for diagnosing nosocomial pneumonia remains elusive. Clinical features, chest radiographs and culture of respiratory secretions have been used to establish the diagnosis. However, this approach is likely to overestimate the diagnosis. Fever and leukocytosis are also non-specific. Cough and sputum production are infrequently diagnostic of pneumonia in intubated children. Purulent tracheal secretions may be due to tracheitis, tracheobronchitis or pneumonia; differentiation can be difficult. Conditions such as atelectasis, pulmonary edema, pulmonary hemorrhage and acute respiratory distress syndrome (ARDS) may be confused with pneumonia2 6 Therefore, clinical suspicion has to be strong for diagnosing nosocomial pneumonia. A change in the child's status such as desaturation, increased requirement for supplemental oxygen, increase in ventilator settings or fever that are not explained by other events can be helpful in the diagnosis. In view of these problems and controversies Centers for Disease Control and Prevention have provided clinicians with guidelines for diagnosis of nosocomial LRTI. 1,2 Once nosocomial pneumonia is suspected attempts should be made to identify the etiologic agent. Qualitative cultures obtained from endotracheal tubes do not predict the causative agent of lower respiratory tract infections. Quantitative cultures appear to be superior to qualitative cultures. TM Blood cultures are usually negative. Transtracheal aspiration in non-intubated patients, percutaneous thin needle lung aspirations, bronchoalveolar lavage (bronchoscopic or blind), and protected bronchoscopic samples of the lower airways have all been suggested as methods for diagnosis, where contamination of lower respiratory secretions with upper airway flora is prevent-ed29~~ In the absence of gold standard criteria for the diagnosis of ventilator-associated pneumonia, quantitative cultures and microscopic examination of the lower respiratory tract secretions are the diagnostic tests of choice. This can provide accurate diagnosis and identification of causative organism. These can also help in diagnosis of ventilator-associated pneumonia in children with ARDS. 21 The colonization of upper airways by pathogenic microbes and thereby, the risk of nosocomial pneumonia can be reduced by several measures. Effective hand washing by the health care personnel can reduce the risk of nosocomial pneumonias. 22 Various chemicals such as chlorhexidine or rubs containing alcohol may be used. The reduction in the number of microorganisms on hands is related to the volume and number of times they are used. 23 In addition, the hospital workers should comply with hospital infection control policies. The gastrointestinal tract is an important source for endogenous upper airway colonization. Use of antacids and H2 blockers raise gastric pH and facilitate gastric microbial colonization. When indicated, instead of H2 blockers and antacids, sucralfate may be used for prophylaxis against gastric bleeding as the gastric pH remains low with its use. 24 The use of selective decontamination of the gut using antimicrobial such as tobramycin, gentamycin, polymyxin and nystatin is controversial and is not recommended. 25 Contaminated respiratory therapy equipments have been implicated in nosocomial pneumonias. 25 Resuscitation bags, ventilator tubings, nebulizers should be disinfected. Only sterile fluids should be nebulized or used in humidifiers. Personnel taking care of intubated children should wash their hands before and after delivering care. The ventilator circuit tubings should be changed no more often than every 48 hours? 7,25 Care should be taken to prevent contamination during suctioning; endotracheal suctioning should be performed as needed to remove secretions. 26 Positioning of patients with head end elevation does reduce the risk of aspiration and nosocomial pneumonia. 27 Bacterial tracheitis usually is secondary to a primary viral upper respiratory tract infection, most often parainfluenza virus. 17 The data on nosocomial bacterial tracheitis is scant. 14 Most nosocomial upper respiratory tract infections are viral and appear 2 weeks after admission. 28 Bacteria are implicated in sinusitis and otitis media. Sinusitis may occur in a significant number of patients who have undergone nasotracheal intubation. 29 Nasogastric tubes also predispose to sinusitis. The diagnosis usually has to be confirmed by radiology. While intravascular catheters provide lifesaving therapy, they also provide a route for microorganisms to bypa~ normal host defenses and can cause serious infections. Primary bacteremia is defined as a bloodstream infection occurring in a patient with no evidence of localized infection while secondary bacteremia is defined as a bloodstream infection with evidence of infection at another site that is the source of the bloodstream infection. More than 90% of all nosocomial bloodstream infections are in children with central venous lines? Infections may occur due to microbes from the skin moving along the catheter surface where catheter enters the skin or due to microbes gaining access to the catheter through the catheter hub and moving down the endoluminal surface of the catheter to the bloodstream. ~1 The former mechanism is more often seen in short-term catheters and the latter in long-term catheters. Formation of biofilms over the implanted devices also may have a role in occurrences of the infections. The most common organisms in bloodstream infections are coagulase negative staphylococcus, Staphylococcus aureus and enterococci. 3 Among the gramnegative bacteria Enterobacter, Pseudomonas aeruginosa, Klebsiella pneumoniae, and E. coli are the most important organisms. 3 In immunocompromised children and those who have received a variety of broad spectrum antibacterials, fungal infections are more frequent. The most important risk factor for catheter related bloodstream infections is the type of catheter used. Central venous catheters account for about 2% of all catheters inserted and more than 90% of all catheterrelated bloodstream infections. 3 The risk is probably greater with multilumen central venous catheters. 32 Sub optimal care of central venous catheters especially when used for total parenteral nutrition (TPN) is another risk factor. Lipid infusions have specifically been associated with risk of catheter-related bloodstream infections due to coagulase negative staphylococcus? 3 The risk of infection increases linearly with the duration of catheterization. The site of insertion is an important determinant of the risk of infection; rates for femoral catheters are higher than that for jugular or subclavian catheters. 3a Peripherally inserted central catheters (PICC lines) may have lower infection rates. Inadvertent contamination during insertion may be an important risk factor for infection. This is highlighted by an inverse relation between the total number of catheters inserted by the physician inserting the catheter and the risk of significant catheter colonization. 3s Improper management of catheter after insertion significantly increases the risk of infection. Transparent dressings may be associated with a higher rate of blood stream infections. 36 Local catheter-related infections usually manifests with local inflammation erythema, tenderness and/or purulent discharge from the catheter tract. The presentation of bloodstream infections may be either acute or insidious. There may be signs of sudden deterioration, elevated body temperature, chills and tachycardia or there may be intermittent fever and failure to improve from their basic illness. Whenever catheter related bacteremia is suspected, blood cultures should be obtained from peripheral blood as well as all catheter sites to correlate and differentiate colonization from infection. Catheter related bloodstream infection is defined as the isolation of same organism from blood cultures that is shown to be significantly colonizing the catheter of a patient with clinical features of bloodstream infection in the absence of any other local infection caused by the same organism that could give rise to bloodstream infection. 1,2 The major factors associated with development of catheter-related nosocomial infections are : (i) the sterility of the technique of insertion and maintenance of the catheter throughout its life, (ii) type of solution being administered through the intravenous line, (iii) number of "break ins" into the catheters system and intravenous tubing, (iv) the presence of infection elsewhere in the body. 37 Largely, the origin of the organisms causing the UTI can be traced either to the patient's own large bowel, perineum or to the hands of care providers. Contamination of the urinary tract by microbes occurs either through the catheter lumen or by ascending up along the catheter during or after insertion. 46 Extraluminal contamination is the commonest; it can occur by direct inoculation when the catheter is inserted or later, by the ascent of microbes from the perineum by capillary action in the thin mucus film contiguous to the external catheter surface. 47 Intraluminal contamination occurs by reflux of microorganisms gaining access to the catheter lumen because of failure of closed drainage or contamination of urine in the collection bag. Pyelonephritis from bloodstream infections are rare but may occur in newborns and infants. The most important risk factor for nosocomial UTI is catheterization. The timing, purpose and duration of catheterization are also important. Malnutrition, renal dysfunction, urological procedures and stenting, open drainage, diarrhea, periurethral skin contamination also play a role in nosocomial UTIs. The criteria for the diagnosis of an UTI would depend on the catheterization status as follows. Some uncertainty still exists in the diagnosis in catheterized children. The catheter, by simple irritation to the bladder, may cause pyuria; the drainage provided by the catheter may mask the clinical symptoms, and in some patients, the underlying disease process may cause fever or render the patient incapable of indicating the symptoms. The following are the guidelines for diagnosis of UTI 9 Clean catch mid stream urine growing >10 5 bacteria/ml of urine. ~ 9 Any growth in a suprapubic sample (gold standard for confirmation of diagnosis). 9 Bacterial counts of >102/ml in samples aspirated with a needle from the catheter in those patients with indwelling catheters. 49 A multitude of practices have been recommended and used to prevent the occurrence of UTIs. Controlled trials are yet to prove the efficacy of some of these. The catheterizations should be kept to a minimum. The need for catheterization must be strictly evaluated and catheterization must be replaced by a closed condom drainage whenever possible, s~ Suprapubic catheterization may be linked to a lesser risk of a CAUTI and may be more comfortable to some patients, s~ When thought to have fulfilled their need the catheters must be immediately removed, sl Strict asepsis should be maintained during insertion of the catheter using sterile gloves, drapes, and local antiseptics. Closed drainage must be strictly maintained and this has been shown to bring down the rates of infection to less than 25% for up to 2 weeks of catheterization, s2 The closed drainage must be maintained with the collection tubing and bag below the level of the patient's bladder and the tubing must always be above the level of the bag. Other positions, by allowing backflow of urine, increase the risk of infection by two-fold. 53 When in place the closed drainage system must be handled and manipulated as infrequently as possible. Antibiotic prophylaxis does reduce the frequency of infections but is not universally recommended as it selects multidrug resistant strains when the infection occurs. Antiinfective lubricants, sealed catheter tubing junctions, antireflux valves, bladder or bag irrigation with antiinfective solution, antibiotic, silver hydrogel impregnated catheter materials are the newer techniques being studied for their role in reducing the risk of nosocomial UTIs. 46 For reducing the incidence of nosocomial infection, each PICU should have an infection control program. There should be a written description of the goals, objectives, and structure of program. A team of health professionals should ensure implementation of the policies and compliance on the part of the PICU team. Well-directed infection control activities can reduce the nosocomial infection rates by up to 50%. u The importance of hand washing and hand disinfection is well understood. The appropriate hand washing technique includes wetting the hands, taking soap, rubbing hands to produce a lather, and performing wash movements that include rubbing palm to palm, right palm over left dorsum and vice versa, palm to palm with fingers interlaced, backs of fingers to opposing palm with fingers interlocked, rotational rubbing of right thumb clasped in left palm and vice versa, rotational rubbing with clasped fingers of fight hand in palm of left hand and with changed roles. 5s The whole procedure should not take less than 30 seconds. After washing, hands should be dried with disposable paper or cloth towel. It has been noticed that health personnel practice hand washing in only 25-50% of the opportunities? 6 In order to improve compliance, various hygienic hand rubs can be used. Rubbing of 3-5 ml of a fast acting antiseptic preparation on to both hands can be an effective substitute to hand washing. The various preparations available include n-propanol, isopropanol, ethanol, and chlorhexidine diacetate. 55 In addition to the specific measures mentioned earlier for prevention of specific nosocomial infections, proper sterilization/disinfection of various medical items is mandatory. Aseptic precautions should be followed strictly whenever any invasive procedure is being carried out. A well-nourished child is less likely to acquire nosocomial infection than a malnourished one. Even in PICU, nutrition should be given due attention. Enteral nutrition appears to be better than parenteral nutrition. Enteral nutrition may have a favorable impact on gastrointestinal immunologic function and infectious morbidity. 57 There has been considerable interest in the role of immune-enhancing enteral diets (containing glutamine, arginine, mRNA, omega-3 fatty acids from fish oil) in reduction of nosocomial infections and mortality in ICUs . 58, 59 Appropriate and rational prescription of antibiotics is essential to prevent emergence of resistant strains, s6 There should be constant surveillance and periodic review of the antibiotic policies and prescriptions. With careful microbiologic monitoring, cycling of antibiotics for empiric therapy can help in reducing the emergence of drug resistance. 56 Adequate and well trained staff-both nursing staff and physicians-are essential for infection control. Various studies have demonstrated the adverse effects of understaffing on nosocomial infection rates. 6~ Education of the staff about various infection control practices and procedure-specific guidelines has an important role in the reduction of incidence of nosocomial infections. The education program should be on a continuing basis with periodic evaluation of the knowledge and practices. Surveillance of nosocomial infections is an essential element of any infection control program. The most important goal of surveillance is to reduce the risk of acq~g nosocomial infections. This provides data useful for identifying infected patients, determining the site of infections and identifying the factors that contribute to nosocomial infections. Use of uniform definitions is critical for proper collection of data and inter-hospital comparisons. Standard CDC definitions that include laboratory and clinical criteria may be used. 1,2 The major purpose of surveillance is to establish baseline infection rates and identifying outbreaks. This data can be used effectively to convince health care workers to accept recommended preventive practices. Control measures can be evaluated objectively if the surveillance is good. CDC definitions for nosocomial infections Surveillance of nosocomial infections The National Nosocomial Infection Surveillance System 9 Nosocomial infections in pediatric intensive care units in the United States Risk factors for nosocomial infection in critically ill children: A prospective cohort study Infections in a pediatric intensive care unit Nosocomial infections in medical ICUs in the United States Nosocomial colonization and infection in a pediatric respiratory intensive care unit Environmental services Nosocomial infections in a pediatric intensive care unit Klebsiella pneumoniae bacteremia in children Consequences of candidemia for pediatric patients Nosocomial infection in children Risk factors for pneumonia and fatality in patients receiving continuous mechanical ventilation Nosocomial pneumonia and tracheitis in a pediatric intensive care unit: a prospective study Sources of gram negative bacilli colonizing the trachea of intubated patients Epidemiologic study of 4684 hospital acquired infections in pediatric patients Nosocomial bacterial infections of the central nervous system, upper and lower respiratory tracts, and skin in pediatric patients Specificity of endotracheal aspiration, protected specimen brush, and bronchoalveolar lavage in mechanically ventilated patients Diagnostic efficiency of endotracheal aspirates with quantitative bacterial cultures in intubated patients with suspected pneumonia: comparison with protected specimen brush Blind protected specimen brush and bronchoalveolar lavage in ventilated children Ventilator-associated pneumonia or not? 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Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomized trial Epidemiology of nosocomial infections in pediatric patients Incidence of sinusitis in patients with nasotracheal intubation Aprospective study of the mechanisms of infection associated with hemodialysis catheters Risk factors for central venous catheter related infections in surgical and intensive care units Infection rate for single lumen vs triple lumen subclavian catheters Potentiation of Staphylococcus epidermidis catheter-related bacteremia by lipid infusions Prospective multicenter study of vascular catheter-related complications and risk factors for positive patients Prospective study of catheter replacement and other risk factors of infection of hyperalimentation catheters A prospective, randomized study comparing transparent and dry gauze dressings for central venous catheters Nosocomial infections in the pediatric intensive care unit Prevention of central venous catheter related infections by using maximal sterile precautions during insertion New technologies to prevent intravascular catheter-related bloodstream infections Bacteriologic surveillance of indwelling urinary catheters in pediatric intensive care unit patients Urinary tract etiology of bloodstream infections in hospitalized patients Catheter-associated urinary tract infections in surgical patients: a controlled study on the excess morbidity and costs Urinary tract infection: economic considerations Mortality associated with nosocomial urinary tract infection Hospitalacquired urinary tract infections in pediatric patient: a prospective study Engineering out the risk for infection with urinary catheters A prospective study of the pathogenesis of catheter-associated with urinary tract infection Asymptomatic infections of the urinary tract Bacteriuria in the catheterized patient Urethral catheters, condom catheters, and nosocomial urinary tract infections Early catheter removal decreases incidence of urinary tract infections in renal transplant receipients Prevention of catheter-induced urinary tract infections by sterile closed drainage Risk factors for catheterassociated urinary tract infection: a prospective study showing the minimal effects of catheter care violations on the risk of CAUTI (Abstract) The efficacy of infection surveillance and control programs in preventing nosocomial infections in US hospitals Hand washing and hand disinfection Controlling antimicrobial resistance in hospitals: infection control and use of antibiotics Enteral nutrition in the critically ill patient: a critical review of the evidence An immune-enhancing enteral diet reduces mortality rate and episodes of bacteremia in septic intensive care patients Randomised trial of glutamine-enriched enteral nutrition on infectious morbidity in patients with multiple trauma The role of understaffing in central venous catheter-associated bloodstream infections Patient density, nurse-to-patient ratio and nosocomial infection risk in a pediatric cardiac intensive care unit At least one of the following: a. new onset of purulent sputum or change in character of sputum b. organisms cultured from blood c. isolation of an etiologic agent from a specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy. Criterion 2 : Patient has a chest radiographic examination that shows new or progressive infiltrate, consolidation, cavitation, or pleural effusion Criterion 4And At least one of the following: a. new onset of purulent sputum or change in character of sputum b. organisms cultured from blood c. isolation of an etiologic agent from a specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy. d. isolation of virus or detection of viral antigen in respiratory secretions e. histopathologic evidence of pneumonia.: Patient < 1 year of age has at least two of the following signs or symptoms: apnea, bradycardia, wheezing, rhonchi, or cough And At least one of the following : a. increased production of respiratory secretions b. new onset of purulent sputum or change in character of sputum c. organisms cultured from blood d. isolation of an etiologic agent from a specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy. e. isolation of virus or detection of viral antigen in respiratory secretions f. histopathologic evidence of pneumonia : Patient < 1 year has a chest radiographic examination that shows new or progressive infiltrate, consolidation, cavitation, or pleural effusion At least one of the following : a. increased production of respiratory secretions b. new onset of purulent sputum or change in character of sputum c. organisms cultured from blood d. isolation of an etiologic agent from a specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy. isolation of virus or detection of viral antigen in respiratory secretions histopathologic evidence of pneumonia. *Expectorated sputum cultures are not useful in diagnosis of pneumonia *Findings from serial chest x-rays may be more useful than a single x-ray. A Symptomatic urinary tract infection must meet at least one of the following criteria: Criterion I : Patient has at least one of the following sign or symptoms with no other recognized cause : fever (>38 ~ C), urgency, frequency, dysuria or suprapubic tenderness and Patients has a positive urine culture that is >10 s microorganisms per cm 3 of urine with no more than two species of microorganisms. Patients has at least two of the following signs or symptoms with no other recognized cause: fever (>38 ~ C), Urgency, frequency, dysuria, or suprapubic tenderness and at least one of the following : a. pyuria (urine specimen with >10 WBC/mm 3 or >3 WBC/high power field of unspun urine) b. organism seen on Gram stain of unspun urine c. at least two urine culture with repeated isolation of the same uropathogen (gram-negative bacteria or S.saprophyticus) with >102 colonies mL in non voided specimens d. < 10 s colonies/mL of a single uropathogen (gram negative bacteria or S. saprophyticus) in a patient being treated with an effective antimicrobial agent for a urinary tract infection e. physician diagnosis of a urinary tract infection f. physician institutes appropriate therapy for a urinary tract infection Patient < 1 year of age has at least one of the following signs or symptoms with no other recognized cause: fever(>38 ~ C), hypothermia (<37~ apnea, bradycardia, dysuria, lethargy, or vomiting and patient has a positive urine culture, that is >10 s microorganisms per cm 3 of urine with no more than two species of microorganisms. Patient < 1 year of age has at least one of the following signs or symptoms with no other recognized cause: fever (>38 ~ C), hypothermia (<37~ apnea, bradycardia, dysuria, lethargy, or vomiting And At least one of the following: a. pyuria (urine specimen with > 10 WBC/mm 3 or > 3 WBC/high power field of unspun urine) b. organisms seen on Gram stain of unspun urine c. atleast two urine culture with repeated isolation of the same uropathogen (gram-negative bacteria or S. saprophyticus) with > 102 colonies/mL in nonvoided specimens d. < 105 colonies mL of a single uropathogen (gram negative bacteria or S. saprophyticus) in a patient being treated with an effective antimicrobial agent for a urinary tract infection e. physician diagnosis of a urinary tract infection f. physician institutes appropriate therapy for a urinary tract infection