The Diagnostic Utility of Induced Sputum Microscopy and Culture in Childhood Pneumonia.

BACKGROUND.: Sputum microscopy and culture are commonly used for diagnosing the cause of pneumonia in adults but are rarely performed in children due to difficulties in obtaining specimens. Induced sputum is occasionally used to investigate lower respiratory infections in children but has not been widely used in pneumonia etiology studies. METHODS.: We evaluated the diagnostic utility of induced sputum microscopy and culture in patients enrolled in the Pneumonia Etiology Research for Child Health (PERCH) study, a large study of community-acquired pneumonia in children aged 1-59 months. Comparisons were made between induced sputum samples from hospitalized children with radiographically confirmed pneumonia and children categorized as nonpneumonia (due to the absence of prespecified clinical and laboratory signs and absence of infiltrate on chest radiograph). RESULTS.: One induced sputum sample was available for analysis from 3772 (89.1%) of 4232 suspected pneumonia cases enrolled in PERCH. Of these, sputum from 2608 (69.1%) met the quality criterion of <10 squamous epithelial cells per low-power field, and 1162 (44.6%) had radiographic pneumonia. Induced sputum microscopy and culture results were not associated with radiographic pneumonia, regardless of prior antibiotic use, stratification by specific bacteria, or interpretative criteria used. CONCLUSIONS.: The findings of this study do not support the culture of induced sputum specimens as a diagnostic tool for pneumonia in young children as part of routine clinical practice.

Microscopy and culture of sputum specimens are standard techniques commonly used by diagnostic laboratories to evaluate pneumonia in adults. Despite difficulties interpreting results [1], carefully collected and processed sputum specimens have been shown to be useful diagnostic tools in some contexts [2]. Nonetheless, ongoing controversy continues about the value of routinely examining sputum [3-7]. Furthermore, sputum microscopy and culture are not routinely performed in children, who are typically unable to expectorate, making it difficult to obtain specimens [8].

Induced sputum is widely used to investigate lower respiratory infections in immunocompromised adults, especially for diagnosing Pneumocystis jirovecii infection [9]. It has also been used to diagnose pneumonia in children from settings with a high prevalence of tuberculosis [10]. However, few studies have collected induced sputum routinely from children with pneumonia. Recent studies of children hospitalized with community-acquired pneumonia from Finland, Kenya, and New Caledonia showed that collection of induced sputum was well tolerated, with a diagnostic yield from culture ranging from 12% to 65% using different interpretative criteria [11-14].

We made a decision to include microscopy and culture of induced sputum as part of the Pneumonia Etiology Research for Child Health (PERCH) study, a large case-control study involving 9 sites in 7 countries from sub-Saharan Africa and south Asia [15, 16]. The expectation was that this approach may help overcome the inherent difficulties with obtaining specimens from the lower respiratory tract in children with pneumonia and facilitate the diagnosis of pneumonia etiology. In an accompanying article we show that low numbers of squamous epithelial cells (SECs) was the best measure of induced sputum quality in children with pneumonia from the PERCH study, as evidenced by low quantities of oropharyngeal flora and higher prevalence of putative pathogens. A large proportion of induced sputum samples met this criterion for good quality, suggesting that most specimens originated from the lower respiratory tract [17]. Here, we evaluate the diagnostic utility of induced sputum microscopy and culture in the PERCH study. A specific objective was to determine whether sputum culture results should be included in the primary etiology analysis of the study. Other companion articles in this supplement focus on the agreement of polymerase chain reaction results between induced sputum and nasopharyngeal/oropharyngeal specimens, safety of induced sputum collection, and utility of induced sputum for diagnosing tuberculosis [18-20].

METHODS

Participants

Participants were children aged 1–59 months who were hospitalized with World Health Organization (WHO)–defined severe or very severe pneumonia as part of the PERCH case-control study, details of which have been described elsewhere [21, 22].

Chest Radiography

Chest radiographs (CXRs) from each child were interpreted by a panel of radiologists and pediatricians trained in the standardized interpretation of pediatric CXRs [23]. CXRs were classified as demonstrating consolidation, other infiltrate, both consolidation and other infiltrate, or as being normal or uninterpretable.

Specimen Collection

Induced sputum was obtained from cases at enrollment as described in detail in an accompanying article [17].

Laboratory Methods

Gram stain smears were made from the most visually purulent portion of each induced sputum specimen. The quality of sputum was assessed microscopically as outlined elsewhere [17], and only specimens with <10 SECs per (100×) low-power field (LPF) were included in further analyses. Microorganisms seen in the smear under (1000×) high power were described according to classic Gram stain morphotypes, and relative numbers of each type were recorded within the following categories: 1 (scanty), 2–9 (1+), 10–99 (2+), ≥100 (3+) per representative high-power field.

The most purulent portion of each specimen was inoculated onto sheep or horse blood, chocolate, and MacConkey agars; streaked out using a standard 4-quadrant streaking method; and incubated at 35°C for 48 hours. Cultures were examined at 24 hours and 48 hours, and predominant organisms were identified and quantified according to the furthest quadrant with visible colonies (first quadrant = scanty; second quadrant = 1+; third quadrant = 2+; fourth quadrant = 3+).

In order to standardize reporting across sites, uniform standard operating procedures, on-site training, and internal and external quality checks were established [24].

Study Definitions The following definitions were used in the study.

Sputum Culture Positivity. Sputum culture results can be interpreted in a variety of ways and no one consistent approach is used by diagnostic laboratories. In general, it is recommended that potential pathogens must be present as a predominant isolate, usually with a compatible Gram stain appearance [25, 26]. For the interpretative criteria used in this study, we reported separately both organisms cultured in any amount and organisms cultured as the predominant isolate with compatible Gram stain morphotype seen on microscopy.

CXR+ Cases and Nonpneumonia Cases. CXR+ pneumonia was defined by the presence of consolidation and/or other infiltrate on CXR [23]. Given that WHO-defined severe or very severe pneumonia has poor specificity for CXR+ pneumonia, a proportion of the enrolled cases likely did not have true pneumonia. Using baseline clinical and laboratory characteristics and the absence of CXR changes, a group of “control” children unlikely to have pneumonia (nonpneumonia) were identified. Children who met all of the following 3 criteria were defined as “nonpneumonia”: presence of a normal CXR, negative blood cultures, either normal respiratory rate or nonhypoxic in the absence of crackles or normal respiratory rate and nonhypoxic in the presence of crackles. We compared pneumonia to nonpneumonia cases for all analyses.

Prior Antimicrobial Therapy. Prior antimicrobial therapy was defined as antibiotic activity in serum by bioassay or documentation of antibiotic administration before induced sputum sample collection [27].

Microbiologically Confirmed Cases. Cases were defined as having microbiologically confirmed pneumonia if they had a bacterium that was not regarded as a contaminant isolated from blood, lung aspirate, or pleural fluid [27].

Statistical Analyses

We hypothesized that pneumonia pathogens are more likely to be detected in sputum samples from children with radiographic pneumonia compared to sputum samples from children in the nonpneumonia group. Also, we hypothesized that pathogens that cause pneumonia are likely to be present in high enough quantities that they should be detected by both culture and microscopy, and thus pediatric induced sputum cultures should be interpreted in conjunction with Gram stain findings.

To assess whether pathogen detection was associated with CXR+ pneumonia among hospitalized infants and young children, we calculated the prevalence of specific bacteria cultured from high-quality induced sputum specimens from CXR+ cases and nonpneumonia cases, stratified by site and prior antimicrobial therapy. Comparisons were made using the χ2 test. Odds ratios were calculated for associations of pneumonia status with organism presence using different interpretive criteria in order to examine the effect of Gram stain results on observed associations.

Ethical Considerations

The institutional review board or ethical review committee at each study site institution and at the Johns Hopkins Bloomberg School of Public Health approved the PERCH study protocol. Parents or guardians of participants provided written informed consent.

RESULTS

Induced sputum culture results were available for analysis from 3772 (89.1%) of 4232 children enrolled in PERCH. Sputum from 2608 (69.1%) met the quality criterion of <10 SECs per LPF; of these, 1162 (44.6%) had radiographic pneumonia, 398 (15.3%) were nonpneumonia cases, and 1048 (40.2%) did not meet either definition.

Of the 1162 CXR+ cases with high-quality induced sputum, 866 (74.5%) had severe pneumonia and 296 (25.5%) had very severe pneumonia. A total of 197 (17.0%) were from the Gambia, 126 (10.8%) from Mali, 233 (20.1%) from Kenya, 194 (16.7%) from Zambia, 198 (17.0%) from South Africa, 142 (12.2%) from Bangladesh, and 72 (6.2%) from Thailand. The median age of these children was 8 months (interquartile range, 4–17), 493 (42.4%) were female, and 90 (7.8%) had human immunodeficiency virus infection. Among this group, 908 (80.6%) had prior antimicrobial therapy before collection of induced sputum, although the frequency varied by site as follows: 43 (21.8%) at the Gambia, 112 (88.9%) at Mali, 213 (91.4%) at Kenya, 190 (97.9%) at Zambia, 178 (89.9%) at South Africa, 104 (73.2%) at Bangladesh, and 68 (94.4%) at Thailand.

Of the 398 nonpneumonia cases, 67 (16.8%) were from the Gambia, 50 (12.6%) from Mali, 157 (39.5%) from Kenya, 48 (12.1%) from Zambia, 22 (5.5%) from South Africa, 28 (7.0%) from Bangladesh, and 26 (6.5%) from Thailand. Relative to the CXR+ cases, the nonpneumonia cases were slightly older (median age 10 months; interquartile range, 3–20), less likely to be female (34.4%), and less likely to have human immunodeficiency virus (1.0%) infection or to have evidence of prior antimicrobial use (68.2%).

Table 1 shows the prevalence of bacteria cultured from induced sputum samples with <10 SECs per LPF from CXR+ cases, by study site, using the 2 culture interpretative criteria (ie, organisms cultured in any amount and organisms cultured as the predominant isolate with compatible Gram stain morphotype). Tables 2 and 3 show the prevalence of organisms cultured from both CXR+ and nonpneumonia cases using the 2 culture interpretative criteria, by antibiotic exposure status. Haemophilus influenzae, Streptococcus pneumoniae, and Moraxella catarrhalis were the predominant organisms isolated when measured as organism detected in any amount (Table 2) or as the predominant organism (Table 3); their prevalence was similar in CXR+ and nonpneumonia cases. Klebsiella pneumoniae was more commonly isolated from cases from South Africa and Zambia, although this regional predominance was less evident when the more rigorous interpretative criterion (predominant organisms with compatible Gram stain morphotype) was used (Table 1). There was no predominant organism in 323 (27.8%) high-quality induced sputum specimens from cases with radiographic pneumonia.

Table 1.

Prevalence of Bacteria Cultured in Any Quantity or as the Predominant Isolate With Compatible Gram Stain From High-Quality Induced Sputum from Children Aged 1–59 Months With World Health Organization–Defined Severe or Very Severe Radiographic Pneumonia, by Study Site

	Study Site (n, %)
	Kenya N a = 233		Gambia N = 197		Mali N = 126		Zambia N = 194		South Africa N = 198		Bangladesh N = 142		Thailand N = 72		All Sites N = 1162
Bacteria	Any Quantity	Predominantb	Any Quantity	Predominant	Any Quantity	Predominant	Any Quantity	Predominant	Any Quantity	Predominant	Any Quantity	Predominant	Any Quantity	Predominant	Any Quantity	Predominant
Streptococcus pneumoniae	58 (24.9)	39 (16.7)	126 (64.0)	79 (40.1)	17 (13.5)	10 (7.9)	36 (18.6)	18 (9.3)	47 (23.7)	26 (13.1)	59 (41.5)	49 (34.5)	23 (31.9)	19 (26.4)	366 (31.5)	240 (20.7)
Staphylococcus aureus	2 (0.9)	0 (0.0)	6 (3.0)	3 (1.5)	17 (13.5)	4 (3.2)	21 (10.8)	1 (0.5)	32 (16.2)	11 (5.6)	7 (4.9)	3 (2.1)	9 (12.5)	7 (9.7)	94 (8.1)	29 (2.5)
Other streptococci and enterococci c	0 (0.0)	0 (0.0)	1 (0.5)	0 (0.0)	3 (2.4)	3 (2.4)	0 (0.0)	0 (0.0)	2 (1.0)	1 (0.5)	1 (0.7)	1 (0.7)	0 (0.0)	0 (0.0)	7 (0.6)	5 (0.4)
Haemophilus influenzae	86 (36.9)	33 (14.2)	146 (74.1)	105 (53.3)	56 (44.4)	36 (28.6)	62 (32.0)	22 (11.3)	53 (26.8)	10 (5.1)	58 (40.8)	49 (34.5)	12 (16.7)	7 (9.7)	473 (40.7)	262 (22.5)
Moraxella catarrhalis	97 (41.6)	70 (30.0)	121 (61.4)	68 (34.5)	30 (23.8)	19 (15.1)	57 (29.4)	29 (14.9)	30 (15.2)	8 (4.0)	6 (4.2)	5 (3.5)	22 (30.6)	16 (22.2)	363 (31.2)	215 (18.5)
Enterobacteriaceae d
All	11 (4.7)	4 (1.7)	8 (4.1)	3 (1.5)	19 (15.1)	11 (8.7)	24 (12.4)	8 (4.1)	35 (17.7)	6 (3.0)	5 (3.5)	2 (1.4)	1 (1.4)	0 (0.0)	103 (8.9)	34 (2.9)
Klebsiella pneumoniae only	0 (0.0)	0 (0.0)	5 (2.5)	2 (1.0)	7 (5.6)	5 (4.0)	20 (10.3)	6 (3.1)	20 (10.1)	4 (2.0)	2 (1.4)	2 (1.4)	1 (1.4)	0 (0.0)	55 (4.7)	19 (1.6)
Mixed gram-negative rods	5 (2.1)	2 (0.9)	10 (5.1)	1 (0.5)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)	6 (3.0)	4 (2.0)	19 (13.4)	8 (5.6)	2 (2.8)	1 (1.4)	42 (3.6)	16 (1.4)
Other nonfermentative gram-negative rods e
All	3 (1.3)	2 (0.9)	1 (0.5)	1 (0.5)	6 (4.8)	3 (2.4)	2 (1.0)	1 (0.5)	1 (0.5)	0 (0.0)	14 (9.9)	1 (0.7)	0 (0.0)	0 (0.0)	27 (2.3)	8 (0.7)
Pseudomonas aeruginosa	2 (0.9)	2 (0.9)	0 (0.0)	0 (0.0)	1 (0.8)	1 (0.8)	0 (0.0)	0 (0.0)	1 (0.5)	0 (0.0)	1 (0.7)	1 (0.7)	0 (0.0)	0 (0.0)	5 (0.4)	4 (0.3)

High-quality induced sputum defined as <10 epithelial cells per low-power field. Radiographic pneumonia defined as any abnormal chest radiograph (consolidation and/or other infiltrates).

aNumber of cases at each site who had high-quality induced sputum and radiographic pneumonia.

bIsolated as the predominant organisms with compatible Gram stain morphotype.

cOther streptococci and enterococci includes Streptococci (other than S. pneumoniae) and Enterococci species.

dEnterobacteriaceae includes Escherichia coli, Enterobacter species, Klebsiella species, Citrobacter species, and Serratia species, excluding mixed gram-negative rods. Klebsiella pneumoniae also reported separately.

eOther nonfermentative gram-negative rods includes Acinetobacter species and Pseudomonas species. Pseudomonas aeruginosa also reported separately.

Table 2.

Prevalence of Bacteria Cultured in Any Quantity From High-Quality Induced Sputum Among Radiographic Pneumonia Cases and Nonpneumonia Cases, by Antibiotic Exposure Status

	Regardless of Antibiotic Exposure a			No Antibiotic Exposure			Antibiotic Exposure
Bacteria	CXR+ b (N = 1162) n (%)	Nonpneumoniac(N = 398) n (%)	P Value d	CXR + (N = 219) n (%)	Nonpneumonia (N = 124) n (%)	P Value	CXR + (N = 908) n (%)	Nonpneumonia (N = 266) n (%)	P Value
Streptococcus pneumoniae	366 (31.5)	149 (37.4)	.03	141 (64.4)	76 (61.3)	.64	210 (23.1)	68 (25.6)	.41
Staphylococcus aureus	94 (8.1)	27 (6.8)	.45	13 (5.9)	12 (9.7)	.20	80 (8.8)	15 (5.6)	.10
Other streptococci and enterococci e	7 (0.6)	3 (0.8)	.72	2 (0.9)	2 (1.6)	.62	4 (0.4)	1 (0.4)	>.99
Haemophilus influenzae	473 (40.7)	168 (42.2)	.60	148 (67.6)	84 (67.7)	>.99	302 (33.3)	77 (28.9)	.21
Moraxella catarrhalis	363 (31.2)	156 (39.2)	.005	111 (50.7)	55 (44.4)	.26	238 (26.2)	96 (36.1)	.002
Enterobacteriaceae f
All	103 (8.9)	33 (8.3)	.76	12 (5.5)	5 (4.0)	.62	89 (9.8)	27 (10.2)	.91
Klebsiella pneumoniae	55 (4.7)	15 (3.8)	.49	4 (1.8)	3 (2.4)	.71	50 (5.5)	12 (4.5)	.64
Mixed gram-negative rods	42 (3.6)	8 (2.0)	.14	12 (5.5)	1 (0.8)	.04	28 (3.1)	7 (2.6)	.84
Other nonfermentative gram-negative rods g
All	27 (2.3)	11 (2.8)	.58	1 (0.5)	2 (1.6)	.30	26 (2.9)	9 (3.4)	.68
Pseudomonas aeruginosa	5 (0.4)	3 (0.8)	.43	0 (0.0)	0 (0.0)	N/A	5 (0.6)	3 (1.1)	.39

High-quality induced sputum defined as <10 epithelial cells per low-power field.

Abbreviation: CXR, chest radiograph.

Prior use of antibiotics defined as bioassay positive, antibiotic administration at the referral facility, antibiotic administration prior to induced sputum specimen collection at the study facility.

bRadiographic pneumonia (CXR+) defined as any abnormal CXR (consolidation and/or other infiltrates).

cNonpneumonia case defined as a case with a normal CXR, blood culture pathogen negative, and normal respiratory rate or nonhypoxic in the absence of crackles, or normal respiratory rate and nonhypoxic in the presence of crackles.

d P value from χ2 or Fisher exact test.

eOther streptococci and enterococci includes Streptococci (other than S. pneumoniae) and Enterococci species.

fEnterobacteriaceae includes Escherichia coli, Enterobacter species, Klebsiella species, Citrobacter species, and Serratia species, excluding mixed gram-negative rods. Klebsiella pneumoniae also reported separately.

Other nonfermentative gram-negative rods include Pseudomonas aeruginosa, Acinetobacter species, Pseudomonas species. Pseudomonas aeruginosa also reported separately.

Table 3.

Prevalence of Bacteria Cultured as the Predominant Organism With Compatible Gram Stain From High-Quality Induced Sputum Among Radiographic Pneumonia Cases and Nonpneumonia Cases, by Antibiotic Exposure Status

	Regardless of Antibiotic Exposure a			No Antibiotic Exposure			Antibiotic Exposure
Bacteria	CXR+ b (N = 1162) n (%)	Nonpneumoniac(N = 398) n (%)	P Value d	CXR + (N = 219) n (%)	Nonpneumonia (N = 124) n (%)	P Value	CXR + (N = 908) n (%)	Nonpneumonia (N = 266) n (%)	P Value
Streptococcus pneumoniae	240 (20.7)	94 (23.6)	.23	90 (41.1)	55 (44.4)	.57	139 (15.3)	37 (13.9)	.63
Staphylococcus aureus	29 (2.5)	9 (2.3)	>.99	3 (1.4)	4 (3.2)	.26	26 (2.9)	5 (1.9)	.52
Other streptococci and enterococci e	5 (0.4)	2 (0.5)	>.99	2 (0.9)	1 (0.8)	>.99	3 (0.3)	1 (0.4)	>.99
Haemophilus influenzae	262 (22.5)	92 (23.1)	.84	104 (47.5)	60 (48.4)	.91	141 (15.5)	27 (10.2)	.03
Moraxella catarrhalis	215 (18.5)	93 (23.4)	.04	62 (28.3)	29 (23.4)	.37	147 (16.2)	61 (22.9)	.01
Enterobacteriaceae f
All	34 (2.9)	11 (2.8)	>.99	1 (0.5)	1 (0.8)	>.99	32 (3.5)	10 (3.8)	.85
Klebsiella pneumoniae	19 (1.6)	6 (1.5)	>.99	1 (0.5)	0 (0.0)	>.99	17 (1.9)	6 (2.3)	.62
Mixed gram-negative rods	16 (1.4)	2 (0.5)	.27	2 (0.9)	0 (0.0)	.54	12 (1.3)	2 (0.8)	.75
Other nonfermentative gram-negative rods g
All	8 (0.7)	7 (1.8)	.07	0 (0.0)	2 (1.6)	.13	8 (0.9)	5 (1.9)	.19
Pseudomonas aeruginosa	4 (0.3)	3 (0.8)	.38	0 (0.0)	0 (0.0)	N/A	4 (0.4)	3 (1.1)	.20

High-quality induced sputum defined as <10 epithelial cells per low-power field.

Abbreviation: CXR, chest radiograph.

Prior use of antibiotics defined as bioassay positive, antibiotic administration at the referral facility, antibiotic administration prior to induced sputum specimen collection at the study facility.

bRadiographic pneumonia (CXR+) defined as any abnormal CXR (consolidation and/or other infiltrates).

cNonpneumonia case defined as a case with a normal CXR, blood culture pathogen negative, and normal respiratory rate or nonhypoxic in the absence of crackles, or normal respiratory rate and nonhypoxic in the presence of crackles.

d P value from χ2 or Fisher exact test.

eOther streptococci and enterococci includes Streptococci (other than S. pneumoniae) and Enterococci species.

fEnterobacteriaceae includes Escherichia coli, Enterobacter species, Klebsiella species, Citrobacter species, and Serratia species, excluding mixed gram-negative rods. Klebsiella pneumoniae also reported separately.

Other nonfermentative gram-negative rods include Pseudomonas aeruginosa, Acinetobacter species, Pseudomonas species. Pseudomonas aeruginosa also reported separately.

Table 4 shows the organisms cultured from high-quality induced sputum samples from the cases with microbiologically confirmed pneumonia. The same organism was isolated from a normally sterile site and induced sputum in a minority of these cases overall; the exception being M. catarrhalis for which 4 of 5 cases with positive cultures from a normally sterile site also had this organism isolated from induced sputum.

Table 4.

Bacteria Cultured From High-Quality Induced Sputum Samples From Children Aged 1–59 Months With Microbiologically Confirmed Pneumonia

Bacteria Isolated from Normally Sterile Site		Same Bacteria Isolated from Induced Sputum		Other Bacteria Cultured from Induced Sputum in Any Quantity
	N	Isolated in Any Quantity (n, %)	Isolated as the Predominant Organism With Compatible Gram Stain (n, %)	Haemophilus influenzae	Moraxella catarrhalis	Streptococcus pneumoniae	Mixed Gram- Negative Rods	Pseudomonas aeruginosa	Staphylococcus aureus	Escherichia coli	Enterobacter cloacae	Streptococcus Group A	Klebsiella Species
Streptococcus pneumoniae	35	17 (48.6)	9 (25.7)	15	14	N/A	1	2	2	1	0	0	0
Staphylococcus aureus	11	4 (36.4)	1 (9.1)	1	3	2	0	0	N/A	0	0	0	0
Haemophilus influenzae	12	8 (66.7)	4 (33.3)	N/A	3	5	0	0	0	0	1	1	1
Moraxella catarrhalis	5	4 (80.0)	4 (80.0)	2	N/A	2	1	0	0	0	0	0	0
Klebsiella pneumoniae	1	0 (0.0)	0 (0.0)	1	1	0	0	0	0	0	0	0	N/A

Microbiologically confirmed pneumonia defined as a bacterium detected by blood culture or polymerase chain reaction/culture in lung aspirates or pleural fluid.

High quality defined as <10 epithelial cells per low-power field.

Table 5 shows the odds ratios associated with CXR+ case status for detection of the major potential pathogen groupings in induced sputum with varying culture interpretative criteria. For all organisms there was either no association or a negative association between CXR+ pneumonia and the isolation of a pathogenic organism from induced sputum. For all organisms there was either no association or a negative association with the isolation of a pathogenic organism from induced sputum and CXR+ pneumonia (Table 5). This pattern was consistent across all levels of interpretative criteria (Supplementary Table 1).

Table 5.

Odds Ratio Associated With Radiographic Pneumonia Case (N = 1162) Versus Nonpneumonia Case (Reference) (N = 398) as a Predictor of Organism Presence Among Cases With High-Quality Induced Sputum Samples

	Haemophilus influenzae		Streptococcus pneumoniae		Staphylococcus aureus		Moraxella catarrhalis		Other Gram-Negative Rods a
Sputum Culture Interpretative Criteria	OR (95% CI)	P Value	OR (95% CI)	P Value	OR (95% CI)	P Value	OR (95% CI)	P Value	OR (95% CI)	P Value
Present in any quantity	0.94 (0.75,1.18)	.60	0.77b (0.61,0.97)	.03	1.21 (0.78,1.89)	.40	0.69b (0.54,0.87)	<.01	1.61 (0.91,2.85)	.10
Present in any quantity with compatible Gram stain	0.98 (0.76,1.26)	.87	0.86 (0.67,1.1)	.22	0.97 (0.51,1.85)	.94	0.72b (0.55,0.93)	<.01	1.38 (0.66,2.89)	.39
Present in any quantity without compatible Gram stain	0.91 (0.65,1.27)	.57	0.62b (0.4,0.98)	.04	1.41 (0.78,2.57)	.25	0.77 (0.52,1.13)	.18	1.91 (0.79,4.59)	.15
Predominant organism	0.91 (0.72,1.16)	.46	0.73b (0.57,0.94)	<.01	1.19 (0.72,1.96)	.50	0.67b (0.52,0.86)	<.01	1.42 (0.73,2.77)	.31
Predominant organism with compatible Gram stain	0.97 (0.74,1.27)	.81	0.84b (0.64,1.1)	.21	1.11 (0.52,2.36)	.79	0.72b (0.55,0.95)	.02	1.26 (0.51,3.13)	.62
Predominant organism without compatible Gram stain	0.86 (0.61,1.23)	.42	0.51b (0.31,0.83)	<.01	1.24 (0.65,2.37)	.52	0.68 (0.45,1.04)	.07	1.59 (0.6,4.2)	.35

Abbreviations: CI, confidence interval; OR, odds ratio.

High-quality induced sputum defined as <10 epithelial cells per low-power field. Radiographic pneumonia (CXR+) defined as any abnormal chest radiograph (CXR) (consolidation and/or other infiltrates). Nonpneumonia case defined as a case with a normal CXR, blood culture pathogen negative, and normal respiratory rate or nonhypoxic in the absence of crackles, or normal respiratory rate and nonhypoxic in the presence of crackles.

aOther nonfermentative gram-negative rods include Pseudomonas aeruginosa, Acinetobacter species, Pseudomonas species.

bP < .05.

None of the reported findings changed when another, more rigorous, sputum culture interpretative criterion was used, namely, requiring that organisms be isolated in quantities of 2+ or 3+, with or without compatible Gram stain appearance.

DISCUSSION

The key finding of this study is that culture of a potential pathogen from induced sputum was not clearly associated with radiographic pneumonia in young children compared to a group of hospitalized children unlikely to have pneumonia, even when a sputum quality standard was applied.

When sputum culture is used in pneumonia etiology studies, predefined criteria have been traditionally used to determine results thought to be associated with pneumonia causation [11, 13, 28, 29]. Only high-quality specimens that contain low numbers of SECs are typically accepted for analysis, and potential pathogens are required to be present as a predominant isolate, usually with a compatible Gram stain appearance [25, 26]. These criteria are derived from expert opinion, and their usefulness has been regularly debated [3–7, 30]. Had we applied this traditional approach to using sputum culture results in the PERCH study, the prevalence data shown in the second column of Table 3 would have been simply incorporated into the main etiologic analysis without further scrutiny. However, there was sufficient concern about the reliability of this approach with pediatric induced sputum specimens that we sought additional evidence of diagnostic utility.

Without a suitable comparator gold standard, it is difficult to determine the diagnostic accuracy of sputum culture for identifying pneumonia etiology. In this study, we compared cases of CXR+ pneumonia with a group of patients who (despite fulfilling the WHO case definition for severe or very severe pneumonia) were unlikely to have pneumonia. This approach is based on the assumption that true bacterial pneumonia pathogens will be overrepresented in induced sputa from children with CXR+ pneumonia compared to children unlikely to have pneumonia. We found no clear association between positive sputum culture results and pneumonia status. Indeed, for S. pneumoniae and M. catarrhalis, microorganisms that can also be part of the normal oropharyngeal flora, isolation tended to be associated with nonpneumonia status, especially in the absence of a compatible Gram stain smear. In addition, among children with microbiologically confirmed pneumonia, culture of induced sputum often detected a different organism than that detected from the sterile-site culture. While it is certainly possible that some of these children had polymicrobial pneumonia, this finding further highlights concerns about the nonspecificity of induced sputum culture in this age group, even when restricted to high-quality specimens that meet a rigorous definition of culture positivity. It may be possible that induced sputum does not adequately capture what is in the lung and/or that there is inevitable contamination with oropharyngeal flora that compromises even high-quality sputum.

It is standard laboratory practice to interpret sputum culture results in conjunction with the Gram stain smear of the same specimen [25, 26]. This follows the principle that, in general, an organism that acts as a pathogen rather than as a colonizer will be present in sufficient quantity to be seen on direct microscopy as well as to be detected by culture. Greater significance is given to organisms that grow in large amounts and are seen in the Gram stain. Despite a trend for the odds ratios of most organisms associated with CXR+ pneumonia to be higher when there was a compatible Gram stain compared to when there was not, this did not alter the fact that no culture results were associated with radiographic pneumonia.

This study has several limitations. Most importantly, the alternative diagnoses in the nonpneumonia cases (all of whom had respiratory symptoms) were largely unknown and there is residual uncertainty about the appropriateness of using this group as a comparator. It is possible that a large proportion of these cases actually did have pneumonia that was yet to be detected radiographically and that the lack of association between sputum culture results and pneumonia may simply indicate misclassification of “nonpneumonia” episodes. Also, nonpneumonia cases were not equally represented across sites [20]. In addition, about three quarters of cases had received antibiotics before collection of induced sputum, and isolation of potential pathogens in specimens from these children was less common than in those who had not received antibiotics. We may not have had the statistical power to detect associations with case status in those who did not receive antibiotics given the relatively smaller number in this group. We were also reliant on an imperfect definition of prior antibiotic use that may have failed to identify all the cases who had received antibiotics [27]. Another potential limitation is interobserver variability in reporting microscopy and culture results. However, uniform standard operating procedures, on-site training, and internal and external quality checks were incorporated into the PERCH study in an effort to standardize reporting across sites, and quality reviews indicated that these procedures were being followed in a consistent manner [24]. Despite these efforts to standardize methods and to collect all relevant data, there is still a subjective element to sputum culture interpretation that may not have been captured by the variables collected and used in the analyses.

In summary, isolation of bacteria from induced sputum did not reflect CXR+ pneumonia in young children hospitalized with WHO-defined severe or very severe radiographic pneumonia. Despite potential confounding by antibiotic use and the limitations of the study design, these findings did not provide sufficient evidence to incorporate induced sputum culture results into the primary etiology analysis of the PERCH study. Furthermore, the findings of this study do not support the culture of induced sputum specimens as a diagnostic tool for pneumonia in young children as part of routine clinical practice.

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