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Supervised and induced sputum among patients with smear-negative pulmonary tuberculosis

K. C. Chang, C. C. Leung, W. W. Yew, C. M. Tam
European Respiratory Journal 2008 31: 1085-1090; DOI: 10.1183/09031936.00122907
K. C. Chang
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C. C. Leung
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W. W. Yew
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C. M. Tam
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Abstract

Sputum culture is essential for monitoring drug resistance. Although sputum induction may optimise culture yield, better selection criteria and simpler algorithms are needed for countries with intermediate tuberculosis burdens.

From a cohort of 660 patients who registered for antituberculosis treatment in a government chest clinic from May 21, 2005 to February 28, 2007, 187 patients with pulmonary disease and a negative smear in two unsupervised sputum specimens were enrolled prospectively for collection of one specimen each of supervised and induced sputum in succession.

Among enrolled patients, induced sputum significantly improved ease of expectoration on a subjective five-point scale. Among 78 patients with culture-proven pulmonary tuberculosis, analysis of matched sputum culture results showed that: 1) induced sputum outperformed supervised sputum; 2) the second unsupervised sputum was significantly inferior to the first and redundant in the presence of the others; 3) adding one specimen each of supervised and induced sputum to two unsupervised specimens increased culture yield significantly; and 4) patients with either extent of disease less than right upper lobe or no respiratory symptoms were more likely to benefit.

In summary, it may be practical to collect a sample of unsupervised, supervised and induced sputum for smear-negative patients with extent of disease less than the right upper lobe, especially when respiratory symptoms are absent.

  • Culture
  • diagnosis
  • induced sputum
  • supervised sputum
  • tuberculosis

Sputum culture, useful for confirming pulmonary tuberculosis (TB), is essential for drug susceptibility testing 1, which is becoming increasingly important in an era of increasing drug-resistance 2, multidrug-resistant TB 3 and extensively drug-resistant TB 4.

Introduced >40 yrs ago 5–9, sputum induction has been advocated for improving diagnostic yield in patients with difficulty in expectorating 10, 11. Its efficacy is probably comparable with bronchoalveolar lavage 12–15. It is uncertain whether sputum induction may owe its efficacy to supervision. Although several studies 12, 14, 16, 17 showed sputum induction was cost-saving, it may be difficult for countries with intermediate TB burdens to spend 30 min on sputum induction indiscriminately and virtually impossible to spend up to 2 h 18 to induce sputum three times 14, 18. Better selection criteria and simpler algorithms are needed.

Hong Kong (China) has been classified as having an intermediate TB burden 19. In 2005, TB notifications and rate were ∼6,000 cases and 90 cases per 100,000 population, respectively, 20. Approximately one-third of pulmonary TB cases were smear-positive, whereas two-thirds were culture-proven 20. Despite a common practice of collecting up to four sputum specimens before treatment, the prevalence of culture-positive cases among smear-negative patients was only 52% 20. Although sputum induction might enhance diagnostic yield, it has never been evaluated in Hong Kong.

In view of a lack of systematic studies of supervised and induced sputum for countries with intermediate TB burden, a prospective study was conducted among patients with smear-negative pulmonary TB disease to identify an optimal algorithm for sputum collection.

METHODS

From May 21, 2005 to February 28, 2007, patients suspected of pulmonary TB disease with negative acid-fast bacilli smear in two unsupervised sputum specimens were enrolled prospectively from a government chest clinic (Yaumatei Chest Clinic, Hong Kong) for collecting one specimen each of supervised and induced sputum in immediate succession. Thus, each participant had four sputum specimens. TB was diagnosed based upon clinical and radiographical findings coupled with absence of response to empirical antibiotics. Public health nurses instructed all patients on how to cough and produce sputum 21. Sputum specimens were sent to the Supranational TB Reference Laboratory in Hong Kong for processing. All specimens were examined macroscopically according to a published guide 21. Only empty bottles and specimens that were dried up or considered insufficient were rejected.

Some specimens were excluded from enrolment due to: TB occurring only in nonpleural extrapulmonary sites; positive smear or culture in any respiratory specimen; anti-TB treatment received for >1 week before sputum induction; practical difficulty in inducing sputum; or lack of consent.

Before or within 1 week after commencement of treatment, supervised expectoration followed immediately by sputum induction was performed inside a transparent local exhaust ventilation booth, which was built in accordance with published guidelines 22, 23. Patients fasted for ≥2 h beforehand. Nebulised hypertonic saline (5.85% (weight/volume)) delivered with a high-flow jet nebuliser for 20 min was used to induce sputum. Blood pressure and peak expiratory flow rate (PEFR) were measured before and after sputum induction. The patients' ease of sputum production was measured before and after sputum induction on a subjective five-point scale, comprising the following items ranking 1–5, respectively: “no sputum”, “difficult”, “okay after effort”, “easy” and “effortless”. Wilcoxon signed rank test was used to compare ranks obtained before and after sputum induction.

Paired culture results obtained by alternative sputum collection methods were compared among patients with culture-proven pulmonary TB. Factors that might associate with culture gain from supervised and induced sputum relative to two unsupervised specimens were evaluated by univariate and multivariable analyses. For multivariable analysis, factors with p-values <0.05 by univariate analysis were included by default, whereas those with p-values <0.2 were included by forward stepwise selection using p-values of 0.05 and 0.10 as cut-offs for entry and removal, respectively.

Approval and informed consent were obtained from the institutional review board and each participant, respectively.

RESULTS

Figure 1⇓ shows enrolment from a cohort of 660 patients who registered for anti-TB treatment from May 21, 2005 to February 28, 2007. There was no significant difference between 187 enrolled patients and 32 eligible patients that were excluded due to oversight or unwillingness to participate.

Fig. 1—
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Fig. 1—

Flow diagram showing enrolment of patients from a cohort of 660 patients. TB: tuberculosis.

Among 187 enrolled patients, sputum induction increased ease of expectoration significantly as compared with supervised collection on a subjective five-point scale (median score 3 versus 2, respectively; p<0.001). Sputum induction was aborted in two (1.1%) patients owing to transient numbness or dizziness with chest pain, which disappeared spontaneously. A total of nine (4.8%) patients had minor adverse events that did not require termination of sputum induction or treatment: nausea (n = 1), chest pain (n = 1), dizziness (n = 2), numbness (n = 2), epigastric discomfort (n = 1) and transient asymptomatic fall in PEFR (n = 2).

Table 1⇓ shows comparison of paired culture results obtained by alternative sputum collection methods among 78 patients with culture-proven pulmonary TB. The second unsupervised sputum was significantly inferior to the first. Induced sputum significantly outperformed supervised sputum. Adding one specimen each of supervised and induced sputum to two unsupervised specimens increased culture yield significantly.

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Table 1—

Comparison of paired culture results obtained by alternative sputum collection methods among 78 patients with culture-proven pulmonary tuberculosis

Table 2⇓ shows the results of univariate analysis of factors that may associate with culture gain from supervised and induced sputum, relative to two unsupervised specimens among the 78 patients with culture-proven pulmonary TB. Only extent of disease less than right upper lobe and lack of respiratory symptoms were significantly associated with culture gain in both univariate and multiple logistic regression analyses; the adjusted odds ratios (95% confidence interval) were 7.2 (1.9–28.0) and 3.0 (1.0–8.9), respectively.

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Table 2—

Univariate analysis of factors that may associate with culture gain from supervised and induced sputum relative to two unsupervised specimens among the 78 patients with culture-proven pulmonary tuberculosis (TB)

Table 3⇓ shows the sensitivity of smear and culture in different sputum collection methods stratified by disease extent and respiratory symptoms. By including a specimen of supervised and induced sputum to two unsupervised specimens, the sensitivity for culture in descending order of magnitude was: from 26 to 95% when the extent of disease was less than the right upper lobe with no respiratory symptoms; from 50 to 100% when the extent of disease was less than right upper lobe with respiratory symptoms; and from 86 to 100% when the extent of disease exceeded right upper lobe. The corresponding changes for sputum smear, which occurred in the reverse direction, were 0–0%, 0–8% and 0–19%, respectively. The second unsupervised specimen was redundant in the presence of the other specimens.

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Table 3—

Sensitivity of smear and culture in different sputum collection methods among a cohort of 78 patients with culture-proven pulmonary tuberculosis

DISCUSSION

The present study has provided more evidence supporting the use of sputum induction in smear-negative pulmonary TB disease. First, induced sputum significantly outperformed supervised sputum. It is probable that hypertonic saline works by improving sputum transportability, enhancing mucociliary clearance and inducing cough 24, 25. Secondly, by adding one specimen each of supervised and induced sputum to two unsupervised specimens the culture yield was significantly increased. Although the reference group comprised two unsupervised specimens instead of the current standard of three, the difference could be negligible given the significantly inferior performance of the second unsupervised specimen relative to the first. The latter is consistent with previous studies 26. It is probably unnecessary to request more than one unsupervised specimen if both supervised expectoration and sputum induction are contemplated.

The present study may also help to refine selection criteria for sputum induction. Smear-negative patients with either extent of disease less than right upper lobe or no respiratory symptoms were more likely to benefit from supervised expectoration and sputum induction. This is consistent with previous findings supporting the role of sputum induction for tuberculous pleural effusion 27, in which lung disease is often minimal.

In accordance with a previous study 28, which showed no significant difference between induced sputum and routine-expectorated sputum in establishing a diagnosis of smear-positive TB disease, the present study showed that only 8% of symptomatic patients with smear-negative disease of extent less than right upper lobe would become smear-positive after collecting additional supervised and induced sputum. When the initial sputum smear is negative, additional supervised and induced sputum would mainly enhance culture yield and drug susceptibility testing without establishing a rapid bacteriological diagnosis. Treatment would still need to be initiated on clinical and radiographical grounds.

Inaccessibility to data on disease extent and respiratory symptoms in the published literature may make it difficult to compare supervised and induced sputum with multiple sputum induction. Reorganisation of data from a recent study 15 showed that two additional induced sputum specimens increased culture yield of two spontaneous sputum specimens from 74 to 100% among 27 patients with culture-proven TB. This order of gain may be less than that for extent of disease less than right upper lobe but comparable with that for more extensive disease.

In countries of intermediate TB burden, a triplet of unsupervised, supervised and induced sputum may be more practicable than three induced sputum specimens. Thus, the current authors recommend the following algorithm. For lesions less than right upper lobe, check unsupervised sputum once, especially when respiratory symptoms are absent, and prescribe antibiotics empirically 29. If smear-negative TB disease is suspected, collect one specimen each of supervised and induced sputum in immediate succession inside a local exhaust ventilation device 22, 23. Costs may be outweighed by savings on laboratory consumables, manpower and bronchoscopy.

In summary, the present study has reaffirmed the role of sputum induction, refined its selection criteria and provided a practicable algorithm for optimising culture yield in smear-negative pulmonary tuberculosis disease.

Statement of interest

None declared.

Acknowledgments

The authors would like to thank C. Chan (Tuberculosis & Chest Service, Hong Kong, China), our senior nursing officer, and all colleagues of Yaumatei Chest Clinic for their dedicated and professional support in the study. The authors would additionally like to thank T.Y. Lau, D.H.C. Lam, K.Y.K. Lau, W.L. Law, F. Cheung, S.P. Wong, A. Fung and S. Sin (Tuberculosis & Chest Service). Finally, the authors would also like to thank C.K. Chan (Tuberculosis & Chest Service) for conducting a small pilot study of sputum induction in another chest clinic (Wanchai Chest Clinic, Hong Kong) before this study was conceived.

  • Received September 17, 2007.
  • Accepted December 25, 2007.
  • © ERS Journals Ltd

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Supervised and induced sputum among patients with smear-negative pulmonary tuberculosis
K. C. Chang, C. C. Leung, W. W. Yew, C. M. Tam
European Respiratory Journal May 2008, 31 (5) 1085-1090; DOI: 10.1183/09031936.00122907

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Supervised and induced sputum among patients with smear-negative pulmonary tuberculosis
K. C. Chang, C. C. Leung, W. W. Yew, C. M. Tam
European Respiratory Journal May 2008, 31 (5) 1085-1090; DOI: 10.1183/09031936.00122907
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