Nontuberculous mycobacteria, Zambia.
Mycobacterial infections (Diagnosis)
Mycobacterial infections (Care and treatment)
Buijtels, Patricia C.A.M.
van der Sande, Marianne A.B.
de Graaff, Cas S.
Verbrugh, Henri A.
Petit, Pieter L.C.
van Soolingen, Dick
|Publication:||Name: Emerging Infectious Diseases Publisher: U.S. National Center for Infectious Diseases Audience: Academic; Professional Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2009 U.S. National Center for Infectious Diseases ISSN: 1080-6040|
|Issue:||Date: Feb, 2009 Source Volume: 15 Source Issue: 2|
|Topic:||Event Code: 310 Science & research|
|Geographic:||Geographic Scope: Zambia Geographic Code: 6ZAMB Zambia|
Clinical relevance of nontuberculous mycobacteria (NTM) isolated
from 180 chronically ill patients and 385 healthy controls in Zambia was
evaluated to examine the contribution of these isolates to tuberculosis
(TB)--like disease. The proportion of NTM-positive sputum samples was
significantly higher in the patient group than in controls; 11% and 6%,
respectively (p<0.05). NTM-associated lung disease was diagnosed for
1 patient, and a probable diagnosis was made for 3 patients.
NTM-positive patients and controls were more likely to report vomiting
and diarrhea and were more frequently underweight than the NTM-negative
patients and controls. Chest radiographs of NTM-positive patients showed
deviations consistent with TB more frequently than those of controls.
The most frequently isolated NTM was Mycobacterium avium complex.
Multiple, not previously identified mycobacteria (55 of 171 NTM) were
isolated from both groups. NTM probably play an important role in the
etiology of TB-like diseases in Zambia.
Tuberculosis (TB) is a problem of enormous dimensions in Africa, and Mycobacterium tuberculosis is the most important causative agent. However, in industrialized countries, nontuberculous mycobacteria (NTM) also play a key role in etiology of TB-like syndromes. In Africa, the contribution of NTM to such disease has been examined on a small scale only (1-6).
Zambia is a country with historically high prevalence rates of TB. Patients with acid-fast bacilli (AFB)-positive sputum, or those with chest radiographic findings suggestive of active TB, who do not respond to general antimicrobial drugs, are generally presumed to have pulmonary TB. In general, these patients are treated empirically for 6 months with a combination of drugs recommended by the World Health Organization. However, several TB-like syndromes in Africa could be caused by NTM. Thus, inconclusive diagnosis of pulmonary TB would lead to overdiagnosis of TB and in some cases, to inappropriate treatment for NTM infections.
When NTM are isolated from a usually sterile site (e.g., blood, bone marrow, lymph nodes, synovial fluid), diagnosis of true disease is generally straightforward. However, when NTM are isolated from nonsterile sources, such as sputum or bronchoalveolar lavage samples, the diagnosis is less definitive, especially when the colony numbers are low or NTM are isolated from only I cultured specimen. Therefore, it is a challenge to differentiate true NTM lung disease from contamination and colonization. Thus, finding AFB by microscopy of respiratory specimens or by culture may pose a diagnostic problem for the clinician. In 1997, the American Thoracic Society (ATS), published useful criteria for determining the clinical relevance of NTM isolates (7). In 2007, the ATS guidelines were revised to include more lenient diagnostic criteria (8). Clinical criteria include a symptomatic patient with pulmonary symptoms, nodular or cavitary opacities on chest radiographs, or a high-resolution computed tomography scan that shows multifocal bronchiectasis with multiple small nodules. In addition, the microbiologic criteria comprise positive culture results from [greater than or equal to] 2 separate sputum samples, or positive culture results from [greater than or equal to] 1 bronchial wash or lavage, or a lung biopsy specimen with mycobacterial histopathologic features (granulomatous inflammation or AFB) and positive culture for NTM, or lung biopsy specimen showing mycobacterial histopathologic features and [greater than or equal to] 1 sputum or bronchial washing culture positive for NTM.
In a pilot study performed in 3 hospitals in Zambia in 2001, high rates of NTM culture-positive sputum samples were obtained (P.C.A.M. Buijtels et al., unpub, data). Therefore, we studied the clinical relevance of and risk factors for isolation of NTM from HIV-positive and HIV-negative patients with chronic productive cough and from randomly selected community controls in Zambia.
Materials and Methods
The study was conducted in St. Francis Hospital in the district of Katete in Zambia from August 2002 through March 2003. Informed consent was obtained from all patients and controls before enrollment. The study was reviewed and approved by the research ethics committee of the University of Zambia, the Central Board of Health, and the Ministry of Health in Zambia.
The study population was composed of adults ([greater than or equal to] 15 years of age) with chronic (defined as [greater than or equal to] 2 weeks) signs and symptoms and a productive cough who were admitted to the department of internal medicine at the hospital. Most (96%) of the included patients had respiratory tract symptoms. The other 4% of the patients had skin infections/abscesses or lymphadenopathy.
For each eligible patient who consented to participate in the study, 2 healthy community controls were recruited randomly from the neighboring community. These controls were not matched for age or other characteristics of the patients. Nested within this case-control study, the characteristics of NTM-positive and NTM-negative persons were analyzed separately.
At the time of enrollment, patients and controls were interviewed in their own language, and their medical records were reviewed by using a standard form. A detailed physical examination was conducted. Chest radiographs were evaluated in a blinded manner in the Netherlands without any additional clinical information. Radiographs were scored for mediastinal adenopathy, cavitation, pleural and pericardial fluid, miliary pathologic changes, alveolar infiltration, interstitial pathologic changes, other lung pathologic changes, or no pathologic changes. Results of the scoring system were chest radiographs with no pathologic changes, pathologic changes not suggestive of TB, and pathologic changes consistent with TB. Over 3 consecutive days, sputum was collected from patients with a productive cough. Controls were asked to gargle with normal saline if they could not produce sputum. The first 2 sputum samples or gargle specimens were cultured for mycobacteria, and a third sample was stored at -20[degrees]C until used.
Sputum or gargle specimens were divided into 2 equal parts: half was decontaminated with N-acetyl-L-cysteine-NaOH and half was decontaminated by using 6% sulfuric acid to compare these decontamination procedures for culture of mycobacteria (9). Specimens were cultured in Mycobacteria Growth Indicator Tubes (Becton Dickinson Microbiology Systems, Cockeysville, MD, USA) according to the manufacturer's instructions and guidelines reported by Master (10). Mycobacterium isolates were identified by using the Accuprobe culture confirmation test for the M. tuberculosis complex (Accuprobe; bioMerieux, Marcy l'Etoile, France) or by 16S rRNA gene sequencing (11). Serologic testing for HIV was performed by using a qualitative immunoassay (Determine HIV-1/2; Abbott Laboratories, Abbott Park, IL, USA) and the Vidas HIV DUO assay (bioMerieux).
Data were entered into SPSS version 6 software (SPSS Inc., Chicago, IL, USA) and analyzed by using STATA version 8.0 (StataCorp., College Station, TX, USA). Student t-tests were used to assess different means between groups; proportions were compared by using [chi square] tests. Univariate odds ratios with 95% confidence intervals were calculated to assess associations of potential risk factors for NTM positivity. A stepwise backward regression approach was used for multivariate analysis.
Body mass index (BMI) was calculated as weight in kilograms divided by squared height in meters. Underweight was defined as a BMI <18.
Clinical Diagnosis of NTM Lung Disease
NTM lung disease was diagnosed if patients had respiratory symptoms, abnormal chest radiographic results suggestive of Mycobacterium infection, and 2 positive sputum cultures with the same NTM. Patients or controls with positive NTM cultures who did not meet these criteria were considered colonized.
From August 2002 through February 2003, 180 patients and 385 controls were enrolled in the study. Two sputum samples were cultured from 154 patients and 383 controls, and from 1 sample of the remaining participants. The median age of the patients and controls was 35 years (range 16-80 years) and 30 years (range 15-78 years), respectively. Female participants represented 55% (99/180) of the patient group and 69% (265/385) of the control group. A total of 128 (71%) of the patients were HIV positive, and 87 (23%) of the controls were HIV positive. Statistically significant differences in age, sex, and HIV status were observed between patients and controls.
Culture Results for Patients
Of 180 patients, 60 (33%) had only M. tuberculosis isolates in their sputum samples, 12 (7%) had M. tuberculosis and NTM, and 19 (11%) had only NTM (Table 1). Microscopic results of Ziehl-Neelsen-stained smears of sputum samples were positive in 46 (67%) of 69 patients with M. tuberculosis isolates and in 1 patient with an NTM-positive culture.
Of the 31 NTM-positive patients, 29 had 2 consecutive sputum samples subjected to culture. In 22 of the 29 patients, only 1 of 2 cultures was positive. Four NTM-positive patients had 2 positive NTM cultures; 1 of these patients had pulmonary disease. M. intracellulare was isolated twice from 2 of these 4 patients, M. avium was isolated from both samples from 1 patient, and NTM of 2 species and M. tuberculosis was isolated from 1 patient. One of 2 sputum cultures from 3 other NTM-positive patients contained mycobacteria that could not be identified. Two of these 3 patients had M. intracellulare in 1 sputum sample; M. porcinum was isolated from 1 patient.
Case Reports for Patients with Suspected NTM Disease
Characteristics of the 4 patients with NTM isolates in both sputum samples and of the 3 NTM-positive patients from whom 1 of the 2 sputum samples contained mycobacteria that could not be identified are shown in Table 2. For 3 patients (1, 2, and 4), NTM-associated disease was suspected because of the combination of symptoms, positive cultures, and pathologic changes consistent with TB seen on chest radiographs. However, only 1 patient (patient 4) fulfilled the ATS criteria for NTM lung disease. M. intracellulare was isolated from all 3 of these patients.
The first patient (patient 4) was a 32-year-old HIV-positive man who reported having had a productive cough with hemoptysis for 17 weeks. He also was vomiting and had diarrhea. His BMI was 15. He had been treated for TB. Results of a chest radiograph were consistent with TB and showed alveolar infiltration and interstitial pathologic changes. His condition did improve after treatment with antimicrobial drugs (chloramphenicol and tetracycline), and he was again given treatment for TB. Mycobacteria were cultured from 2 sputum samples and identified as M. intracellulare. The patient died 5 weeks later.
The second patient (patient 1), who had M. intracellulare pulmonary disease, was a 55-year-old HIV-positive man. He was admitted because of a productive cough with hemoptysis for 17 weeks. Diarrhea was also reported; his BMI was 17. He had been receiving treatment for TB for 4 months. Sputum obtained before treatment was AFB negative. Radiographic investigation of the chest showed cavities and alveolar consolidation. No improvement was seen after he was treated with antimicrobial drugs (chloramphenicol, amoxicillin, gentamicin, and metronidazole). Sputum was examined again and was smear positive for AFB. The first sputum culture showed M. intracellulare. In the second sputum culture, the isolated mycobacteria could not be identified because of logistic reasons. The patient died 3 weeks later.
The third patient (patient 2), who had M. intracellulare pulmonary disease, was a 45-year-old HIV-positive woman who had had respiratory signs and symptoms for >1 year. She was known to have asthma. Physical examination found enlarged submandibular, supraclavicular, and axillary lymph nodes. Her BMI was 20. Alveolar infiltration was seen on a chest radiograph. Treatment with chloramphenicol was started. Culture of the first sputum sample showed mycobacteria that could not be identified; the second sputum showed M. intracellulare. Three days after admission, the patient was taken home by her family and was lost to follow-up.
Culture Results for Controls
M. tuberculosis was cultured from sputum or gargle specimens from 3 (0.8%) of the 385 controls; in 1 of these 3 controls, NTM and M. tuberculosis were isolated (Table 1). In 61 (16%) controls, only NTM were isolated; this number was comparable with the proportion of patients among whom only NTM were isolated (11%; p = 0.2). In 61 of 62 NTM-positive controls, only 1 sputum or gargle specimen was culture positive for NTM. In 1 control, who was HIV negative, 2 mycobacteria, M. porcinum and an unknown Mycobacterium sp., were isolated. No chest radiographs suggestive of TB were observed for any of the controls.
From 383 controls, 2 sputum or gargle samples were cultured for Mycobacterium spp. Significantly fewer controls (1/383) than patients (4/154) had 2 sputum or gargle cultures positive for NTM (p<0.05).
Mycobacterium spp. Isolated
To compare the influence of the decontamination method on the yield of mycobacteria, we divided sputum or gargle samples from all patients and controls into 2 equal parts before decontamination (9). A total of 635 sputum samples were cultured from 180 patients, and 1,532 sputum or gargle samples were cultured from 385 controls. The results of the cultures are shown in Table 3. The number of NTM (72) isolated from 635 sputum samples of patients was significantly higher than the number of NTM (99) isolated from 1,532 sputum or gargle samples from controls (11% and 6%, respectively, (p<0.001).
Mycobacteria were isolated from 273 (43%) of 635 sputum samples from patients; M. tuberculosis isolates were found in 201 (74%) of the 273 positive sputum specimens, and NTM were found in 72 (26%). The most frequently isolated NTM was M. intracellulare, which was found in 12 specimens.
Mycobacteria were isolated from 104 (6.8%) of 1,532 sputum or gargle samples cultured from the controls. M. tuberculosis was found in 5 (4.8%) of the 104 positive cuptures, and NTM were found in 99 (95%). The predominant NTM isolated from the controls were M. avium (5 specimens), M. goodii (4 specimens), and M. peregrinum (4 specimens).
A total of 55 (32%) of 171 NTM isolated from patients and controls were not identified because their 16S rDNA sequences were absent in the BLAST (National Center for Biotechnology Information, Bethesda, MD, USA, www. ncbi.nlm.nih.gov) database. These 55 NTM species were closely related to various Mycobacterium spp. such as M. intracellulare, M. malmoense, M. fortuitum, M. smegmatis, and M. terrae.
Comparison of Persons with and without NTM in Sputum or Gargle Samples
The 93 patients and controls with NTM-positive cultures had different clinical and radiographic features than the 472 patients and controls without NTM in sputum samples (Table 4). These persons were more likely to report vomiting and diarrhea, were more often underweight (BMI
Independent risk factors for NTM culture-positive sputum were determined by using multivariate analysis. Two factors, underweight (BMI<18) and use of tap water, were independently associated with having an NTM-positive sputum culture (Table 6).
The purposes of this study were to compare the prevalence of NTM in sputum between hospitalized chronically ill patients and community controls and to determine the clinical importance of isolation of NTM. The proportions of patients and controls with positive sputum or gargle cultures for NTM were comparable (11% and 15%, respectively). However, the proportion of NTM-positive sputum samples was higher for patients than for controls (11% and 6%, respectively). This finding suggests that persistent NTM are associated with chronic illness in these patients. It is not known whether culture results were influenced by the method of obtaining specimens. A gargle specimen contains flora of the oropharyngeal mucosa, whereas a sputum sample contains flora of the lower airways. In the patient group, more persons were capable of producing sputum, which may have influenced the yield of positive NTM-positive cultures.
NTM lung disease was definitively diagnosed for 1 patient and probable diagnosis was made for 3 patients (nos. 1, 2, and 4; Table 2). M. intracellulare was isolated from the sputum samples of these HIV-positive patients. These patients had respiratory symptoms, and chest radiographs showed pathologic changes compatible with TB. Unfortunately, in 2 of these patients, 1 of 2 sputum samples with mycobacteria could not be identified because of contamination and reculture problems.
The combination of symptoms, positive cultures, and pathologic changes seen on chest radiographs are characteristics of NTM infection and suggestive of NTM pulmonary disease. However, the ATS criteria valid at the time of the study were not completely fulfilled because only 2 sputum samples were cultured for mycobacteria on consecutive days, instead of the 3 samples recommended. Furthermore, 2 of these patients suspected of having NTM lung disease had been treated for TB. Because these sputum samples were not tested with molecular amplification techniques for multidrug-resistant M. tuberculosis, the possibility that they had multidrug-resistant TB could not be excluded (12,13). Conversely, performance of these nucleic acid amplification tests is generally good for clinical respiratory specimens that are AFB smear positive but less so for specimens that contain fewer organisms or are AFB negative. Moreover, because sputum specimens were not cultured on solid medium, it was not possible to count the number of colony-forming units to distinguish colonization and infection from disease.
Many risk factors for NTM have been identified (14-16). In this study in a setting in Africa, HIV, sex, and age were not risk factors for NTM. The 2 risk factors for a positive NTM culture were being underweight and having consumed tap water. NTM are natural inhabitants of municipal water systems and soil. A biofilm may form in the water distribution system and be a source of replicating NTM (17). Consequently, availability of clean tap water may introduce a serious danger, in particular, to immunosuppressed human populations. Therefore, tap water in Zambia should be tested for NTM.
In this study, patients and controls with NTM in sputum or gargle samples more often had symptoms and signs of general malaise, including diarrhea, vomiting, and being underweight, and chest radiographs for these NTM-positive persons more often showed pathologic changes than did those for NTM culture-negative persons. These symptoms and signs may not be specific for NTM infection, but they may reflect the patients' poor health in general.
Differences in geographic distribution of NTM species have been reported (16,18,19). The most commonly encountered NTM from clinical specimens in industrialized countries are M. avium complex (MAC) and M. kansasii (20-24). Despite limited studies conducted in Africa, the distribution of NTM is not known. In our study, the most commonly isolated NTM in patients and controls was M. avium complex. However, 32% of NTM found in both groups in Zambia have not been identified on a species level. This study indicates that the distribution of NTM in Africa may differ from that in Europe and the United States. NTM in Africa may have diverged from NTM in industrialized countries. This hypothesis could be tested by extensive DNA sequencing of semiconserved genes such as those for RNA polymerase B and 65-kD heat-shock protein. Unidentified NTM colonize persons in Africa and can cause disease in some instances. The magnitude of this problem, in addition to the problem of TB, is unknown but deserves more attention.
Rates of NTM colonization and disease that have been reported vary in different areas. In North America and Europe, rates of colonization and disease in the general population range from [approximately equal to] 1-15/100,000 persons to 0.1-2 /100,000 persons, respectively (20-23,25-28). These rates are largely unknown for most countries in Africa. In South Africa, prevalence rates of NTM colonization of 1,400-6,700/100,000 persons have been reported (29,30). In gold miners in South Africa, rates of infection were 101/100,000 persons for NTM, 66/100,000 persons for M. kansasii, and 12/100,000 persons for M. scrofulaceum (31,32). Although numbers of cases were small, the estimated rate of colonization in our study in the patient population was 9% (14/154) and the rate of disease was [approximately equal to] 2% (3/154). Two sputum or gargle specimens were collected and cultured from 383 controls in our study. NTM were isolated from both specimens for 1 of 61 controls with [greater than or equal to] 1 sample being culture positive for NTM. This control was not suspected of having NTM pulmonary disease. The estimated rate of colonization in the general population on the basis of this result is 16% (61/383).
NTM probably play a role in the etiology of TB-like disease in Zambia. More extended studies, in terms of duration and size, will be needed to determine the true prevalence of NTM infection in Africa.
We thank Shirley Visser-Triep and Astrid Bos-Grit for excellent laboratory assistance, Wouter Tietge and Ilse van den Berg for sampling a subgroup of the controls, the staff of St. Francis Hospital in Katete for their teamwork and cooperation, and Margoth Petit-Vijgen for managing the extended patient database.
This study was supported by the partnership of microbiologists at the Medical Centre Rijnmond-South in Rotterdam and The Netherlands Society of Tropical Medicine and International Health.
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Author affiliations: Medical Centre Rijnmond-Zuid, Rotterdam, the Netherlands (P.C.A.M. Buijtels); University Medical Center Rotterdam, Rotterdam (P.C.A.M. Buijtels, H.A. Verbrugh); National Institute of Public Health and the Environment, Bilthoven, the Netherlands (M.A.B. van der Sande, D. van Soolingen); Medical Centre Alkmaar, Alkmaar, the Netherlands (C.S. de Graaff); St. Francis Hospital, Katete, Zambia (S. Parkinson); and Vlietland Hospital, Schiedam, the Netherlands (P.L.C. Petit)
Address for correspondence: Patricia C.A.M. Buijtels, Meander Medical Centre, Location Lichtenberg, Laboratory for Medical Microbiology and Immunology, Utrechtseweg 160, 3818 ES Amersfoort, the Netherlands; email: email@example.com
Dr Buijtels is a medical microbiologist at the University Medical Centre in Utrecht. Her research interests include the clinical relevance of NTM in Africa.
Table 1. Culture results for 180 hospitalized chronically ill patients and 385 controls, Zambia, August 2002-March 2003 * Results Patients Culture exclusively Mycobacterium 60 (33) tuberculosis, no. (%) Culture M. tuberculosis and NTM, no. (%) 12 (7) Culture exclusively NTM,([dagger]) no. (%) 19 (11) Culture NTM, ([double dagger]) no. (%) 31 (17) 2 sputum or gargle samples cultured 154 2 sputum or gargle samples cultured from 29 of 31 NTM-positive NTM-positive person patients 1 NTM-positive culture in NTM-positive 22 of 29 NTM-positive person with 2 samples cultured patients 1 NTM-positive cultures in NTM-positive 4 of 29 NTM-positive person with 2 samples cultured patients 2 NTM-positive cultures in persons with 4 of 154 patients with 2 2 samples cultured ([section]) samples cultured Results Controls Culture exclusively Mycobacterium 2 (0.5) tuberculosis, no. (%) Culture M. tuberculosis and NTM, no. (%) 1 (0.3) Culture exclusively NTM,([dagger]) no. (%) 61 (16) Culture NTM, ([double dagger]) no. (%) 62 (16) 2 sputum or gargle samples cultured 383 2 sputum or gargle samples cultured from 62 of 62 NTM-positive NTM-positive person controls 1 NTM-positive culture in NTM-positive 61 of 62 NTM-positive person with 2 samples cultured controls 1 NTM-positive cultures in NTM-positive 1 of 62 NTM-positive person with 2 samples cultured controls 2 NTM-positive cultures in persons with 1 of 383 controls with 2 2 samples cultured ([section]) samples cultured * NTM, nontuberculous mycobacteria. ([dagger]) Proportion of patients with exclusively NTM was comparable with controls (p = 0.2). ([double dagger]) NTM isolated with or without M. tuberculosis. ([section]) Significantly more patients than controls had 2 sputum or gargle cultures positive for NTM (p<0.05). Table 2. Data for 4 patients with NTM in 2 consecutive sputum samples and 3 NTM-positive patients from whom 1 of 2 sputum samples contained mycobacteria that could not be identified, Zambia, August 2002-March 2003 * Isolate from Ziehl- Patient Isolate from first second sputum Neelsen no. sputum sample sample staining 1 ([dagger]) Mycobacterium AFB not 1+ intracellulare identified 2 ([dagger]) AFB not M. intracellulare - identified 3 M. intracellulare M. intracellulare - 4 ([dagger]) M. intracellulare M. intracellulare - 5 AFB not M. porcinum - identified 6 M. avium M. avium - 7 M. avium M. peregrinum, - M. tuberculosis Patient HIV Temp, Duration, no. Sex Age, y status [degrees]C wk 1 ([dagger]) M 55 + 34.6 17 2 ([dagger]) F 45 + 36.1 487 3 M 43 + 36.3 3 4 ([dagger]) M 32 + 36.8 17 5 F 50 - 36.6 8 6 M 33 + 37.4 17 7 F 24 + 35.0 13 Chest Patient radiograph no. result Died BMI 1 ([dagger]) Suspected TB Yes 17 2 ([dagger]) Suspected TB No 20 3 No pathologic No 19 changes 4 ([dagger]) Suspected TB Yes 15 5 No suspected TB No 21 6 No radiograph No 16 7 No pathologic Yes NK changes * NTM, nontuberculous mycobacteria; Temp, temperature at time of enrollment; Duration, duration of symptoms from time of coming to the hospital to enrollment in the study; BMI, body mass index; AFB, acid-fast bacilli; TB, tuberculosis; NK, not known. All patients had respiratory symptoms. ([dagger]) Patients assumed to have pulmonary NTM disease. Table 3. Results from cultures of sputum samples taken from hospitalized chronically ill patients and controls, Zambia, August 2002-March 2003 Patients, Controls, Result no. (%) no. (%) Negative 362 (57) 1,428 (93) Mycobacterium tuberculosis 201 (32) 5 (0.3) M. avium complex 15 (2) 5 (0.3) M. intracellulare 12 (2) 0 M. avium 3 (0.5) 5 (0.3) M. gordonae 4 (0.6) 0 M. peregrinum 2 (0.3) 4 (0.3) M. goodie 1 (0.2) 4 (0.3) M. porcinum 1 (0.2) 3 (0.2) M. lentiflavum 1 (0.2) 0 Unknown Mycobacterium spp. 13 (2) 42 (3) Other Mycobacterium spp. * 3 (0.5) 7 (0.5) Unidentified acid-fact bacilli 32 (5) 34 (2) Total no. sputum samples 635 1,532 * Other Mycobacterium spp. in patients were M. fortuitum, M. neoaurum, and M. simiae. Other Mycobacterium spp. in controls were M. fortuitum, M. asiaticum, M. aurum, and M. conspicuum. Table 4. Clinical data for samples obtained from NTM-positive and NTM-negative persons, Zambia, August 2002-March 2003 * NTM-positive NTM-negative Characteristic samples samples Persons, no. (%) 93 (16.5) 472 (83.5) HIV positive, no. (%) 41 (45.6) 174 (38.5) Mycobacterium tuberculosis, 13 (14.0) 62 (13.1) no. (%) BMI, mean (SD) 20.2 (4.2) 20.8 (3.7) Underweight, no. (%) 26 (29.6) 92 (20.6) Vomited, no. (%) 8 (8.6) 18 (3.8) Diarrhea, no. (%) 12 (12.9) 11 (2.3) Lymph nodes analyzed, no. (%) 21 (22.8) 146 (30.9) Chest radiograph compatible 5 (26.3) 28 (7.1) with TB but culture negative for M. tuberculosis, no. (%) Died, no. (%) 9(9.7) 26(5.5) Characteristic p value All samples Persons, no. (%) -- 565 HIV positive, no. (%) 0.2 215 (39.7) Mycobacterium tuberculosis, 0.8 75 (13.3) no. (%) BMI, mean (SD) 0.2 20.7 (3.8) Underweight, no. (%) 0.06 118 (22.1) Vomited, no. (%) 0.04 26 (4.6) Diarrhea, no. (%) <0.001 23 (4.7) Lymph nodes analyzed, no. (%) 0.1 167 (29.6) Chest radiograph compatible 0.003 33 (8.0) with TB but culture negative for M. tuberculosis, no. (%) Died, no. (%) 0.1 35(6.21 * NTM, nontuberculous mycobacteria; BMI, body mass index; TB, tuberculosis. Table 5. Backqround characteristics of NTM-positive and NTM-negative persons, Zambia, Auqust 2002-March 2003 * NTM positive, NTM negative, Characteristic no. (%) no. (%) Persons 93 (16.5) 472 (83.7) Female 61 (65.6) 303 (64.2) Age, y, mean (SD) 36.7 (13.1) 34.8 (14.6) Farmer 48 (51.6) 245 (51.9) Used tap water 23 (25.0) 62 (13.2) Used unboiled milk 15 (16.1) 62 (13.1) Smoker 5 (5.7) 41 (8.9) Used alcohol 9 (10.3) 51 (11.2) Hospitalized 31 (33.3) 149 (31.6) Previously treated for TB 9 (9.7) 28 (5.9) Characteristic p value All persons, no. (%) Persons -- 565 Female 0.8 364 (64.4) Age, y, mean (SD) 0.2 35.1 (14.4) Farmer 1.0 293 (51.9) Used tap water 0.004 85 (15.1) Used unboiled milk 0.4 77 (13.6) Smoker 0.3 46 (8.4) Used alcohol 0.8 60 (11.0) Hospitalized 0.7 180 (31.9) Previously treated for TB 0.2 37 (6.6) * NTM, nontuberculous mycobacteria; TB, tuberculosis. Table 6. Crude and adjusted risk factors for isolation of NTM from sputum samples, Zambia, August 2002-March 2003 * Univariate Multivariate analysis, analysis, OR Factor OR (95% CI) (95% CI) ([dagger]) Hospitalized 1.1 (0.7-1.7) NS Age [greater than or equal 1.3 (0.8-2.5) NS to] 25 y Sex (female) 1.1 (0.7-1.7) NS Underweight (BMI <18) 1.6 (1.0-2.7) 1.7 (1.0-2.9) Mycobacterium tuberculosis 1.1 (0.6-2.0) NS infection Previous treatment for TB 1.7 (0.8-3.7) NS HIV positive 1.3 (0.8-2.1) NS Used tap water 2.2 (1.3-3.8) 2.0 (1.1-3.5) Used alcohol 0.9 (0.4-1.9) NS Smoker 0.6 (0.2-1.6) NS Used unboiled milk 1.3 (0.7-2.3) NS Farmer 1.0 (0.6-1.5) NS Chest radiograph compatible 4.7 (1.6-13.9) NS with TB but culture negative for M. tuberculosis * NTM, nontuberculous mycobacteria; OR, odds ratio; CI, confidence interval; NS, not significant; BMI, body mass index; TB, tuberculosis. ([dagger]) Stepwise backward elimination.
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