Between 2004 and 2013, all patients who experienced major ADR due to first-line antituberculosis drugs provided on ambulatory basis by our Pulmonology Diagnostic Centre (PDC) were identified and all demographic and clinical data were retrospectively collected. Data from a group control consisting of a matched population by sex, age and year of initiation of treatment were also assembled for comorbid conditions analysis.

Inclusion criteria were as follows: age of 17 years or older; established diagnosis of active TB, either pulmonary or extrapulmonary, or proven LTBI; treatment regimen with first-line antituberculosis drugs; confirmed ADR to at least one of the antituberculosis drugs.

TB was defined as a clinically compatible illness confirmed by microbiological analysis or, when negative, a case with compatible clinical, radiologic, and/or histologic findings, and exhibiting positive response to treatment. LTBI was defined by the absence of clinical features suggestive of TB, normal chest radiographic examination and a positive tuberculin skin test (TST) induration. Since 2008, after the acquisition of laboratory means to perform the interferon gamma release assay (IGRA) using the ELISA method (Quantiferon-TB® Gold In-tube), this highly specific test was implemented as an active screening routine to confirm all positive TST reactions from patients suspected of having TB infection and support treatment decision.

Once having started antituberculosis treatment, all patients were closely monitored for surveillance of possible ADR and other disease-related complications. The first appointment occurred 15 days after beginning treatment, the second appointment at 1-month of treatment and the following ensued at monthly intervals.

Blood tests including complete blood count (CBC), liver transaminases, bilirubin (total and partial) and creatinine, were routinely checked at 15, 30 and 60 days of treatment and, afterwards, once each 2 months until the treatment was completed. Viral serology for hepatitis and HIV were routinely assessed, mostly before starting antituberculosis treatment.

Whenever necessary, as in the event of a serious side effect or complication, the patient was consulted or serum analyses were done beyond the usual routine. Also, if required, other complementary studies were added to the standard evaluation.

From patient's clinical records and national registration forms, information was collected regarding sex, age, nationality, residency, career occupation, symptoms, risk factors such as intravenous drug abuse, alcoholism or residence in a social support community, comorbidities, site of disease, diagnostic tests, initial treatment, adverse effects and outcomes.

Major ADR were defined as those that required discontinuation of one or more drugs, shift to second-line drugs or hospital admission. When all drugs were suspended, they were restarted after clinical and/or laboratory complete resolution, in a sequential way to possibly isolate the drug that caused the toxicity. A second-line treatment was initiated when a slow resolution was anticipated or treatment interruption was not desirable.

Hepatitis was defined as liver transaminases more than three times higher than the upper limit of normal in the presence of symptoms such as nausea, vomiting or abdominal pain, or transaminases more than five times the upper limit of normal without symptoms.

Significant episodes of cutaneous toxicity related to extensive eruption, symptoms like fever and mucous membrane involvement, or to sustained complaints while on medication with anti-histaminic drugs.

Gastrointestinal disturbance was considered major when there was no improvement despite measures such as combining the timing of administration to main meals or proton pump inhibitor medication.

Loss of visual acuity was routinely assessed by a careful ophthalmologic examination and related to anti-TB drugs when all other causes had been excluded.

Data analysis was executed by IBM SPSS® for Windows version 20.0. All demographic and clinical features were reported using frequency and descriptive analyses. Qualitative data were evaluated by chi-square test and quantitative data by Student's t test.

Demographic and clinical characteristics of the population are described in Table 1. From a total of 764 patients treated with antituberculosis regimens, 55 experienced at least one major ADR (7.2%). Six patients experienced a second ADR, for a total of 61 advents. The majority were male (52.7%) with a mean age of 50.8 years (range 17 to 94 years). Most of them were European (92.7%) and a small cluster belonged to Portuguese-spoken language African countries (7.3%), such as Cape Verde, Mozambique and Guinea Bissau.

Fourteen patients (25.5%) had at least one important comorbidity. The most frequent was malignant disease, followed by HIV and hepatitis C co-infection.

Five patients were currently living in community centres, two of which for treatment of drug addiction. One other patient was also a drug addict and five patients were alcoholic.

Of all 55 patients with severe ADR, 40 (72.7%) had been diagnosed with active TB, either pulmonary or extrapulmonary, while the remaining 15 (27.3%) had confirmed LTBI. Pulmonary TB was the most frequent form of the disease, accounting for more than half of the patients. Extrapulmonary TB was diagnosed in 10 patients: 5 ganglionic, 3 pleural and 1 each of genitourinary and cutaneous TB.

TB was detected mainly through passive screening of symptomatic patients (69.1%). Those remaining were diagnosed by active screening (30.9%), either by the investigation of contacts or assessment of other groups, such as patients submitted to anti-tumour necrosis factor (TNF)-alpha treatment.

All patients with LTBI or extra-pulmonary TB had normal chest radiographs. Pulmonary cavity TB was recognized in 13 patients while other radiographic patterns occurred in the remaining 17 patients with pulmonary TB and also in all patients with pleural TB.

Pulmonary TB was diagnosed mainly by smear microscopy and/or culture analysis from respiratory sample specimens (93.5%). Positive microbiological test results were obtained from sputum samples in 17 of these patients and from bronchial lavage samples in the other 10 patients. The remaining three patients with pulmonary TB had negative microbiological tests and were diagnosed through histological analysis from lung biopsies. Genitourinary TB was diagnosed by urine culture examination. All other cases of extrapulmonary TB (pleural, lymphatic and cutaneous) were diagnosed by specimen biopsy from the corresponding tissue sample. All 15 cases of LITB were confirmed by positive IGRA tests.

The most common initial treatment, prescribed to 24 patients, was the combination of four first-line anti-TB drugs: INH, RIF, PZA and EMB. One patient was treated with the same regimen except that SM replaced EMB. Nine patients with pulmonary cavity lesions were included in the four-drug standard treatment with EMB because of SM in-hospital absence. Fifteen patients initiated treatment with a three-drug regimen that included INH, RIF and PZA. EMB was not integrated in this group once drug susceptibility was already known and M. tuberculosis was fully susceptible.

The chosen therapeutic regimen for all patients with LTBI included in our study was the combination of INH and RIF administered on a daily basis during a 3-month period. However, the best therapeutic approach was determined on an individual basis and the patient characteristics. Other options included 9 months of INH or 4 months of RIF.

Whenever possible, fixed-doses combination tablets of rifater (INH, RIF and PZA) and rifinah (INH and RIF) were prescribed on a daily continuous basis. However, the emergence of an ADR frequently meant suspension of the combination treatment to remove or assess the ADR-related antituberculosis drug.

Only two patients with pulmonary TB did not undergo directly observed therapy (DOT), which was strictly related to accessibility difficulties. Neither of the patients with genitourinary and cutaneous TB and none of the patients with LTBI were treated with DOT strategy. Ultimately, a total of 36 patients (65.5%), 28 with pulmonary TB, all 5 patients with lymphatic TB and all 3 patients with pleural TB, were submitted to DOT.

The majority of patients who suffered severe ADR experienced a deviation from the total predicted time of treatment with a mean variation of 1.0±2.6 months (range −3.4 to 10.6) due to treatment suspension or termination (Tables 2 and 3).

The most frequent ADR was hepatitis. Five of these patients were alcoholic, two had a previous history of chronic liver disease and one was HIV-positive. Asymptomatic hepatotoxicity occurred in 35 cases and the remaining 18 were symptomatic. The most common symptoms were nausea, vomiting and abdominal pain. One female patient with no history of comorbid conditions had a poor outcome and needed liver transplantation while all others had complete liver transaminases normalization.

Rash occurred in five cases, with itchiness in three of them, and was the second most frequent adverse reaction.

One patient with chronic inflammatory arthritis and LTBI suffered gastrointestinal toxicity associated to RIF. One other patient with LTBI and no significant comorbid conditions had an episode of angioedema 25 days after initiating INH plus RIF anti-TB regimen which was subsequently interrupted. EMB was responsible for one single case of ocular toxicity in a patient with genitourinary TB whose visual acuity was never restored.

Side effects emerged mainly after 2 months of anti-TB drug regimen and more than half of these patients had their treatment stopped before completing the total number of doses and had, on average, a total time of treatment 0.7 months less than the predicted one. The remaining had an increase in the overall time of treatment due to one or more interruptions. Only seven cases of side effects during this period had LTBI and the majority had pulmonary TB (n=26).

A small proportion of ADR developed during the initial phase of treatment, that is, before completing 2 months of treatment. Eight of those had a decrease and 11 had an increase in the total number of months of treatment. Nine had LTBI.

It was not possible to identify which specific drug was responsible for the ADR in 82% of the cases since the drug rechallenge occurred with only minor residual effects, allowing treatment to continue, or it was definitively suspended with no further rechallenge. In these situations, all drugs that could have caused that effect were considered responsible.

The combination of INH and RIF was largely responsible for the incidence of side effects, specifically for 41 hepatotoxicity events and 3 cutaneous reactions. Those two drugs plus PZA accounted for six more cases of drug-induced hepatitis.

PZA, INH, RIF, and EMB were responsible for 5, 3, 2 and 1 major side effect, respectively. SM was not associated to any major ADR.

No correlation was found between age or sex and the overall incidence of ADR. However, when considering each category of ADR, younger age was meaningfully related to an increased risk of hepatotoxicity (P=0.035), which was 0.96 times smaller for each year that the age increased. In this group of patients, mean age was 49.0±19.4 years while those that had no drug-related hepatitis had a mean age of 64.6±16.4 years. On the other hand, an important association was found between male gender and toxicity to both INH and PZA but this did not achieve statistical significance (P=0.055).

Diabetes mellitus and major ADR were significantly associated (P=0.042) but the same could not be stated for other comorbidities or multidrug resistance risk factors. One diabetic patient had his treatment with oral anti-diabetic drugs changed to insulin therapy after being diagnosed with TB for an optimal glycaemic control, while the remaining were already being treated with insulin.

The authors declare that no experiments were performed on humans or animals for this study.

The authors declare that they have followed the protocols of their work centre on the publication of patient data.

The authors declare that no patient data appear in this article.