# Navigating Tuberculosis in Pregnancy and Lactation: A Review of Maternal and Neonatal Considerations

**Authors:** Tiago Lima, Sandra Trigo, Eduarda Silveira, Gabriela Jorge da Silva, Sara Domingues

PMC · DOI: 10.3390/diseases14030102 · Diseases · 2026-03-11

## TL;DR

This review discusses the challenges and considerations of managing tuberculosis during pregnancy and breastfeeding to ensure safe treatment for mothers and prevent neonatal complications.

## Contribution

The paper provides a comprehensive review of maternal and neonatal considerations in TB treatment during pregnancy and lactation, emphasizing drug safety and diagnostic challenges.

## Key findings

- First-line anti-TB drugs are considered safe during pregnancy and lactation.
- Second-line drugs have limited evidence on safety during breastfeeding, requiring individualized risk-benefit assessments.
- Routine TB screening in prenatal care is crucial in high-prevalence regions to improve maternal and neonatal outcomes.

## Abstract

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis. Despite the availability of effective treatments and advances in diagnostic methods, TB remains the leading cause of death from infectious disease globally, with its incidence tending to increase. Pregnant women constitute a population group with particular characteristics, as the diagnosis and treatment of certain conditions can be challenging. Early diagnosis and monitoring of TB by a multidisciplinary team are crucial to guide treatment and reduce complications. Congenital TB, although uncommon, is a serious complication that should be assessed in neonates, especially when the mother has previously been diagnosed with the disease. First-line anti-TB drugs are considered safe during pregnancy and lactation. In contrast, second-line drugs have a less well-established safety profile during breastfeeding, and the available evidence regarding their excretion in breast milk remains limited; therefore, their use requires individualised risk-benefit assessment. Data on this specific population group are limited, as physiological changes during pregnancy alter the pharmacokinetics/pharmacodynamics (PK/PD) of drugs and the inclusion of pregnant women in clinical trials remains contentious. Routine TB screening in prenatal care, particularly in high-prevalence regions, is crucial to improving maternal and neonatal outcomes. This narrative review was based on a structured search of PubMed, Scopus, and Web of Science (January 2000–June 2025), using the keywords tuberculosis, Mycobacterium tuberculosis, pregnancy, and breastfeeding. Eligible articles included original studies, reviews, and international guidelines.

## Linked entities

- **Diseases:** Tuberculosis (MONDO:0018076)
- **Species:** Mycobacterium tuberculosis (taxon 1773)

## Full-text entities

- **Genes:** RHOF (ras homolog family member F, filopodia associated) [NCBI Gene 54509] {aka ARHF, RIF}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** granuloma (MESH:D006099), complex (MESH:D048090), non- (MESH:C580335), meningitis (MESH:D008580), stillbirth (MESH:D050497), perinatal death (MESH:D066087), respiratory distress (MESH:D012128), COVID-19 (MESH:D000086382), insomnia (MESH:D007319), petechiae (MESH:D011693), sepsis (MESH:D018805), postpartum (MESH:D006473), congenital TB meningitis (MESH:D014390), congenital (MESH:D008209), MDR-TB (MESH:D018088), mediastinal lymphadenopathy (MESH:D008477), peripheral neuropathy (MESH:D010523), cyanosis (MESH:D003490), preterm birth (MESH:D047928), diabetes mellitus (MESH:D003920), intracranial tuberculomas (MESH:D016862), lethargy (MESH:D053609), acute infantile hepatitis (MESH:D017114), weight loss (MESH:D015431), maternal disease (MESH:D000079262), cold abscess (MESH:D000038), congenital musculoskeletal abnormalities (MESH:D009139), seizures (MESH:D012640), Infection with M. tuberculosis (MESH:D014376), inflammatory (MESH:D007249), renal failure (MESH:D051437), mastoiditis (MESH:D008417), haemophagocytic syndrome (MESH:D013577), hepatosplenomegaly (MESH:C535727), miliary pneumonia (MESH:D011014), postnatal infection (MESH:D019052), death (MESH:D003643), failure to thrive (MESH:D005183), paralysis (MESH:D010243), thrombocytopenia (MESH:D013921), nontuberculous mycobacterial infection (MESH:D009165), malnutrition (MESH:D044342), bacterial pneumonia (MESH:D018410), abortion (MESH:D000026), tuberculous mastitis (MESH:D008413), skin lesions (MESH:D012871), vomiting (MESH:D014839), omphalocele (MESH:D006554), hyperhidrosis (MESH:D006945), pruritus (MESH:D011537), cutaneous lesions (MESH:D009059), alcoholism (MESH:D000437), ascites (MESH:D001201), cleft palate (MESH:D002972), otitis media (MESH:D010033), anencephaly (MESH:D000757), fatalities (MESH:C565541), disseminated intravascular coagulation (MESH:D004211), jaundice (MESH:D007565), apnoea (MESH:D001049)
- **Chemicals:** PAS (MESH:D010131), pyridoxamine (MESH:D011733), PZA (MESH:D011718), bilirubin (MESH:D001663), Rifampicin (MESH:D012293), Ethionamide (MESH:D005000), fluoroquinolones (MESH:D024841), vitamin B6 (MESH:D025101), vitamin K (MESH:D014812), rifapentine (MESH:C018421), levofloxacin (MESH:D064704), linezolid (MESH:D000069349), BDQ (MESH:C493870), moxifloxacin (MESH:D000077266), aspirin (MESH:D001241), Ciprofloxacin (MESH:D002939), Pyridoxine (MESH:D011736), EMB (MESH:D004977), clarithromycin (MESH:D017291), clofazimine (MESH:D002991), streptomycin (MESH:D013307), delamanid (MESH:C516022), terizidone (MESH:C100142), INH (MESH:D007538), pretomanid (MESH:C410767), pyridoxal phosphate (MESH:D011732), Macrolides (MESH:D018942), metformin (MESH:D008687), Cycloserine (MESH:D003523), amines (MESH:D000588), uric acid (MESH:D014527), vitamin D (MESH:D014807), 1HP (-)
- **Species:** Mycobacterium tuberculosis subsp. tuberculosis (subspecies) [taxon 182785], Human immunodeficiency virus 1 (no rank) [taxon 11676], Mycobacterium tuberculosis complex (species group) [taxon 77643], Mycobacterium tuberculosis (species) [taxon 1773], Mycobacteriales (order) [taxon 85007], Homo sapiens (human, species) [taxon 9606], Bacillus sp. CG (species) [taxon 1196795]

## Full text

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## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC13025932/full.md

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Source: https://tomesphere.com/paper/PMC13025932