Background
Tuberculosis (TB) remains a major public health problem globally and poses a considerable threat to human health [
1]. Globally, approximately 3.2 million women suffer from clinical TB each year [
2]. Pregnancy-related TB endangers the health of both women and their fetuses and is considered an important cause of morbidity and mortality [
3‐
5]. TB more rapidly progresses in pregnant women than in nonpregnant ones [
5] and can lead to miscarriage [
3‐
5]. Furthermore, women who survived from TB are often dissuaded from having children or, even worse, can no longer conceive again.
Acute miliary TB, a more serious and potentially lethal form of the disease, results from massive hematogenous dissemination of
Mycobacterium tuberculosis. The miliary pattern in the lungs has been radiologically described as “a collection of tiny discrete pulmonary opacities that are generally uniform in size and widespread in distribution, each of which measures 2 mm or less in diameter” [
6,
7]. If untreated, miliary TB is uniformly fatal. Relative to all forms of TB, the incidence of miliary TB ranges from 0.15 to 10 % [
1,
6,
7]. Additionally, approximately 15–30 % of patients with pulmonary TB during pregnancy exhibit hematogenous dissemination and have miliary TB [
8]. Because clinical symptoms such as fever and cough are nonspecific and chest X-ray (CXR) and chest computed tomography (CT) scan during pregnancy are associated with a risk of radiation exposure, the diagnosis of miliary TB during pregnancy is often delayed.
With the increasing application of in vitro fertilization and embryo transfer (IVF-ET), the incidence of TB during pregnancy has gradually increased, posing a serious threat to the health of pregnant women and fetuses [
1,
9,
10]. There have been occasional case reports of TB with hematogenous dissemination, miliary TB, and/or meningitis during pregnancy after IVF-ET, leading to abortion, fetal malformation, or increased risk of mortality [
10,
11]. Therefore, correct and timely diagnosis and management of TB during pregnancy are important. Therefore, in this study, we aimed to describe the clinical features of TB and its impact on pregnancy outcomes after IVF-ET. We retrospectively analyzed the data of patients who underwent IVF-ET and showed clinical signs of miliary TB during pregnancy between January 2012 and December 2017 at the reproductive center of our hospital. Additionally, we summarized the clinical manifestations and pregnancy outcomes of these patients.
Methods
This was a retrospective study of patients who underwent IVF-ET for infertility between January 1, 2012, and December 31, 2017, at Peking University Third Hospital, a tertiary referral hospital in Beijing, China. Data on patients undergoing IVF-ET, including causes of infertility, serum hormone concentrations, the controlled ovarian hyperstimulation protocol, and CXR results, were recorded. CXR was routinely performed for each patient, and active TB cases were excluded before IVF-ET was started. A medical team was assigned to follow up the pregnancy outcomes.
During the 6-year period, 62,755 patients, who were all HIV-negative, had received IVF-ET at our center. Among these patients, seven with active TB during pregnancy were identified. Active TB was diagnosed according to the national guidelines [
12]. Miliary TB was diagnosed based on the size, distribution, and density of miliary-like nodules that were bilaterally distributed on CXR or chest CT scan [
13,
14]. Baseline data and CXR and laparoscopy results before IVF-ET were retrieved. A respiratory physician contacted the seven patients via phone call and reviewed the medical records. Live birth was defined as the delivery of a living fetus (or living fetuses) beyond 28 weeks of gestation, whereas miscarriage was defined as pregnancy loss before 28 weeks of gestation.
This study was approved by the Ethics Committee of Peking University Third Hospital [batch number: (2019)327-02]. The retrospective nature of the study resulted in a waiver regarding the signing of the informed consent form.
IVF-ET protocol
IVF-ET was performed as previously described [
15]. Briefly, controlled ovarian hyperstimulation was achieved, oocytes were fertilized, and ETs were subsequently performed [
15]. Among seven patients who developed TB during pregnancy, one had undergone a frozen cycle transfer, whereas the remaining six had undergone fresh cycle transfer. After ET, 60 mg of progesterone was injected intramuscularly for 14 days. Blood human chorionic gonadotropin concentration was monitored at 2 weeks after transplantation, and the status of the embryo sac was examined by ultrasonography at 4 weeks after transplantation.
Statistical analysis
Continuous variables are expressed as mean ± standard deviation or as median with interquartile range. Statistical analysis was performed using SPSS version 23 (IBM Corp., Armonk, NY).
Discussion
In this retrospective study, we identified seven cases of active TB during pregnancy from 62,755 cases of IVF-ET carried out at our hospital. All of these seven cases were diagnosed with acute miliary TB, with two cases complicated by TB meningitis. Notably, signs of prior TB on CXR were detected in 11.4 % of our study population (7137/62,755), and six out of the seven patients with acute miliary TB had prior TB signs identified on CXR before IVF-ET.
Our data indicated that TB in pregnancy after IVF-ET mostly occurred during the first 8–12 weeks of pregnancy. Fever was the main symptom, and the time interval between fever onset and definitive diagnosis was 2–4 weeks or more. An important finding of our study was that all seven patients with active TB during pregnancy after IVF-ET developed hematogenous dissemination, which is the most serious condition of TB. Two out of the seven patients had tuberculous meningitis as a complication. This finding is consistent with the result of a previous report. We conducted a literature review on patients with TB during pregnancy after IVF-ET using the keywords “infertility,” “in vitro fertilization and embryo transfer,” “tuberculosis,” and “pregnancy” to search for articles published from 1980 to 2019 in PubMed, MEDLINE, EMBASE, and Chinese Wanfang databases. Furthermore, we summarized 37 cases of TB during pregnancy after IVF-ET [
10,
16‐
24] (Table
3). Addis et al. reported the first case in 1988 [
10]. Since then, more cases have been described, the majority of which were from developing countries, [
17‐
21,
24]. The results from our study and from these previous studies indicated that women with TB during pregnancy after IVF-ET were prone to hematogenous dissemination.
Table 3
Summary of reported cases of TB during pregnancy after IVF-ET
1 | 33 | 10 | Denial of TB history | Fever, cough, shortness of breath | Miliary TB (1/1) | Cured | Spontaneous abortion | U.K. | |
5 | 25–33 | 5–9 | Denial of TB history; Laparoscopy showed bilateral oviduct obstruction (5/5) | Fever (5/5) | Miliary TB (5/5) | Cured | Spontaneous abortion (5/5) | China | |
4 | NA | 5–15 | Denial of TB history | Fever (4/4) | Miliary TB (4/4); ARDS (1/4) | Died (1/4); Cured (3/4) | Spontaneous abortion (4/4) | China | |
1 | 29 | 11 | Denial of TB history; laparoscopy showed bilateral oviduct obstruction | Fever, shortness of breath | Miliary TB (1/1) | Cured | Spontaneous abortion | China | |
6 | 27–32 | 6–9 | One case had a history of tuberculous pleuritis, and 1 case had a history of pelvic TB | Fever (6/6), slight cough and expectoration (6/6) | Miliary TB (6/6) | Cured | Spontaneous abortion (5/6); induced abortion (1/6) | China | |
11 | 26–36 | 6–14 | Denial of TB history | Fever (11/11) | Miliary TB (11/11); TB meningitis (4/11) | Cured | Spontaneous abortion (8/11); induced abortion (3/11) | China | |
6 | 29–39 | 5–16 (5/6); 26 (1/6) | One case had a history of TB, one case had no history of TB, but chest radiograph showed sclerotic calcification in the lung(s), and the other 4 cases had no manifestation of TB | Fever, cough, shortness of breath (6/6); Headache (1/6) | Miliary TB (6/6); TB meningitis (1/6) | Cured | Spontaneous abortion (3/6); induced abortion (3/6) | China | |
1 | 38 | 14 | Denial of TB history, and laparoscopy showed bilateral oviduct obstruction | Fever, cough | Miliary TB with TB meningitis (1/1) | Cured | Spontaneous abortion | Israel | |
1 | NA | 8 | Denial of TB history; Laparoscopy showed bilateral oviduct obstruction | Fever, cough | Miliary TB (1/1) | Cured | Spontaneous abortion | Belgium | |
1 | 31 | 8 | Denial of TB history; Laparoscopy showed bilateral oviduct obstruction | Fever, cough | Miliary TB (1/1) | Cured | Premature delivery | China | |
TB activation and dissemination may be related to latent infection, IVF-ET intervention, and immune dysregulation in pregnancy [
25]. Studies have shown that estrogen, progesterone, and human chorionic gonadotropin have a direct inhibitory effect on T-cells [
26,
27]. High estrogen levels are conducive to the proliferation of
M. tuberculosis. Increased vascular permeability after pregnancy may also facilitate bacterial spread throughout the body, resulting in hematogenous dissemination [
28]. The prognosis of miliary TB during pregnancy after IVF-ET was poor and may have caused the spontaneous abortion or may have resulted in premature delivery. More seriously, respiratory failure and even acute respiratory distress syndrome might occur in pregnant women [
14,
16]. Furthermore, fetuses might suffer from intrauterine growth retardation or be stillborn due to hypoxia, or acquire infection via hematogenous dissemination or aspiration of contaminated amniotic fluid [
11]. Moreover, those with miliary TB during pregnancy were less likely to achieve pregnancy, even with IVF-ET.
Identifying patients at high risk for TB activation should be an important evaluation before IVF-ET, especially in regions with a high TB burden. From our observation, we speculate that the coexistence of primary infertility, untreated prior pulmonary TB, and fallopian tube obstruction may be a risk factor for active TB during an IVF-ET pregnancy. Signs of fibrotic scarring, calcified nodules, and/or pleural thickening on CXR indicate previous infection with
M. tuberculosis [
29‐
31]. In our series, among the 7137 patients who had “old TB” lesions on CXR, six developed miliary TB during pregnancy. Liu et al. reported a similar case in which untreated prior pulmonary TB developed into miliary TB during pregnancy [
18]. Our previous study revealed that the clinical pregnancy and live birth rates were significantly lower in infertile patients with untreated prior pulmonary TB than in those without signs of prior TB, highlighting the adverse effects of TB in this specific patient population [
32].
Genital TB (GTB) is a form of extrapulmonary TB and a major cause of primary infertility among women in TB-endemic countries [
33], with a prevalence rate of 28.4 % in our hospital, as observed in previous studies [
34,
35]. GTB may cause fallopian tube obstruction, reduced endometrial receptivity, and ovarian dysfunction, leading to infertility. However, manifestations of GTB are nonspecific, and confirmation of diagnosis relies on invasive procedures. Our seven patients showed unilateral or bilateral oviduct obstruction, which suggested chronic infections such as GTB. Further studies are required to clarify whether the IGRA test and TST are necessary for the assessment of latent TB infection prior to IVF-ET and whether preventive anti-TB therapy can improve the pregnancy outcomes of infertile women with latent TB infection or untreated prior pulmonary TB on CXR. Moreover, screening for latent TB infection during pregnancy can provide an excellent opportunity for prevention.
Imaging plays a pivotal role in the diagnosis of pulmonary diseases, including TB [
31,
36]. Clinical diagnosis of active TB in pregnant women is often delayed, which is largely attributable to the concern about radiation exposure from chest radiography. The IGRA test is an important diagnostic method for active TB detection and is safe for use during pregnancy [
37‐
40]. Both the IGRA test and TST have a high consistency of 77.3–88.0 % [
39]. The
IGRA test has a high sensitivity of 100% and a moderate specificity of 80.0% for detecting
active TB during pregnancy [
40], which are not affected by previous vaccination with
bacillus Calmette–Guérin. Further studies on the use of the IGRA test for TB detection
during pregnancy, particularly in high-risk patients from TB-endemic regions, are warranted.
Our study has some limitations. First, this was a single-center study; however, as the largest reproductive center in China, we perform more than 10,000 cycles of IVF-ET annually on women from all over the country. Therefore, the population in this study was representative. Second, we inquired whether active TB had occurred during pregnancy through telephone follow-up, which might have led to an underdiagnosis of the disease.
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