Recent Advances in Diagnosis and Management of Female Genital Tuberculosis.

Female genital tuberculosis (FGTB) is an important cause of significant morbidity and infertility. Gold-standard diagnosis by demonstration of acid fast bacilli on microscopy or culture or detection of epithelioid granuloma on histopathology of endometrial or peritoneal biopsy is positive in only small percentage of cases due to its paucibacillary nature. Use of gene Xpert on endometrial or peritoneal biopsy has improved sensitivity of diagnosis. Composite reference standard (CRS) is a significant landmark in its diagnosis in which combination of factors like AFB on microscopy or culture, positive gene Xpert, epithelioid granuloma on endometrial or peritoneal biopsy, demonstration of definite or probable findings of FGTB on laparoscopy or hysteroscopy. There have been many advances and changes in management of FGTB recently. The program is now called National Tuberculosis Elimination Program (NTEP), and categorization of TB has been stopped. Now, patients are divided into drug-sensitive FGTB for which rifampicin (R), isoniazid (H), pyrazinamide (Z) and ethambutol (E) are given orally daily for 2 months followed by three drugs (rifampicin, isoniazid and ethambutol (RHE) orally daily for next 4 months. Multi-drug-resistant FGTB is treated with shorter MDR TB regimen of 9-11 months or longer MDR TB regimen of 18-20 months with reserved drugs. In vitro fertilization and embryo transfer have good results for blocked tubes and receptive endometrium, while surrogacy or adoption is advised for severe grades of Asherman's syndrome. © Federation of Obstetric & Gynecological Societies of India 2021.

Introduction

Tuberculosis remains a major public health problem globally [1]. Female genital tuberculosis (FGTB) is a chronic infectious disease of female genital tract due to Mycobacterium tuberculous (rarely Mycobacterium bovis from unpasteurized infected milk) [2, 3]. It causes significant morbidity, especially irregular menstruation, pelvic pain, tubo-ovarian mass and infertility particularly in South East Asia and Africa [4-9]. The disease is making a comeback even in the developed countries like Europe and USA due to more liberal migration, concomitant immunocompromising diseases like human immunodeficiency virus coinfection, diabetes mellitus, chronic kidney and other systemic diseases [8-10]. FGTB is usually secondary to pulmonary TB through hematogenous route or lymphatic route but can occur through contagious spread from adjacent ileocaecal TB and rarely through infected semen from tuberculous orchitis in males [5, 6]. FGTB can cause permanent damage to female genital tract in advanced stages. Hence, early diagnosis and treatment in subclinical stage can prevent permanent damage and sequelae of female genital tract with successful pregnancy outcome [11, 12]. A high index of suspicion is needed for diagnosis which includes past or family history of TB or anti-tubercular therapy [4]. There have been recent changes in diagnosis and treatment of all types of TB including FGTB [13, 14]. Although FGTB is a paucibacillary disease, still all efforts should be made to arrive at a microbiological diagnosis and to do drug sensitivity test as treatment of TB including FGTB is now drug sensitivity test (DST) based using oral daily 4 drugs (rifampicin, isoniazid, pyrazinamide and ethambutol, RHZE for 2 months) followed by three drugs (RHE) daily orally for next 4 months. For drug-resistant TB, MDR drug regimens (shorter and longer) are used [2, 13–15].

Epidemiology

FGTB is an important variety of EPTB which causes significant morbidity, especially menstrual dysfunction and infertility (both primary and secondary) in affected women [2-6]. The prevalence of FGTB in infertility patients varies from country to country being only 0.72% in Portugal, 1% in USA and Europe to 20% in Pakistan and 6–25% in India being more in tertiary referral centers and in assisted reproduction centers [16-20]. It also causes significant infertility in other south East Asian countries like Indonesia [21] FGTB is observed in younger age group (20–40 years) in South East Asia and Africa as compared to older (pre-menopausal) age group in Europe and USA possibly due to early child bearing in the developing countries [2, 5, 6, 10]. Genital tuberculosis has significantly impacted both male and female reproduction in India [22, 23]. HIV coinfection has fueled the epidemic of TB all over the world with risk of TB in 10–20% [24, 25]. Now, the COVID-19 pandemic has exerted deleterious effect on control of TB including EPTB and FGTB [26-28]. People ill with COVID-19 and pulmonary TB show similar symptoms such as cough, fever and difficult breathing, and both are transmitted through droplets infection. WHO has observed 25% global reduction in TB detection due to less attention to TB as all the resources went into control of COVID-19. It may be responsible for 26% increase in TB deaths in near future. WHO has advised all member nations to urgently maintain continuity of essential services for people affected with TB during the COVID-19 pandemic [27, 28].

WHO estimates that TB may have caused more than double the number of death of COVID-19 in 2020 but yet has not received much attention or funding. In fact, COVID-19, tuberculosis and poverty may be a potential destructive synergism causing a storm like situation [27, 28].

Etiopathogenesis

FGTB is caused by Mycobacterium tuberculosis but can also be rarely caused by Mycobacterium bovis due to consumption of unpasteurized milk in villages [2, 4]. Genital infection is usually secondary to pulmonary TB or intestinal TB through hematogenous or lymphatic route and is more common in immunocompromised people or with chronic medical diseases including HIV and COVID-19 [2, 5, 6, 24–28]. Among the various sites, fallopian tubes are mostly affected (90–100%) followed by uterus (70%), ovaries (30%), cervix (10%) and rarely vulva and vagina (1% each) [2, 5, 6, 29]. Abdomino-pelvic TB may cause peritoneal adhesions, nodules and ascites and may simulate ovarian cancer [30]. Similarly, cervical TB may mimic cervical cancer causing abnormal vaginal discharge or vulval and vaginal ulcer or cancer [31].

Tuberculous of vulva may present as vulvul tumor or hypertrophic TB, while vaginal or vulval TB can present as genital fistula [2, 32].

In abdomino-pelvic TB, we have observed various types of adhesions on laparoscopy as TB is notorious to cause thick and vascular adhesions which may make laparoscopy and laparotomy hazardous with more risk of injury to the bowel [4]. We have described perihepatic adhesions with hanging gall bladder sign in abdomino-pelvic TB [33]. We have also observed Sharma’s ascending colon adhesion, Sharma’s sigmoid colonic adhesive band, Sharma’s compartmentalization sign in abdomino-pelvic TB [34-36]. We have described Sharma’s parachute sign in abdomino-pelvic TB with ascending colon being adherent to anterior abdominal wall making putting second port of laparoscope risky and hazardous on right side [37]. Abdomino-pelvic TB may sometimes be coexistent with malignancies or endometriosis [38, 39].

Symptomatology

The clinical features of FGTB vary as per involvement of different genital organs and are shown in Table 1 [2-6]. It is important to know that up to 10–12% of women may be asymptomatic or may have no obvious signs on clinical examination. As in Table 1, commonest symptoms are menstrual dysfunction and infertility (both primary and secondary).

Table 1

Clinical feature of FGTB [2–5]

Symptoms	Signs
1. No symptoms (10–12%)	1. No signs (10–12%)
2. Constitutional symptoms (some time)	2. Pallor
(i) Fever
(ii) Weight loss
(iii) Anorexia
(iv) Malaise
(v) Night sweats
(vi) Feeling unwell
3. Menstrual symptoms	3. Swollen and inflammed bones with discharge (TB osteomyelitis)
(i) Abnormal uterine bleeding (in early stages)
(ii) Postmenopausal bleeding
(iii) Oligomenorrhea
(iv) Hypomenorrhea
(v) Opsomenorrhea
(vi) Amenorrhea
(vii) Dysmenorrhea
4. Infertility (common)	4. Swollen and inflammed joints (skeletal TB)
(i) Primary
(ii) Secondary
5. Lower abdominal pain	5 Lymphadenopathy (in lymph node TB)
6. Pelvic pain	6. On chest auscultation (in pulmonary TB) Rales
7. Abdominal distension	7. Abdominal distension and ascites (abdominal TB)
8 Abnormal vaginal discharge	8. Bartholin enlargement vulval TB
9. Symptoms of TB of other areas (as per site)	9. Swelling of vagina (Vaginal TB)
	10. Swelling or growth or ulcer on vulva (vulval TB)
(A) Pulmonary TB	11. Cervical growth or ulcer (cervical TB)
(i) Cough	12. Unhealthy vaginal discharge
(ii) Sputum
(iii) Hemoptysis
(iv) Chest pain
(B) Tuberculous lymphadenitis of neck, axilla or groin	13. Pus discharge through cervix (pyometra)
Enlarged lymph nodes in different areas
(C) Skeletal TB	14. Enlarged uterus (in pyometra)
(i) Pain and swelling in joints
(ii) Pain, swelling and discharge from bones
(D) Intestinal TB	15. Tubo-ovarian mass and tenderness
(i) Constipation	(i) Unilateral
(ii) Loose motion	(ii) Bilateral
(iii) Abdominal distension
(iv) Abdominal swelling
10. Acute abdominal pain due to rupture of abscess or flare-up of lesions usually after some procedure	16. Unusual features
	(i) Vesicovaginal fistula
	(ii) Rectovaginal fistula

Causes of Infertility

Fallopian tubes are involved in almost all cases of FGTB. It is often bilateral causing exosalpingitis and endosalpingitis with tubal blockage.

Uterus: TB affects endometrial receptivity with damage of endometrium and formation of intrauterine synechiae (Asherman’s syndrome). Latent FGTB can cause recurrent implantation failure and recurrent miscarriages due to endometrial hostility through increased TNF alpha (tumor necrosis factor alpha) and interleukin 2 (IL-2) levels [17]. It also shifts T helper cells response from T1 to T2.

TB causes oophoritis with poor ovarian reserve and increased need of gonadotrophins for ovulation induction. It can also destroy ovaries [8, 9].

Differential Diagnosis

Abdomino-pelvic TB and FGTB are great mimickers and may be confused with other genital diseases like ovarian cyst, vulval or vaginal cyst, ectopic pregnancy, endometriosis genital malignancies and other intestinal diseases (appendicitis, Crohn’s disease) actinomycosis and various miscellaneous conditions (Schistosomiasis, filariasis, silicosis, leprosy, granuloma inguinale). Hence, history taking, meticulous clinical examination and judicious investigations are required to make the appropriate diagnosis of FGTB and to rule out other diseases.

Diagnosis of FGTB

As FGTB can be asymptomatic and may mimic many other diseases, its diagnosis may be missed in many women, especially in early stages. Hence, a high index of suspicion is needed. A careful and detailed history of anti-tubercular past tuberculosis (especially pulmonary) including in childhood, family history of TB and past history of treatment, history of other chronic diseases or conditions causing poor immunity (including HIV, immunosuppressive treatment, diabetes) is crucial to make the diagnosis. A meticulous general and gynecological examination as per Table 2 is crucial to make the diagnosis of FGTB. Clinicians should be particularly vigilant to make the diagnosis of FGTB in non-sexually active women with tubo-ovarian masses (adnexal masses) after ruling out germ cell tumors. Similarly, chronic pelvic inflammatory disease or abdominal or pelvic pain not responding to routine treatment should also be suspected to have FGTB. A careful examination for TB at other sites can give an active diagnosis. We have observed discharging sinus on knee or cervical or axillary lymphadenopathy in adolescent girls with tubo-ovarian masses in FGTB patients. One can easily collect specimen from such sites for demonstration of acid fast bacilli as compared to poorly accessible adnexal masses, especially in non-sexually active women where endometrial biopsy cannot be done.

Table 2

Laboratory investigations and diagnostic modalities for FGTB [2–4, 11, 12, 29]

S. no
1. Hematological tests	Complete hemogram: anemia, total leucocyte count may be increased. Lymphocytosis and raised erythrocyte sedimentation rate may be present
2. Coinfection testing	i) Human immunodeficiency virus testing ii) HbsAg iii) HCV
3. Blood sugar test	Blood sugar fasting and postprandial for diabetes mellitus
4. Other blood tests	Renal function tests: to rule out chronic kidney dresses
5.	CA-125 levels on patient serum: A level of > 35 IU/L may be seen in FGTB but is not reliable
	Mantoux test: a value of > 10 mm may give some clue but is not reliable
6.	Interferon gamma release assay (IGRA) has been approved by US FDA for diagnosis of latent TB and is available as Quantiferon TB-Gold which is done on whole blood
7.	X ray chest for any active or old healed pulmonary TB
8.	Endometrial aspirate or biopsy or peritoneal or lesion biopsy It is the most important test. Various tests can be done on it [2–4]
	(i) AFB microscopy
	(ii) AFB culture
	(iii) Cartridge-based nucleic acid amplification test (CBNAAT) or gene Xpert
	(iv) PCR (polymerase chain reaction)
	(v) Epithelioid granuloma on histopathology
	(vi) Newer molecular tests (Xpert Ultra, TB-LAMP)
9. Radiological tests	(i) Hysterosalpingography: It is avoided in acute disease to avoid flare-up. Various findings of FGTB can be blocked tubes, (usually cornual block) tobacco-pouch appearance of tubes, beaded tubes, filling defects in uterine cavity. (Asherman’s syndrome)
	(ii) Ultrasound: Cogwheel appearance due to hydrosalpinx is visible as tubal dilatation with septae due to tubal mucosal thickening. Endometritis due to TB causes thin, diffuse endometrial images with irregular borders
	(iii) Computerized tomography (CT), magnetic resonance imaging (MRI) and positron emission tomography (PET): one of the three modalities can be used for tuberculous tubo-ovarian masses. MRI has higher resolution especially for TB lymphadenitis. PET-CT can demonstrate increased FDG uptake of tuberculous tubo-ovarian masses
10. Endoscopic modalities	(i) Diagnostic laparoscopy: best diagnostic tool to detect FGTB by direct visualization of TB lesions on tubes like tubercles and caseous nodules and to take biopsy
	(ii) Hysteroscopy: to visualize endometrial disease like tubercles, pale endometrium and intrauterine adhesions

Investigations

Various detailed laboratory investigations and diagnostic modalities used in diagnosis of FGTB are shown with commonly used investigations being discussed here:

Endometrial aspirate or sampling or peritoneal biopsy

It is the most important investigation which should be done whenever possible especially in all sexually active women. It is done in premenstrual phase (day 21–24 of regular cycle) with patient having maintained abstinence (or used condoms) in the current cycle to avoid inadvertent pregnancy. It can be done with no 4 Karman cannula or pipelle or with endometrial biopsy curette. The sample should preferably be without blood and should be homogenized and sent in saline for following investigations.

AFB microscopy using Ziehl–Neelsen (ZN) staining is a traditional, rapid and economic method to detect bacteria but lacks sensitivity [3, 29].

Auramine and rhodamine fluorescent dyes with LED microscopy improve sensitivity. Gabbett cold staining method is economic and fast [2, 3, 12, 29].

Mycobacterial culture: It is the gold standard for diagnosis of tuberculosis and is particularly useful for drug sensitivity testing with various media being discussed below [2, 3, 12, 29]

Traditional egg-based solid media like Lowenstein Jensen (LJ) medium and agar-based 7H10 or 7H11 broth have been used for decades. They take up to 6 weeks to grow M. tuberculosis [2, 3, 12, 29]

BACTEC 460 radiometric culture system: is not used in current practice due to risk of needle stick injury and radiation hazard.

BACTEC-MGIT 960 system (Mycobacterium Growth Indicator Tube): It is a non-radio-active, noninvasive and fluorometric culture medium which uses Middlebrook 7H9 broth and fluorescent compound in a silicone sensor [2, 3, 12].

Versa TREK: It is a US FDA-approved liquid-based culture for M. tuberculosis with much higher detection rate of FGTB of up to 46.7% and uses special Myso bottle. Its advantages are higher specificity, sensitivity testing and for identification of Mycobacteria species. Limitations is longer time (weeks) for results with delay in treatment.

Cartridge-based nucleic acid amplification test (CBNAAT): It is also called gene Xpert which uses heminested real-time PCR to magnify Mycobacterium tuberculosis. It can be chip-based (Truenat). It can detect as low as 133 colony-forming units (CFU)/ml of specimen and is used to diagnose TB and can detect rifampicin resistance within 2 h. It has been approved by WHO. We observed a sensitivity of 30% and specificity of almost 100% in FGTB patients with gene Xpert [29, 40, 41]. Xpert Ultra has much higher sensitivity. Disadvantages are lower sensitivity, higher cost, negative report due to blood contamination and inability to know resistance to other drugs.

Although PCR is a rapid, sensitive and specific tool to diagnose FGTB, it has many drawbacks. It cannot differentiate between live and dead bacteria and may remain positive during anti-tuberculous therapy or after completion of therapy. It thus has high false positivity and may be false negative also. Instead of uniplex PCR, multiplex PCR using multi-gene or multi-primer PCR has higher sensitivity. However, in clinical practice, PCR is not used to diagnose FGTB or to start anti-tubercular therapy but as a method to investigate further for FGTB using endoscopic techniques [3, 29, 41].

Loop-mediated isothermal amplification (LAMP): It is quicker and inexpensive with sensitivity of about 40% in detection of FGTB but cannot diagnose drug resistance [42]. Various studies are ongoing on it, and it is still not routine test for diagnosis of FGTB.

Molecular line probe assays (LPA): They have been recommended by WHO for rapid diagnosis of multi-drug-resistant TB including FGTB on positive liquid culture and can detect drug sensitivity also.

Histopathology: A part of endometrial (or peritoneal) biopsy specimen is taken in 10% formalin for detection of epithelioid granuloma or granulomatous disease on histopathology with almost 100% specificity but very low sensitivity [29]. Typical caseation is rare in FGTB due to shedding of endometrium during menstruation.

Newer Molecular Methods in Pipeline

Newer generation sequencing (NSG) technology can allow increasingly rapid and accurate sequencing of entire Mycobacterial genome and has the potential for amplifying the diagnosis and management of drug-sensitive and drug-resistant pulmonary and extra-pulmonary TB (including FGTB) but is not yet routinely available [43].

Nuclear Receptors: As nuclear receptors have important role in maintenance of uterine receptivity and immune modulation, they can be used as a biomarker for early detection of FGTB, especially latent FGTB and as a therapeutic drug target, but are still experimental [44].

Laparoscopy

It is a very valuable tool for infertility and FGTB with the dual advantage of pelvic organ visualization and sample collection even from inaccessible sites for laboratory diagnosis as biopsy can be taken under direct vision [2, 12, 45]. One should carefully visualize the pelvic organs (uterus, ovaries, tubes) and entire peritoneal cavity including upper abdomen for any TB lesions [3, 4]. We have observed various new signs perihepatic adhesions and Sharma’s hanging gall bladder sign, Sharma’s ascending colonic adhesion, Sharma’s sigmoid colonic adhesive band and Sharma’s parachute sign (adhesions of ascending colon to abdominal wall) and Sharma’s compartmentalization sign (multiple compartments are formed by omental adhesions to contain infection) [33-37]. We have also observed fallopian tubes distended with alternate constrictions and dilatations on laparoscopy and dye test resembling blue python in FGTB cases (Sharma’s blue python sign) [46] and fusion of both fallopian tubes due to FGTB (Sharma’s kissing fallopian tubes sign) [47]. Figure 1 shows laparoscopy showing perihepatic adhesions (Fitz Hugh Curtis Syndrome) with Sharma’s hanging gall bladder sign in a case of FGTB, while Fig. 2 shows laparoscopy showing Sharma’s blue python sign with distended hydrosalpinx in left fallopian tube and tubercles on right fallopian tube and ovary in a case of FGTB..

Fig. 1

Laparoscopy showing perihepatic adhesions (Fitz–Hugh–Curtis syndrome) (single arrow) with Sharma’s hanging gall bladder sign (double arrow) in a case of FGTB

Fig. 2

Laparoscopy showing Sharma’s blue python sign with distended hydrosalpinx in the left fallopian tube (single arrow) and tubercles (double arrow) on the right fallopian tube and ovary in a case of FGTB

Hysteroscopy

It is an endoscopic visualization of endometrial cavity using a distension medium (saline or glycine) and is often done concomitantly with laparoscopy for better results. The various TB lesions on hysteroscopy are pale endometrium, tubercles, caseous nodules, chronic endometritis, edema, micropolyps, varying grades of intrauterine adhesions and distorted and shrunken uterine cavity with obliterated ostia [2, 12, 20]. Figure 3 shows pale endometrium and intrauterine adhesions on hysteroscopy in a case of FGTB.

Fig. 3

Hysteroscopy showing pale endometrium and intrauterine adhesions in a case of FGTB

Use of Composite reference standard (CRS) and diagnostic algorithm for FGTB (Fig. 4)

In the absence of availability of any single sensitive and specific test for detection of FGTB, combination of tests can be used to increase the sensitivity and detection rate of FGTB and to avoid false positivity. High degree of clinical suspicion from the past or family history of TB or anti-tuberculous therapy, menstrual dysfunction, especially oligomenorrhea and infertility along with combination of reliable tests, can detect higher number of FGTB cases as has been done for other extra-pulmonary TB (EPTB) cases like pleural TB [48]. Index TB guideline is an example of use of composite reference standard for various EPTB cases including FGTB [48]. It combines positive detection of acid fast bacilli on microscopy or culture, positive gene Xpert or positive epithelioid granuloma on histopathology of endometrial or peritoneal biopsy and definite findings of TB like tubercles, caseous nodules or beaded tubes on laparoscopy or hysteroscopy (tubercles, caseous nodules) [48].

An algorithm for diagnosis of FGTB is shown in Fig. 4. Thus, PCR alone is not used for diagnosis of FGTB.

Fig. 4

Use of composite reference standard (CRS) and diagnostic algorithm for FGTB

Medical treatment

There have been changes in the treatment of both pulmonary and extra-pulmonary TB including FGTB, shown in Table 3. Treatment of FGTB is similar to pulmonary TB and is given for total 6 months. It consists of four drugs regimen with rifampicin (r), isoniazid (h) [1, 2, 13] pyrazinamide (z) and ethambutol (E) daily orally for first 2 months of intensive phase [1, 2, 13]. In the continuation phase, three-drug regimen (unlike 2 drugs in past) is given using rifampicin (R), isoniazid (I) and ethambutol (E) orally daily for next 4 months [1, 2, 13] Categories are no longer used. Even patients with irregular treatment or defaulters are treated with the above regimen in the case of drug-sensitive TB.

Table 3

Drug treatment of drug-sensitive and isoniazid-resistant FGTB as per WHO and National TB Elimination Program (NTEP) (13–15)

Drug-sensitive FGTB (rifampicin- and isoniazid-sensitive new previously treated or retreatment TB cases)
Daily dose regimen for adults as per weight bands
Number of tablets of fixed drug combination (FDC)
Weight category	Intensive-phase HRZE 75 mg /150 mg/400 mg/275 mg Per FDC tablet (2 months) oral daily treatment	Continuation-phase HRE 75 mg /150 mg/275 mg per FDC tablet (4 months) oral daily treatment	Streptomycin* (g)
25–39 kg	2	2	0.5
40–54 kg	3	3	0.75
55–69 kg	4	4	1
≥ 70 kg	5	5	1

*Streptomycin is given only for adverse drug reaction to first-line drugs like drug-induced hepatitis when HRZ are withheld and streptomycin, ethambutol and levofloxacin are given till liver function tests (LFT) return to normal, when RHZ are added sequentially under LFT monitoring

On an average a woman with 50 kg weight (45–54 kg) will receive 225 mg isoniazid (H), 450 mg of rifampicin ®, 1200 mg pyrazinamide (Z) and 825 mg ethambutol (E) while a 60-kg woman (55–69) will receive 300 mg (H), 600 mg ®, 1600 mg (Z) and 1100 mg (E), respectively

Isoniazid-Resistant Rifampicin-Sensitive (Hr-TB)**

REZ + levofloxacin: uniphasic orally daily for 6 months (LRZE for 6 months daily orally)

i. Regimen to be modified if polyresistance detected

ii. **Regimen extended to 9 months in the case of poor response, provided other resistance ruled out

iii. Levofloxacin to be replaced with moxifloxacin if strain resistant to levofloxacin but sensitive to moxifloxacin

For primary or secondary drug-resistant FGTB, longer oral regimen with reserve drugs is given for 18–20 months or shorter regimen is given for 9–12 months in selected category of patients as shown in Table 4 [2, 13, 14, 49]. All women should be carefully monitored for adherence to treatment and any side effects, especially hepatotoxicity with rifampicin, isoniazid and pyrazinamide, ocular toxicity (ethambutol) and peripheral neuritis (isoniazid). Pyridoxine can be given for any neuritis, and liver function tests should be performed on suspicion of hepatotoxicity.

Table 4

Drug treatment of drug-resistant FGTB as per WHO and National TB Elimination Program (NTEP) (13–15)

(A) Longer all oral regimen (18–20 months)
Indications: (II MDR FGTB):
1. Disseminated RR/MDR FGTB with pulmonary or other extra-pulmonary TB sites/involvements
2. RR/MDR with resistance to other reserve drugs
3. History of intake of reserve drugs for ≥ one month
4. Intolerance or adverse drug reactions on shorter MDR regimen
5. HIV-positive patients with RR/MDR FGTB
6. Pregnant women with MDR TB. It can be given to all patients of MDR
S No	Name of drug	Dose
1	Tab bedaquiline	400 mg daily for 2 weeks then 200 mg thrice weekly for 22 weeks ( total 24 weeks)
2	Tab levofloxacin or Tab moxifloxacin	750 mg or 600 mg
3	Tab linezolid	600 mg
4	Tab cycloserine	500–750 mg
5	Tab clofazimine	100 mg
6	Tab ethionamide*	750 mg
These 6 drugs are given orally daily for 6–8 months in intensive phase
In continuation phase, 4 drugs: Tab levofloxacin /moxifloxacin, linezolid, cycloserine and clofazimine are given for 12 months for MDR TB and 14 months for XDR TB. (Resistance to fluoroquinolones with or without resistance to other group A drugs)
Linezolid can be given on alternate days during continuation phase
*Ethionamide in some cases (not all cases) Replacement sequence in case of drug intolerance is as follows: delamanid, aminoglycoside, pyrazinamide, ethionamide, pas, ethambutol, carbapenem
(B) Shorter drug-resistant TB regimen (total 9–12 months regimen) (7 drugs for 4–6 months followed by 4 drugs for 5 months) (Total 9–11 months)
Indications:
1 Localized RR/ MDR FGTB
2. History of intake of reserve drugs ≤ one month
3. Sensitivity to fluoroquinolones, second line injectables, Z (inhA or kat G mutation but not both)
Intensive phase (4–6 months Am-Mfx-Cfz-Eto-High H-Z-E)
1	Injection amikacin# (Km) (intramuscular)	750 mg
2	Tab moxifloxacin (Mfx)	600 mg
3	Tab clofazimine ( Cfz)	100 mg
4	Tab ethionamide (Eto)	750 mg
5	High dose isoniazid (high H)	1000 mg
6	Tab pyrazinamide (Z)	1500 mg
7	Tab Ethambutol (E)	1200 mg
Continuation phase (5 months of daily oral Mfx–Cfz–Z–E)
1	Tab moxifloxacin (Mfx)	600 mg
2	Tab clofazimine (Cfz)	100 mg
3	Tab pyrazinamide (Z)	1500 mg
4	Tab ethambutol (E)	1200 mg

Pyridoxine 40 mg is given daily for prophylaxis (100 mg for treatment) for adverse drug effects in all cases for all drug-sensitive and drug-resistant regimens. # Bedaquiline replaced shorter all oral regimen is being pilot-tested for RR and MDR TB with replacement of amikacin with bedaquiline with total duration of 9–12 months in eligible patients

Treatment should preferably be directly observed treatment short course (DOTS) with quality assured free medicines from government DOTS centers present all over India under National TB Elimination program (previously called Revised National TB Control Program).

TB Notification

India TB notification policy mandates that all patients with TB including FGTB are notified through Nikshay (TB notification portal).

Patients of TB including FGTB can also take benefit of government’s Nikshay Poshan yojana in which TB patients gets Rs. 500 per months to buy food till patient continues treatment.

Surgical Treatment

Surgery is best avoided in FGTB due to more complications and need to give ATT. Only limited surgery in the form of drainage of abscesses can be done [2]. However, diagnostic laparoscopy and hysteroscopy is done at beginning to diagnose the disease and later after completion of full treatment of TB to prognosticate the patient and to plan further treatment for infertility. Treatment is planned as follows.

If tubes are patent on laparoscopy and endometrium is normal on hysteroscopy, normal conception is tried or ovulation induction drugs are given.

If tubes are blocked, but endometrium is receptive (normal), IVF ET (in vitro fertilization and embryo transfer) is performed with good outcome and conception rate of up to 25%.

If tubes are blocked and endometrium is not receptive with more than grade 3 adhesions (not amenable to surgical treatment), then gestational surrogacy is advised.

If tubes are blocked and endometrium is not receptive and ovaries are also damaged, then adoption is advised.

TB and Pregnancy

Both pulmonary and extra-pulmonary TB can occur in pregnancy. Drug-sensitive TB must be treated with all the four drugs (RHZE) for 2 months and the three drugs (RHE) for 4 months even in first trimester of pregnancy [2]. Drug-resistant TB patients should not conceive while on reserve drugs. Medical termination of pregnancy (MTP) is advised for MDR TB in first trimester as reserve drugs can be teratogenic. If patient refuses MTP, then treatment is modified by excluding injections (kanamycin, amikacin, gentamycin, as they are fetotoxic) avoiding ethionamide till 32 weeks and after counseling the patient. Use of bedaquiline though safe is still debatable in pregnancy.

Summary and Conclusions

FGTB is a significant factor to cause reproductive and genital morbidity, especially infertility in the developing nations. The clinicians should always keep FGTB in mind and should take detailed history and careful examination and perform appropriates investigations to reach to a diagnosis of FGTB. Use of composite reference standard increases detection rate. Treatment of drug sensitivity FGTB is essentially medical using four drugs (RHZE) daily orally for 2 months followed by three drugs (RHE) daily orally for next 4 months (total 6 months). For drug-resistant FGTB, all oral longer regimens (18–20 months) or shorter regimen (9–12 months) are used under careful supervision. In vitro fertilization and embryo transfer and surrogacy have a role in selected cases. Newer molecule tests like genomics and nucleus receptors are being developed for early diagnosis of TB including FGTB [50]. Novel biotechniques, nanoparticles and stem cell transplantation are being developed for regeneration of endometrium (in Asher man’s syndrome), fallopian tubes (fallopian tubes blockage and damage) and for ovaries (damaged ovaries).