Revista Brasileira de Ginecologia e Obstetrícia

Screening, diagnosis and management of hypothyroidism in pregnancy: Number 10 – October 2022

DOI: s-0042-1758490 - volume 44 - 2022

Sara Toassa Gomes Solha, Rosiane Mattar, Patrícia de Fátima dos Santos Teixeira, Maria Izabel Chiamolera, Carlos Alberto Maganha, Alberto Carlos Moreno Zaconeta, Renato Teixeira Souza

Abstract

Key points Recommendations

Full Text

There is an increase in the stimulation of the hypothalamic-pituitary-thyroid axis during pregnancy through different mechanisms:(1)

This stimulus to the axis explains why pregnant women have lower TSH concentrations than non-pregnant women, especially in the first trimester.(1) In the first trimester of pregnancy, there are greater metabolic demands and given the changes in the stimulation of the gland, this a critical period for the occurrence of thyroid dysfunctions. All described changes in the physiology of the hypothalamic-pituitary-thyroid axis ensure the supply of THs to the fetus, especially in the period when the fetal thyroid is not yet functionally mature. Although the development of the gland begins at week 8, it functions fully only between weeks 18-20 of pregnancy. Therefore, until that moment, the fetus is totally dependent on the placental transfer of maternal THs. Note that this is a critical period for the formation of the fetal nervous system.(1) There is a compensatory mechanism, via feedback, between the thyroid, pituitary and hypothalamus that regulates glandular functioning. Knowing this mechanism helps in signaling where the cause of a possible dysfunction may be (Figure 1).

 

Figure 1
Schematic representation of the hypothalamic-pituitary-thyroid axis indicating the types of hypothyroidism

TRH: thyrotropin releasing hormone; TSH: thyroid stimulating hormone; T4: thyroxine; T3: triiodothyronine

 

Primary hypothyroidism is the most common form of the disease and occurs due to failure in the production and/or release of thyroxine (T4) and triiodothyronine (T3) hormones by the thyroid gland. (2–4) When central hypothyroidism is secondary to a failure in the production or release of TSH by the pituitary gland, manifestations from other pituitary sectors often occur. As gonadotropic or corticotrophic impairment is common, patients usually need to replace other hormones before they need TH replacement.(5) More rarely, central hypothyroidism has a tertiary origin resulting from hypothalamic disorders impairing the production or release of thyrotropin releasing hormone (TRH). In this document, we will address primary hypothyroidism during pregnancy. As in non-pregnant women, Hashimoto's thyroiditis is its main cause, as well as the most prevalent among organ-specific autoimmune diseases, affecting about 12-13% of the population.(6,7) In approximately 85-90% of cases, Hashimoto's thyroiditis presents with circulating antithyroid antibodies; the most common is the ATPO.(2,6) Primary hypothyroidism caused by Hashimoto's thyroiditis may present with progressive thyroid failure, in which, initially, small elevations in serum TSH levels may compensate for slight reductions in the production of T4 and T3 by the thyroid.(3,4) Other causes of hypothyroidism include previous thyroidectomy and/or radioiodine therapy for definitive treatment of hyperthyroidism. Less commonly, primary hypothyroidism is caused by glandular infiltrative diseases (amyloidosis, hemochromatosis, sarcoidosis), drug use, and severe deficiency or excess of iodine.(2–4) A critical point in the investigation of hypothyroidism in pregnant women refers to what TSH elevation should be considered, defining the presence of primary hypothyroidism. When local reference values specific for pregnant women are unavailable, reference values from other centers that have been determined in a population of similar characteristics using the same TSH measurement methodology can be adopted.(8) According to the latest North American guideline, the upper limits of normality for TSH in the first trimester of pregnancy can be calculated by reducing 0.5 mIU/L from the upper limit of TSH reference values for non-pregnant women.(8) Such a strategy was confirmed in a study conducted with a population of pregnant women in the city of Rio de Janeiro.(9) Therefore, for most centers, the upper limit of TSH for pregnant women will be around 4.0 mIU/L, since most laboratory kits present a value of 4.5 mIU/L as the upper limit of normal for non-pregnant women. When treatment of primary hypothyroidism is indicated, LT4 replacement is required with the aim to reduce TSH levels to appropriate values for the patient's age group and health condition.(2–4) These values are different for pregnant women compared to non-pregnant women in the same age group.(2–4, 10)

 

Common scenarios in clinical practice

When addressing hypothyroidism in pregnancy, the main scenarios present patients previously diagnosed with hypothyroidism and those who received this diagnosis during pregnancy. The following conditions are possible for patients with a previous diagnosis:

In general, patients with hypothyroidism who get pregnant, even if compensated, need an increase in LT4 dose to maintain adequate TSH concentrations. Regarding diagnosis during pregnancy, we may have:

The laboratory finding that combines TSH levels above reference values considered normal for a given population with normal circulating levels of THs is called subclinical hypothyroidism (mild or initial).(10) Overt hypothyroidism is considered when TSH levels during pregnancy are above 10.0 mIU/L(11,12) or when TSH levels are > 4 mIU/L and ≤ 10.0 mIU/L and the patient has TH levels below the lower limits of the respective reference values.(8) By knowing that most of the hormone produced by the thyroid is T4, which circulates preferentially linked to TBG and the latter is under direct interference from different factors, it is appropriate to measure FT4 as a way of estimating thyroid hormone production. Measurement of FT4 concentrations is performed to differentiate subclinical from clinical thyroid dysfunction. Obstetricians and endocrinologists must be familiar with thyroid function and dysfunction, as the correct diagnosis and treatment of thyroid diseases surely leads to better maternal and fetal outcomes.

 

What are the possible maternal-fetal repercussions of hypothyroidism?

Overt hypothyroidism has been consistently associated with a higher risk of pregnancy complications, and impaired neurocognitive development of the conceptus.(8,12,13) Normal TH levels are essential for neuronal migration, myelination, and proper brain formation of the fetal brain.(8,14,15) Complications more commonly associated with overt hypothyroidism are:(8,11,13,16)

Although there are controversies regarding the causal relationship of subclinical hypothyroidism with all situations mentioned above, many studies indicate that women with subclinical hypothyroidism are also at a higher risk for:

With regard to fetal neurocognitive development, overt hypothyroidism should be considered a risk factor for its alteration, and logic suggests that subclinical hypothyroidism, in the same way, can cause intellectual impairment in a variable spectrum.(8) However, some studies argue there is no neurocognitive benefit associated with treatment of subclinical hypothyroidism in pregnancy.(17) Some limitations of these studies, such as fixed or excessive dose of LT4, as well as late initiation of treatment should be considered. Further research is needed to determine if early initiation of treatment (before week 13) is beneficial.(11,17)

Note that women with circulating ATPO, even with TSH within normal limits, are at a higher risk of pregnancy complications compared to women with negative antibodies.(8,12,13)

Regarding the timing of delivery, there is no evidence to support the resolution of pregnancy before 40 weeks for women with hypothyroidism.

 

In places with complete technical and financial conditions, for which pregnant women and when to request an evaluation of thyroid function?

Considering the possible complications of hypothyroidism during pregnancy, all women with pregnancy plans who known they have thyroid disease, should have their TSH levels evaluated, preferably before conception. On the other hand, there is no consensus on the best form of screening women without known thyroid disease. Despite the scarcity of robust evidence supporting universal screening, which proposes the evaluation of thyroid function for all pregnant women in the first trimester, several authors recommend this strategy under justification that different studies have shown the ineffectiveness of selective screening in diagnosing cases of hypothyroidism during pregnancy.(18,19) In a systematic review with meta-analysis, the two strategies were compared and almost half of cases of thyroid dysfunction went undiagnosed when only high-risk women were investigated.(20) In a recent study conducted in the city of Rio de Janeiro, 41.2% of pregnant women would remain undiagnosed because they did not meet any criteria for selective screening.(21) Thus, thyroid dysfunction during pregnancy presents high prevalence and is usually asymptomatic or oligosymptomatic. On the other hand, the serum TSH measurement, considered the test of choice for the diagnosis of thyroid dysfunction, is a sensitive, simple, robust, low-cost and widely available test, in addition to not offering risks to the patient when applied. Furthermore, the treatment of hypothyroidism, LT4, is an effective, inexpensive, available, and safe drug.(8,22) The benefits of treating overt hypothyroidism during pregnancy are crystal clear. According to recommendations of the World Health Organization (WHO), the only point that still lacks evidence for the complete inclusion of TSH in criteria establishing a screening test regards the lack of reported benefits of treating subclinical hypothyroidism during pregnancy.(22) Considering these premises, the present group recommends that under complete financial and technical conditions, the evaluation of thyroid function should be performed universally during pregnancy, as early as possible, at the beginning of antenatal care.

 

In places where there are no complete financial and technical conditions, for which pregnant women and when to request the evaluation of thyroid function?

If technical and/or financial limitations exist, criteria should be used to select those at greater risk for developing hypothyroidism during pregnancy. Evaluation of thyroid function should be performed as early as possible, preferably at the beginning of the first trimester of pregnancy. According to the latest recommendation from the American Thyroid Association (ATA), the physician should identify patients at greater risk of developing thyroid dysfunction according to criteria presented in chart 1. In these selected cases, TSH dosage will be recommended before conception or at the first antenatal visit.(8) Considering that some factors, especially age > 30 years and ≥ 2 pregnancies, significantly increase the number of pregnant women selected for screening, in situations of even more limited economic and technical conditions, this group suggests the priority evaluation of thyroid function for women with the following risk factors:

 

Chart 1   Risk criteria for thyroid dysfunction during pregnancy according to the American Thyroid Association

*History of head/neck irradiation
*Previous thyroid surgery or radioiodine therapy
*Type 1 diabetes mellitus or other autoimmune disease
*Previously known thyroid autoimmunity or presence of goiter
*History of hypo/hyperthyroidism
- Signs/symptoms of thyroid dysfunction
- Morbid obesity (BMI ≥ 40 kg m²)
- History of fetal loss, premature birth or infertility
- Use of amiodarone or lithium, or recent administration of iodinated contrast
- Family history of autoimmune thyroid disease or thyroid dysfunction
- Resident in an area with moderate to severe iodine insufficiency
- Age > 30 years
- ≥2 pregnancies

 

 

In the presence of symptoms such as fatigue, constipation, anemia and weight gain in addition to the expected during pregnancy, the possibility of evaluating thyroid function should be considered (Figure 2).

 

Figure 2
Hypothyroidism: evaluation of thyroid function

TSH: thyroid stimulating hormone; BMI: body mass index.

 

 

How to laboratory evaluate hypothyroidism?

Measurement of TSH is considered the test of choice for screening for thyroid dysfunction (Chart 2). Given the known physiological reduction in TSH levels during pregnancy, elevations in these levels are highly sensitive and suggestive of dysfunction. Preferably, the trimester-specific reference values provided by the laboratory for the local pregnant population should be taken into account. However, this group suggests that in the absence of validated references in local populations, a TSH level ≤ 4.0 mIU/L should be considered as a normal value. When TSH levels are at concentrations above 10.0 mIU/L, the diagnosis of overt hypothyroidism is confirmed and the patient should be treated with LT4 immediately, regardless of FT4 levels. Thus, there is no need to measure FT4 or ATPO to guide management. If TSH values are > 4.0 mUI/L and ≤ 10.0 mUI/L, FT4 must be requested, with two possibilities:

 

Chart 2   Laboratory evaluation in the investigation of hypothyroidism in pregnancy

  TSH T4L Diagnosis ATPO
HYPOTHYROIDISM DIAGNOSED PRIOR TO PREGNANCY ≤2.5 mUI/L Do not request (Result will not change management) Properly treated hypothyroidism during pregnancy Do not request (Result will not change management)
>2.5 mUI/L Hypothyroidism not properly treated during pregnancy
HYPOTHYROIDISM DIAGNOSED IN PREGNANCY >10.0 mUI/L Do not request (Result will not change management) Overt hypothyroidism Do not request (Result will not change management)
>4.0 and ≤10.0 mUI/L Within reference values informed by the laboratory Subclinical hypothyroidism Do not request (Proposed management in subclinical hypothyroidism is independent of ATPO)
>4.0 and ≤10.0 mUI/L Below the lower limit of reference informed by the laboratory Overt hypothyroidism Do not request (Result will not change management)
>2.5 until ≤4.0 mUI/L Within reference values informed by the laboratory Euthyroidism ATPO positive case (above the upper limit of reference informed by the laboratory), consider treatment
≤2.5 Do not request (Result will not change management) Euthyroidism Do not request (Result will not change the proposed management for the first trimester in most patients)

 

Therefore, the ideal is to have immediate access to FT4 levels to determine the management, as its value defines the subclinical or clinical condition of hypothyroidism.(8,12,13) However, if this access is unavailable, our group suggests immediate initiation of LT4 treatment.

However, if ATPO testing is unavailable, the recommendation for the range of TSH > 2.5 mIU/L and ≤ 4 mIU/L, is as follows:

 

If the TSH level is normal in screening, should the test be repeated as the pregnancy progresses?

There is no need to repeat the evaluation of thyroid function throughout pregnancy. It should be performed at the beginning of antenatal care, preferably in the first trimester. If TSH concentrations are ≤ 2.5 mIU/L or > 2.5 and ≤ 4 mIU/L with negative ATPO, the patient is considered to be euthyroid. The dosage will only be repeated when there is any clinical suspicion of thyroid dysfunction or, exceptionally, in the presence of more relevant risk factors (Figure 1).

 

How to calculate the LT4 dose to start hypothyroidism treatment?

Recent studies have shown that the timing of introduction of TH can play an important role in the effectiveness of the intervention, and treatment in the first trimester has shown effectiveness in reducing the overall rate of pregnancy complications and the rate of preterm births.(23–25) Pregnant women with hypothyroidism should be treated with LT4 starting with doses of 1-2 mcg/kg daily. Since the objective is to reach euthyroidism as quickly as possible, the ideal is not to use the strategy of dose staggering, but to start with a full dose immediately. In a practical way, we recommend the following scheme (Figure 3):(13)

 

Figure 3
Hypothyroidism: management during pregnancy

 

What should be the type of antenatal care for pregnant woman with hypothyroidism?

Patients with hypothyroidism prior to pregnancy and those with a diagnosis of overt hypothyroidism in pregnancy screening should be followed up in high-risk antenatal care (preferably together with an endocrinologist). High surveillance is recommended for these patients.(8) Furthermore, in patients with more relevant risk factors for decompensation of thyroid metabolism during pregnancy, the same procedure should be followed. Such factors are:

In this differentiated follow-up, continuous interaction between obstetrician and endocrinologist is recommended, with serial laboratory measurements to obtain adequate and early metabolic control.

Cases of subclinical hypothyroidism without major risk factors should be followed up in Primary Care in usual risk antenatal care.

 

How to perform dose adjustment for women with hypothyroidism who are planning to get pregnant or in early stages of pregnancy?

Different cutoff points for TSH have been advocated as a target for preconception, ranging from < 1.2 mIU/L to < 2.5 mIU/L. It has already been found that only 17% of women with TSH < 1.2 mIU/L had to increase their LT4 dose during pregnancy. However, from a practical point of view, the recommendation so far is that women with hypothyroidism undergoing treatment optimize the dose in preconception, aiming to obtain TSH < 2.5 mIU/L (Figure 4).(8,26) Pregnancy is associated with a higher need for TH in approximately one third of women already undergoing treatment.(26,27) This increased demand is believed to be related to greater estrogen production.(28) Clinical studies have confirmed that the higher need for exogenous LT4 occurs as early as weeks 4 to 6 of pregnancy.(26,27) This need gradually increases throughout weeks 16-20 of pregnancy and stabilizes thereafter until the time of delivery. For this reason, most pregnant women need to receive a higher dose of exogenous LT4 during pregnancy.(29) The importance of correcting doses early in pregnancy is noteworthy. The increase in LT4 dose varies depending on a number of factors:

 

Figure 4
Hypothyroidism: dose adjustment and therapeutic goal

TSH: thyroid stimulating hormone.

 

 

After starting treatment, what is the goal to be achieved? How often should exams be requested?

The treatment target is to achieve TSH in the lower half of the specific reference range of the pregnancy trimester. When this reference value is unavailable, it is reasonable to target maternal TSH concentrations below 2.5 mIU/L (Figure 3). The TSH level should be evaluated every four weeks during dose adjustment.(8,13,31)

 

What should be the guidelines for prescribing LT4?

Preparations containing T3 should be avoided during pregnancy, as they increase T3 levels in comparison with T4, generating supraphysiological levels of maternal T3 and low levels of T4; maternal T4 is essential for the development of the fetal central nervous system.(8) As concomitant administration of LT4 and food can impair hormone absorption, LT4 administration is recommended 30-60 minutes before breakfast or at bedtime (three or more hours after the evening meal) for optimal and consistent absorption. In addition, LT4 should be taken separately from other potentially interfering drugs and supplements (eg ferrous sulfate, calcium carbonate, aluminum hydroxide, and sucralfate).(32) Switching LT4 brands can result in variations in the administered dose and should be avoided.(32,33)

 

How should postpartum dose adjustment be done?

After delivery, the maternal dose of LT4 should be adjusted to the dose used before pregnancy, and serum TSH should be measured after six weeks (Figure 5). Some patients with Hashimoto's thyroiditis who required an increase in the dose of TH during pregnancy may continue to need an additional dose in the postpartum period, in case of postpartum exacerbation of autoimmune thyroid dysfunction. On the other hand, some women with autoimmune thyroid disease who started taking LT4 during pregnancy may not need LT4 after delivery, especially when the dose is ≤ 50 mcg/d. If LT4 is discontinued, serum TSH should be re-evaluated in approximately six weeks.(34) When the dose used is greater than 50 mcg/d, a 25-50% reduction with further laboratory evaluation is recommended.(35)

 

Figure 5
Hypothyroidism: postpartum

 

Final considerations

Proper screening, diagnosis and management of hypothyroidism during pregnancy are essential, especially given the risks to fetal neurocognitive development and obstetric complications caused by improper treatment. Early identification is one of the major challenges, ideally at the beginning of the first trimester, allowing the initiation of therapy at the stage when the conceptus’ neuronal structures are developing. This way, the window of opportunity for real neurocognitive benefits for the offspring is reached. Thyroid hormones are essential for proper myelination and neuronal migration. The fetal thyroid is functionally mature only after week 20 of pregnancy; until then, the conceptus depends on the transfer of maternal THs. Furthermore, obstetric complications, especially those linked to first trimester abortion, preeclampsia, placental abruption and prematurity are at greater risk, especially when overt hypothyroidism is untreated. The laboratory test that guides the diagnosis of hypothyroidism is TSH, but there are several methodological limitations for the assertive establishment of TSH reference values representative of the local population. Current recommendations state that in this scenario, the normality value for TSH adopted during pregnancy should be ≤ 4.0 mIU/L. Universal screening is recommended provided that complete technical and financial conditions are available and should be carried out as early as possible. In adverse conditions, screening is reserved for cases with higher risk criteria for thyroid function decompensation during pregnancy. An important risk group is of women previously thyroidectomized or who underwent radioiodine therapy for the treatment of hyperthyroidism and who are already on LT4 therapy. Other critical factors include type 1 diabetes mellitus or other autoimmune diseases, the presence of goiter, a history of previous hypo or hyperthyroidism, or even the presence of autoimmunity. The T4L dosage helps to elucidate the overt or subclinical context of hypothyroidism. The role of autoimmunity –mainly ATPO positivity – is currently much studied. Women in this condition, even in euthyroidism, are at higher risk for adverse maternal-fetal outcomes. Although the literature is still controversial about the real benefits of treating subclinical hypothyroidism during pregnancy, evidence points to a relevant role of autoimmunity in the occurrence of potential complications in pregnancy and neurocognitive impairment of the offspring. Furthermore, the risk of occurrence of postpartum thyroiditis is greater in the presence of this autoimmune condition. In the preconception period, women who are known to be hypothyroid, especially those with positive ATPO, should be advised to adjust their LT4 therapy in advance, in order to enter the pregnancy-puerperal cycle under compensated conditions. De-escalation of LT4 in the postpartum period should be judicious and adequately monitored. It is a drug for use during breastfeeding. The challenges for coping with this pathology involve, above all, excessive diagnosis based on erroneous laboratory values that guide erroneous treatments and determine a non-existent gestational risk. At the other extreme, important conditions of thyroid dysfunction deserve adequate attention and guidance in high-risk antenatal care, receiving early and assertive treatments that avoid serious maternal-fetal complications.


References

1 Korevaar TI, Medici M, Visser TJ, Peeters RP. Thyroid disease in pregnancy: new insights in diagnosis and clinical management. Nat Rev Endocrinol. 2017;13(10):610-622


2 Garber JR, Cobin RH, Gharib H, Hennessey JV, Klein I, Mechanick JI. Clinical practice guidelines for hypothyroidism in adults: cosponsored by the American Association of Clinical Endocrinologists and the American Thyroid Association. Thyroid. 2012;22(12):1200-1235


3 Almandoz JP, Gharib H. Hypothyroidism: etiology, diagnosis, and management. Med Clin North Am. 2012;96(02):203-221


4 McDermott MT. Hypothyroidism. Ann Intern Med. 2020;173(01):ITC1-ITC16


5 Fleseriu M, Hashim IA, Karavitaki N, Melmed S, Murad MH, Salvatori R. Hormonal replacement in hypopituitarism in adults: an Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2016;101(11):3888-3921


6 Caturegli P, De Remigis A, Rose NR. Hashimoto thyroiditis: clinical and diagnostic criteria. Autoimmun Rev. 2014;13(4-5):391-397


7 Sichieri R, Baima J, Marante T, Vasconcellos MT, Moura AS, Vaisman M. Low prevalence of hypothyroidism among black and Mulatto people in a population based study of Brazilian women. Clin Endocrinol (Oxf). 2007;66(06):803-807


8 Alexander EK, Pearce EN, Brent GA, Brown RS, Chen H, Dosiou C. 2017 Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and the postpartum. Thyroid. 2017;27(03):315-389


9 Morais NS, Assis AS, Corcino CM, Saraiva DA, Berbara T, Ventura CD. Recent recommendations from ATA guidelines to define the upper reference range for serum TSH in the first trimester match reference ranges for pregnant women in Rio de Janeiro. Arch Endocrinol Metab. 2018;62(04):386-391


10 Pearce SH, Brabant G, Duntas LH, Monzani F, Peeters RP, Razvi S. 2013 ETA Guideline: management of subclinical hypothyroidism. Eur Thyroid J. 2013;2(04):215-228


11 Lazarus J, Brown RS, Daumerie C, Hubalewska-Dydejczyk A, Negro R, Vaidya B. 2014 European Thyroid Association Guidelines for the Management of Subclinical Hypothyroidism in Pregnancy and in Children. Eur Thyroid J. 2014;3(02):76-94


12 . ACOG Practice Bulletin, Number 223. Obstet Gynecol. 2020;135(06):e261-e274


13 Ross DS. . Hypothyroidism during pregnancy: clinical manifestations, diagnosis, and treatment [Internet]. 2022;:-


14 Spencer L, Bubner T, Bain E, Middleton P. Screening and subsequent management for thyroid dysfunction pre-pregnancy and during pregnancy for improving maternal and infant health. Cochrane Database Syst Rev. 2015;2015(09):-


15 Ausó E, Lavado-Autric R, Cuevas E, Del Rey FE, Morreale De Escobar G, Berbel P. A moderate and transient deficiency of maternal thyroid function at the beginning of fetal neocorticogenesis alters neuronal migration. Endocrinology. 2004;145(09):4037-4047


16 Abalovich M, Gutierrez S, Alcaraz G, Maccallini G, Garcia A, Levalle O. Overt and subclinical hypothyroidism complicating pregnancy. Thyroid. 2002;12(01):63-68


17 Lazarus JH, Bestwick JP, Channon S, Paradice R, Maina A, Rees R. Antenatal thyroid screening and childhood cognitive function. N Engl J Med. 2012;366(06):493-501


18 Vaidya B, Anthony S, Bilous M, Shields B, Drury J, Hutchison S. Detection of thyroid dysfunction in early pregnancy: Universal screening or targeted high-risk case finding?. J Clin Endocrinol Metab. 2007;92(01):203-207


19 Chang DL, Pearce EN. Screening for maternal thyroid dysfunction in pregnancy: a review of the clinical evidence and current guidelines. J Thyroid Res. 2013;2013:851326-851326


20 Jouyandeh Z, Hasani-Ranjbar S, Qorbani M, Larijani B. Universal screening versus selective case-based screening for thyroid disorders in pregnancy. Endocrine. 2015;48(01):116-123


21 Berbara TM, Morais NS, Saraiva DA, Corcino CM, Schtscherbyna A, Moreira KL. Selective case finding versus universal screening for detecting hypothyroidism in the first trimester of pregnancy: a comparative evaluation of a group of pregnant women from Rio de Janeiro. Arch Endocrinol Metab. 2020;64(02):159-164


22 Wilson JM, Jungner YG. Principles and practice of mass screening for disease. Bol Oficina Sanit Panam. 1968;65(04):281-393


23 Dong AC, Stephenson MD, Stagnaro-Green AS. The need for dynamic clinical guidelines: a systematic review of new research published after release of the 2017 ATA Guidelines on thyroid disease during pregnancy and the postpartum. Front Endocrinol (Lausanne). 2020;11:193-193


24 Nazarpour S, Ramezani Tehrani F, Simbar M, Tohidi M, Minooee S, Rahmati M. Effects of levothyroxine on pregnant women with subclinical hypothyroidism, negative for thyroid peroxidase antibodies. J Clin Endocrinol Metab. 2018;103(03):926-935


25 Casey BM, Thom EA, Peaceman AM, Varner MW, Sorokin Y, Hirtz DG. Treatment of subclinical hypothyroidism or hypothyroxinemia in pregnancy. N Engl J Med. 2017;376(09):815-825


26 Abalovich M, Alcaraz G, Kleiman-Rubinsztein J, Pavlove MM, Cornelio C, Levalle O. The relationship of preconception thyrotropin levels to requirements for increasing the levothyroxine dose during pregnancy in women with primary hypothyroidism. Thyroid. 2010;20(10):1175-1178


27 Alexander EK, Marqusee E, Lawrence J, Jarolim P, Fischer GA, Larsen PR. Timing and magnitude of increases in levothyroxine requirements during pregnancy in women with hypothyroidism. N Engl J Med. 2004;351(03):241-249


28 Arafah BM. Increased need for thyroxine in women with hypothyroidism during estrogen therapy. N Engl J Med. 2001;344(23):1743-1749


29 Mandel SJ, Larsen PR, Seely EW, Brent GA. Increased need for thyroxine during pregnancy in women with primary hypothyroidism. N Engl J Med. 1990;323(02):91-96


30 Loh JA, Wartofsky L, Jonklaas J, Burman KD. The magnitude of increased levothyroxine requirements in hypothyroid pregnant women depends upon the etiology of the hypothyroidism. Thyroid. 2009;19(03):269-275


31 Yassa L, Marqusee E, Fawcett R, Alexander EK. Thyroid hormone early adjustment in pregnancy (the THERAPY) trial. J Clin Endocrinol Metab. 2010;95(07):3234-3241


32 Jonklaas J, Bianco AC, Bauer AJ, Burman KD, Cappola AR, Celi FS. Guidelines for the treatment of hypothyroidism: prepared by The American Thyroid Association task force on thyroid hormone replacement. Thyroid. 2014;24(12):1670-1751


33 Mayor GH, Orlando T, Kurtz NM. Limitations of levothyroxine bioequivalence evaluation: analysis of an attempted study. Am J Ther. 1995;2(06):417-432


34 Galofré JC, Haber RS, Mitchell AA, Pessah R, Davies TF. Increased postpartum thyroxine replacement in Hashimotos thyroiditis. Thyroid. 2010;20(08):901-908


35 Melmed S, Auchus RJ, Goldfine AB, Koenig RJ, Rosen CJ. . Williams texbook of endocrinology. 2020;:-