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|Year : 2015 | Volume
| Issue : 5 | Page : 484--490
Psychopharmacoteratophobia: Excessive fear of malformation associated with prescribing psychotropic drugs during pregnancy: An Indian perspective
Dushad Ram1, Basavnna Gowdappa2, HG Ashoka2, Najla Eiman1,
1 Department of Psychiatry, JSS Medical College, JSS University, Mysore, Karnataka, India
2 Department of Medicine, JSS Medical College, JSS University, Mysore, Karnataka, India
Dr. Dushad Ram
Department of Psychiatry, JSS Medical College, JSS University, Mysore, Karnataka
"Psychopharmacoteratophobia is the fear or avoidance of prescribing psychotropic medicine to a pregnant woman on a given indication in anticipation of fetal malformation." It is rooted in the tragedy associated with thalidomide use and is increasing due to the inability to predict accurately, strict legal provision of consumer protection, ethical and legal issues involved, and pitfalls in the available evidence of teratogenicity. In the Indian setting, the physicians face more challenges as the majority of the patients may ask them to decide, what is the best for their health. Most guidelines emphasize more on what not to do than what to do, and the locus of decision is left to the doctor and the patient. In this review, we have focused on relevant issues related to psychopharmacoteraophobia that may be helpful to understand this phenomenon and help to address the deprivation of a mentally ill woman from the required treatment.
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Ram D, Gowdappa B, Ashoka H G, Eiman N. Psychopharmacoteratophobia: Excessive fear of malformation associated with prescribing psychotropic drugs during pregnancy: An Indian perspective.Indian J Pharmacol 2015;47:484-490
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Ram D, Gowdappa B, Ashoka H G, Eiman N. Psychopharmacoteratophobia: Excessive fear of malformation associated with prescribing psychotropic drugs during pregnancy: An Indian perspective. Indian J Pharmacol [serial online] 2015 [cited 2022 May 18 ];47:484-490
Available from: https://www.ijp-online.com/text.asp?2015/47/5/484/165186
Teratophobia is an excessive fear of giving birth to a malformed child while psychopharmacoteratophobia (psychofarmakoteratofobi) is the trepidation of prescribing psychotropic medicine to pregnant woman on given indication in anticipation of fetus malformation., The word has Greek origin and is the combination of four words - psȳkhē (breath, life, soul); pharmakon (drug); teras (monster) and phobos (fear). This phenomenon can be traced back to the thalidomide tragedy that first launched in 1950s for morning sickness and as a sedative during pregnancy. The use of this medication caused phocomelia in about 10,000 newborn and was banned since 1961 in most part of the world.
Five percent of all live births have major congenital anomalies. In only 0.25% of all births, the major congenital anomalies can be attributed to medication., Benzodiazepine is the commonly used psychotropic drug (85% of all psychotropic) during pregnancy. In comparison to the general population, the teratogenic event increase is by 0.2% with benzodiazepine, 1–3% with antidepressant, 0.5% with lithium, up to 5% with carbamazepine, and up to 10% with valproate.,,,, Prevalence of malformation in India is about 2%.,,
Approximately, half a million women become pregnant each day, and up to 35% of them use a psychotropic medication at least once before delivery. 15–20% of pregnant women suffer from mental illness, of which 86% remained untreated, and psychopharmacoteratophobia is one reason for the deprivation from treatment.,,,
Most of the published reports are case reports, case series, prospective or comparative cohort studies, case–control studies, prescription database studies, and national birth registries done in Western countries. Except for case reports, there is no comprehensive study from India about psychotropic drugs related malformation. Most Indian psychiatrists agree that in India the incidence of malformation associated with psychotropic medication may be less compared to Western population due to the less dose requirement for Indian patients, high discontinuation of psychotropic medication during pregnancy, availability of good social support, and less population psychiatrists' ratio. Obstetricians prefer to withdraw psychotropic medication (due to the risk involved) resulting in the development of withdrawal syndrome, self-medication with complementary medicine, substance abuse, and termination of pregnancy. In India, prescription of psychotropic drugs during pregnancy face many barriers such as stigma of mental illness, fear of adverse outcome of pregnancy, ambiguous guidelines, biased harm reporting, fear of legal issue, misconception of risk, media reports, and lack of clear professional guidelines.
Most guidelines emphasize more on what not to do, and the locus of decision is left to the doctor and patient. In this review, we have focused on relevant issues related to psychopharmacoteratophobia that may be helpful to understand this phenomenon and help to address the deprivation of a mentally ill women from required treatment.
Pitfalls in the Available Evidence
Drawback of Previous Human Teratogenic Studies
The concept of first trimester as the critical period is outdated. Age of the gestation is calculated from beginning of last menstrual cycle, and with this calculation, blastocyst gets a place in the uterus during the 4th week. Thus, only the 2nd and 3rd months of the first trimester can be considered as a critical period. However, for some congenital anomalies, the critical period exceeds the end of the 3rd month. Most studies on malformation of newborn did not consider the chemical structures, routes of administration and indication, and reasons for the teratogenic evaluation.
The birth of a child with an anomaly is traumatic, and mothers may attribute to drug use during pregnancy while ignoring infection, fever, and other medical conditions known to cause similar malformation.
Benefits of Medication Use is Underestimated
Published literature is more in favor of not giving psychotropic medication during pregnancy that may result in unfavorable impact on the outcome of the pregnancy and maternal and fetal mental health.
The Teratogenic Risk of Medication is Overemphasized
The most published literature addressing relationships of medication and malformations was carried out a few decades ago when traditional gender role was emphasized, and malformation or disability was associated with curtailed social activity, stigma, and superstitions. Other reasons for exaggeration are an extrapolation of animal finding to human fetus despite species specificity, higher false positive finding due to methodological shortcoming and recall bias, publication bias of positive finding or selected case report, and self-defensive attitude of health care professionals regarding the use of medication during pregnancy.
Factors Contributing to Psychopharmacoteratophobia
In India, paternalistic model of doctor-patient relationship is prevalent, and patients expect and request the doctor to decide the best treatment. The most common but difficult question, a pregnant patient with mental illness asked, is whether she should continue the medication. In the absence of an accurately predictable test, answering such question is constrained by clinical, legal, ethical, and psychosocial issues.
Impact of psychotropic medication in pregnancy outcome
Psychotropic medications that are commonly reported with teratogenic effect are:
Benzodiazepines may increase the incidence (<1%) of cleft lip or palate, infantile hypotonia, and neonatal abstinence syndromeSelective serotonin/norepinephrine reuptake inhibitors and tricyclic antidepressants may increase malformation by 1–3% compared to the general population Mood stabilizes may increase the malformation from the baseline general population. The increase is <1% for lithium (Ebstein's anomaly), <5% for the carbamazepine (neural tube defects) and lamotrigine (oral clefts), and highest is 5–10% for valproate (neural tube defects),,,,Antipsychotic medications may also increase malformation (<1%), particularly second generation antipsychotics Currently, there is no effective nonpharmacological intervention except for electroconvulsive therapy that can be used as treatment in severe illness.
Obstetricians have the dual responsibility of safety for mother and fetus. Untreated mental illness poses a problem for both mother and fetus while pharmacotherapy may harm the fetus. If mental illness is untreated, it may affect the health of patients in the form of poor self-care (malnutrition, infection, and poor pregnancy care), self-harm (abdominal injury), impulsive acts (excessive physical activity), self-medication with indigenous method, and substance abuse.
Consequences of psychiatric illness on outcome of pregnancy
Untreated mental illness in pregnant women may adversely affect the outcome of pregnancy depending upon the diagnosis, severity, and patients' physical health status. Anxiety disorders have been associated with fetal distress, spontaneous abortion or preterm delivery or prolong the labor, assisted (forceps) delivery, decrease developmental scores, and slow mental development. Similarly, major depression and bipolar disorder are associated with decreased fetal growth/low birth weight, postnatal complications, increased crying, and more admission to neonatal intensive care units. Schizophrenia has also been linked to decreased fetal growth/low weight at birth, placental abnormalities, antenatal hemorrhage, postnatal death, and congenital cardiovascular malformations.
Indian Consumer Protection Act, 1986
Patients are protected by the Consumer Protection Act. The applicable clauses of this act are: (1) An unfair trade practice or a restrictive trade practice that has been adopted by any trader or service provider; (2) the services hired or availed of or agreed to be hired or availed of by him, suffer from deficiency in any respect; and (3) services which are hazardous or likely to be hazardous to life and safety of the public when used are being offered by the service provider, which such person could have known with due diligence to be injurious to life and safety.
Any untoward event in pregnancy in patients with mental illness with or without treatment may be stretched to medical negligence. Medical negligence comprises of: (1) The defendant owes a duty of care to the plaintiff; (2) the defendant has breached this duty of care; and (3) the plaintiff has suffered an injury due to this breach.
The Medical Termination of Pregnancy Act, 1971
During treatment with psychotropic medication in pregnancy, before considering for termination of pregnancy, it is necessary to ascertain that condition falls under required conditions specified in the act, that is: (1) The continuance of the pregnancy would involve a risk to the life of the pregnant woman or of grave injury to her physical or mental health. (2) There is a substantial risk, which if the child were born, it would suffer from such physical or mental abnormalities so as to be seriously handicapped.
Mental Health Act, 1987 and Protection of Human Rights Act, 1993, Mental Health Care Bill, 2013
Involuntary treatment, competency to take a decision about treatment, and freedom to live her life as she wants are important issues encountered.,
The Guardians and Wards Act, 1890
When pregnancy takes place before the legal age of marriage.
The Pre-Natal Diagnostic Technique, 1994
When medication may affect gender-specific deformity e.g. genital deformity or malformations.
The most common ethical dilemmas that a clinician or obstetrician's may face are: (1) Conflict between the interest of the mother and fetus; (2) autonomy of patient decision when decision making is compromised; (3) during the decision making limited information can be provided (due to lack of adequate data) and there is ambiguity of absolute risk; (4) coercion by family members; and (5) conflicts between patient and spouse or significant others.
The common issues encountered in Indian setting are: (1) Stigma - related to mental illness, birth of a female child or birth defect; (2) loss of support - loss of emotional and family support from husband and in-laws, physical and psychological abuse, and increased family burden; and (3) Cultural disadvantages - lower status of women and belief that mental illness is punishment of God or evil makes them vulnerable for termination of pregnancy and discrimination, etc.
According to Indian culture, all individuals are indebted to three things: (1) The God (dev rin), (2) ancestors (pitri rin), (3) the teachers (risi rin), and raising of a normal child is the dharma (sacred duty). One's own child can relieve the parents from these debts or bondages. A son can directly prevent parents from entering into a specific kind of hell (called pum). Such values are strongly transmitted to next generations by cultural practices that are organized both before and after the infants' births. Traditionally, the children are the backbone of parents, who support them whole life.
Most guidelines leave the final decision to patient and physician. According to Food and Drug Administration (USA), most of the psychotropic drugs fall under Category C (to be used after assessment of risk and benefit). In an Indian setting, in the face of ambiguous evidence and guidelines, obstetricians face difficulty when most Indian patients request the doctors to decide the best treatment for them.
Teratogenic Risk Factors in Indian Women
There is a paucity of studies in this area, except for environmental factors such as water pollution, bio-hazards such as Bhopal gas tragedy, etc. Some of the common risk factors are:
Use of indigenous treatment for physical or mental illness, with uncertain safety and efficacy of treatment during pregnancyDelay in treatment-seeking behavior in the face of physical illness, e.g., rubella infection ,,Malnutrition, anemia and other common physical illness, e.g., diabetes, phenylketonuriaInadequate health literacy, including reproductive healthInadequate preventive care at community level, e.g., water pollution, high level of hazardous metal in drinking water.
Safety Concerns That May Be Associated With Mental Illness during Pregnancy
Risk factors for suicide includes a family history of suicide attempts, psychiatric disorders requiring hospitalization; a history of suicidal behavior in the past (attempted or aborted suicide/self-injurious behavior), currently a diagnosis of mood disorders, psychotic disorders, alcohol/substance abuse, attention deficits and hyperactive disorder, traumatic brain injury, posttraumatic stress disorder and acute stress reaction, and personality disorders (dramatic, emotional, and erratic cluster). Some symptoms that have been associated with suicidal behavior are anhedonia, impulsivity, hopelessness, anxiety/panic, insomnia, command hallucination, intense feeling of humiliation, shame or despair, and abuse or isolation.
Risk factors associated with violence and aggression are characterized by history of childhood/adult abuse (physical or sexual), disorganized behavior or recurrent violent behavior or dissocial behavior, and severe anxiety or agitation or motor restlessness and other severe psychopathologies such as psychotic symptoms (paranoid delusions, command hallucination), poor impulse control, low intelligence, suicidal behavior, absconding or defiant behavior, and severe substance abuse.
Teratogenic Aspect of Psychotropic Medications in Pregnancy
Effect of Pregnancy on Psychotropic Drugs
Medication efficacy may be altered as volume of distribution increases, plasma proteins concentration decreases, hepatic function is enhanced, and metabolic enzymes are influenced by hormone. Increase in isozyme CYP2A6, 2D6, and 2C9 may decrease the levels of medication such as levels of risperidone, aripiprazole, and iloperidone while decreased activity of CYP1A2 and 2C19 may increase the level of clozapine and olanzapine.
Criteria to Ascertain Teratogenicity of a Drug
Numerous attempts have been framed to ascertain causality. Teratogenicity is not an idiosyncratic effect and follows some scientific principle (e.g., vulnerable timing of pregnancy, toxicological dose response curve, and specific teratogenic effect not any type of malformation, etc.). However, in the court of law, it may not require to determine absolute certainty, but reasonable certainty (more likely than not or more than 50% likelihood) about given child's abnormality may be sufficient to consider as the cause. Some of the important proposed criteria that have been cited during medico legal trials or during expert witness are:
James Wilsons criteria
Initially, James Wilson put forward the principles of teratology in 1977 and is well-accepted even now., They were: (1) Susceptibility to teratogenesis depends on the genotype of the conceptus, and the manner in which it interacts with environmental factors; (2) susceptibility to teratogenic agents varies with the developmental stage at the time of exposure; (3) teratogenic agents act in specific ways (mechanisms) on developing cells and tissues to initiate abnormal embryogenesis (pathogenesis); (4) the final manifestations of abnormal development are functional disorder, malformation, growth retardation and death; (5) the access of adverse environmental influences to developing tissues depends on the nature of the influences (agent); and (6) manifestations of deviant development increase in degree as dosage increases from the no-effect to the totally lethal level.
Sir Austin Bradford Hill modified criteria
In 1965, Sir Austin Bradford Hill proposed criteria for causation in teratology during his address to Royal Society of Medicine.,, He proposed that a teratogenic effect should satisfy the following criteria: (1) Degree of association (degree of significant statistical association); (2) consistency of the association (same observation across studies); (3) specificity of the association (whether the specific defect is consistent); (4) appropriate timing (timing of exposure during pregnancy); (5) dose-response relationship; and (6) biological plausibility.
In 1995, Brent after extensive review of literature proposed a more comprehensive criteria., The criteria were: (1) Strong epidemiological evidence of congenital malformation (or syndrome) in exposed population; (2) incidence of congenital malformations vary with degree of exposure; (3) appropriate animal model demonstrated similar results with equivalent exposures; (4) the appropriate animal model has demonstrated teratogenesis (frequency and severity) to be dose dependent; and (5) the observed teratogenic effect can be explained with the principles of embryology and teratology.
Shepard published a catalogue of teratogenic agent in 2001, and proposed a comprehensive criteria., He offered the following criteria: (1) Proven exposure to agent at critical time in prenatal development; (2) consistent findings of two or more epidemiologic studies of high quality: (a) Control of confounding factors, (b) sufficient numbers, (c) exclusion of positive and negative bias factors, (d) prospective studies, if possible, and (e) relative risk of six or more; (3) careful delineation of the clinical cases; (4) rare environmental exposure associated with rare defect; (5) teratogenicity in experimental animals is important, but not essential; and (6) the association should make biologic sense.
Principles of Determining Teratogenic Causality in Litigation
It is very difficult to ascertain the cause-effect relationship when inadequate information is available, and level of exposure is uncertain. However, in litigation, common principles employed  to ascertain causality are: (1) Based on scientific evidence; (2) biologically plausible; (3) evidence of exposure; (4) protective level of exposure can be considered causative if evidence exist; (5) causal relationship of an outcome is agent and outcome-specific; (6) conclusions are based on human data; and (7) single case report is not sufficient to conclude as established causal relationship.
Factors That May Increase the Teratogenic Effect of a Psychotropic Medication
Drug profiles that may enhance the teratogenic effects of a medicine are:  (a) Chemical and pharmacological properties of the drug (less plasma binding, high placental crossing, the active metabolite, inhibition of folate metabolism, etc.), (b) potency and dose reaching the fetus (low potency, high quantity drug reaching to fetus), and (c) duration of exposure (longer duration of exposure particularly during the first trimester). Patient characteristics that may be associated with increased teratogenic incidence are: (a) Co-morbid physical illness (e.g., endocrinal or metabolic); (b) individual susceptibility (family history of malformation; patient having malformation; medication for the comorbidity; repeated infection; immune-compromised status; and medical illness such as obesity, diabetes mellitus, hypothyroidism, hyperthyroidism, hyperparathyroidism, cretinism, and iodine and folate deficiency). During pregnancy, teratogenic susceptibility also depends upon: (a) The critical stage at the time of administration (first trimester); (b) high placental permeability to the medication used; (c) Increased medication dose exposed to the fetus; (d) disposition within the conceptus; and (e) susceptibility of the fetus. Possible environmental factors associated with teratogenicity during pregnancy are frequent intake of fast food, synthetic additive in food, and pollution or contamination of air or water.
Pathophysiology of Teratogenicity
Medication may affect the fetus by direct metabolic or indirect toxic effect mediated by anti-metabolites, anti-vitamins, disruption of placental permeability, and alteration of endocrinal function. The drug may directly affect fetoplacental unit leading to placental spasm, changes in the volume of amniotic fluid, alteration in fetal or maternal blood flow, or alteration in the transfer of nutrients. The drug may also impair the maternal absorption of nutrients; induce metabolic changes such as hyperglycemia, endocrinal alteration, cardiovascular changes such as hypotension or hypertension. At cellular level, psychotropic drugs may result in mutation and cell division abnormality; disturbance in structure (composition of nucleic acid) or function of cells (biosynthesis, enzyme system) or enzyme system or cell interaction; inadequate energy supply for embryo (vascular disruption); and changes in membrane characteristics (specific receptor- or enzyme-mediated teratogenesis), oxidative stress, endocrine disruption, and fluid and electrolyte balance.,
Outcome of Teratogenic Effect of Psychotropic Medication
The teratogenic effect of psychotropic medicine may result into variable outcomes such as major malformation (first trimester exposure); miscarriage (spontaneous abortion) or still birth; toxic or withdrawal effects to neonate (third trimester exposure); and long-term neurobehavioural difficulty and growth retardation.
Food and Drug Administration (Usa) Classification of Teratogenic Risk of Psychotropic Medication
None of the psychotropic medication falls under Category A (no risk in pregnancy). Antipsychotic clozapine and antidepressant buspirone, mirtazapine, venlafaxine, mianserin, reboxetine and bupropion, and zolpidem are listed under Category B (no risk in animal study, but inadequate study in human). Most psychotropic medications fall under Category C (adverse effect on animal study and inadequate study in human). High-risk medications that are listed under Category D (evidence of the human fetal risk present) are carbamazepine, lithium, valproic acid, paroxetine, alprazolam, chlordiazepoxide, clonazepam, clorazepate, diazepam, lorazepam, and oxazepam.
Screening of the Teratogenic Effect in Patients With Psychotropic Medication during Pregnancy
All patients receiving psychotropic drugs should be screened for the reported teratogenic effect of the given drug and other malformation. The common method of examination includes: (a) Ultrasonography may be considered for all pregnancies with mental illness and on psychotropic medication to rule out the neural tube defect or any other malformation; (b) amniocentesis may be considered for high-risk patient such as past or family history of malformation or genetic disorder. Some indicators that have been reported are changes in serum human chorionic gonadotropin (hCG) (low total free beta-hCG and higher total hCG) and low levels of α feto protein, unconjugated estriol-3, dimeric inhibin-A and pregnancy-associated plasma protein A. (c) Chorionic villi sampling may be considered for family history of known genetic disorder.
Starting, Maintaining or Discontinuing a Psychotropic Medication during Pregnancy in Indian Setting
General Treatment Principle
In general, maternal safety is considered first. If pregnancy can cause life-threatening risk to the mother, termination of pregnancy should be consideredWhen a mother wants to continue a pregnancy at her own risk, regular safety monitoring of the mother and the fetus is needed. Investigate for fetal teratogenic effect and on presence, consider for the termination of pregnancy if fetus is unlikely to surviveWhen a mother does not have any safety concern, let the decision to continue the medication be made by the patient alone or with her guardian or joint decision by the physician (panel of physician-obstetrician, pediatrician, and psychiatrist) and the patientWhen there is an anatomical evidence of defect and the child's life is compatible to life, explain the outcome of pregnancy and advise to review the continuation of pregnancy, however final decision to be made by the patient alone or with her guardian or joint decision by the patient and the physician (panel of physician-obstetrician, pediatrician, and psychiatrist).
Prescribing a Psychotropic Medication in Indian Setting
It should be ideally decided by the patient. In India, the patient usually asks their physician to decide for her, and appropriate way could be a joint decision by the patient (with her husband and other family member), obstetrician, psychiatrist and pediatrician. Obtain written consent before starting a medication.
Establish a clear indicationSelect a drug (prefer monotherapy):
Lowest known risk or prior exposure in previous pregnancyAvailable reproductive safety dataKnown effectivenessHigher protein bindingHigh potencyShort period of exposure (e.g. during peak of the symptoms) or intermittent dosingLowest effective dose and smaller multiple divided doses, andOptimize if necessary rather than switching or combining.Provide adequate information - this is most important before starting any medication. Explain about teratogenic potentials in simple terms (e.g., in percentage), efficacy of medication, nonpharmacological optionSafety monitoring - close monitoring of fetus (appropriate fetal screening and monitoring) and mother (severity of illness, level of personal social and occupational impairment)Good practice - be familiar with risks of medication, risks of maternal illness, and treatment guidelines. Adequate document appropriately communicates and collaborates with the patient referred to a specialist if required.
Threshold for Initiating or Maintaining on Medication
There is no general guideline as to when the medication should be started during pregnancy. Establish that severity of illness that requires active supervision or behavior posing/or invariably may lead to a safety issue to the patient or the fetus. A score below 30 on the global assessment of functioning may be considered as a gross threshold when specific assessment cannot be done. Some of the symptom severity indicators are severe insomnia and loss of appetite, being immobile or very hyperactive, impaired judgment, severe impairment in personal care, patient requiring active supervision for daily routine, inability to follow the recommendation by an obstetrician, or any risk that poses threat to the safety of self or to the growing fetus. In other words, without treatment, there is a high chance of poor outcome of pregnancy and safety issues may invariably arise. Other factors that are often considered before prescribing psychotropic are: Imminent safety issue (suicidality, harm to others), poor support system, severe relapse in the past, causing safety issues, a malformation in children or first degree relative, history of substance use during illness, and mental illness during a past pregnancy and more than 12 weeks gestation.
Dilemma for Asymptomatic Patient on Medication, But at Risk of Relapse During Pregnancy
Most guidelines are in opinion that if the patient is asymptomatic, reduce dose and high teratogenic medicine should be switched to a less teratogenic medication. In general, folate supplement should be given. In depression and anxiety disorder, single antidepressant may be continued at the lowest effective, dose except for paroxetine and venlafaxine. Benzodiazepine can be used intermittently or on requirement basis. Patients with schizophrenia should continue their typical antipsychotic, atypical antipsychotic may be changed to typical antipsychotics, and if the patient has a poor response to typical, reduce to lowest effective dose of atypical antipsychotics, do not give depot antipsychotics. Anticholinergic should not be used routinely. Valproate, carbamazepine, lithium, and lamotrigine should not be used unless there is no alternative. Antipsychotics can be an alternative option to mood stabilizers in the management of bipolar disorder during pregnancy. If clinician/obstetrician has decided to stop the medication, it should not be abrupt. There is no clear guideline regarding the discontinuation of psychotropic medication, and general term that gradual tapering has been used in literature. Usually, discontinuation of psychotropic medication depends on many factors such as duration of illness, duration of remission, diagnosis, possibility of withdrawal symptoms, psychosocial issues, etc. Attempt has been made as to how a psychotropic medication may be discontinued,, in such situation, an appropriate approach may be:
If the patient is asymptomatic for more than 6 months and on single medication - If the medication is a high potency then quarter dose reduction weekly with continuous observation of symptoms of relapseIf the patient is asymptomatic for more than 6 months and on single medication - If medication is lower potency than half dose reduction weekly with continuous observation of symptoms of relapseIf the patient is asymptomatic for more than 6 months and on single medication - If medication is more than one, both high potency and low potency, then simultaneous quarter dose reduction for high potency and half dose reduction for low potency medication every week with continuous observation of symptoms of relapseIf the patient is asymptomatic for less than 6 months and on single medication - If the medication is a higher potency then 20% dose reduction weekly with continuous observation of symptoms of relapse.
Choice of Psychotropic Medication during Pregnancy
After extensive review, National Institute for Health and Care Excellence provided with medication with a better safety record as drugs of choice. These medications are:
Hypnotic and sedative: Zolpidem or promethazineAntipsychotics: Chlorpromazine, haloperidol, and trifluoperazineAntidepressant: Nortriptyline, amitriptyline, imipramine, and fluoxetineMood stabilizers: High potency typical antipsychotics may be considered as a mood stabilizer during pregnancy.
Preventing the Teratogenic Effect of Psychotropic Medication
One-third of major physical anomalies can be prevented (primary prevention). The most advocated measures are folic acid and multivitamin supplementation, use of drug with better safety and prevention of infection, and other physical disorder during pregnancy.,,
Physicians in India are more likely to face psychopharmacoteratophobia and issues related to this phenomenon are distinct in India. Clear guidelines is required to address this issue for Indian setting.
The authors would like to thank Yahosa A, Shamaya T, Asther M, Yasuas J, Marias P, Ashish T, Akash M and Mini T for their moral help.
Financial Support and Sponsorship
Conflicts of Interest
There are no conflicts of interest.
|1||Robertson JG. An Excess of Phobias and Manias: A Compilation of Anxieties, Obsessions, and Compulsions that Push Many Over the Edge of Sanity. Los Angeles: Senior Scribe Publications; 2003.|
|2||Henry CO. Avoiding the Fear Trap: Learning to Neutralize and Overcome the Power of Fear. Mustang, Oklahoma: Tate Publishing and Enterprises, LLC; 2010.|
|3||Kim JH, Scialli AR. Thalidomide: The tragedy of birth defects and the effective treatment of disease. Toxicol Sci 2011;122:1-6.|
|4||Webster WS, Freeman JA. Is this drug safe in pregnancy? Reprod Toxicol 2001;15:619-29.|
|5||Hancock RL, Koren G, Einarson A, Ungar WJ. The effectiveness of Teratology Information Services (TIS). Reprod Toxicol 2007;23:125-32.|
|6||Marchetti F, Romero M, Bonati M, Tognoni G. Use of psychotropic drugs during pregnancy. A report of the international co-operative drug use in pregnancy (DUP) study. Collaborative Group on Drug Use in Pregnancy (CGDUP). Eur J Clin Pharmacol 1993;45:495-501.|
|7||Bellantuono C, Tofani S, Di Sciascio G, Santone G. Benzodiazepine exposure in pregnancy and risk of major malformations: A critical overview. Gen Hosp Psychiatry 2013;35:3-8.|
|8||Einarson A, Vega CP. The safety of psychotropic drug use during pregnancy: A review. MedGenMed 2005;7:3.|
|9||Mawhinney E, Campbell J, Craig J, Russell A, Smithson W, Parsons L, et al. Valproate and the risk for congenital malformations: Is formulation and dosage regime important? Seizure 2012;21:215-8.|
|10||Morrow J, Russell A, Guthrie E, Parsons L, Robertson I, Waddell R, et al. Malformation risks of antiepileptic drugs in pregnancy: A prospective study from the UK epilepsy and pregnancy register. J Neurol Neurosurg Psychiatry 2006;77:193-8.|
|11||Meador KJ, Baker GA, Finnell RH, Kalayjian LA, Liporace JD, Loring DW, et al. In utero antiepileptic drug exposure: Fetal death and malformations. Neurology 2006;67:407-12.|
|12||Suresh S, Thangavel G, Sujatha J, Indrani S. Methodological issues in setting up a surveillance system for birth defects in India. Natl Med J India 2005;18:259-62.|
|13||Taksande A, Vilhekar K, Chaturvedi P, Jain M. Congenital malformations at birth in Central India: A rural medical college hospital based data. Indian J Hum Genet 2010;16:159-63.|
|14||Chinara PK, Singh S. East-West differentials in congenital malformations in India. Indian J Pediatr 1982;49:325-9.|
|15||Matthys A, Ambat MT, Pooh R, Kupesic Plavsic S. Psychotropic medication use during pregnancy and lactation: Role of ultrasound assessment. Donald Sch J Ultrasound Obstet Gynecol 2014;8:109-21.|
|16||Kelly RH, Danielson BH, Zatzick DF, Haan MN, Anders TF, Gilbert WM, et al. Chart-recorded psychiatric diagnoses in women giving birth in California in 1992. Am J Psychiatry 1999;156:955-7.|
|17||Kelly RH, Russo J, Katon W. Somatic complaints among pregnant women cared for in obstetrics: Normal pregnancy or depressive and anxiety symptom amplification revisited? Gen Hosp Psychiatry 2001;23:107-13.|
|18||Andersson L, Sundström-Poromaa I, Bixo M, Wulff M, Bondestam K, Ström M. Point prevalence of psychiatric disorders during the second trimester of pregnancy: A population-based study. Am J Obstet Gynecol 2003;189:148-54.|
|19||Vesga-López O, Blanco C, Keyes K, Olfson M, Grant BF, Hasin DS. Psychiatric disorders in pregnant and postpartum women in the United States. Arch Gen Psychiatry 2008;65:805-15.|
|20||Einarson A, Selby P, Koren G. Abrupt discontinuation of psychotropic drugs during pregnancy: Fear of teratogenic risk and impact of counselling. J Psychiatry Neurosci 2001;26:44-8.|
|21||Einarson A, Davis W. Barriers to the pharmacological treatment of women with psychiatric disorders during pregnancy and breastfeeding: Results of a survey. J Obstet Gynaecol Can 2013;35:504-5.|
|22||Bánhidy F, Lowry RB, Czeizel AE. Risk and benefit of drug use during pregnancy. Int J Med Sci 2005;2:100-6.|
|23||ACOG Committee on Practice Bulletins – Obstetrics. ACOG Practice Bulletin: Clinical management guidelines for obstetrician-gynecologists number 92, April 2008 (replaces practice bulletin number 87, November 2007). Use of psychiatric medications during pregnancy and lactation. Obstet Gynecol 2008;111:1001-20.|
|24||NPSA. National Patient Safety Agency. With Safety in Mind: Mental Health Services and Patient Safety. Patient Safety Observatory Report 2; 2006. Available from: http://www.npsa.nhs.uk/patientsafety/alerts-and-directives/directives-guidance/mental-health. [Last retrieved on 2014 Dec 23].|
|25||CPA. The Consumer Protection Act, 1986. (Act 68 of 1986). Government of India. Available from: http:// ncdrc. nic.in/1_1.html. [Last accessed on 2014 Dec 28].|
|26||IPC. Indian Penal Code 304-A. India; 1897.(Section 304-A of 1897). Government of India. Available from: http://www.indianpenalcode.in/ipc-243/. [Last accessed on 2014 Dec 28].|
|27||MTPA. The Medical Termination of Pregnancy Act. India; 1971. Government of India. Avilable from: http://tcw. nic.in /Acts/MTP-Act-1971.pdf. [Last accessed on 2014 Dec28].|
|28||MHA. Mental Health ACT 1987. Available from: http://www. disabilityindia.org /mentalact.cfm. [Last accessed on 2014 Dec 28].|
|29||PHRA. Protection of Human Rights Act. India; 1993. Available from: http://nhrc. nic.in/. [Last accessed on 2014 Dec 28].|
|30||GWA. The Guardians and Wards Act. India; 1890. Government of India. Available from: http://wcd.nic.in/ gawaact. htm. [Last accessed on 2014 Dec 28].|
|31||PNDT. The Pre-Natal Diagnostic Technique. India; 1994. Government of India. http://pndt. gov.in/index2.asp ?slid =49&sublinkid=31. [Last accessed on 2014 Dec 28].|
|32||Mishra RC, Mayer B, Trommsdorff G, Albert I, Schwarz B. The value of children in urban and rural India: Cultural background and empirical results In: Trommsdorff G, Nauck B, editors. The Value of Children in Cross-cultural Perspective. Case Studies from Eight Societies. Lengerich: Pabst Science; 2005. p. 143-70.|
|33||Collier SA, Rasmussen SA, Feldkamp ML, Honein MA; National Birth Defects Prevention Study. Prevalence of self-reported infection during pregnancy among control mothers in the National Birth Defects Prevention Study. Birth Defects Res A Clin Mol Teratol 2009;85:193-201.|
|34||Acs N, Bánhidy F, Puhó E, Czeizel AE. Maternal influenza during pregnancy and risk of congenital abnormalities in offspring. Birth Defects Res A Clin Mol Teratol 2005;73:989-96.|
|35||Acs N, Bánhidy F, Puhó EH, Czeizel AE. Acute respiratory infections during pregnancy and congenital abnormalities: A population-based case-control study. Congenit Anom (Kyoto) 2006;46:86-96.|
|36||Jacobs DG. Suicide assessment, five-step evaluation and triage. In: Best Practices Registry (BPR) for Suicide Prevention. SPRC (Suicide Prevention Resource Center). Available from: http://www.sprc.org/library/safetpcktcrdredc.pdf. [Last accessed on 2014 Dec 22].|
|37||Dubin WR, Jagarlamudi K. Safety in the evaluation of potentially violent patients. Psychiatr Times 2010;27:15-7.|
|38||Robakis T, Williams KE. Atypical antipsychotics during Pregnancy: Make decisions based on available evidence, individualized risk/benefit analysis. Curr Psychiatry2013;12:12-8.|
|39||Brent RL. Bendectin: Review of the medical literature of a comprehensively studied human nonteratogen and the most prevalent tortogen-litigen. Reprod Toxicol 1995;9:337-49.|
|40||Wilson JG. Current status of teratology. General principles and mechanisms derived from animal studies. In: Wilson JG, Fraser FC, editors. Handbook of Teratology. General Principles and Etiology. Vol. 1. New York: Plenum Press; 1977. p. 47-74.|
|41||Scialli AR. Causation in teratology-related litigation. Birth Defects Res A Clin Mol Teratol 2005;73:421-3.|
|42||Hill AB. The environment and disease: Association or causation? Proc R Soc Med 1965;58:295-300.|
|43||Scialli AR. A clinical guide to reproductive and developmental toxicology. Boca Raton, FL: CRC Press; 1992.|
|44||Shepard TH. Catalogue of Teratogenic Agents. 10th ed. Baltimore: Johns Hopkins University Press; 2001. p. xxiv.|
|45||Wilson RD, Johnson JA, Summers A, Wyatt P, Allen V, Gagnon A, et al. Principles of human teratology: Drug, chemical, and infectious exposure. J Obstet Gynaecol Can 2007;29:911-26.|
|46||van Gelder MM, van Rooij IA, Miller RK, Zielhuis GA, de Jong-van den Berg LT, Roeleveld N. Teratogenic mechanisms of medical drugs. Hum Reprod Update 2010;16:378-94.|
|47||Wilson JG. Environment and Birth Defects. New York, London: Academic Press; 1973.|
|48||Niesink RJ, de Vries J, Hollinger MA. Toxicology Principles and Applications. New York, London, Tokyo, Boca Raton: CRC Press; 1996.|
|49||Nowbar A. What challenges do clinicians face when prescribing psychotropic medication in pregnancy? Perinatal Psychiatry Essay. 2013. Publication of Royal Psychiatric Association. Available from: https://www.rcpsych.ac.uk /pdf/Perinatal %20Psychiatry%20Essay2013.pdf. [Last accessed on 2014 Dec 28].|
|50||Viguera AC, Baldessarini RJ, Hegarty JD, van Kammen DP, Tohen M. Clinical risk following abrupt and gradual withdrawal of maintenance neuroleptic treatment. Arch Gen Psychiatry 1997;54:49-55.|
|51||Hoga DB. Strategies for Discontinuing psychotropic medications. Can Geriatr Soc J CME 2014;4:14-8.|
|52||NICE. National Institute for Clinical Excellence. Antenatal and Postnatal Mental Health. Clinical Management and Service Guidance (Reissued April 2007); 2007. Available from: http://www.nice.org.uk/. [Last accessed on 2014 Dec 22].|
|53||Taruscio D. Folic Acid: From Research to Public Health Practice. In: Report of WHO Regional Office for Europe and the Instituto Superiore di Sanita, Rome; November 11-12, 2002.|
|54||Blom HJ, Shaw GM, den Heijer M, Finnell RH. Neural tube defects and folate: Case far from closed. Nat Rev Neurosci 2006;7:724-31.|
|55||Moh W, Graham JM Jr, Wadhawan I, Sanchez-Lara PA. Extrinsic factors influencing fetal deformations and intrauterine growth restriction. J Pregnancy 2012;2012:750485.|
|56||Taruscio D, Arriola L, Baldi F, Barisic I, Bermejo-Sánchez E, Bianchi F, et al. European recommendations for primary prevention of congenital anomalies: A joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans. Public Health Genomics 2014;17:115-23.|