27 Gangguan Irama JTG
27 Gangguan Irama JTG
27 Gangguan Irama JTG
ANDALAS UNIVERSITY
By:
Mentor:
Prof. Dr. dr. Hj. Yusrawati, SpOG, Subs-KFM
(K)
Dr. Dr. dr. Joserizal Serudji SpOG, Subs-KFM
(K)
LEMBAR PENGESAHAN
MENGETAHUI
Prof.Dr.dr.Hj.Yusrawati,SpOG(K)
CHAPTER 1
INRODUCTION
Case: Mrs. Syahrani 27 years old 01107860 with G1P0A0H0 15-16 weeks
gestational ages presents to fetomaternal. This patient referral from Secondary
hospital. She had had history of bradycardia diagnosed since a teenager but had
not undergone tests nor received treatments. Now she has diagnosed by
cardiologist with AV block on peace maker.
2.1 Introduction
Bradycardia in pregnancy due to total atrioventricular block is a rare yet serious
occurrence [1]. In most cases, it is often asymptomatic but symptomatic cases
would require urgent and definitive management [1]. Total atrioventricular block
may be a congenital disorder or stem from an acquired pathology [2]. Lack of
awareness often delays diagnosis with some patients presenting late during labour
[3]. Definitive management requires pacemaker implantation but there has been
controversy in the past regarding its necessity [3].
Unfortunately, due to its rarity, only few cases have been described in the
literature and guidelines on optimal management have been sparse. As a result, no
uniform management recommendations are available and, in some cases,
clinicians have had to explore the best form of management for their patient. In
Indonesia, to the best of the authors’ knowledge, there have been no case reports
so far of bradycardia in pregnancy due to a congenital disorder. This case report
wishes to highlight the rare cases, the challenges we had, the lack of experience
we encountered and the solutions we undertook using the best clinical evidence
available so far.
2.2 Discussion
Bradyarrhythmia among female of reproductive age is rare, even rarer is
bradyarrhythmia in pregnancy [1]. It is estimated that the prevalence of
bradyarrhythmia is in 1/20,000 women of reproductive age [1]. However, this
figure may also be an estimation as the true prevalence remains unknown. In this
case, the bradyarrhtyhmia is caused by TAVB. There are various etiologies to
TAVB in pregnancy [2]. The most common is congenital TAVB, in which
patients are born with a disconnected cardiac electric conduction system with no
communication between the sinoatrial (SA) node and the AV node [2] (1). Other
causes are often acquired including ischemic heart diseases, drug toxicity, nodal
ablation, electrolyte imbalance and post-operative heart blocks due to past cardiac
surgeries [2]. Systemic diseases such as amyloidosis, sarcoidosis and systemic
lupus erythematosus (SLE) may also cause TAVB [2]. The two cases in this
report had congenital TAVB as they had no history toward acquired TAVB.
Fig 1.
Complete atrioventricular block and its ECG waveforms Complete
atrioventricular block and its ECG waveforms [5].
Screening, early recognition, risk stratification and thorough planning are required
to successfully manage TAVB in pregnancy. Bradycardia in pregnancy due to
total atrioventricular block (TAVB) is a rare occurrence, often asymptomatic and
may arise from a congenital disorder. Pacemaker is often required. Cases are few
and management is not yet standardised. TAVB in pregnancy requires a concerted
effort involving obstetricians, cardiologists, and intensivists. Pacemaker
implantation is recommended. Whilst vaginal delivery remains first-choice,
caesarean section is indicated under obstetric indications.
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