TRIPLETS A Rare Case Report Lt Col PD SHARMA *, Lt Col GSN MURTHY +, Lt Col (Mrs) V PADMINI #, Maj (Mrs) N CHHABRA **, Lt Col MA KHAN ++, Brig Be RAY # MJAFI 2001; 57: 66·67

KEY WORDS:Multiple Pregnancies; Triplets; Twins.

Introduction he term "Triplets" is used when three babies are born to a mother at one time. Twin deliveries are quite common but triplets are rare. Amongst multiple pregnancies, estimated incidence of twins is I 0 86, triplets 1 of 862 and quadruplets 1 of 863 and so on, which is called Helin's law. [I]. Incidence of multiple gestations has increased in recent past due to frequent use of ovarian stimulant drugs such as clomiphene and gonadotropins for treatment of infertility. Clomiphene increases the occurrence of dizygotic pregnancies by 5 to 10% [1,2]. Perinatal mortality rate for twins and triplets is as high as 4 to 11 times that of singleton [3]. One such case is reported here and related problems discussed.

T

tube. Prophylactic dexamethasone was given to mother before delivery and 10 babies after birth to prevent hyaline membrane disease. The first one, who had a separate placenta, had feed intolerance and poor thermo regulation and succumbed on fOUJ1h day of life to apnoea of prematurity. TI1C second and third of the triplets remained stable and are growing well.

Case Report Triplets were born to a 29 year old primigravida mother, married for past 9 years and treated for primary infertility with clomiphene in civil, where no sonography was done. She reported to the out patient department of a zonal service hospital at 34 weeks of gestation and was advised sonological work up. Ultrasonography (Fig-I) revealed three live foetuses with vertex presentation. There was no family history of twins or triplets and her ante-natal period was uneventful. She was hospitalised and all necessary arrangements were made for the delivery and management of three preterm babies. On third day of admission, she went into labour and three male babies (Fig-2), each weighing 1500 grams were delivered by emergency lower segment Caesarean section. Three resuscitation teams were kept ready to receive the babies. Babies were asphyxiated at birth and were successfully resuscitated. There was no evidence of foetofoetal or Ioeto-rnaternal transfusion and no congenital anomaly was found in them, The first of the triplet had separate placenta, whereas second and third one shared a common chorion. All of them had their own amniotic sacs. Their blood groups were B positive, same as that of their mother. They were managed in neonatal intensive care unit (NICU) in thermo-neutral environment, using incubator and radiant heat warmer, under complete asepsis. Expressed breast milk and reconstituted powder milk were given to them through nasogastric

Fig. 1: Ultrasonogram of triplets

Fig. 2: Triplet born to a primigravida

"Classified Specialist (Paediatrics), "Classified Specialist (Radiology), #... Classified Specialist (Gynae & Obst), ++Classified Specialist (Anaesthesiology), ## Commandant, Military Hospital, Jabalpur-482 001 (MP)

Triplets

Disussion Management in pregnancy and labour in triplets is done on the same lines as that in twins [4]. Real time ultrasonological examination is the key diagnostic tool for confirmation of diagnosis and can be done as early as five to six weeks of gestation [5]. Simultaneous birth of three pre term babies is a challenge to medical attendants as well as to parents. Ante natal diagnosis helps in the preparedness for their successful management. Congenital malformations are more common in triplets and twins as compared to singletons. The common congenital anomalies reported are vertebral, anorectal, tracheoesophageal, renal and cardiac defects [1,2,6]. The incidence of foeto-foetal and foeto-maternal transfusion is as common as 15 to 50%, where donor baby is born anaemic and may even require blood transfusion [2,6]. The triplets reported by us had none of these problems. Neonatal problems related to prematurity and intra uterine growth retardation are no different in triplets from singletons of same gestation and birth weight [2]. These problems include hypothermia, hypoglycaemia hyaline membrane disease, apnoea of prematurity, feed intolerance and hyperbilrubinaernia, They should be anticipated and managed on time. In our case, first neonate had feed intolerance and aponea of prematurity. In multiple pregnancies, usually first delivered baby is at low risk as compared to babies delivered subsequently, probably due to higher chances of hypoxia, but in our case, first of the triplets had more problems and did not survive which is unusual. The triplets reported here had same sex, same features and same blood groups, and hence they are likely to be monozygotic, however only immunological studies can con-

MJAFI. VOL 57, NO.1, 2001

67

firm their zygosity. Since first neonate had a separate placenta while second and third babies shared a common one, possibility of diamnotic monochorionic twins cannot be excluded. Clompiphene usually produces polyzygotic multiple pregnancies and they may not be of same sex. However, this was not found in our case. Polyhydraminos is a common problem in mothers with multiple gestations [4] but that was not found by us. There are different schools of thought regarding trial of normal delivery in such pregnancies, however interlocking of foetuses, knotting of cords, delayed delivery of second and third babies causing hypoxia may jeopardize foetal outcome and hence Caesarean delivery may be better to overcome these problems. Energetic resuscitation and neonatal care under the supervision of a neonatologist produce rewarding outcome and good prognosis in twins/triplets. References I. Nelson WE, Behrarnan RE, Kliegman RM and Arvin AM. Multiple pregnancies in Nelson text book of Paediatrics, 15th ed, Prism Books, Bangalore, 1996;453-4. 2. Pursley DM and Slark AR. Multiple gestation. In Manual of Neonatal care, 3rd ed. Little Brown and Company, London, 1991; 104-8. 3. Benson RC Multiple pregnancy. In Current Obstetric and Gynaecologic Diagnosis and Treatment. 4th ed. Lange Medical Publications, California 1982;755-63. 4. Dawn CS. High Risk Pregnancies In : Text book of Obstetrics and Neonatology. 10th ed. Dawn Books, Calcutta 1987;407-9. 5. Sanders RC. Obstetric Sinology. In Clinical Sonography- A Practical guide. 2nd ed, Little Brown and Company, Boston, 1991 ;124-6. 6. Meharban Singh. Haematological problems. In: Care of New born. 4th ed. Sagar publications, New Delhi, 1991;335-

6.

TRIPLETS - A Rare Case Report.

TRIPLETS - A Rare Case Report. - PDF Download Free
743KB Sizes 4 Downloads 14 Views

Recommend Documents


Case report of multiple valve disease found in triplets.
Valvular heart disease is a multifactorial disorder. Twin studies may help to better understand both genetic and environmental determinants contributing to the development of valve lesions. We describe the case of a 45-year-old female asymptomatic tr

Dioctophymiasis: A Rare Case Report.
Dioctophyma renale commonly known as "giant kidney worm' is found in the kidney of carnivorous mammals. Human infestation is rare, but results in destruction of the kidneys. Very few cases have been reported worldwide. We are here reporting a case of

Ainhum - A Rare Case Report.
The term 'AINHUM' is derived from the African word meaning 'to saw or cut'. True ainhum otherwise called dactylolysis spontanea is a condition involving soft tissue or digits with constricting rings commonly presenting in fifth toes, usually bilatera

Melorheostosis: a rare entity: a case report.
Melorheostosis is a rare entity belonging to the group of sclerotic bone dysplasias. Described for the first time in 1922 by Leri, it remains imperfectly known as clinical presentations are highly variable, and the etiological diagnosis is not fully

Perrault syndrome - a rare case report.
Perrault syndrome is a rare disease comprising pure gonadal dysgenesis (46 XX) and sensorineural hearing loss in females and deafness alone in affected males. It is an autosomal recessive disorder. Over the years many additional features like marfano

Ascher's syndrome: A rare case report.
An 18-year-old Indian girl with upper lip deformity presented with on and off painless swelling of her both upper eyelids for 3 years. Clinical evaluation revealed bilateral blepharochalasis, narrowing of horizontal palpebral fissure, decreased outer

Klippel Feil Syndrome: A Rare Case Report.
In Klippel Feil syndrome, classically there is a triad of short neck, a low posterior hairline and a limited range of neck movements especially of lateral bending. In fewer than 50% of cases have all the three elements.