سندرم محرومیت ترامادول در نوزاد: گزارش موردی

Authors

  • برنا, صدیقه دانشکده پزشکی، دانشگاه علوم پزشکی تهران
Abstract:

Background: Tramadol is a synthetics 4-phenyl-piperidine analogue of codeine used for treating moderate to severe pain. Tramadol is a FDA pregnancy category C medication which induces release of serotonin and inhibits the reuptake of norepinephrine. Chronic use of this drug during pregnancy may lead to physical dependency and withdrawal syndrome in the neonate.Case presentation: We report the newborn of a woman admitted in the delivery ward of Mostafa Khomeini Hospital in Tehran, Iran in 2011. The mother suffered from chronic low back pain and headache and frequently took tramadol during pregnancy. The infant had a gestational age of 38.5 w, a birth weight of 2950 gr and an Apgar score of 9/10 at 1 and 5 minutes after birth. The first signs of withdrawal syndrome occurred after 24 h with nausea, vomiting, poor feeding, and tremor. Later, agitation, tremor, hyprertonicity, and repeated multifocal myoclonus, and generalized tonic-clonic seizures developed. Clinical signs of withdrawal syndrome waned under phenobarbital therapy.Conclusion: Drug withdrawal syndrome should be considered in the neonates of pregnant mothers who chronically take tramadol. Tramadol administration during pregnancy should be restricted to carefully selected cases.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

گزارش یک مورد سندرم دندی واکر در یک نوزاد

ABSTRACT Dandy-Walker syndrom was described by blackfan, dandy in 1914. Dandy-Walker syndrome is characterized by a triad of complete or partial agenesis of the cerebellar vermis, cystic dilatation of the forth ventricle and enlarged posterior fossa with upward displacement of the transvers sinus, tentorium and torcular. The most striking abnormality is the presence of a huge dilated f...

full text

سندرم  Gitelman:  گزارش موردی

Background: Gitelman syndrome is a rare autosomal recessive disorder that typically presents with recurrent muscle cramps, carpopedal spasms, hypokalemic metabolic alkalosis, hypocalciuria and hypomagnesemia and high urine magnesium during adolescence. Mutation in the gene encoding for sodium chloride co-transporter in distal convoluted tubule causes electrolyte imbalance.Case presentation: We ...

full text

گزارش یک مورد سندرم دندی واکر در یک نوزاد

سندرم دندی واکر در سال 1914 توسط dandy، blackfan توصیف شد. این سندرم بوسیله یک تریاد، مشخص می شود که شامل آژنزی کامل یا نسبی ورمیس مخچه، دیلاتاسیون کیستیک بطن چهارم و بزرگی حفره خلفی با جابجایی سینوس ترانسورس ـ تنتوریوم و torcular به طرف بالا می باشد. مهمترین ناهنجاری در این سندرم وجود اتساع وسیع بطن چهارم است که به شکل کیست در آمده و سقف آن توسط یک غشای نوروگلیال عروقی پوشیده می شود. این کیست ...

full text

آترزی کوآن دو طرفه در یک نوزاد: گزارش موردی

ABSTRACT Choanal atresia is the most common congenital anomally of the nose and has a frequency of aproximately 1/7000 live births. It consists of a unilateral or bilateral bony (29%) or bony-membranous(71%) wall. Nearly 50% of affected infants have other congenital anomalies or CHARGE syndrome that include: coloboma, heart disease, choanal atresia, growth and development retardation, ...

full text

سندرم پلاک مکونیوم در نوزاد بدنبال مصرف سولفات منیزیوم در مادر (گزارش یک مورد)

The meconium plug syndrom is a benign form of colon obstruction in the neonate caused by a firm white plug of mucus. These babies usually present with abdominal distention. Abdominal X ray film reveals distended loops of bowels. Barium enema shows a long radiolucency within the desending colon. The plug is passed after the barium enema or a saline rectal irrigation. Although meconium plug syndr...

full text

گزارش یک مورد سندرم گوردون در یک زن 35 ساله با حاملگی طبیعی و نوزاد ترم

Gordon syndrome is a familial autosomal dominant syndrome with hyperkalemia, increased extracellular volume, hypertension, normal kidney function, and metabolic acidosis. It is also called type II Pseudohypoaldosteronism due to usually normal aldosterone and low renin levels. In this report a 35 years old woman is presented with 2-year history of hypertension, eclampsia, and fetal death. Labora...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 70  issue None

pages  389- 392

publication date 2012-09

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023