Sabtu, April 30, 2011

Proud of You by Fiona Fung





Love in your eyes
Sitting silent by my side
Going on Holding hand
Walking through the nights
Hold me up Hold me tight
Lift me up to touch the sky
Teaching me to love with heart
Helping me open my mind
I can fly
I'm proud that I can fly
To give the best of mine
Till the end of the time
Believe me I can fly
I'm proud that I can fly
To give the best of mine
The heaven in the sky
Stars in the sky
Wishing once upon a time
Give 
me love Make me smile
Till the end of life
Hold me up Hold me tight
Lift me up to touch the sky
Teaching me to love with heart
Helping me open my mind
I can fly
I'm proud that I can fly
To give the best of mine
Till the end of the time
Believe me I can fly
I'm proud that I can fly
To give the best of mine
The heaven in the sky
Can't you believe that you light up my way
No matter how that ease my path
I'll never lose my faith
See me fly
I'm proud to fly up high
Show you the best of mine
Till the end of the time
Believe me I can fly
I'm singing in the sky
Show you the best of mine
The heaven in the sky
Nothing can stop me
Spread my wings so wide

Jumat, April 29, 2011

Aku dan Rasa Lelahku (Honda: Kartini Muda Indonesia) [Karena setiap manusia itu spesial]

Aku iseng buka-buka facebook
Ketemu kontes ini ...
Menarik! Tentu saja... Setiap orang bisa jadi inspirasi, setiap manusia itu selalu punya cerita, karena itu setiap manusia adalah spesial :)

click here ... Read and Vote :)

Aku dan Rasa Lelahku (Honda : Kartini Muda Indonesia)

Aku yang dulu hingga jadi aku yang sekarang
Meski kegagalan dan semua yang sedih-sedih itu terus masih datang karena gak akan mungkin pernah berakhir ... Aku akan terus tetap berusaha berdiri ...

Kamupun harusnya begitu ... Karena kita spesial :)


Hidup yang spesial


Dan teman teman yang spesial ... 

Kamis, April 28, 2011

Let Me In by Eyes Set to Kill

When will I find the light in day
I'm tired of learning
Of tossing and turning
When will I find the perfect words to say
I'm tired of burning papers
I didn't mean to throw away,
I didn't mean to throw away

I'm tired of writing the same old song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in
Yeah, ah, yeah, ah, ah, ah

I'm tired of writing this song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in

Come on let me in

When will I find the exit of this maze
I'm sick of retracing
Of rotting and wasting
When will I find the perfect words to say
I'm tired of burning papers
I didn't mean to throw away
(away, away)

I'm tired of writing the same old song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in
Yeah, ah, yeah, ah, ah, ah

I'm tired of writing this song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in

Come on let me in

If you let me in
You'll only want me out
But at least you'll share
The pain with someone else
You will live the life you haven't lived
Hear the voice you kept within
I will turn you inside out

I'm tired of writing the same old song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in
Yeah, ah, yeah, ah, ah, ah

I'm tired of writing this song
'cause there's no way out
There's no way out 'til you let me in,
'til you let me in

Come on let me in




Two Letter Sins by Eyes Set to Kill





Will you climb up to get me, release your grip
I've got time to be wasted don't try to leave, don't try to leave
It seems to me that I'm never sober, I can't rely on living lies
I really wish we could start it over just you and me

When we touched you initialed into my skin
With the scratch of a nail carve two letter sins, two letter sins
It seems to me that I'm never sober, I can't rely on living lies
I really think we should start it over just you and me

It seems to me that I'm never sober, my tongue is dry and doused with lies
I really think we should start it over just you and me
Just you and me

Will you climb up to get me, release your grip
Will you climb up to get me, release your grip
It seems to me that I'm never sober, I can't rely on living lies
I really think we should start it over just you and me

It seems to me that I'm never sober, I can't rely on living lies
I really wish we could start it over just you and me
It seems to me that I'm never sober, my tongue is dry and doused with lies
I really think we should start it over just you and me, just you and me
Just you and me

Rabu, April 27, 2011

Aku Mengingatnya.



Setiap detail tentangmu, aku ingat


Setiap hal yang terakumulasi ditelingaku, suara dan kata-katamu... Aku mengingatnya
Setiap hal yang tergambar oleh mataku, senyum dan bahasa tubuhmu ... Aku mengingatnya
Setiap hal yang terhidu oleh indera pembauku, tubuhmu dan bau rambutmu .... Aku mengingatnya
Setiap hal yang mungkin bisa terkecap oleh lidahku, manis dan pahit kalimatmu ... Aku mengingatnya
Bahkan setiap hal yang menyentuh kulitku ... Hingga sekarang aku mengingatnya ..
Seakan baru kemarin!


Dan satu hal yang paling aku ingat adalah air mata itu .... Bagaimana air mata itu jatuh kewajahku dan menyentak seluruh pikiranku.... Terasa hangat, namun pedih dan dingin disaat yang sama ....


Saat ini, aku menangis.... Tapi malam ini bukan karena sedih! Aku menangis karena aku merasa begitu dicintai...


Meski aku mendengar, aku melihat, aku menghidu, aku merasa, dan aku meraba ... Tapi ada hal-hal yang bisa kurasakan tanpa kelima inderaku... Ada sesuatu yang aku rasakan tanpa perlu apapun selain perasaan ...


Saat ini aku menangis... Bukan karena sedih. Aku menangis karena aku merasa begitu dicintai dan diterima apa adanya .....
Entahlah ... Tiba-tiba saja aku merasa seperti itu!

Senin, April 25, 2011

Boy's Crying for Girl ....

RT @IDoThat2: If a guy cries over a girl he must really love her


And girls really love to believe this quote............




Pas buka twitter, follow satu account itu, dan baca 'wew' ....
I'm not really know about 'guy' , they all just one of the introvert ... Maksud aku, rata" cowok itu tertutup entah karena aku cewek atau emang mereka hanya terbuka sama cowok atau gimana ... Tapi yang aku ingat cowok kalo ngumpul tu pasti seru-seruan aja sambil ketawa-ketawa .. Entah mereka seperti lebih senang sendiri atau mengungkapkan dalam komunitas yang sedikit.


Aku? aku juga introvert, tertutup tapi dalam sebuah artian yang 'pemilih' aku seorang pemilih, just that ... Kalo untuk emosi tetap sama kayak orang lain malah kadang berlebihan. Ketika mau nangis ya nangis, ketika mau ngakak ya ngakak, ketika galau ya galau .... Kalo cowok tu kesannya, sedih but! It's too precious ketika kamu bisa liat mereka nangis ....


Penting gak sih! Kalo menurutku sih penting ....
Kamu tahu rasanya nangis sendirian sama nangis dihadapan seseorang yang bisa ngerti kita tu beda, lebih bikin kita lega kalo ada orang lain tapi kadang bikin sebel kalo kita nangisnya didepan orang yang salah, yang gak ngerti kita dan nganggap remeh masalah kita ....


Mungkin itu ya sebabnya?
Mereka 'kaum cowok' juga punya emosi yang sama, tapi mereka lebih memilih untuk sendiria atau dengan komunitas kecil, terus menahan emosi itu didalam karena 'mind set' yang sudah tertanam di masyarakat sehingga rasanya sebuah tangisan tu murah untuk diri sendiri tapi terlalu mahal untuk orang lain melihatnya!


Mungkin! I'm not really know about that, about guy, about boy, about man, just try to understand but I have limit too ----


Tapi, untuk quote diatas, kayaknya beberapa cowok mungkin akan setuju!
Cewek? Entahlah!
Banyak hal yang sulit dijelaskan ...
Beberapa, mungkin sebagian besar cewek bakal setuju kalo cewek tu firasatnya kuat


Dia akan tahu jika ada yang gak beres
Dia akan tahu jika sesuatu itu bohong atau tidak, hanya saja kadang dia pura-pura merasa normal! Mereka jago membohongi diri sendiri
Entah kenapa, even ketika cewek baru kenalan sama orang, meski dia gak kenal orang itu, hatinya akan secara perlahan menolak orang itu JIKA nantinya orang itu akan mengancam posisinya
Cewek itu pasif, iya. Tapi, Give them one, they will reply thousand times... Give them one flower, they will give you thousand flowers back
Jadi, ketika mereka melihat sesuatu dan dia merasa itu jujur, dia akan setuju! DAn untuk quote diatas, almost agree ....


You know guys ...
They never even afraid to cry over you
But they always afraid to see you cry over them, why? Because they know it must be bad thing already happened when you cry out. Because they know that something that makes you cry only one, something that makes you feel bad and alone!


They never even afraid to tell why they cry
But, at the last they will regret to make you worry with that crying....


They think that, crying is the one easy way to make their heart relieve but! They always deem that your crying is the precious and the hard thing to see


Geezzz ,,... And once they see your crying, it will make them afraid, because it will makes them love you more...
And twice they see your crying, they wont be bored, they even will love you over and over, and makes them feel that you need them too much, they wont go away!
And third crying ... They will really afraid to see your third crying because, they will do anything to make your crying stop!


You have to know, how afraid girl with 'the person who she love's crying' not because she hate to make you happy, but they afraid to see you sad over and over!


They will happy if you trust them to crying over them, but will more than happy if there's nothing in this world that can makes you cry!


My New Room and Diary

Pusang! -_-"
Pusing ada obatnya
Kalo pusang, gak ada ....


Tapi .... Yo wes lah ...
Ah sekalian pamer kamar baru deng!
Pertama kali liat pas selesai make over sebulan yang lalu, rasanya kayak habis kedatangan 'Bedah Rumah' ... Eh ganti ding .. 'Bedah Kamar Kos' trus pas buka tirai, tereak-tereak sambil nangis berlutut .. --__--"


Kayak kamar anak SD habis ulang taunan (Emang kan niat awalnya gitu, tapi ada Tuhan yang selalu bisa menjadikan maupun menggagalkan segala hal ;'/ ) ... ckck 
BTW tu yang nempel di dinding (merah muda sama hijau di pojok foto) namanya 'Glow In the Dark' jadi kalo matiin lampu
OhMyGawdddd ... Cantik sumpah! (Lebay ah)
Kayak liat bintang-bintang dehhh <3

Eh satu lagi ...
Sekarang aku mau mulai nulis diari lagi ...
Denger gak DIARI! Emak!
Itu kan mainan SMP-SMA yah,.. Udah hampir 2 tahun gak ngubek diari manual berupa buku dengan dekorasi cantik dan diperibet dengan kunci gembok seakan isinya rahasia banget gitu padahal cuma uneg-uneg anak kecil labil lagi jatuh cinta wkwkwkwk ....

Tapi sekarang serius, disamping memang ada hal-hal yang gak mungkin aku muntahin di blog, juga karena ingin meningkatkan skill nulis ....

Bukunya lucu deng ... Winnie The Pooh gitu


Isinya? Belum ada sih ...
Masih bingung juga mau mulai darimana, ya dicoba dulu deh :)

Dadah Gutbay kalo gitu
And well!

Semoga besok lebih baik .. Karena aku selalu yakin besok akan lebih baik... .Kau harusnya juga yakin, kau lebih baik kan besok? Kalian lebih baik besok ... Kita semua akan lebih baik besok ...... Tuhan selalu baik! Amin :)




Buat yang jauh disana (Ya ampun gue serasa punya Long Distance Relationship gini sih haha), you always get your place here in my heart, never change whatever happened... Anyone couldn't changes your place but the perfect person who only in my mind, my imagination. Even, he only change you for a while and I have to back to the reality that no one could changes your position here in my heart! Tomorrow will be better, and of course it always be :) ~Gak ngerti juga kenapa pengen ngomong ini sekarang, secara gak nyambung sama tema awal tulisan hagh! Mungkin karena lagi si cewek labil ini sedang galau dan kangen~

Jumat, April 22, 2011

Kado .......



Kado adalah sesuatu yang digunakan sebagai hadiah untuk seseorang dengan tujuan tertentu seperti ulang tahun, hari raya, hari besar, naik kelas, ucapan selamat karena berhasil dalam sebuah pencapaian, bahkan tanpa tujuan apapun kado masih bisa diberikan untuk mengekspresikan pikiran dan perasaan kita terhadap sesuatu, seseorang atau sekumpulan orang.


Ketika sesuatu diciptakan, maka ia pasti berharap memiliki manfaat
menjadi berguna, dan tidak sia-sia....


Seonggok kado, ia berdebu, diam sendirian di pojokan ruangan tanpa tahu harus melakukan apa. Diciptakan namun hanya untuk merasakan kesia-siaan. Sendirian terpuruk dalam gelap diantara semut kecil. Menangis namun tak didengar, meminta untuk dibuang tapi sang tuan tak bisa merelakannya untuk dibuang. Diberikan? Kemana?
Lalu kenapa dia dibuat. Untuk mengekspresikan perasaan. Untuk mengucapkan sesuatu, namun ternyata tidak tersampaikan.


Seperti seorang bayi, kenapa dia dilahirkan? Karena dia akan melakukan sesuatu yang hebat nantinya, sesuatu yang bermanfaat, dia akan menjadi jodoh seseorang, dia akan berbuat baik atau jahat untuk membantu jalannya takdir yang telah Tuhan buat, begitu banyak manfaat dia dilahirkan ke dunia tapi tahukah dia dan orang-orang yang ada disekitarnya bahwa kelak jika dia dilahirkan ayahnya sebenarnya sudah tiada dan ibunya ternyata akan meninggal setelah melahirkan dia. Dia tak akan tahu itu sebelum hal itu terjadi, dan ketika dia telah lahir dan menjadi sebatang kara, lantas apakah dia berhak menuntut Tuhan agar mengambil nyawanya lagi sebelum apa yang harus dia lakukan terlaksana? Tidak


Apa yang terjadi pada si kado kecil juga sama seperti itu.
Pada akhirnya ia harus menerima dirinya yang kini sendirian dan merasa kosong disana. Dipojok ruangan yang dingin dan kotor berdebu.


Bagaimana jika kau diciptakan ke dunia untuk sebuah manfaat tapi ternyata kau tidak bisa menjalankan manfaatmu sesuai tujuan awal kau diciptakan? Sakit!


Itu pula yang dia rasakan jika dia punya hati.
Siapa yang bisa jamin benda mati itu tak punya perasaan. Tidak ada yang tahu jika dia diam-diam menangis. Tidak ada yang tahu jika nantinya dia mulai menua dalam keputusasaan dan kekosongan.


Itulah yang terjadi padanya. Si kado yang malang. Si kado yang cantik dan berharga tapi ternyata sangat malang.


Itulah yang terjadi padaku sekarang... Aku si kado yang malang!


Aku terpuruk sendiri dipojok ruangan.
Dibuat untuk hadiah kepada temannya 'tuanku'
Tapi hingga sekarang aku masih berada disini. Berdebu.
Diam-diam aku menangis, tapi tidak ada yang bisa mendengar karena aku sebuah benda mati
Kadang aku berharap dikeluarkan, dibuka, dipeluk, lalu disimpan sebagai hadiah. Tapi sekarang aku berada di kantong kresek.
Aku diam-diam meminta kepada Tuhan.
Tidak jarang aku mengeluh.
Aku kotor, dan berdebu.
Ya ... Meskipun kadang 'tuanku' masih sering mengeluarkan aku dari sudut ruangan berdebu itu untuk membersihkan permukaan tubuhku, semuanya tidak ada bedanya, karena setiap melihat aku, 'tuanku' juga menangis, tubuhku jadi basah dan rapuh. Kertasnya jadi mudah robek dan aku akan jadi jelek.
Penampilanku sekarang manis tapi didalam sini menyedihkan.
Akupun tidak bisa meminta kepada 'tuanku' agar membuangku, dia terlalu sayang padaku dan menganggapku berharga.
Aku pernah dengar dia bilang akan simpan aku sampai fungsiku tercapai. Sungguh aku terharu, aku sedih!
Sekarang aku berada disini, dalam kantong kresek, menunggu seperti benda yang bodoh.
Aku tertawa kadang!
Aku bingung apakah sekarang aku merasa bahagia oleh karena 'tuanku' yang sering memluku, menimangku, menyayangiku karena aku begitu berharga. Ataukah aku harus merasa tersiksa karena dibiarkan berada di pojok ruangan yang sumpek itu, menunggu ketidakpastian.


Aku sedikit banyak bisa mengerti sekarang tentang manusia. Aku hanya diberikan Tuhan sepotong perasaan, dan itu sudah cukup rumit untukku.


Mungkin karena itulah manusia jadi sering menangis. Mereka kadang terus saja menangis setiap hari dengan alasan yang sama yang itu itu saja, padahal mereka tidak pernah tertawa pada sebuah lelucon yang sama lebih dari dua kali, lalu kenapa mereka harus menangis untuk masalah yang sama berkali-kali. Manusia memang rumit.


AKu, si kado kecil ini hanya bisa menonton dan menunggu!
Paling tidak aku punya hiburan
dan patokan untuk belajar....


Aku, si kado kecil yang malang...............




"Broken gift" by J E. Stรฅlberg


oleh : Kado kecil pada bulan april ...
nb : Pada awalnya aku punya teman, tapi sekarang semua kado telah sampai pada fungsinya, kecuali aku :') ... Tuanku... Cepat Lakukan sesuatu!!!

Unfaithful by Rihanna





Story of my life, searching for the right
But it keeps avoiding me
Sorrow in my soul cause it seems that wrong
Really loves my company

He's more than a man and this is more than love
The reason that the sky is blue
But clouds are rolling in because I'm gone again
And to him I just can't be true

And I know that he knows I'm unfaithful
And it kills him inside
To know that I am happy with some other guy
I can see him dying

I don't wanna do this anymore
I don't wanna be the reason why
Every time I walk out the door
I see him die a little more inside

I don't wanna hurt him anymore
I don't wanna take away his life
I don't wanna be a murderer

I feel it in the air as I'm doing my hair
Preparing for another date
A kiss up on my cheek, he's here reluctantly
As if I'm gonna be out late

I say I won't be long just hanging with the girls
A lie I didn't have to tell

Because we both know where I'm about to go
And we know it very well

?Cause I know that he knows I'm unfaithful
And it kills him inside
To know that I am happy with some other guy
I can see him dying

I don't wanna do this anymore
I don't wanna be the reason why
Every time I walk out the door
I see him die a little more inside

I don't wanna hurt him anymore
I don't wanna take away his life
I don't wanna be a murderer

Our love, his trust
I might as well take a gun
And put it to his head
Get it over with
I don't wanna do this
Anymore, anymore

And I don't wanna do this anymore
I don't wanna be the reason why
And every time I walk out the door
I see him die a little more inside

And I don't wanna hurt him anymore
I don't wanna take away his life
I don't wanna be a murderer
A murderer, no no no
Yeah

Rabu, April 20, 2011

NEONATAL ABSTINENCE SYNDROME (NAS)



OVERVIEW
Neonatal withdrawal syndrome, generically termed neonatal abstinence syndrome (NAS), is a complex disorder. It is defined as a constellation of behavioral and physiological signs and symptoms that are remarkably similar despite marked differences in the properties of the causative agent. Two major types of neonatal abstinence syndrome are recognized: neonatal abstinence syndrome due to prenatal or maternal use of substances that result in withdrawal symptoms in the newborn and postnatal neonatal abstinence syndrome secondary to discontinuation of medications such as fentanyl or morphine used for pain therapy in the newborn.
Postnatal neonatal abstinence syndrome results when an abrupt discontinuation of opioid analgesia occurs, usually after prolonged drug exposure. Fentanyl is the most commonly used analgesic drug in the neonatal intensive care unit (NICU). It is a potent, rapid-acting, synthetic opioid with a relative lack of hemodynamic side effects. Clinical studies have found that continuous infusions of fentanyl and morphine produce a high rate of opioid withdrawal when administered to critically ill infants. Tolerance and physical dependence are thought to develop more rapidly with shorter acting drugs and after continuous infusions rather than with intermittent administration. Tolerance and withdrawal symptoms may occur after 5 or more days of continuous infusion of fentanyl. This occurs more often with fentanyl than morphine.[1, 2] This article focuses on prenatal or maternal use of illicit drugs, although symptoms and therapy for postnatal neonatal abstinence syndrome are similar.
Maternal substance abuse, the cause of prenatal neonatal abstinence syndrome, is a leading preventable cause of mental, physical, and psychological problems in infants and children. Substance use by pregnant women has both medical and developmental consequences for the newborn, in addition to the legal, health, and economic consequences for the mother.
Drug abuse in pregnancy and neonatal psychomotor behavior consistent with withdrawal from opiate and polydrug withdrawal is currently a significant clinical and social problem. Approximately 3% of the 4.1 million women of child-bearing age who abuse drugs are believed to continue drug use during pregnancy.[3]
Drugs frequently associated with neonatal problems include the following:
  • Opiates and narcotics
    • Codeine
    • Fentanyl
    • Heroin
    • Methadone
    • Meperidine (Demerol)
    • Oxycodone
    • Morphine
    • Hydromorphone (Dilaudid)
    • Butorphanol (Stadol)
    • Pentazocine
    • Propoxyphene (Darvon)
    • Chlordiazepoxide
    • Buprenorphine[4]
  • Other drugs
    • Barbiturates
    • Caffeine
    • Cocaine
    • Selective serotonin reuptake inhibitors (SSRIs)
    • Antihistaminics (Diphenhydramine, Hydroxyzine)
    • Ethanol
    • Marijuana
    • Nicotine
    • Phencyclidine
    • Meprobamate
    • Glutethimide
    • Ethchlorvynol
    • Diazepam and lorazepam


    PATHOPHYSIOLOGY 

    Most illicit drugs cause an addiction in both the mother and the infant. Addiction or tolerance in the latter is due to passage of the drugs across the placental barrier; this occurs in varying degrees, depending on the pharmacokinetic properties of the individual drugs. Substances that act on the CNS are usually highly lipophilic and have relatively low molecular weight. These characteristics facilitate crossing from maternal to fetal circulation, with rapid equilibration of free drug between mother and fetus. Once drugs cross the placenta, they tend to accumulate in the fetus because of the immaturity of the renal function and the enzymes used for metabolism. Disruption of the transplacental passage of drugs at birth results in the development of a withdrawal syndrome.
    Neonatal abstinence syndrome is often a multisystem disorder that frequently involves the CNS, GI system, autonomic system, and respiratory system. Manifestations of neonatal abstinence syndrome depend on various factors, including the drug used, its dose, frequency of use, and the infant's own metabolism and excretion of the active compound or compounds. In addition, prenatal neonatal abstinence syndrome depends on the infant's last intrauterine drug exposure and the mother's drug metabolism and excretion. Withdrawal is generally a function of the drug's half-life; the longer the half-life, the later the onset of withdrawal. A longer half-life is also associated with a decreased likelihood of neonatal abstinence syndrome in the infant.
    Opiates produce the most dramatic effects on both the mother and fetus. Aside from the withdrawal symptoms, common findings in infants exposed to opiates include low birth weightprematurity, and intrauterine growth retardation (IUGR). Because of its short half-life, heroin withdrawal may start as early as 24 hours after birth and usually peaks within 48-72 hours in 50-80% of infants born to mothers who are dependent on heroin. Some delayed withdrawal may occur as long as 6 days after birth. Sedative-hypnotics such as benzodiazepines and barbiturates have an even longer half-life, and withdrawal may not start until after the infant has been discharged from hospital (age 2 wk).
    Methadone maintenance has been an acceptable form of therapy for opiate-addicted pregnant women since the late 1960s. Methadone has been shown to decrease illicit behaviors, improve prenatal care and obstetric outcomes, and prevent acute maternal withdrawal that is associated with fetal death.[5]However, maternal methadone use is also associated with neonatal abstinence syndrome, and its effects on the fetus are similar to the effects of heroin. Methadone's half-life is longer than 24 hours, and acute withdrawal may occur within the first 48 hours after birth and as long as 7-14 days later. The withdrawal may even be delayed for as long as 4 weeks after birth, with subacute signs developing as long as 6 months after birth. Neonates face an increased risk of fetal distress and demise, impaired fetal growth, and an increased risk of sudden infant death syndrome (SIDS). Thrombocytosis may occur in the second week of life and may continue until age 4 months.
    The relationship between maternal methadone dosage and neonatal abstinence syndrome is controversial, and the available data are conflicting. However, articles have showed that higher maternal doses are associated with an increase in the risk of preterm birth, the risk of symmetrically smaller infants, and longer hospital stays; the need for treatment for neonatal abstinence syndrome indicates more significant withdrawal symptoms.[6, 5, 7]
    Cocaine and amphetamines are stimulants with potent vasoconstrictor effects that stimulate the release and block the reuptake of the neurotransmitters dopamine, epinephrine, norepinephrine, and serotonin. Cocaine is a potent CNS stimulant that alters the major neurotransmitters and rapidly crosses the placenta. Early studies suggested that neonates exposed to cocaine exhibited a hyperactive Moro reflex, jitteriness, and excessive sucking. More recent studies do not support that neonates who have been exposed to cocaine differ behaviorally from unexposed infants. The unresolved question is whether or not cocaine acts to limit head growth or disrupt brain development. A synergistic effect between cocaine and other CNS toxins is still possible.
    Methylxanthine accumulates in the blood of breastfed infants whose mothers regularly consume caffeine substances. Nicotine is transferred through the placenta and may reach concentrations 15% higher than maternal levels. In utero exposure impairs neonatal habituation, orientation, autonomic regulation, and orientation to sound. Exposure also affects the infant's ability to be comforted and is associated with exaggerated startle reflex and tremor.
    No evidence suggests neonatal withdrawal problems associated with maternal use of marijuana during pregnancy. Fetal exposure to marijuana has been associated with hypoglycemiahypocalcemiasepsis, hypoxic encephalopathy, intracranial hemorrhage, and jitteriness. Effects on the fetus depend on the dose, with evidence of IUGR noted in cases of heavier usage.
    Neonates exposed to marijuana while in utero may also exhibit signs of nicotine toxicity, such as tachycardia, poor perfusion, irritability, and poor feeding. Growth inhibition is pronounced at birth and affects weight, length, and head circumference. Catch-up growth occurs within the first year in each growth category. Cognitive effects may persist to school age. However, withdrawal symptoms are generally not noted in infants in the newborn period. Extended follow-up does not show any effect in children aged 5-6 years.
    Several studies have demonstrated that maternal cigarette smoking during pregnancy increases the risk of having a low birth weight infant.[8] Neonates born to mothers who smoke during pregnancy weigh an average of 150-250 g less at birth than neonates born to mothers who do not smoke during pregnancy. Research findings also suggest that infants of mothers who smoke during pregnancy may develop nicotine withdrawal in a pattern that is related to the magnitude of in utero exposure. Infants who have been exposed to tobacco have been found to be more excitable and hypertonic and demonstrate more stress and abstinence signs.
    Neonates who are exposed to antidepressant medications during gestation are at increased risk of neonatal abstinence syndrome. SSRIs (eg, fluoxetine, paroxetine, sertraline, citalopram) are used to treat depression and a wide spectrum of other mood and behavioral disorders. Infants exposed to SSRIs during the last trimester of pregnancy may exhibit neonatal adaptation syndrome. This is primarily manifested as CNS (eg, irritability), motor (eg, agitation, tremors), respiratory (eg, increased respiratory rate, nasal congestion), and GI signs (eg, emesis, diarrhea). These manifestations are self-limiting and usually disappear by age 2 weeks. Symptoms are more commonly reported with fluoxetine and paroxetine exposure.
    A prospective study showed no statistically significant differences between tricyclic antidepressants and SSRIs. It also revealed that women using antidepressants often use other medications as well during pregnancy, making the interpretation of antidepressant withdrawal symptoms difficult. A decrease in maternal SSRI and tricyclic antidepressant use during the third trimester may lower the neonatal risk of developing withdrawal syndrome; however, this needs to be balanced against the harmful effects of depression during pregnancy.
    EPIDEMIOLOGY

    Frequency

    United States

    Neonatal drug withdrawal is a common problem in populations in which drugs taken for therapeutic, recreational, or addiction purposes are readily available to pregnant women. However, the incidence is difficult to determine because of unreliable histories of maternal drug abuse and limited health provider skills in eliciting drug histories and diagnosing nonopiate drug exposure in the newborn period. In addition, maternal use of more than one drug makes ascribing a given effect on the neonate to a specific drug difficult.
    In the United States, substance use among pregnant and postpartum women is a public health issue. In 2002-2003, the National Survey on Drug Use and Health (NSDUH) in the United States found that 4.3% of pregnant women aged 15-44 years reported using illicit drugs, compared with 10.4% of nonpregnant women in this age group.[9] The rate of illicit drug use among pregnant women aged 15-25 years was 8%. The rate for nonpregnant women of the same age was 16.8%.[9] A later report , primarily evaluating methamphetamine use in a nonselected population, reported that 10.7% of mothers had used illicit drugs during pregnancy.
    A more recent NSDUH report examined past month use of alcohol, cigarettes, and marijuana among pregnant and parenting women aged 18-44.[10] Combined 2002-2007 data showed that past-month alcohol use among women aged 18-44 was highest for those who were not pregnant and who did not have children living in the household (63%). The rate was comparatively low for those in the first trimester of pregnancy (19%) and even lower for those in the second (7.8%) or third (6.2%) trimester. Similar patterns were noted across these 4 subgroups of women for past-month binge alcohol use, cigarette use, and marijuana use.
    Data from the 2009 NSDUH report provide indirect evidence of dramatic increases in the prevalence of substance use following childbirth. Marijuana use was higher for recent mothers with children younger than 3 months in the household (3.8%) than for women in the third trimester of pregnancy (1.4%), suggesting resumption of use among mothers in the first 3 months after childbirth.[10]
    Overall the incidence of drug-exposed newborns is reportedly 3-50%, depending on the specific patient population, with urban centers usually reporting higher rates. An estimated 10–11% of the 4.1 million live births (in 2005) involved prenatal exposure to alcohol or illegal drugs. When tobacco data are included more than one million children are affected by prenatal exposure. Among offspring exposed to opioids or heroin in utero, withdrawal signs develop in 55-94%.

    International

    No accurate data are available concerning worldwide incidence. Data from the UK Advisory Council on the Misuse of Drugs suggests 6,000 babies are born to mothers who abuse drugs each year (1% of all UK deliveries).[11, 12] In the past, heroin was the most commonly abused drug. Women are now more likely to use cocaine, methadone, or more than one illicit drug.
    In Europe, each year as many as 30,000 pregnant women use opioids, and the number of pregnant women using drugs other than opioids may be equally as high.[13]

    Mortality/Morbidity

    Death is rarely associated with withdrawal alone but occurs as a consequence of prematurity, infection, and severe perinatal asphyxia.
    Long-term mortality rate is likely to be extremely low, although the risk for SIDS is significantly higher among infants who are exposed to opiates. Infants exposed to methadone have a 3.7-fold higher risk of SIDS compared with controls. Infants exposed to cocaine have a 2.3-fold higher risk for SIDS compared with infants with no exposure. This increased risk is related to a complex interplay of factors; the compromised home environment associated with a mother who is drug addicted is an important variable.

    Race

    Pregnant white women and Hispanic women had lower rates of illicit drug use (4.4% and 3%, respectively) than black women (8%).[9] Among women aged 15-44 years, the rate of cigarette use is higher among pregnant white women than among pregnant black or pregnant Hispanic women.[9]

    Age

    Rates of substance use among pregnant women vary by age group, with past-month illicit drug and alcohol use highest among teenagers. Pregnant women aged 15-25 years (8%) are more likely to use illicit drugs than pregnant women aged 26-44 years (1.6%).[9] The NSDUH report on 2003-2004 annual averages of substance use by pregnant women showed that 16% of pregnant teens aged 15-17 years reported past month illicit drug use compared with 7.8% of those aged 18-25 years and 2.1% of pregnant women aged 26-44 years.[14]

    HISTORY
    When assessing potential neonatal abstinence syndrome (NAS), the most reliable method of determining the extent of drug use in pregnancy is maternal history as part of routine antenatal assessment, with a structured interview providing a greater yield than an informal interview.
    The amount of information obtained from the mother about prenatal drug exposure widely varies and may not be reliable. How the mother is questioned and the specificity of the questions are the most important factors. Maternal interviews have been reported to be the least sensitive method of identifying drug use in pregnancy when compared with maternal hair and meconium drug testing. Maternal self-report was found to underestimate in utero drug exposure by as much as 44% when compared with data from meconium analyses.[15]
    Despite concerted efforts by health care professionals to promote prenatal care, the mother may not have received such care and the delivery hospitalization may be the only opportunity to elicit information on the nature and extent of the infant's in utero exposure to drugs and alcohol. The mother's concern for her infant's health may encourage valid responses; conversely, fear of legal reprisals or loss of custody of the infant may cause the mother to deny drug use.
    The Committee on Substance Abuse of the American Academy of Pediatrics recommends obtaining a comprehensive medical and psychological history that includes specific information regarding maternal drug use as part of every newborn evaluation.[16]
    The relationship between maternal cocaine use and placental abruption is well established. Therefore, a perinatal history of abruption should alert the medical caretaker that prenatal exposure to cocaine is a possibility.

    PHYSICAL
    A thorough physical examination of the neonate should include accurate assessment of weight, length, and head circumference and a standardized assessment of gestational age. Special attention should be paid to signs of intrauterine growth retardation (IUGR), microcephaly, prematurity, congenital infection, and major and minor congenital malformations.
    Infants are suspected of having neonatal abstinence syndrome if they exhibit any of the following signs:
    • CNS dysfunction
      • High-pitched cry
      • Restlessness, with sleep duration less than 1-3 hours after feeding
      • Hyperactive reflexes
      • Jitteriness
      • Tremors
      • Hypertonia
      • Myoclonic jerks
      • Generalized convulsions
    • Metabolic, vasomotor, and respiratory disturbances
      • Sweating
      • Fever
      • Mottling
      • Frequent yawning
      • Sneezing (>3 times per interval)
      • Nasal flaring
      • Respiratory rate greater than 60 breaths per minute without retractions
      • Apnea
    • GI dysfunction
      • Excessive (frantic) sucking or rooting
      • Poor feeding
      • Hyperphagia, usually associated with poor weight gain
      • Regurgitation or projectile vomiting
      • Loose or watery stools
    • Alcohol-specific symptoms
      • Withdrawal that presents within the first 24 hours of life is reported among infants with the dysmorphic features of fetal alcohol syndrome.
      • Neonates also exhibit irritability, tremors, seizures, opisthotonus, and abdominal distention.
    • Lysergic acid (LSD) symptoms
      • The effect of LSD on the fetus is clouded by the high incidence of polydrug abuse.
      • Withdrawal symptoms manifest as hypertonia, tremors, poor feeding, and abnormal feeding patterns.
    • Other symptoms
      • Nicotine may produce withdrawal symptoms in infants, including increased excitability and hypertonicity.
      • Caffeine withdrawal includes feeding difficulties, vomiting, excessive crying, irritability, and poor sleep patterns. Onset of symptoms may occur as long as 5 days after birth and persist for weeks or months.
    The timing of onset of the symptoms gives an indication of the maternal drug abuse. Withdrawal from high levels of maternal alcohol can occur within a day or 2 of birth. Heroin has a short half-life and withdrawal also occurs within 48–72 h of birth, whereas methadone withdrawal occurs at 7–14 days.
    Different scoring systems have been developed for assessing the severity of neonatal abstinence syndrome, such as those by Finnegan, Ostrea, Lipsitz, Rivers, and the Neonatal Intensive Care Unit Network Neurobehavioral Scale (NNNS).[17, 18, 19] These are based on opiate withdrawal and may not be entirely appropriate for the infant exposed to cocaine or other drugs.
    The most widely used system is the Finnegan scoring system, in both its original and modified forms. A neonatal abstinence syndrome scoring form is shown below.
    Neonatal abstinence syndrome scoring form. Neonatal abstinence syndrome scoring form.
    The Finnegan scale assesses 21 of the most common signs of neonatal drug withdrawal syndrome and is scored on the basis of pathological significance and severity of the adverse symptoms, which sometimes requires pharmacological treatment. Despite the number of items that can be scored, it is nevertheless a relatively easy and reliable system to use once staff have been adequately trained. However, the potential for bias and subjectivity may affect the scores, and the thresholds for treatment reported in the literature vary. This scale can also be used to assess the resolution of signs and symptoms after initiating treatment.
    To obtain a daily average score, measurements are performed every 4 hours until the patient is stable. If 3 consecutive scores are equal to or greater than 8, treatment for withdrawal is started. The decision to commence treatment can depend on factors other than this score alone, including the reported exposure, the age of the infant, consideration of comorbidities that might influence the score, whether an inpatient or outpatient strategy is used, and the experience of the clinician making treatment decisions.
    The infant is best cared for in a unit with experienced personnel who can recognize problems, perform constant evaluations, and institute the necessary interventions.

    CAUSES
    Current resurgence in heroin use is associated with the introduction of a cheap, smokeable form that is comparable to crack cocaine, only more potent. Cocaine's current popularity is related to increased availability and the presence of newer, cheaper forms.
    Depression is common in reproductive age women, and continued pharmacologic treatment of depression during pregnancy may be necessary to prevent relapse. Neonates who are exposed to antidepressant medications during gestation are at increased risk to have neonatal abstinence syndrome.

    DIFFERENTIAL DIAGNOSE
    • Hyperthyroidism
    • Hypocalcemia
    • Hypoglycemia
    • Sepsis
    LABORATORY STUDIES
    Health care professionals, hospitals, and clinics have an obligation to assess newborns who exhibit signs and symptoms of drug exposure, whose mothers have been identified as probable substance users, or whose mothers have signs and symptoms of drug use.
    Clear evidence suggests that recognizing the substance exposed infant and implementing early intervention services for the child and mother are keys to minimizing the acute and long-term effects of prenatal substance exposure. Thus, even if the infant exhibits no clinically significant difficulties in the neonatal period, identification of the substance exposed infant can improve the long-term outcome.
    Specific clinical conditions for which urine or meconium toxicology testing is indicated are noted. Commonly accepted indications for toxicology analysis include no prenatal care, intrauterine growth retardation (IUGR), preterm delivery, abruptio placentae, or cardiovascular accidents in mother or child, especially in those cases in which no other reasons for poor outcome are noted.[20]
    The following studies may be necessary to prevent or diagnose cases of neonatal abstinence syndrome (NAS):
    • Radioimmunoassay and enzyme immunoassay
      • These are the most commonly used drug screens. Both are semiquantitative and highly sensitive, but enzyme immunoassay takes less time to perform and is less expensive.
      • These tests inform the clinician about the presence or absence of substance abuse, rather than quantifying the drug level, as in toxicology screens.
    • Blood tests: The usefulness of neonatal blood samples varies. Blood samples are of limited value because the window of detection is narrow because of the rapid effects of metabolism and the low concentrations of drugs present in blood.
    • Urine toxicology assays
      • Urine was traditionally the specimen of choice for neonatal drug testing, although collection is difficult. The adhesive for the collection bag causes skin irritation and frequently fails to adhere. Another disadvantage is the short detection window; urine provides maternal drug use data only for a few days prior to delivery.
      • Urine toxicology screening is useful for clinical and research purposes. Urinary excretion of metabolites may be detectable only for a few days (eg, benzoylecgonine) to a few weeks (eg, cannabinoids). One cannot expect to ascertain early pregnancy use or even relatively recent use if the metabolite concentration does not reach the detection threshold.
      • Urine is relatively easy to obtain, requires minimal preparation (provided samples are not contaminated by meconium or feces), and can be analyzed using numerous laboratory techniques. Although urine samples generally contain a higher drug concentration than serum samples, the detection of compounds depends on obtaining an appropriate sample as close as possible to birth and also depends on the timing of maternal drug ingestion prior to delivery.
      • These tests detect recent use of cocaine and its metabolites, amphetamines, marijuana, barbiturates, and opiates. Cocaine can be detected in urine 6-8 hours after use in the mother and as long as 48-72 hours after use in the newborn.
      • Detection of drugs depends on many variables, including individual drug metabolism, hydration status of the subject, route of administration, and frequency of ingestion.
      • No drugs are known to crossreact with the immunoassays for cocaine and marijuana. Several over-the-counter remedies and herbal preparations may contain ephedrine and phenylpropanolamine (recalled from US market), which can produce false-positive enzyme immunoassay test results for amphetamines. Therefore, confirmatory testing is required.
      • Immunoassay for opiates does not distinguish between codeine, morphine, or their glucuronide conjugates.
    • Meconium analysis
      • Meconium analysis is currently considered the best method for detecting drug exposure in pregnancy. It provides a wider window of detection of gestational exposure, presumably as remote as the second trimester, when drugs begin to accumulate in meconium (by direct deposition from the biliary tree or when the fetus ingests amniotic fluid).
      • Meconium analysis is reliable for detecting opioid and cocaine exposure after the first trimester and can be used to detect a range of other illicit and prescribed medications.
      • Meconium can be contaminated by infant urine, although only cocaine or opiate use within approximately 72 hours of birth is reflected.
      • False positive results occur if meconium is contaminated with urine, reflecting antepartum and perinatal exposure. Theoretically, lidocaine can cause a positive result, but a large amount is required.
      • When a meconium sample is stored at room temperature, it decreases cocaine and cannabinoid levels by 25% per day.
  • Hair analysis
    • Neonatal hair testing can also identify prenatal drug exposure. Hair begins to form at approximately 6 months' gestation; a positive result indicates use during the last trimester. Hair testing is advantageous because the specimen can be collected at any point during the first 3 months of life, after which time infant hair replaces neonatal hair.[21]
    • This method is useful in detecting narcotics, marijuana, cocaine, and cocaine-alcohol metabolites, but the technique is expensive, is not widely available, and is limited by the procedures required to quantify the very small amounts of drug present. Obtaining an adequate sample may be difficult, and recent exposure might not be detected because hair growth is slow.
    • Analysis of 1.5 cm of maternal hair reveals the maternal drug use pattern during the previous 3 months. Drug metabolites can be detected in infant hair for 2-3 months after birth

    IMAGING STUDIES
    Cranial ultrasonography is not routinely recommended, but literature is suggestive of CNS abnormalities, including hemorrhagic ischemic lesions in some drug-exposed infants.
    Evidence is insufficient to support a mandate for cranial ultrasonography in all cocaine-exposed infants. Smit et al studied 154 neonates exposed to cocaine in utero and found that none of the infants had severe abnormalities on cranial ultrasonography. Also, the detected abnormalities were not correlated with the duration or maximum amount of cocaine use. Given these findings, they recommended that routine cranial ultrasonography in this population is not warranted.[22] However, special consideration should be given to specific neuroimaging of cocaine-exposed preterm infants, infants whose head circumference falls below the 10th percentile on standardized fetal growth curves, and infants with abnormal neurologic signs, neurobehavioral dysfunction, or seizure activity.

    OTHER TEST
    A recent report has suggested that detecting drug exposure from umbilical cord tissue has similar sensitivity and specificity to meconium samples and may have some advantages over collection of meconium.[23] Testing umbilical cord tissue enables analysis to occur immediately after birth, compared with meconium testing, which is delayed as long as 3 days prior to specimen availability. Umbilical cord is easily and noninvasively collected and may reflect a long window of drug detection; however, because few studies have examined cord tissue analysis to date, interpreting results is difficult.
    Drug-exposed infants are at increased risk of acquiring infections transmitted from mothers whose lifestyles include unsafe sexual practices or intravenous drug abuse. Assessment of the mother who abuse drugs and their infants forhepatitis B and hepatitis C and sexually transmitted diseases including human immunodeficiency virus (HIV) should be incorporated into the prenatal care setting and delivery hospitalization.

    MEDICAL CARE
    The large number of infants who suffer from neonatal abstinence syndrome (NAS) and the associated long-term morbidity mandate that affected infants be accurately identified and their treatment and support should be optimized.
    • The assessment and management of neonatal abstinence syndrome pose difficulties for staff and families and have been hampered by a lack of prospective studies and by few research studies that specifically assess the merits of one management approach over another.
    • Vomiting and diarrhea leading to dehydration and poor weight gain, in the absence of other diagnoses, are indications for treatment, even in the absence of a high drug-withdrawal score.
    • In the delivery room, naloxone use is contraindicated in infants whose mothers are known to be dependent on opioids because of the risk of neonatal seizures from abrupt drug withdrawal. However, in the absence of a specific history of opioid abuse in a mother who has recently received narcotics, naloxone treatment remains a reasonable option in the delivery room management of a depressed infant if the infant continues to demonstrate respiratory depression after positive pressure ventilation has restored normal heart rate and color.
    • Primary treatment of neonatal symptoms related to prenatal substance exposure should be supportive because pharmacologic therapy can prolong hospitalization and exposes the infant to additional agents that are often not necessary. The treatment for morphine administration has been reported to last 8-79 days.[24] This length of hospitalization interferes with maternal bonding, has potential for nosocomial infection, and is a major use of resources.[25]
    • Pharmacotherapy for infants with more severe expression of neonatal abstinence syndrome is necessary to allow them to feed, sleep, gain weight, and interact with care givers. Approximately 30-91% of infants who exhibit signs of neonatal abstinence syndrome receive pharmacological treatment.

      Nonpharmacologic approaches include the following:
      • Assess daily for signs of withdrawal, including sleeping habits, feeding patterns, and weight gain.
      • Reduce the degree of ambient light exposure, minimize excessive noise, avoid unnecessary handling, and provide swaddling for settling.
      • Provide frequent small feeds of hypercaloric formula




MEDICATION SUMMARY
Medications used in patients with neonatal abstinence syndrome (NAS) should be considered when supportive measures fail to ameliorate the infant's withdrawal. This may be manifested early on as difficulty with feeding, extreme irritability, and poor sleeping. If a scoring system is used, pharmacological treatment is commonly started when the average of 3 scores is 8 or more on the Finnegan scale[17] or 4 or more on the Lipsitz scale.
The optimal treatment for neonatal abstinence syndrome has not been established. This is reflected in the considerable heterogeneity in the pharmacologic treatment of neonatal abstinence syndrome among different institutions. Many pharmacological agents have been used to treat neonatal abstinence syndrome. However, few randomized trials have compared the efficacy of the various pharmacological treatments. For opioid related neonatal abstinence syndrome, morphine and methadone are given as substitutes. Nonmorphine treatments (eg, phenobarbital, chlorpromazine, diazepam, clonidine) provide symptomatic relief.
Agthe et al studied 80 infants who were exposed in utero to methadone or heroin and subsequently had neonatal abstinence syndrome to determine if oral clonidine would reduce the duration of opioid detoxification.[26] Each infant received oral diluted tincture of opium (dosage according to standardized algorithm) and also either oral clonidine (1 mcg/kg every 4 h) or placebo. Duration of opioid therapy was measured. Median length of therapy was 27% shorter in the clonidine group (11 d) compared with placebo (15 d).
Seven infants in the clonidine group required restarting opium after initial discontinuation, compared with none in the placebo group, although the total length of treatment was significantly less in the clonidine group. Higher opium doses were required by 40% of infants in the placebo group compared with 20% in the clonidine group. Treatment failures occurred in 12.5% of the infants in the placebo group compared with none in the clonidine group. The addition of clonidine to standard opioid therapy reduced the duration of pharmacotherapy for NAS.
A US survey reported that opioid medications are the most commonly used medications for the treatment of both opioid and polydrug withdrawal.[27]Diluted tincture of opium is recommended by the American Academy of Pediatrics for the treatment of neonatal abstinence syndrome due to opioid withdrawal.[28] Diluted tincture of opium is a 25-fold dilution of deodorized tincture of opium. Deodorized tincture of opium is equivalent to anhydrous morphine 10 mg/mL, whereas diluted tincture of opium is equivalent to anhydrous morphine 0.4 mg/mL. As a tincture, opium contains a high amount of alcohol. Diluted tincture of opium (Paregoric) contains 45% alcohol. The Institute for Safe Medication Practices considers this a high alert medication because of the confusion if abbreviated as DTO because the abbreviation could mean deodorized or diluted tincture of opium.
Many neonatal units use proprietary oral or intravenous morphine solutions, and methadone is also used. A recent study showed chlorpromazine to be efficacious, with no adverse effects in neonates with neonatal abstinence syndrome and shorter treatment time when compared with morphine. A large multicenter trial was recommended by the author to confirm the safety and efficacy of chlorpromazine.[29]
Buprenorphine is the first prescription drug approved under the 2000 US Drug Addiction Treatment Act for office based treatment of addiction to narcotics.[30] Buprenorphine has numerous characteristics that make it an attractive agent in the treatment of neonatal abstinence syndrome. Buprenorphine has a ceiling effect for respiratory depression. It does not have the cardiovascular liability associated with methadone and has an established safety profile in adults. Finally, abuse liability is limited, which makes consideration of outpatient treatment for neonatal abstinence syndrome a possibility for carefully screened caregivers. A pilot study showed that the treatment of neonatal abstinence syndrome with sublingual buprenorphine is feasible, has acceptable safety margin, and may represent a novel treatment.[31]
Currently, many infants are exposed to polydrug abuse. Unfortunately, evidence from randomized studies is insufficient to determine the best management for these patients. In 2 randomized trials, phenobarbital (rather than diazepam or paregoric) was best at controlling symptoms in infants exposed to polydrugs. The results of another study suggested that the combination of phenobarbital with diluted tincture of opium may be more effective than diluted tincture of opium alone because the combination was associated with a shorter hospital stay.[23]
DRUGS
hese drugs have a long half-life and can be orally administered, allowing for the neonate to be discharged and treated as an outpatient.
Disadvantages include lack of effect on GI symptoms and ineffectiveness in treating seizures secondary to withdrawal. In addition, antiepileptics contain 14-25% alcohol, and larger doses are required to achieve the desired effect.


 
Phenobarbital (Luminal)

Interferes with transmission of impulses from thalamus to cortex of brain. Used as a sedative. Irritability and insomnia are controlled. Available in PO and IV preparations.

OPIATE
These agents are the mainstay of treatment for opiate withdrawal, either alone or in combination with other medications. These agents are CNS depressants with advantages that include oral administration, mild sedation that improves the effectiveness of sucking, and effectiveness in treating seizures secondary to opiate withdrawal.


 
Morphine sulfate (Roxanol, Astramorph PF)

PO solutions are available in concentrations of 2 mg/mL, 4 mg/mL, and alcohol-free 20 mg/mL. Administered to neonates as diluted PO solution containing 0.4 mg/mL.
Bioavailability is 20-40% when administered orally. Elimination half-life is approximately 9 h. Recommended that Neonatal Abstinence Scoring System be used to guide treatment management of NAS.


 
Methadone

Long-acting narcotic analgesic. PO bioavailability is 50%, with peak plasma levels obtained in 2-4 hours. Serum half-life ranges from 16-25 hours in neonates and is prolonged in patients with renal failure. Available as PO solutions in 1-mg/mL and 2-mg/mL concentrations containing 8% alcohol and 10-mg/mL alcohol-free solution.

SOURCE :
http://emedicine.medscape.com
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