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Transcript
Neonatal Abstinence Syndrome
MENU
Introduction
Incidence and risk factors
1. Risk factors for illicit drug use
2. Risk factors for adverse pregnancy outcomes
3. Risk factors for neonatal abstinence syndrome
Consequences
1. Tobacco
2. Alcohol
3. Amphetamines
4. Cocaine and derivatives
5. Marijuana
6. Opiates
7. Polydrug use
Diagnosis
1. Drug use in pregnancy
2. Testing of newborns
3. Diagnosis of withdrawal
Interventions
1. Antenatal care
a. Treatment of pregnant users of illicit drugs
b. Smoking in pregnancy
c. Support from caregivers for pregnant women abusing drugs
2. Postnatal care
3. Pharmacological treatment
a. Opioid withdrawal: MORPHINE REGIMEN
b. Non-opioid CNS depressants: PHENOBARBITONE REGIMEN
c. Management of the vomiting baby
Discharge
The Drug use in pregnancy team
Infant protection issues
Follow-Up
Keypoints
References
Introduction:
Pregnant women using drugs have the same anxieties and expectations as other pregnant women. All
women using drugs are entitled to accurate information, and to be treated sensitively in a non-judgmental
manner.
Maternal illicit drug use is a risk factor for adverse pregnancy and neonatal outcomes including preterm
birth. Infants born to mothers using illicit drugs (and alcohol and tobacco) are at risk of the toxic effects of
the drugs both in-utero and ex-utero; adverse pregnancy and neonatal outcomes related to the poor
socioeconomic situations and lifestyle factors associated with illicit drug use; neonatal drug withdrawal; and
the subsequent poor outcomes of infants reared in a socioeconomically disadvantaged environment.
The Report of the US Preventative Services Task Force 1996 1 and the monograph review by Bell and Lau
2 1995 are used as background for the content of this guideline.
Incidence and risk factors:
The incidence of illicit drug use appears to be on the increase in the Australian National Drug Strategy
Household Survey (NDSHS 1998) 3 with nearly 50% of people reporting having used an illicit drug in their
lifetime and > 20% reporting use in the last 12 months. Drugs used by pregnant women (% of pregnant
women surveyed) included alcohol (73.1%), tobacco (25.9%), marijuana (17.2%), and injected illegal drugs
(1.3%).
1. Risk factors for illicit drug use: The prevalence of illicit drug use in pregnancy is highest among
mothers who smoke and drink, are unmarried, are not working, who have public or no health
insurance, who live in urban areas, or receive late or no prenatal care 1 . The Australian NDSHS 3
found that unemployed persons, persons with low educational qualifications, persons working in blue
collar jobs, and persons who were never married were more likely than others to be using drugs.
2. Risk factors for adverse pregnancy outcomes: Adverse pregnancy and neonatal outcomes may
be associated with a variety of illicit drugs. However, much of the contribution to these outcomes
may be the result of problems associated with drug use, including the use of alcohol or cigarettes,
poverty, poor nutrition and inadequate prenatal care 1 . Infections associated with intravenous drug
use also have an impact on the mother and infant. The incidence of hepatitis C virus infection (antiHCV positive) in a cohort of 131 pregnant women from the methadone clinic at RPA Hospital was
95% (125/131). None of the women were positive for HIV antibodies. Of 61 women followed up, 38
(62%) had evidence of past hepatitis B infection (HepBcAb positive) 4 .
3. Risk factors for neonatal abstinence syndrome: Withdrawal symptoms in the neonate may occur
as a result of a variety of drugs including opiates, cocaine and derivatives, amphetamines, and
alcohol 2 . With less certainty, abnormal neurobehavioral patterns have also been reported in
newborn infants of mothers with high intakes of caffeine 5 , cigarettes, marijuana 1 and volatile
substances6 .
Studies have found conflicting results in their ability to relate methadone dose and severity of
withdrawal 2 . Withdrawal appears to be greater in infants born to mothers on higher doses of
opiates7, 56 . Withdrawal is less severe in infants of mothers taking less than 20-mg methadone a
day8 . Withdrawal from heroin usually occurs earlier (within 24 hours of birth) and is less severe
than from methadone (usually 2 to 7 days after birth) 2 .
Consequences:
The consequences of drug use in pregnancy may be a result of the direct toxic or teratogenic effect of the
drug on the fetus, drug withdrawal or toxicity in the neonate, or the lifestyle and maternal health issues that
are associated with illicit drug use. The following reviews the consequences of abuse of six of the most
commonly used drugs in pregnancy.
1. Tobacco: infants of mothers who smoke weigh less on average than infants of non-smoking
mothers in direct proportion to the number of cigarettes smoked. An increased rate of fetal loss 9,
10, 11 and prematurity 12 have been documented in pregnancies of mothers who smoke although
the effect was not significant in all studies 10 . Pregnant women who stop smoking in the first
trimester have babies that are of comparable size to non-smoking mothers 12
The long-term effects of prenatal cigarette smoking remain unclear 2 . Infants of parents who smoke
are at increased risk of SIDS 13, 14, 15, 16 .
2. Alcohol: The Fetal alcohol Syndrome consists of prenatal and/or postnatal growth restriction, CNS
involvement, and specific craniofacial dysmorphic features2, 17, 18 . Excess alcohol use in
pregnancy is associated with second trimester abortion and infants with FAS have a high incidence
of premature delivery 2 . Subtle neurobehavioral changes have been observed in infants of mothers
who were moderate to heavy drinkers in pregnancy 2 . Population based studies have cast doubt on
the relationship between light alcohol consumption during pregnancy and subsequent abnormal
neurodevelopment in the infant19, 55 .
3. Amphetamines: Infants born to mothers using low dose therapeutic amphetamines have not had
any abnormalities 20 . Decreased head circumference, length, birth weight, increased rates of
abruption, prematurity and growth restriction have been reported in pregnancies of mothers abusing
amphetamines 2 . In utero amphetamine exposure may lead to intracranial lesions including
haemorrhage, infarction and cavitatory lesions 21 .
4. Cocaine and derivatives: Adverse pregnancy and neonatal outcomes have been reported in
mothers using cocaine during pregnancy 2, 21, 22 . However, a meta-analysis of studies examining
the effect of cocaine use in pregnancy on pregnancy outcomes found that the independent effect of
cocaine on adverse outcomes of cocaine was small, and that similar effects were seen in polydrug
users whether or not they used cocaine 23 . A meta-analysis examining the association between
Sudden Infant Death Syndrome suggests that SIDS appears to be more common in cocaineexposed infants although, again, the risk was similar to that of polydrug users 24 .
5. Marijuana: use of marijuana in pregnancy does not appear to increase the risks of obstetric
complications 25 . It has been associated with reduced birth length and low birth weight. No
consistent morphological abnormality has been found in infants of mothers who use marijuana.
Subtle neurobehavioural abnormalities have been described in infants whose mothers are heavy
users of marijuana although the relationship remains unproven 2 .
6. Opiates: there has been no documented increase in incidence of congenital abnormalities in infants
of opiate using mothers. However, increases in the incidences of sexually transmitted diseases, low
socioeconomic status, poor environment and family instability have been reported in opiate using
women, and hyperbilirubinaemia in the infants of opiate using women 2 .
Withdrawal from maternal opiate use is present in 42-68% of infants of heroin users, and 68-85% of
methadone exposed newborns. Withdrawal from heroin typically starts within 24 hours of birth, whilst
methadone withdrawal usually occurs between 2 and 7 days after birth. A subacute withdrawal may
persist for 4-6 months2 .
Seizures have been documented in 7.8% of infants born to mothers on methadone and 1.2% of
infants born to mothers using heroin 26 .
In a population based cohort study 27 , Kandall found after controlling for known associated highrisk variables, the risk ratio for SIDS in each individual drug group (methadone, 3.6; heroin, 2.3;
methadone and heroin, 3.2; cocaine, 1.6; cocaine and methadone or heroin, 1.1) was higher than in
the non-drug-exposed group.
7. Polydrug use: Users of illicit drugs frequently use more than one drug. In a study of 267 Australian
women undergoing treatment for alcohol or drug use, polydrug use was the norm 28 . Meta-analysis
of studies suggests that polydrug users have an increased risk of abnormal pregnancy outcomes 23 ,
and the infants of polydrug users have an increased risk of SIDS 24 .
Diagnosis:
1. Drug use in pregnancy: The initial diagnosis of drug use and dependence is made by a careful
diagnostic interview. Important information includes the quantity, frequency, and pattern of drug use;
adverse effects of drugs on work, health and social relationships; and any symptoms of dependence
1 . Although a careful history is potentially a sensitive means of detecting drug use and abuse 29, 30
, a history of self-reported drug use identified only 40-60% of pregnant women with positive urine
tests for drugs in US studies 31 . Our experience at RPAH is that it is uncommon for an infant to
have a significant withdrawal without a clinical history of drug or methadone use in pregnancy.
2. Testing of newborns: As compared with a maternal history of drug use, radioimmunoassay (RIA)
of urine has a sensitivity of 52% and RIA of meconium has a sensitivity of 88% for identifying infants
exposed to drugs 30 .
The testing of pregnant mothers and their newborns should be weighed against the rights of
the patient to privacy and autonomy, as well as the potential for adverse effects on
employment, insurance coverage and personal relationships if confidentiality of the results is
lost 1 . In general, a sensitive and thorough history is the mainstay of diagnosis. Testing
should be limited to situations of diagnostic uncertainty and should preferably performed
with the consent of the mother.
Persons who use intravenous drugs should be periodically screened for HIV, hepatitis B and
hepatitis C.
3. Diagnosis of withdrawal: neonatal abstinence syndrome is scored using an NAS score chart (a
modified Finnegan Scoring System) 32 . Infants scoring 3 consecutive abstinence scores averaging
more than 8 (eg 9-7-9) or ³ 12 for 2 scores should be treated as detailed below. The scoring interval
should be 4 hourly until the infant has been stabilised. Infants withdrawing from non-opiates
frequently display similar behaviours to those withdrawing from opiates.
Withdrawal symptoms from opiates include:
Central nervous system: tremors, irritability, sleep disturbance,
Respiratory system: tachypnoea, nasal flare, chest recession,
Autonomic nervous system: sneezing, yawning, fever, sweating,
Gastrointestinal system: poor feeding, vomiting, diarrhoea.
Measuring movement: a commercially available movement sensor with a high level of
accuracy for prediction of need for treatment for NAS (sensitivity 92%, specificity 89%) is
currently under evaluation at RPAH 33
Interventions:
1. Antenatal care:
Management of women using illicit drugs and their infants is by community based services. The
Drug Use in Pregnancy Service (DIPS) at Royal Prince Alfred Hospital co-ordinates the care of the
women in pregnancy, the mother and infant after birth and ensures continuity with community based
services.
Continuity of obstetric and midwifery care 34 , and support from counselors35 is essential for
effective management of substance abuse around pregnancy.
Treatment of pregnant users of illicit drugs: There are few controlled trials to guide interventions
for pregnant women who use illicit drugs. Observational studies suggest that increasing the number
of prenatal visits reduce the risk of low birth weight 1 . Methadone maintenance is the usual
treatment for pregnant women addicted to opiates, as withdrawal during pregnancy is potentially
dangerous 1 , and pregnant women in a supervised methadone program have better outcomes than
women in unsupervised programs or using street heroin or polydrug users 36 . However, methadone
prolongs withdrawal in the infant. Infants whose mothers are on less than 20 mg/day of methadone
tend not to have a significant withdrawal 8 . This should be weighed against the increased risk of
intravenous and other drug use if the woman is not on an adequate and stable dose of methadone.
Tapering the methadone dose compared to methadone maintenance has not been trialled in
pregnant women but results in increased use of heroin in non-pregnant opiate users37 .
All pregnant women should be advised about the potential risks to themselves and the fetus of drug
use during pregnancy. A treatment plan should be developed that is tailored to the drug of use and
the needs of the patient. Withdrawal of opiates in pregnancy may be harmful to the fetus and the
woman should be stabilised on methadone 1 .
Persons who continue to use intravenous drugs should be advised to use a new sterile syringe with
each use, never to share or re-use equipment, use clean water to prepare drugs, to clean the
injection site with alcohol prior to injection, and safely dispose of the syringes after use 1 .
Smoking in pregnancy: Obstetricians and midwives should ensure that information on self-help
behavioural strategies for quitting smoking, prepared specifically for pregnant women, are available
and accessible to all women in their care 38 . Smoking cessation programs in pregnancy appear to
reduce smoking, low birthweight and preterm birth, but no effect was detected for very low
birthweight or perinatal mortality. Behaviourally orientated programs such as the QUIT program are
cost effective 39 .
Support from caregivers for pregnant women abusing drugs: Clinics that offer continuity of care and
which are sensitive to the social circumstances and needs of their clients have no known risks and
may have important benefits for low-income mothers and their children 40 . The DIPS team at King
George V Hospital is integrated into the obstetric antenatal clinics. Women using opiates are referred
to the Drug and Alcohol Service Methadone Clinic for stabilisation on methadone.
2. Postnatal care
An attempt should be made to identify women using potentially harmful drugs antenatally. Discussion
of postnatal care can commence before the infant is born. All mothers using illicit drugs in pregnancy
and their infants should be referred to the DIPS team.
NAS can produce a major disruption to mother infant attachment. Unnecessary separation of mother
and infant should be avoided. Mothercraft techniques such as swaddling, settling, massage,
relaxation baths and dummies can assist in settling babies and reassuring mothers. Nonpharmacological interventions shown to reduce symptoms in infants with NAS include maternal
education teaching comforting and interacting techniques 41 . Although waterbeds have been shown
to comfort the infant 42 , they are associated with an increased risk of SIDS 43 . Use of rocking
beds results in overstimulation of the infant 44 .
Regular post-natal care includes:
Diagnosis of withdrawal: neonatal abstinence syndrome is scored using an NAS score chart
(a modified Finnegan Scoring System) 26 . Infants scoring 3 consecutive abstinence scores
averaging more than 8 (eg 9-7-9) or ³ 12 for 2 scores should be treated as detailed below.
The scoring interval should be 4 hourly until the infant has been stabilised.
Transfer to the nursery if NAS score ³ 8 for 3 scores, or ³ 12 for 2 scores. Further scoring in
nursery is usually appropriate to confirm high scores are due to NAS. Transfer back when
stabilised (scores < 8 for 24 hours).
Education of mother to administer morphine once infant has settled.
Daily assessment for signs of withdrawal, adequacy of feeding, adequacy of weight gain (or
severity of weight loss), assessment of mothercraft abilities of mother and monitoring for signs
of continued drug use.
Teaching mothers comforting and interaction techniques for use with their infants.
Infants should be weighed on day 5 and 2 nd daily thereafter.
Encouragement of breastfeeding if the mother is stable on methadone. Breastfeeding is
discouraged if the mother is on heroin or other sedatives and stimulants.
Liaison with DIPS social worker and nursing staff concerning social situation and need for
DOCS referral.
Hepatitis B vaccine before discharge, or hepatitis B vaccine and immunoglobulin within 72
hours of birth if HepBsAg positive. Hepatitis C is not a contraindication to breast- feeding and
women with hepatitis B may breast feed once their infant is vaccinated and given
immunoglobulin.
3. Pharmacological treatment
If a baby at risk of NAS has 3 consecutive abstinence scores averaging more than 8 (eg 9-7-9), or ≥ 12
for 2 scores , treatment as detailed below should be commenced and the scoring interval should be 4
hourly until the infant has been stabilised.
Opioid withdrawal: If mother uses opioid drugs (e.g. methadone, heroin, and pethidine) +/- other central
nervous system depressant drugs, morphine is the drug of choice. Morphine has been shown in a
randomised-controlled trial to be better than phenobarbitone at preventing seizures in infants with opiate
withdrawal 45 , although it does increase the time infant stays on treatment 46 .
MORPHINE REGIMEN
Pharmacy prepares morphine as a 0.5mg /ml aqueous solution.
NAS score (score every 4 hours)
Action
Score averages ≥ 8 for 3 scores
Morphine 0.5 mg/kg/day in 4 divided doses orally
If score persists ≥ 8 despite morphine 0.5
mg/kg/day
Morphine 0.7 mg/kg/day in 4 divided doses orally
If score persists ≥ 8 despite morphine 0.7
mg/kg/day
Morphine 0.9 mg/kg/day in 4 divided doses orally
When infants are on 0.9 mg/kg/day
Monitor cardiorespiratory function
After scores fall below treatment level for 48 hrs, the dose should be reduced by 0.1ml (0.05 mg) per dose
every 4 days or longer, depending on the scores. The usual length of morphine treatment is 1-2 months.
Cardiorespiratory monitoring should continue for 4 days or until dose is reduced.
Management of the vomiting baby: ensure that the infant is not being overfed and that the infant is being
appropriately postured during and after feeding. Give the morphine before the feed. If baby has a large
vomit after being given morphine:
if vomits within 10 minutes of dose, re-dose,
if vomits after 10 minutes, give ½ dose,
if baby vomits after feed, do not give further morphine (always err on side of caution).
Non-opioid CNS depressant withdrawal: If the mother does not use opioid drugs but central nervous
system depressants (e.g. benzodiazepines, barbiturates, and alcohol) phenobarbitone is the drug of choice.
PHENOBARBITONE REGIMEN
NAS score (score every 4 hours)
Action
Score averages ≥ 8 for 3 scores
Phenobarbitone 15 mg/kg oral or IMI stat, then 6
mg/kg/day in 2 divided doses orally
If score persists ≥ 8 despite phenobarbitone 6
mg/kg/day
Phenobarbitone 8 mg/kg/day in 2 divided doses
orally
If score persists ≥ 8 despite phenobarbitone 8
mg/kg/day
Phenobarbitone 10 mg/kg/day in 2 divided doses
orally
When infants are on 10 mg/kg/day
Monitor cardiorespiratory function
For barbiturate withdrawal, after scores fall below treatment level for 48 hours the dose should be reduced
by 2mg per dose every 4th day or longer depending on scores. For non-barbiturate withdrawal (eg
benzodiazepines), the dose may be reduced more rapidly after withdrawal symptoms settle.
Discharge:
All mothers and infants should be assessed adequately prior to discharge by the DIPS team with respect to
current drug usage and psychological stability, mothercraft abilities, social situation and the infants
wellbeing.
Infants should not be discharged if:
Absolute:
Excessive weight loss (≥ 10% of birth weight),
Before day 5 of life,
Suspected infant neglect or abuse,
Suspected home violence.
Relative:
Poor mothercraft ability of mother, and inadequate home support or acceptance of assistance,
Erratic behaviours or continued intravenous and illicit drug use,
Polydrug use.
Inability of team to monitor welfare of infant.
Mothers on high doses of methadone or other drugs should be discouraged from going home early,
since their babies could withdraw at home. If such mothers insist on going home against medical
advice, a DOCS notification should be considered.
The neonatal consultant on call must be notified, if parents are threatening to take
their baby home with any of the above contraindications to discharge. It will
usually be appropriate to admit the baby to SCBU for ongoing withdrawal
observations, either voluntarily or with support from a DOCS intervention.
Home visiting and early intervention:
Home intervention in high risk families has been demonstrated to improve long term health and
psychosocial outcomes in the families and children 47, 48, 49, 50, 51, . Interventions started in pregnancy,
continued to 2 years of age, used home visiting and provided continuity of care. Although promising, studies
to date have not shown unequivocal benefits of home intervention of families using illicit drugs 52, 53 . In
view of the high risk and poor follow up rates of these families, further research is needed.
Early intervention in high risk populations using daycare intervention in preschool children dramatically
improves children's IQ, has beneficial effects on behavioural development and school achievement. Longterm follow up demonstrates increased employment, lower teenage pregnancy rates, higher socioeconomic
status and decreased criminal behaviour. There are positive effects on mothers' education, employment and
interaction with children. 54 .
The Drug Use in Pregnancy Service (DIPS)
Drug and alcohol services for pregnant women are almost entirely provided by the Drugs in Pregnancy
Service based at the King George V Hospital. The DIPS was the first specialist service for drug dependent
women in New South Wales, established at the Crown Street Womens Hospital in 1979 and subsequently
transferred to the King George V Hospital. The service now functions as a statewide tertiary level referral
and advisory service on drug use in pregnancy.
The current DIPS Team operates according to principles of harm minimisation and offers assessment and
follow-up to all drug-using women who are pregnant or recently delivered. Patients receive assessment and
ongoing review of their drug use problems in combination with antenatal care.
We believe that early referral enables appropriate interventions outlined by best practice models and
accounting for individual patient needs to be instituted with full awareness of the patient.
The DIPS offers assessment and follow-up of infants born with neonatal abstinence syndrome (NAS)
through its morphine clinic, a clinic established to monitor clinical progress of babies on morphine treatment
for opioid withdrawal. It is also accessible to clients of the DIPS whose babies do not develop NAS.
The Drug Use in Pregnancy Team consists of:
A DIPS Social Worker,
Paediatrician specializing in drug usage in pregnancy and the care of infants with neonatal
abstinence syndrome,
Nursing staff of K7W nursery and K7W postnatal ward,
Neonatal early discharge team (NEDP)
Nursing staff from Drug Health Services, CSAHS.
Community Representation from early childhood centers, DoCS, and treatment providers and
community programs specializing in the treatment of drug dependencies where appropriate.
Infant protection issues: Go to separate guideline
DOCS HELPLINE - 24 HOURS:
MANDATORY REPORTERS: 133627
GENERAL PUBLIC: 1332111
Follow-Up Neonatal Abstinence Syndrome (NAS)
Clinic:
Criteria for follow up:
All infants on morphine,
Infants of mothers on methadone,
Infants of mothers using frequent illicit drugs in pregnancy, and
Any mother and her infant with significant social or mothercraft problems on a case by case basis.
The clinic consists of the Paediatrician specialising in drug use in pregnancy and the care of infants with
the neonatal abstinence syndrome and the DUiP team social worker. Appointments are on Thursday
afternoons and can be made by contacting the secretary on 02 9515 8760. The clinic provides the following
service:
Weekly examination of infant for signs of withdrawal, adequacy of weight gain and signs of neglect,
Ensuring adequacy of mothercraft practices,
Addressing all concerns of mother and family,
Counseling by doctor and/or DUiP team social worker,
Discussion of implications and management of hepatitis C status,
Attending to the 6 week baby check,
Referral to community services where appropriate,
Discharge from the clinic when the infant is stable, off morphine, and there are no further concerns
for the welfare of mother and infant.
Key Points
Key Points
Level of Evidence
Drug use in pregnancy may be associated with adverse pregnancy and
neonatal outcomes
23
Where appropriate, informed consent should be obtained when performing
drug screens
1
All pregnant women should be counseled about the potential risks of drug
use in pregnancy
1
Pregnant women reporting the use of potentially harmful drugs in
pregnancy should be informed of the risks and encouraged to stop or cut
down
1
Pregnant women using opiates should be stabilised on methadone
36
Patients with evidence of drug dependence should be referred to
appropriate drug treatment providers and community programs specialising
in the treatment of drug dependency
1
Patients injecting intravenous drugs should be counseled as to the risks of
infection and in methods for preventing infection
1
Infants exposed to opiates, cocaine, amphetamines and alcohol may suffer
from a neonatal abstinence syndrome
Infants, of mothers using opiates, with an NAS score averaging ³ 8 on 3
occasions should be treated with morphine in preference to
phenobarbitone
1, 2
45, 46
References
1. Drug abuse. In: Report of the US Preventative Services Task Force. Guide to clinical preventative
services, 2 nd ed. Baltimore: Williams and Wilkins, 1996; 583-594.
2. Bell GL, Lau K. Perinatal and neonatal issues of substance abuse. Pediatr Clin North Am. 1995 Apr;
42(2): 261-281.
3. Adhikari P, Summerill A 2000. 1998 National Drug Strategy Household Survey: Detailed findings. AIHW
cat. no. PHE 27. Canberra: AIHW (Drug Statistics Series No. 6).
4. Spencer JD, Latt N, Beeby PJ, Collins E, Saunders JB, McCaughan GW, Cossart YE. Transmission of
hepatitis C to infants of human immunodeficiency virus-negative intravenous drug-using mothers: rate of
infection and assessment of risk factors for trans mission. J Viral Hep. 1997; 4: 395-409.
5. McGowan D, Altman RE, Kanto WP Jr. Neonatal withdrawal symptoms after chronic maternal ingestion
of caffeine. South Med J. 1988 Sep; 81(9): 1092-1094.
6. Tenenbein M, Casiro OG, Seshia MM, Debooy VD. Neonatal withdrawal from maternal volatile substance
abuse. Arch Dis Child Fetal Neonatal Ed. 1996; 74(3): F204-207.
7. Malpas TJ. Darlow BA. Lennox R. Horwood LJ. Maternal methadone dosage and neonatal withdrawal.
Australian & New Zealand Journal of Obstetrics & Gynaecology. 35(2): 175-7, 1995
8. Strauss ME, Andresko M, Stryjer J, Wardell JN. Relationship of neonatal withdrawal to maternal
methadone. Am J Drug Alcohol Abuse. 1976; 3(2): 339-345.
9. Armstrong BG, McDonald AD, Sloan M. Cigarette, alcohol, and coffee consumption and spontaneous
abortion. Am J Public Health. 1992; 82(1): 85-87.
10. Harlap S, Shiono PH. Alcohol, smoking, and incidence of spontaneous abortions in the first and second
trimester. Lancet. 1980; 2(8187): 173-176.
11. Kline J, Stein ZA, Susser M, Warburton D. Smoking: a risk factor for spontaneous abortion. N Engl J
Med. 1977; 297(15): 793-796.
12. McDonald AD, Armstrong BG, Sloan M. Cigarette, alcohol, and coffee consumption and prematurity.
Am J Public Health. 1992; 82(1): 87-90.
13. Blair PS, Fleming PJ, Bensley D, Smith I, Bacon C, Taylor E, et al. Smoking and the sudden infant
death syndrome: results from 1993-5 case-control study for confidential inquiry into stillbirths and deaths in
infancy. BMJ 1996; 313: 195-8.
14. Mitchell EA, Ford RPK, Stewart AW, Taylor BJ, Becroft DMO, Thompson JMD, et al. Smoking and the
sudden infant death syndrome. Pediatrics 1993; 91: 893-6
15. McGlashan ND. Sudden infant deaths in Tasmania, 1980-1986: a seven year prospective study. Soc
Sci Med. 29: 1015-26, 1989.
16. Naeye RL, Ladis B, Drage JS. Sudden infant death syndrome. A prospective study. Am J Dis Child.
130: 1207-10, 1976.
17. Jones KL. Fetal alcohol effects. In: Smiths recognizable patterns of human malformation. 4 th ed.
Philadelphia. WB Saunders. 1988; 491-494.
18. Spohr HL, Willms J, Steinhausen HC. Prenatal alcohol exposure and long-term developmental
consequences. Lancet. 1993; 341(8850): 907-910.
19. Walpole I. Zubrick S. Pontre J. Lawrence C. Low to moderate maternal alcohol use before and during
pregnancy, and neurobehavioural outcome in the newborn infant. Developmental Medicine & Child
Neurology. 33(10): 875-83, 1991
20. Briggs GG, Samson JH, Crawford DJ. Lack of abnormalities in a newborn exposed to amphetamine
during gestation. Am J Dis Child. 1975; 129(2): 249-250.
21. Dixon SD, Bejar RJ. Echoencephalographic findings in neonates associated with maternal cocaine and
methamphetamine use: incidence and clinical correlates. Pediatr. 1989; 115(5 Pt 1): 770-778.
22. Oro AS, Dixon SD. Perinatal cocaine and methamphetamine exposure: maternal and neonatal
correlates.J-Pediatr. 1987; 111(4): 571-588.
23. Lutiger B, Graham K, Einarson TR, Koren G. Relationship between gestational cocaine use and
pregnancy outcome: a meta-analysis. Teratology. 1991; 44(4): 405-414.
24. Fares I, McCulloch KM, Raju TN. Intrauterine cocaine exposure and the risk for sudden infant death
syndrome: a meta-analysis. J Perinatol. 1997; 17(3): 179-182.
25. Richardson GA, Day NL, McGauhey PJ. The impact of prenatal marijuana and cocaine use on the
infant and child. Clin Obstet Gynecol. 1993; 36(2): 302-318.
26. Herzlinger RA, Kandall SR, Vaughan HG Jr. Neonatal seizures associated with narcotic withdrawal. JPediatr. 1977; 91(4): 638-641.
27. Kandall SR. Gaines J. Habel L. Davidson G. Jessop D. Relationship of maternal substance abuse to
subsequent sudden infant death syndrome in offspring. J Pediatr. 123(1): 120-6, 1993
28. Swift W, Copeland J, Hall W. Characteristics of women with alcohol and other drug problems: findings
of an Australian national survey. Addiction. 1996; 91(8): 1141-1150.
29. Ostrea EM Jr, Brady M, Gause S, Raymundo AL, Stevens M. Drug screening of newborns by
meconium analysis: a large-scale, prospective, epidemiologic study. Pediatrics. 1992; 89(1): 107-113.
30. Callahan CM, Grant TM, Phipps P, Clark G, Novack AH, Streissguth AP, Raisys VA. Measurement of
gestational cocaine exposure: sensitivity of infants' hair, meconium, and urine. J Pediatr. 1992; 120(5): 763768.
31. Magura S, Kang SY. Validity of self-reported drug use in high risk populations: a meta-analytical
review. Subst Use Misuse. 1996; 31(9): 1131-1153.
32. Finnegan LP, Connaughton JF Jr, Kron RE, Emich JP. Neonatal abstinence syndrome: assessment
and management. Addict Dis. 1975; 2(1-2): 141-158.
33. OBrien CM, Jeffery HE. Measuring movement a more objective, reliable and efficient method to assess
drug withdrawal in newborns. PSANZ 5 th Annual Conference. 2001;43.
34. Hodnett ED. Continuity of caregivers for care during pregnancy and childbirth (Cochrane Review). In:
The Cochrane Library, Issue 2, 2001. Oxford: Update Software.
35. Teague GB, Drake RE, Ackerson TH. Evaluating use of continuous treatment teams for persons with
mental illness and substance abuse. Psychiatric Services 1995; 46: 689-95.
36. Stimmel B, Goldberg J, Reisman A, Murphy RJ, Teets K. Fetal outcome in narcotic-dependent women:
the importance of the type of maternal narcotic used. Am J Drug Alcohol Abuse. 1982-83; 9(4): 383-395.
37. Sees KL. Delucchi KL. Masson C. Rosen A. Clark HW. Robillard H. Banys P. Hall SM. Methadone
maintenance vs 180-day psychosocially enriched detoxification for treatment of opioid dependence: a
randomized controlled trial [see comments]. JAMA. 283(10): 1303-10; 2000.
38. Lumley J, Oliver S, Waters E. Interventions for promoting smoking cessation during pregnancy
(Cochrane Review). In: The Cochrane Library, Issue 2, 2001. Oxford: Update Software.
39. Law M, Tang JL. An analysis of the effectiveness of interventions intended to help people stop smoking.
Arch Intern Med. 1995; 155(18): 1933-1941.
40. Racine A, Joyce T, Anderson R. The association between prenatal care and birth weight among women
exposed to cocaine in New York City. JAMA. 1993; 270(13): 1581-1586.
41. French ED. Pituch M. Brandt J. Pohorecki S. Improving interactions between substance abusing
mothers and their substance-exposed newborns. Journal of Obstetric, Gynecologic, & Neonatal Nursing.
27(3): 262-9, 1998.
42. Oro AS, Dixon SD. Waterbed care of narcotic-exposed neonates. A useful adjunct to supportive care.
Am J Dis Child. 1988; 142(2): 186-188.
43. Nakamura S, Wind M, Danello MA. Review of hazards associated with children placed in adult beds.
Arch Pediatr Adolesc Med 1999; 153: 1019-26.
44. D'Apolito K. Comparison of a rocking bed and standard bed for decreasing withdrawal symptoms in
drug-exposed infants. MCN, American Journal of Maternal Child Nursing. 24(3): 138-44, 1999.
45. Kandall SR, Doberczak TM, Mauer KR, Strashun RH, Korts DC. Opiate v CNS depressant therapy in
neonatal drug abstinence syndrome. Am J Dis Child. 1983; 137(4): 378-382.
46. Carin I, Glass L, Parekh A, Solomon N, Steigman J, Wong S. Neonatal methadone withdrawal. Effect
of two treatment regimens. Am J Dis Child. 1983; 137(12): 1166-1669.
47. Kitzman H, Olds DL, Henderson CR, Jr., Hanks C, Cole R, Tatelbaum R et al. Effect of prenatal and
infancy home visitation by nurses on pregnancy outcomes, childhood injuries, and repeated childbearing. A
randomized controlled trial. JAMA 1997; 278: 644-52.
48. Kitzman H, Olds DL, Sidora K, Henderson CR, Jr., Hanks C, Cole R et al. Enduring effects of nurse
home visitation on maternal life course: a 3-year follow-up of a randomized trial. JAMA 2000; 283: 1983-9
49. Olds DL, Henderson CR, Jr., Kitzman H. Does prenatal and infancy nurse home visitation have
enduring effects on qualities of parental caregiving and child health at 25 to 50 months of life? Pediatrics
1994; 93: 89-98.
50. Olds D, Henderson CR, Jr., Kitzman H, Cole R. Effects of prenatal and infancy nurse home visitation on
surveillance of child maltreatment. Pediatrics 1995; 95: 365-72.
51. Olds D, Henderson CR, Jr., Cole R, Eckenrode J, Kitzman H, Luckey D et al. Long-term effects of
nurse home visitation on children's criminal and antisocial behavior: 15-year follow-up of a randomized
controlled trial. JAMA 1998; 280: 1238-44.
52. Black MM, Nair P, Kight C, Wachtel R, Roby P, Schuler M. Parenting and early development among
children of drug-abusing women: effects of home intervention. Pediatrics 1994; 94: 440-8.
53. Schuler ME. Nair P. Black MM. Kettinger L. Mother-infant interaction: effects of a home intervention
and ongoing maternal drug use. Journal of Clinical Child Psychology. 29: 424-31, 2000.
54. Zoritch B, Roberts I , Oakley A. Day care for pre-school children (Cochrane Review). In: The Cochrane
Library, Issue 2, 2001. Oxford: Update Software.
55. Forrest F. Florey CD. Taylor D. McPherson F. Young JA. Reported social alcohol consumption during
pregnancy and infants' development at 18 months [see comments]. BMJ. 303(6793): 22-6, 1991
56. Doberczak TM. Kandall SR. Friedmann P. Relationship between maternal methadone dosage,
maternal-neonatal methadone levels, and neonatal withdrawal. Obstetrics & Gynecology. 81(6): 936-40,
1993
Last Reviewed: July 2001