Neonatal infection

Signs and symptoms of infection include respiratory distress, temperature instability, irritability, failure to thrive, and skin rashes. ==Etiologies==

Early-onset sepsis (EOS), defined as onset of symptoms within 72 hours of life, is generally caused by transmission of pathogens from the female genitourinary system to the fetus. Pathogens can infect the fetus via vertical transmission (direct transmission through the placenta in utero) or infection during delivery as fetus passes through vaginal canal. Late-onset sepsis (LOS), defined as onset of symptoms after 72 hours of life, is generally caused by transmission of pathogens from the environment after delivery. Infants requiring intravascular catheters and other invasive procedures are at increased risk for developing LOS. Bacteria Bacteria found in the maternal gastrointestinal or gastrourinary tracts can commonly lead to neonatal infection. Bacterial infections may present as fetal distress at birth (including signs of tachycardia, temperature instability or difficulty breathing), neonatal sepsis, or neonatal meningitis. Infections that develop during NICU admissions are more commonly coagulase-negative staphylococci, especially in infants with indwelling catheters. Infections that develop one month after the birth of the infant are more likely due to gram-positive bacteria and coagulase positive staphylococci. ... Group B streptococcus (GBS) Group B streptococcus (GBS), also named Streptococcus agalactiae, is a bacteria typically identified as the cause of the majority of early-onset infections in the neonate. GBS is an encapsulated gram-positive cocci that colonizes the gastrointestinal and genital tracts of pregnant women. Maternal infections are usually asymptomatic. This pathogen is vertically transmitted (transmitted directly from the mother's vagina into the infant's amniotic fluid after onset of labor). Due to the high prevalence of GBS, routine screening for the bacteria occurs during pregnancy. If the bacteria is found in the maternal GI / GU tract, mothers will receive IV antibiotic (usually penicillin or ampicillin). Escherichia coli (E. coli) Escherichia coli is an encapsulated gram-negative bacilli that may cause neonatal infections due to its high prevalence in the GI and GU tracts of pregnant patients. With the advances in preventing group B streptococcus infections, β-lactam-resistant Escherichia coli infections have increased in causing neonatal deaths in very low birthweight and premature infants. Common complications of neonatal E.coli infection include neonatal sepsis and neonatal meningitis. Neisseria gonorrhoeae Neisseria gonorrhoeae is a common sexually transmitted infection which may be present in pregnant women at time of delivery. This pathogen is usually acquired during delivery, occurring in 30-40% of cases with known maternal infection. Additionally, untreated maternal gonorrhea may increase the risk of preterm delivery. The most common manifestation of gonococcal infection in a newborn is neonatal conjunctivitis, an infection of the eyes that presents with green-yellow exudate and eyelid swelling. Without treatment, this infection can lead to permanent visual impairment. Treatment of Neisseria gonorrhoeae conjunctivitis consists of a single dose of ceftriaxone (antibiotic). Typically, all neonates (regardless of symptoms or risk factors) receive erythromycin ointment applied to both eyes after delivery Listeria monocytogenes Listeria monocytogenes is a gram-positive bacilli that can cause infection acquired from tainted food and present in the mother. The presence of this pathogen can sometimes be determined by the symptoms that appear as a gastrointestinal illness in the mother. The mother acquires infection from ingesting food that contains animal products such as hot dogs, unpasteurized milk, delicatessen meats, and cheese. Clostridium tetani Clostridium tetani can cause a generalised form of tetanus in the neonate. This usually occurs when the mother has not been vaccinated against tetanus and the baby has not acquired passive immunity. The umbilical cord region is the most susceptible. Other bacterial pathogens Less common bacterial pathogens include Streptococcus pyogenes, Viridans streptococci, Streptococcus pneumoniae, Haemophilus influenzae, and Pseudomonas aeruginosa. Viruses Human immunodeficiency virus (HIV) Human immunodeficiency virus (HIV) infection can occur during delivery of the neonate, in utero through mother-to-child transmission or postnatally by way of breastfeeding. Most transmission occurs during delivery. Transmission depends on multiple risk factors, usually centered around the viral load of HIV in the mother. Strategies for reducing transmission of HIV include: • Anti-retroviral therapy during pregnancy, reducing amount of HIV virus in the maternal bloodstream • Delivery by caesarean section in mothers with plasma viral load > 1000 copies / mL • Using prophylactic anti-retroviral therapy in the newborn infant, especially in mothers with high viral loads • Avoiding breast-feeding Symptoms of HIV in a child will vary depending on the age of presentation. Common symptoms include failure to thrive, recurrent infections such as pneumonia, intermittent diarrhea, swollen lymph nodes and oral thrush. In infants, diagnostic testing for HIV relies of detection of the virus in the bloodstream. For infants born to HIV-infected mothers, diagnostic testing will be performed within days of delivery, at 1–2 months and at 4–6 months of age. Cytomegalovirus (CMV) Cytomegalovirus (CMV) is the most common congenital viral infection, usually transmitted through the placenta during pregnancy. Most neonates with congenital CMV infection will not have any symptoms, but a minority of infected newborns will have symptomatic infection. Common symptoms include rash, microcephaly (small head), low birth weight, jaundice, thrombocytopenia, seizures and retinitis. Long-term complications of congenital CMV infections may include sensorineural hearing loss, developmental delay, and seizures. Due to high prevalence of disease, CMV is not routinely screened in pregnant patients. Herpes simplex virus (HSV) Herpes simplex virus (HSV), which commonly causes cold sores and painful genital blisters can cause congenital infection via direct contact with genital tract lesions during delivery. Neonatal HSV may be classified into three categories based on symptom presentation: • Localized skin, eye and mouth disease: 35–45% of neonatal HSV infections. Presentation includes clustering vesicular lesions (blister-like) with erythematous (skin redness) base in localized area of skin which can spread to the eye or oropharynx. There is risk of progression to CNS or disseminated disease, so infants should be thoroughly evaluated for progression of symptoms. • CNS disease: 30% of neonatal HSV infections. HSV spreads into the brain, leading to seizures, lethargy, irritability, poor feeding, temperature instability within the first six weeks of life. Diagnosis of CNS disease can be made with cerebrospinal fluid analysis or electroencephalogram (EEG) showing lateralized periodic discharges. It can be difficult to distinguish between HSV CNS disease and other causes of neonatal meningitis; therefore, it is recommended to start empiric acyclovir in all cases of neonatal meningitis. • Disseminated disease: 25–30% of neonatal HSV infections. Disease is defined by multi-organ involvement, including liver, lungs CNS, heart, kidney, GI tract, and skin. Neonates with disseminated HSV infection present with nonspecific symptoms of neonatal sepsis. All infants with signs of neonatal sepsis should undergo testing for HSV and empiric antiviral therapy. Rubella Maternal infection with rubella virus during pregnancy can lead to congenital rubella syndrome. The risk of congenital infection is highest during the first trimester (< 12 weeks). Risk of congenital rubella is increased among immigrant women from countries without adequate vaccination programs. Common symptoms include cataracts, hearing impairment, developmental delay and congenital heart disease. Zika Zika virus is an arthropod-borne virus transmitted by mosquitos, and infection during pregnancy can lead to severe congenital abnormalities in a newborn. Congenital infection can lead to fetal growth restriction and CNS abnormalities, including microcephaly, ventriculomegaly and intracranial calcifications. Hepatitis There are five liver specific viruses (hepatitis A, B, C, D, E) that could potentially harm the mother and child. Acute hepatitis A virus or acute hepatitis E virus infection present the greatest risk to maternal and fetal health and increased risk of adverse pregnancy outcomes. Hepatitis B, C and D virus present a risk of mother to child transmission but are dependent on the severity of the underlying disease in the mother. However, hepatitis B virus is the major cause of neonatal infection. • Hepatitis A is a non-enveloped, single-stranded RNA virus that is spread through the fecal-oral route with the main modes of transmission being close personal contact or ingestion of contaminated food or water. During pregnancy, hepatitis A can cause placental abruption, premature rupture of membranes, and increased rates of preterm labor. • Hepatitis C is an enveloped, single stranded RNA virus that is spread by exposure to blood, with the main modes of transmission are blood, sexual transmission, or perinatal. Chronic infection with hepatitis C virus may influence pregnancy outcomes, such as increased rates of small for gestational age, intrauterine death, low birthweight, and preterm delivery, but no clear association between these adverse outcomes and hepatitis C infection have been observed. There is also an increased risk of mother to child transmission and is largely attributable to events during the birth process. Protozoans Infants born with malaria can be infected with a variety of species; Plasmodium vivax, Plasmodium malariae, Plasmodium ovale, and Plasmodium falciparum. In most instances of congenital malaria is caused by P. vivax and P. falciparum. Women living in areas where malaria is prevalent and common are repeatedly exposed to malaria. In response to maternal infection, mothers develop antimalarial antibodies. It is probable that the antibodies present in the mother offers protection for the baby. Bacterial infection can develop with malaria. == Risk factors ==

Preterm neonates are at greater risk of infection, including severe complications such as sepsis and meningitis. Preterm neonates usually have ineffective immune systems, due to decreased IgG antibodies and decreased complement activation. Additionally, preterm neonates require longer hospital admissions, including the placement of invasive devices that increase risk of infection. Maternal risk factors for neonatal infection include: • Chorioamnionitis - acute inflammation of amniotic fluid and fetal membranes during pregnancy, usually caused by polymicrobial bacterial infection. Signs of infection include maternal fever, vaginal discharge, tender uterus or pain with urination. • GBS Colonization - group B streptococcus is a bacterial pathogen commonly found in the gastrointestinal and vaginal membranes of healthy women. Presence of this bacteria is usually asymptomatic; therefore, pregnant patients will routinely be screened for presence of GBS prior to delivery. • Delivery Before 37 Weeks - premature infants require more medical intervention and have less effective immune defenses, so these neonates are at increased risk of infection • Prolonged Rupture of Membranes (PROM) - the amount of time between the rupture of amniotic membranes and delivery of the neonate is directly correlated with risk of neonatal infection. Prolonged course of labor increases neonatal exposure to bacterial and viral pathogens, increasing chance of infection. ==Mechanism==

Inflammation accompanies infection and is likely to complicate treatment and recovery. Inflammation is linked to reduced growth of the lungs of the premature baby. Pathogenesis The recent identification of the presence of microorganisms in maternal-infant body fluids that were previously thought to be sterile has provided one explanation for the presence of the inflammatory response in both the mother and infant. Sixty-one percent of pregnant women with chorioamnionitis, or inflammation of the amniotic fluid, were found to be infected by microorganisms. Often, more than one pathogen was present. In fifteen percent of pregnant women inflammation was still evident even though there was no evidence of pathogens. This may indicate that there are other causes. A high percentage, 51% to 62%, of pregnant women who had chorioamnionitis also had inflammation of the placenta. ==Diagnosis==

being performed on a newborn to detect presence of infection Diagnosis of infection is based upon the recovery of the pathogen or pathogens from the typically sterile sites in the mother or the baby. Unfortunately, as many half of pregnant women are asymptomatic with a gonorrhea infection and other sexually transmitted infections. Samples are obtained from urine, blood or cerebrospinal fluid. Diagnosis of infection can also be aided by the use of more nonspecific tests such as determining the total white blood cell count, cytokine levels and other blood tests and signs. Protozoan infection Congenital malaria has its own set of signs: Neonatal sepsis Neonatal sepsis of the newborn is an infection that has spread through the entire body. The inflammatory response to this systematic infection can be as serious as the infection itself. Infected sepsis in an infant can be identified by culturing the blood and spinal fluid and if suspected, intravenous antibiotics are usually started. Lumbar puncture is controversial because in some cases it has found not to be necessary while concurrently, without it estimates of missing up to one third of infants with meningitis is predicted. ==Prevention==

To reduce neonatal infection, screening of pregnant women for HIV, hepatitis B, and syphilis, is available in the UK and the United States. Treatment with a vaginal antibiotic wash prior to birth does not prevent infection with group B streptococcus bacteria (GBS). Treatment with vaginal chlorhexidine prior to birth does not prevent neonatal infections. Because GBS bacteria can colonize the lower reproductive tract of 30% of women, typically pregnant women are tested for this pathogen from 35 to 37 weeks of pregnancy. Before delivery treatment of the mother with antibiotics reduces the rate of neonatal infection. Breastfeeding has been shown to protect the neonate from some infections. Breast milk protects against necrotizing enterocolitis. Hepatitis A, B, and D are preventable via vaccination. Hepatitis A can be prevented by immunization against HAV, while Hepatitis B and D can both be prevented by immunization against HBV. The other is vitamin K to prevent vitamin K deficiency bleeding. In cases where the pregnant woman is positive for hepatitis B, the baby will receive an additional dose of hepatitis B immunoglobulin in addition to the hepatitis B vaccine to prevent transmission of the disease from mother to baby. Prevention of hepatitis B is crucial as there is no currently no cure. In general, in an unvaccinated individual, the viral hepatitis family causes liver damage due to a cell-mediated response via cytotoxic lymphocytes. Acute viral hepatitis can lead to jaundice, elevated bilirubin, elevated liver enzymes (aspartate transaminase, alanine transaminase, and alkaline phosphatase), and flu-like symptoms. For both Hepatitis B and Hepatitis D, the most significant long-term complications are progression to cirrhosis and hepatocellular carcinoma, which carries high morbidity and mortality. ==Treatment==

Neonatal infection treatment is typically started before the diagnosis of the cause can be confirmed. Neonatal infection can be prophylactically treated with antibiotics. Maternal treatment with antibiotics is primarily used to protect against group B streptococcus. == Epidemiology ==

Up to 3.3 million newborns die each year and 23.4% of these die of neonatal infection. About half of the deaths caused by sepsis or pneumonia happen in the first week postpartum. In industrialized countries, prophylactic antibiotic treatment of the mothers identified with group B streptococcus, early identification of sepsis in the newborn, and administration of antibiotics to the newborn has reduced mortality. In North America, prior to the 1950s, group A β-hemolytic streptococcus (GAS) was the most common pathogen associated with neonatal sepsis prior to the 1960s. In the past twenty years, the most common pathogen causing sepsis is coagulase-negative staphylococci that exist as biofilms associated with infected central venous or arterial catheters.--> Expectant mothers with HSV have a 75% chance of at least one flare-up during their pregnancy. ==Research==

The susceptibility to risk of infection and immune deficiencies are active areas of research. Studies regarding the role of viruses in neonatal infections are lacking. Research also continues into the role and protective effect of gut, skin and other human microbiomes and the colonization during the neonatal period. The comparison between both resource rich and poor countries makes it difficult to compare the diagnosis success; as industrialized regions are able to confirm the diagnosis and presence of pathogens in the clinical laboratory. Clinical testing may not be available in all settings and clinicians must rely on the signs of infection in the newborn. Research data from Africa and Southeast Asia is scarce. A GBS vaccine is currently being tested but not currently available. Vaccination is estimated to being able to prevent 4% of GBS infections for preterm births and 60–70% for neonatal GBS infections in the US. The projected benefits of maternal vaccination is the prevention of 899 cases of GBS disease and 35 deaths among infants. The cost savings in the prevention of GBS may be over 43 million dollars. Vaccination may be especially beneficial in low to middle income countries where screening and prophylactic treatment is not possible. Analysts project that GBS vaccination would prevent 30–54% of infant GBS cases. Screening, prophylactic antibiotics and vaccine would prevent 48% of infection. ==See also==