1、Patient Presentation Patient Presentation A female infant was born at 38 4/7 week gestation to a 34 year old gravida 2, para 1 mother. The mother was positive on Group B streptococcus screening 2 weeks prior to delivery. Labor was induced because of late-term maternal hypertension. The mother receiv
2、ed antibiotics during labor and delivery was by emergent cesarean section for fetal bradycardia. The baby was vigorous at delivery but then became cyanotic at 4 minutes of age and received blow-by oxygen. Apgar scores were 4 at 1 minute, 6 at 2 minutes, and 7 at 5 minutes. Her initial capillary bloo
3、d gas was pH = 7.13, CO2 = 77, and base excess of +2. She was given oxygen by hood, 2 intravenous boluses of normal saline, and ampicillin and gentimicin after blood cultures were drawn. She continued to have respiratory distress and was intubated and sedated before transfer to a regional hospital.
4、She was later extubated on day of life 1. The pertinent physical exam pertinent physical exam on arrival showed a term infant with temperature of 35.6 degrees Celsius, heart rate = 106, respiratory rate = 40, and blood pressure = 69/40 with no evidence suggesting of coarctation of the aorta on 4 ext
5、remity blood pressures. Her oxygen saturation was 100% on 40% oxygen. She did not appear dysmorphic. Skin showed a few red, blanching 3 mm macules on the face. Lungs were normal. Heart had a regular rate and rhythmn with no murmurs. Upper extremity pulses were equal to lower extremity pulses. Abdome
6、n had no organomegaly, normal bowel sounds and a 3 vessel cord. She had a good tone, strength, and appropriately reacted to handling. The workwork- -up up included a complete blood count that showed a hemoglobin of 15.0, hematocrit of 45%, platelets of 233 with segmented neutrophils of 7889, lymphoc
7、ytes of 5474 and bands of 483. A C-reactive protein was 0.5 mg/dl. Her chest radiograph showed some mild hyperexpansion and general haziness of the lung fields (see below). Over the next day, the patients clinical coursepatients clinical course showed her to be more awake, her respiratory distress r
8、esolved and she was extubated. She had no glucose instability. Her blood cultures locally did not grow an organism. The diagnosis ofdiagnosis of presumed neonatal sepsis was made and she received a 7 day course of ampicillin and gentimicin therapy. Her complete blood count was normal at discharge. F
9、igure 43 - AP radiograph of the chest on the first day of life demonstrates normally positioned tubes and lines along with diffuse fine interstitial infiltrates. The differential diagnosis for this finding would include transient tachypnea of the newborn versus neonatal pneumonia due to Group B Stre
10、p. DiscussionDiscussion Neonatal sepsis is an important contributor to neonatal morbidity including poor neurodevelopmental outcomes and neonatal death. Early in the 20th century, group A streptococcus was the leading cause, but in the 1970s group B streptococcus (GBS) emerged. In the 1990s universa
11、l antenatal screening was recommended at 35-37 weeks gestation with recommendations for intrapartum prophylaxis for colonized women. These guidelines decreased the rate of early GBS infection from 1.7/1000 live births to 0.34/1000 live births. Although the rate of GBS infection has declined, the pro
12、portion of mothers exposed to intrapartum antibiotics has more than doubled. Concerns of antibiotic-resistance have also been raised. Early-onset neonatal sepsis is defined as occuring within the first 7 days of life. Most (85%) infants present in the first 24 hours. Overall GBS neonatal sepsis has
13、decreased with the use of antibiotic protocols, but the overall incidence of early-onset sepsis has remained stable mainly because of increased sepsis resulting from Escherichia coli. This is especially true for premature infants and the onset may be extremely rapid. The organisms are acquired as an
14、 ascending infection from the cervix or transplacentally from the mother. Most early-onset neonatal sepsis is not culture-proven and many infants are defined as having “clinical sepsis” such as the infant described above. Late-onset neonatal sepsis is defined as occuring between 8-90 days. It is acq
15、uired from the environment by colonization of the conjunctiva, skin, gastrointestinal tract, respiratory tract, or umbilicus. Pneumonia is a common early-onset sepsis presentation, whereas bacteremia and meningitis are more common in late-onset sepsis. Other presentations include metabolic acidosis,
16、 hyper- or hypo-glycemia, jaundice, pulmonary hypertension, decrease cardiac output, necrotizing enterocolitis, thrombocytopenia, neutropenia, or disseminated intravascular coagulation. Workup often includes complete blood count with differential, C-reactive protein, cerebrospinal fluid analysis and
17、 culture, urinalysis and culture, blood culture, chest radiograph, and possibly head imaging and/or other infectious disease markers. Learning PointLearning Point Early-onset neonatal sepsis commonly is associated with GBS (most commonly), Escherichia coli, Haemophilus influenzae, and Listeria monoc
18、ytogenes. Late-onset sepsis syndrome is associated with Staphylococcus epidermidis (most commonly), coagulase-negative staphylococcus, Staphylococcus aureus, E. coli, Klebsiella, Pseudomonas, Enterobacter, Candida, GBS, Serratia, Acinetobacter, and anaerobes. Empiric treatment for early-onset neonat
19、al sepsis is usually begun with and includes combined IV aminoglycoside and expanded-spectrum penicillin antibiotic therapy in the U.S. and Canada. Clinical situation and local pathogen sensitivities must be considered when selecting antibiotic coverage. Questions for Further DiscussionQuestions for Further Discussion 1. What are the local pathogens that cause neonatal sepsis? 2. What are the local pathogens sensitivities to antibiotics? 3. How long should treatment be given for presumed neonatal sepsis, i.e. culture-negative sepsis?
