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Tachycardia
Uterine tenderness on exam
Other localized abdominopelvic tenderness on exam
Purulent or malodorous lochia
Heavy vaginal bleeding
Ileus
Group Aor B streptococcal bacteremia may have no localizing signs.
DIFFERENTIALDIAGNOSIS
“5 Ws”: Wind (pneumonia); Water (UTI); Wound infection; Wow (mastitis); Wonder drug (medication-related fever)
Viral syndrome; dehydration
Thrombophlebitis
Thyroid storm
Appendicitis
DIAGNOSTIC TESTS & INTERPRETATION
Initial Tests (lab, imaging)
CBC: Interpret with care. (Physiologic leukocytosis may be as high as 20,000 WBCs.)
Two sets of blood cultures (especially with suspected sepsis)
Diagnosis often made on clinical grounds. Potential testing includes:
–Genital tract cultures and rapid test for group B streptococci (may be done during labor)
–Amniotic fluid Gram stain: usually polymicrobial
–Uterine tissue cultures: Prep the cervix with Betadine and use a shielded
specimen collector or Pipelle; difficult to obtain without contamination
If patient not responding to antibiotics in 24 to 48 hours:
–Ultrasound for retained products of conception, pelvic abscess, or mass
–CT or MRI looking for pelvic vein thrombophlebitis, abscess, or deepseated wound infection
Diagnostic Procedures/Other
Paracentesis/culdocentesis with culture rarely necessary
Test Interpretation
Superficial layer of infected necrotic tissue in microscopic sections of uterine lining
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>5 neutrophils per high-power field in superficial endometrium; ≥1 plasma cell in endometrial stroma
TREATMENT
MEDICATION
First Line
Clindamycin 900 mg IV q8h + gentamicin 5 mg/kg IV q24h (5)[A]
Potential side effects include nephrotoxicity, ototoxicity, pseudomembranous colitis, or diarrhea (in up to 6%).
Second Line
Ampicillin/sulbactam 3 g IV q6h
Metronidazole 500 mg IV or PO q8–12h + penicillin 5,000,000 U IV q6h, or
Ampicillin 2 g IV q6h + gentamicin 5 mg/kg IV q24h (5)[A]
Cefoxitin 2 g IV q6h. Add ampicillin 2 g IV q6h, if clinical failure after 48 hours (5)[A].
Cefotetan 2 g IV q12h. Add ampicillin 2 g IV q6h, if clinical failure after 48 hours (5)[A].
Note: Base therapy on cultures, sensitivities, and clinical response.
Contraindications
–Drug allergy
–Renal failure (aminoglycosides)
–Avoid sulfa, tetracyclines, and fluoroquinolones before delivery and if breastfeeding. Metronidazole is relatively contraindicated if breastfeeding.
Precautions:
–Clindamycin and other antibiotics occasionally cause pseudomembranous colitis.
–Antibiotic-associated diarrhea (Clostridium difficile)
Note: Consider adding a macrolide antibiotic (for chlamydia coverage) for infections occurring after 48 hours.
Note: Heparin typically indicated for septic pelvic vein thrombophlebitis; requires 10 days of full anticoagulation
SURGERY/OTHER PROCEDURES
Curettage for retained products of conception
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Surgery or image-guided drainage to drain abscess
Surgery to decompress the bowel
Surgical drainage of a phlegmon is not advised unless it is suppurative. Surgical removal of other inflamed tissue is usually not required.
ADMISSION, INPATIENT, AND NURSING CONSIDERATIONS
Inpatient care is recommended for postpartum infections.
Many infections occur after hospital discharge.
IV antibiotics and close observation for severe infections
Open and drain infected wounds.
Optimize fluid status.
ONGOING CARE
FOLLOW-UPRECOMMENDATIONS
Patient Monitoring
Individualize according to severity.
IV antibiotics can be stopped when the patient is afebrile for 24 to 48 hours.
Oral antibiotics on discharge are not necessary, unless patient was bacteremic; then continue oral antibiotics to complete a 7-day course.
DIET
As tolerated, although may be limited by ileus
PATIENT EDUCATION
Advise patient to contact physician with fever >38°C (100.4°F) postpartum, heavy vaginal bleeding, foul-smelling lochia, or other symptoms of infection.
Information available at http://www.healthline.com/health/pregnancy/complications-postpartum- endometritis
PROGNOSIS
With supportive therapy and appropriate antibiotics, most patients improve quickly and recover without complication.
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COMPLICATIONS
Resistant organisms; peritonitis; pelvic abscess
Septic pelvic thrombophlebitis
Ovarian vein thrombosis
Sepsis; death
REFERENCES
1.Smaill FM, Grivell RM. Antibiotic prophylaxis versus no prophylaxis for preventing infection after cesarean section. Cochrane Database Sys Rev. 2014;(10):CD007482.
2.American College of Obstetricians and Gynecologist. ACOG Practice Bulletin No. 120: use of prophylactic antibiotics in labor and delivery. Obstet Gynecol. 2011;117(6):1472–1483.
3.Tita AT, Szychowski JM, Boggess K, et al; for C/SOAPTrial Consortium. Adjunctive azithromycin prophylaxis for cesarean delivery. N Engl J Med. 2016;375(13):1231–1241.
4.Haas DM, Morgan S, Contreras K. Vaginal preparation with antiseptic solution before cesarean section for preventing postoperative infections.
Cochrane Database Syst Rev. 2014;(12):CD007892.
5.French LM, Smaill FM. Antibiotic regimens for endometritis after delivery.
Cochrane Database Syst Rev. 2004;(4):CD001067.
ADDITIONALREADING
Chibueze EC, Parsons AJ, Ota E, et al. Prophylactic antibiotics for manual removal of retained placenta during vaginal birth: a systematic review of observational studies and meta-analysis. BMC Pregnancy Childbirth.
2015;15:313.
Hadiati DR, Hakimi M, Nurdiati DS, et al. Skin preparation for preventing infection following caesarean section. Cochrane Database Sys Rev. 2014; (9):CD007462.
Liabsuetrakul T, Choobun T, Peeyananjarassri K, et al. Antibiotic prophylaxis for operative vaginal delivery. Cochrane Database Syst Rev. 2014; (10):CD004455.
Mackeen AD, Packard RE, Ota E, et al. Antibiotic regimens for postpartum endometritis. Cochrane Database Syst Rev. 2015;(2):CD001067.
Mackeen AD, Packard RE, Ota E, et al. Timing of intravenous prophylactic
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antibiotics for preventing postpartum infectious morbidity in women undergoing cesarean delivery. Cochrane Database Syst Rev. 2014; (12):CD009516.
McKibben RA, Pitts SI, Suarez-Cuervo C, et al. Practices to reduce surgical site infections among women undergoing cesarean section: a review. Infect Control Hosp Epidemiol. 2015;36(8):915–921.
Pevzner L, Swank M, Krepel C, et al. Effects of maternal obesity on tissue concentrations of prophylactic cefazolin during cesarean delivery. Obstet Gynecol. 2011;117(4):877–882.
SEE ALSO
Algorithm: Pelvic Pain
CODES
ICD10
O86.12 Endometritis following delivery
O86.4 Pyrexia of unknown origin following delivery
O86.13 Vaginitis following delivery
CLINICALPEARLS
Postpartum endometritis follows 1–3% of all births.
Infections are typically polymicrobial and involve organisms ascending from the lower genital tract.
Evidence supports antibiotic prophylaxis prior to skin incision for all cesarean deliveries but not for operative vaginal deliveries.
Clindamycin 900 mg IV q8h and gentamicin 5 mg/kg q24h are recommended as first-line therapy for endometritis. Treat until the patient is afebrile for 24 to 48 hours and stop antibiotics completely (unless there is documented bacteremia, which requires a 7-day course of therapy).
If no improvement occurs on antibiotics, consider retained placental products, abscess, wound infection, hematoma, cellulitis, phlegmon, or septic pelvic vein thrombosis.
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ENURESIS
Swati Avashia, MD, FAAP, FACP, ABIHM
BASICS
DESCRIPTION
Classification
–Primary nocturnal enuresis (NE): 80% of all cases; person who has never established urinary continence on consecutive nights for a period of ≥6 months
–Secondary NE: 20% of cases; resumption of enuresis after at least 6 months
of urinary continence
NE: intermittent nocturnal incontinence after the anticipated age of bladder control (age 5 years)
–Primary monosymptomatic NE (PMNE): bed wetting with no history of bladder dysfunction or other lower urinary tract (LUT) symptoms
–Nonmonosymptomatic NE (NMNE): bed wetting with LUT symptoms such as frequency, urgency, daytime wetting, hesitancy, straining, weak or intermittent stream, posturination dribbling, lower abdominal or genital discomfort, or sensation of incomplete emptying
ALERT
Adult-onset NE with absent daytime incontinence is a serious symptom; complete urologic evaluation and therapy are warranted.
System(s) affected: nervous, renal/urologic
Synonym(s): bed wetting; sleep enuresis; nocturnal incontinence; primary NE
EPIDEMIOLOGY
Incidence
Depends on family history
Spontaneous resolution: 15% per year
Prevalence
Very common; 5 to 7 million children in the United States (1)
10% of 7-year-olds; 3% of 11 to 12-year-olds; 0.5–1.7% at 16 to 17-year-olds
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(2)
1.5 to 2 times more common in males than females
Nocturnal > day (3:1)
Geriatric Considerations
Often associated with daytime incontinence (formerly referred to as diurnal enuresis)
ETIOLOGYAND PATHOPHYSIOLOGY
Adisorder of sleep arousal, a low nocturnal bladder capacity, and nocturnal polyuria are the three factors that interrelate to cause NE.
Both functional and organic causes (below); many theories, none absolutely confirmed
Detrusor instability
Deficiency of arginine vasopressin (AVP); decreased nocturnal AVPor decreased AVPstimulation secondary to an empty bladder (bladder distension stimulates AVP)
Maturational delay of CNS
Severe NE with some evidence of interaction between bladder overactivity and brain arousability: association with children with severe NE and frequent cortical arousals in sleep
Organic urologic causes in 1–4% of enuresis in children: UTI, occult spina bifida, ectopic ureter, lazy bladder syndrome, irritable bladder with wide bladder neck, posterior urethral valves, neurologic bladder dysfunction
Organic nonurologic causes: epilepsy, diabetes mellitus, food allergies, obstructive sleep apnea, chronic renal failure, hyperthyroidism, pinworm infection, sickle cell disease
NE occurs in all stages of sleep.
Genetics
Most commonly, NE is an autosomal-dominant inheritance pattern with high penetrance (90%).
1/3 of all cases are sporadic.
75% of children with enuresis have a first-degree relative with the condition.
Higher rates in monozygotic versus dizygotic twins (68% vs. 36%)
If both parents had NE, risk in child is 77%; 44% if one parent is affected. Parental age of resolution often predicts when child’s enuresis should resolve.
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RISK FACTORS
Family history
Stressors (emotional, environmental) common in secondary enuresis (e.g., divorce, death)
Constipation and/or encopresis
Organic disease: 1% of monosymptomatic NE (e.g., urologic and nonurologic causes)
Psychological disorders
–Comorbid disorders are highest with secondary NE: depression, anxiety, social phobias, conduct disorder, hyperkinetic syndrome, internalizing disorders.
–Association with ADHD; more pronounced in ages 9 to 12 years
Altered mental status or impaired mobility
GENERALPREVENTION
No known measures
COMMONLYASSOCIATED CONDITIONS
Obstructive sleep apnea syndrome (10–54%) (1): Atrial natriuretic factor inhibits renin-angiotensin-aldosterone pathway leading to diuresis.
Constipation (33–75%) (1)
Behavioral problems (specifically ADHD in 12–17%) (1)
Overactive bladder or dysfunctional voiding (up to 41%) (1)
Urinary tract infection (18–60%) (1)
DIAGNOSIS
HISTORY
Age of onset, duration, severity
LUT tract symptoms
Daily intake patterns
Voiding diary and stooling patterns (especially constipation)
Psychosocial history
Family history of enuresis
Investigation and previous treatment history
PHYSICALEXAM
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ENT: evaluation for adenotonsillar hypertrophy
Abdomen: enlarged bladder, kidneys, fecal masses, or impaction
Back: Look for dimpling or tufts of hair on sacrum.
Genital urinary exam
–Males: meatal stenosis, hypospadias, epispadias, phimosis
–Females: vulvitis, vaginitis, labial adhesions, ureterocele at introitus;
evidence of abuse
Consider rectal exam: tone, fecal soiling, fecal impaction
Neurologic exam, especially lower extremities
DIFFERENTIALDIAGNOSIS
Primary NE
–Delayed physiologic urinary control
–UTI (both)
–Spina bifida occulta
–Obstructive sleep apnea (both)
–Idiopathic detrusor instability
–Previously unrecognized myelopathy or neuropathy (e.g., multiple sclerosis, tethered cord, epilepsy)
–Anatomic urinary tract abnormality (e.g., ectopic ureter)
Secondary NE
–Bladder outlet obstruction
–Neurologic disease, neurogenic bladder (e.g., spinal cord injury)
DIAGNOSTIC TESTS & INTERPRETATION
Initial Tests (lab, imaging)
Only obligatory test in children is urinalysis.
Urinalysis and urine culture: UTI, pyuria, hematuria, proteinuria, glycosuria, and poor concentrating ability (low specific gravity) may suggest organic etiology, especially in adults.
Urinary tract imaging is usually not necessary.
If abnormal clinical findings or adult onset: renal and bladder US
IV pyelogram, voiding cystourethrogram (VCUG), or retrograde pyelogram are rarely indicated (1).
MRI if spinal dysraphism is suspected
Follow-Up Tests & Special Considerations
Secondary enuresis: serum glucose, BUN, creatinine, thyroid-stimulating
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hormone (TSH), urine culture
In children, imaging and urodynamic studies are helpful for significant daytime symptoms, history of UTIs, suspected structural abnormalities, and in refractory cases.
Diagnostic Procedures/Other
Urodynamic studies may be beneficial in adults and nonmonosymptomatic NE.
Test Interpretation
Dysfunctional voiding
Detrusor instability and/or reduced bladder capacity most common findings
TREATMENT
GENERALMEASURES
Use nonpharmacologic approaches as first line before prescribing medications (1)[A].
Simple behavioral interventions (e.g., scheduled wakening, positive reinforcement, bladder training, diet changes) are effective, although less so than alarms or medications (1)[B]; found to achieve dryness in 15–20% of cases (3)
–Explain the three pathophysiologic factors.
–Encourage normal drinking patterns during daytime hours and reduction of intake 2 hours prior to sleep.
–Emphasize regular bedtime with full night’s sleep.
–Scheduled voiding before bed
–Scheduled waking for nighttime voiding
–Nightlights to light the way to the bathroom
–Reward system for dry nights
–Use pull up over regular underwear or cloth underwear with built in waterproof barrier.
–“Cleanliness training”: Child helps with changing wet bedding.
Do not shame or punish bedwetting but have the child participate in removing and laundering soiled bedding and garments.
Aggressive treatment of constipation, if present, with polyethylene glycol 3350 (MiraLAX); (peds: 0.8 g/kg; adults 17 g/day)
If behavioral interventions alone have no success, combined therapy (e.g.,
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