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Rasha D. Sawaya, MD, Assistant Professor of Clinical Emergency Medicine; Associate Program Director, Emergency Medicine Residency; Director of Pediatric Quality, Department of Emergency Medicine, American University of Beirut Medical Center, Beirut, Lebanon
Imane Chedid, MD, Emergency Medicine Resident, American University of Beirut Medical Center, Lebanon
Imad El Majzoub, MD, Fellow, Emergency Medicine, MD Anderson Cancer Center, Houston, TX
Aaron Leetch, MD, Assistant Professor of Emergency Medicine & Pediatrics; Residency Director, Combined Emergency Medicine & Pediatrics Residency, University of Arizona College of Medicine, Tucson
Pediatric sepsis is a high-stakes diagnosis that requires vigilance to make an early, timely diagnosis. Aggressive resuscitation, including fluids, antibiotics, and vasoactive agents, may be necessary. Rapidly changing standard of care also makes sepsis a critical diagnosis for clinicians.
— Ann Dietrich, MD, FAAP, FACEP, Editor
Pediatric sepsis syndrome is a leading cause of morbidity and mortality, and results in elevated healthcare costs for infants and children worldwide.1,2 Morbidity and mortality from sepsis are related to the causes of systemic inflammatory response syndrome (SIRS), complications of organ failure, and the potential for prolonged hospitalization.1,2,3
According to data from the 2015 SPROUT study, the point prevalence of severe sepsis globally was 8.2% (95% confidence interval [CI], 7.6-8.9).4 In addition, mortality rates associated with sepsis and septic shock in patients admitted to the pediatric intensive care unit (PICU) were 5.6% and 17.0%, respectively.5
Pediatric severe sepsis usually is community-acquired (57%)6 and occurs most often in toddlers (median age of 3 years with interquartile range, 0.7-11.0).4 The most common primary site of infection is the respiratory tract.4 Interestingly, one study noted the most common pathogen retrieved from blood cultures was Staphylococcus aureus.4
SIRS occurs when the body’s inflammatory state is revved up in response to an insult. The SIRS adult criteria have been modified to produce a pediatric-specific definition. In children, SIRS includes two or more of the following, one of which must be an abnormal temperature or leukocyte count:7
As per the 2017 Sepsis-3 guidelines, sepsis in adults no longer is based on the SIRS criteria, but now is defined as an infection with at least one organ dysfunction.8 Currently, the definition of sepsis in the pediatric population remains based on the SIRS criteria, as evidence for change is still weak. However, this may change in future guidelines.9 For example, one study showed that a child with two or more SIRS criteria still lacked sensitivity and specificity for sepsis, and using SIRS alone would miss one in eight patients with sepsis.10 However, in children younger than 18 years of age, sepsis still is defined as a SIRS response caused by an infection that may be suspected or definite, and the cause may be viral, bacterial, or fungal.
Severe sepsis occurs when there is sepsis and organ hypoperfusion or dysfunction, such as an elevated lactate, oliguria, prolonged capillary refill time (CRT), reduced mental status, disseminated intravascular coagulopathy (DIC), acute respiratory distress syndrome, or acute renal failure.11
Although not included in the definition of sepsis, hyperglycemia, altered mental status, high lactate, and a prolonged CRT are all highly suggestive of sepsis and, therefore, should be considered when evaluating a child for sepsis.11
Septic shock is sepsis with fluid refractory hypotension and signs of hypoperfusion.11 Shock can be cold or warm. Definitions of shock are shown in Table 1.12
Clinically, organ dysfunction is an important component of sepsis. Table 2 shows the criteria for organ dysfunction.13
By definition, sepsis and septic shock include an infectious source, which can be bacterial, fungal, or viral. The most common site of infection is the respiratory tract, followed by the bloodstream, with respiratory infections having the highest mortality rates.14
Among the pathogens, bacterial causes, such as S. aureus and methicillin-resistant S. aureus (MRSA), frequently are isolated in the blood cultures and are a rising culprit in the post-vaccination era.15,16,17
In addition, the prevalence of Streptococcus pneumoniae and Neisseria meningitides is decreasing. Gram-negative bacteria, such as Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae, are the most frequently identified organisms in urinary tract infections.17 Viruses, such as influenza, parainfluenza, and adenovirus, also can cause sepsis.18,19
Risk factors for pediatric sepsis and septic shock are similar to those in adults.16 (See Table 3.) Being younger than 1 month of age also is an important risk factor to recall, especially because newborns initially may appear normal on exam.20
The pathophysiology of sepsis and septic shock is not understood precisely but is thought to involve a complex interaction between the pathogen and the host’s immune system. The normal physiologic response to localized infection includes activation of the host defense mechanisms, which results in an influx of activated neutrophils and monocytes, a release of inflammatory mediators, local vasodilation, increased endothelial permeability, and activation of coagulation pathways. These response mechanisms occur during septic shock, leading to diffuse endothelial disruption, vascular permeability and DIC, vasodilation, and thrombosis of end-organ capillaries. This results in the clinical presentation of specific organ injury or multi-organ failure. 21
Given the high mortality of septic shock and the rapid organ deterioration, it is considered a time-critical emergency. As detailed above, sepsis is the presence of SIRS criteria with a probable infection, and septic shock is sepsis with fluid refractory hypotension and signs of hypoperfusion. However, unlike adults, previously healthy children with intact cardiovascular homeostatic mechanisms can compensate extremely well during hypoperfusion states and do so for relatively long periods; their signs and symptoms will reflect this.12 For instance, a child with severe sepsis may be only tachycardic at presentation, maintaining his/her blood pressure within normal ranges for a relatively long period. But if the compensated shock remains unrecognized and untreated, the child will decompensate suddenly with a drop in blood pressure, making recovery more difficult.
Keep in mind, not every child with fever will have a serious infection that leads to sepsis. However, delaying recognition and the management of a septic child will worsen the prognosis significantly; hence, early recognition is crucial.
The typical presentation varies with the age of the patient. Even cursory knowledge of the developmental stages of children will help determine variations in activity by age. In neonates and infants, any change from the patient’s normal behavior, such as somnolence, irritability, or hypoactivity, with or without a fever, raises the possibility of sepsis.22 It is important to ask parents about the child’s baseline activity and what differs. Febrile children will be slightly hypoactive; therefore, it is important to pinpoint the state and activity of the child with and without the fever. Older infants and children typically present with a fever and a localized source of infection.23 (See Table 4.)
Consider using the risk factors of sepsis from Table 3 as a guide to ask further questions about recent surgeries, recent hospitalization, and past medical history. For instance, the provider should inquire about recurrent infections, such as urinary tract infections, and chronic diseases, such as cystic fibrosis, splenic dysfunction, sickle cell disease, and congenital cyanotic heart diseases. It is important to look for the presence of immunodeficiency in children who have cancer or HIV, who are undergoing immunotherapy, who are taking chronic steroids, or who have severe malnutrition. Ask about the patient's vaccination status, with a focus on pneumococcal, Haemophilus, and meningococcal vaccination. In addition, the presence of a foreign body, such as an indwelling intravascular catheter, urinary catheter, or chest tube, increases the risk of infection.19-24
Vital signs are crucial in identifying sick patients. In children, these vary by age.25 (See Table 5.) The physical examination findings of a septic child may be as subtle as isolated tachycardia or as flagrant as hypotension or poor perfusion with an altered mental status. Always consider sepsis, a differential of consequence, in children with persistently abnormal vital signs. Persistent tachycardia often is missed, as it may be attributed to fever or crying. Hypotension is a late finding in children; in this population, the diagnosis of shock cannot be based solely on the presence of the latter. However, hypotension in children with a suspected source of infection is confirmatory for the presence of septic shock.26 It is important to note that although Table 5 offers a normal range of vital signs in children, care needs to be taken when deciding that a child is hypotensive. Having a systolic blood pressure lower than the range does not automatically make a child hypotensive. Table 5 also shows the systolic blood pressure below which a child needs evaluation for hypotension. Also note the use of the term “persistent” for the tachycardia. This reflects the fact that tachycardia secondary to fever, pain, or crying will get better when the cause is treated and will not “persist.”
Other physical exam signs suggestive of sepsis are included in Table 6.22 Physical exam findings also can help differentiate the type of septic shock. (See Table 1.) In cold shock, the child will have mottled skin and prolonged central CRT (> 3 seconds). Patients at this stage will be tachycardic yet still will maintain their blood pressure in the normal age-adjusted range. This type of shock is seen most often in infants and young children. It is due to myocardial hypocontractility along with compensatory peripheral vasoconstriction. 27 Warm shock is more common in older children, and the provider will note a shorter (flash) CRT, warm skin, and bounding pulses. This is due to peripheral vasodilation along with a compensatory high cardiac output state.
The key take-home message is that a child with a suspected infection, persistently abnormal vital signs, or a concerning exam after antipyretics and intravenous (IV) fluids to treat dehydration should be investigated and treated for sepsis or admitted for close observation.
Whenever sepsis or septic shock is diagnosed based on the presentation (history and physical exam), laboratory studies can help determine the type and source of the infection as well as the potential organ damage endured and patient prognosis. Recommended tests are listed below.
Complete Blood Count With Differential. This test can reveal leukocytosis or leukopenia, thrombocytosis (since platelets are an acute inflammatory marker), or thrombocytopenia. In the latter, consider DIC and complete the workup to confirm its presence with elevation of prothrombin time, partial thromboplastin time, international normalized ratio, D-dimer, and decreased fibrinogen.
Glucose. The presence of hypoglycemia or hyperglycemia has been associated with poor short-term outcomes in multiple studies.28,29,30 Therefore, providers should recognize and correct an abnormal blood glucose level promptly. Hypoglycemia is the most prevalent because of the high metabolic demand in sepsis and the decreased oral intake due to the illness, especially in neonates. Neonates should receive maintenance fluid with dextrose. 31 Correct hyperglycemia to a goal of ≤ 180 mg/dL.31
Electrolytes. Several electrolyte derangements secondary to the underlying illness can accompany sepsis and septic shock. Among them are hyponatremia or hypernatremia from severe dehydration because of gastrointestinal losses or decreased oral intake; hypophosphatemia, hypocalcemia, and hypomagnesemia also may be present. Providers should pay attention to serum calcium. In cases of hypocalcemia, replete calcium to prevent any further decreases in myocardial contractility. The American College of Critical Care still recommends this practice despite acknowledging the absence of solid evidence.27
Anion Gap. Calculate the anion gap (AG) using the following formula: AG = Na+ - (HCO3- + Cl-). In children, an anion gap > 14 to 16 mEq/L is considered high, and in neonates a high anion gap is > 16 mEq/L.32,33 In septic children, the acid-base status varies. Patients might present with respiratory alkalosis due to tachypnea, or respiratory or metabolic acidosis. When metabolic acidosis is present, it is usually a high anion gap metabolic acidosis, due to lactic acidosis. If the anion gap is normal, look for other causes mimicking sepsis (e.g., renal tubular acidosis, certain drug ingestions, and hypernatremic dehydration).34
Urinalysis. The presence of pyuria, nitrites, or leukocyte esterase is suggestive of a urinary tract infection. 35
Blood Urea Nitrogen (BUN) and Creatinine. BUN would be elevated in the case of dehydration, and creatinine can reflect prerenal azotemia. However, a twofold increase in creatinine from baseline may indicate sepsis-induced kidney injury, a sign of end-organ hypoperfusion.36,37
Serum Total Bilirubin and Alanine Aminotransferase. A total bilirubin ≥ 4 mg/dL or alanine aminotransferase > 2 times the upper limit of normal for age indicates liver dysfunction in the setting of sepsis.13
Blood Gas (Arterial or Venous). A blood gas may assist with evaluation of three important factors: tissue oxygenation, adequacy of ventilation, and acid-base disturbances. At times, it can be unreliable to assess ventilation and oxygenation status by noninvasive methods, such as pulse oximetry, as it is affected by other factors such as weak pulses or cold extremities. Thus, an arterial blood gas (venous blood gas or capillary blood gas) in a nonhypotensive child will help detect impending respiratory failure and the need for invasive ventilation.38 An arterial blood gas, venous blood gas, or capillary blood gas also will help determine the type and severity of the acid-base derangement in a nonhypotensive child.39
Microbiology. When possible, draw the cultures before initiating antibiotic therapy but do not delay antibiotics in a critical child; all patients require a blood culture. The other cultures depend on the age of the child, the presentation, and the suspected source of infection. For example, all children younger than 3 months of age with septic shock need a full septic workup that includes blood, urine, and cerebrospinal fluid cultures. Do not delay antibiotics if the child is unstable for a lumbar puncture. Send a deep tracheal aspirate on patients with tracheostomies, and send a wound culture if cellulitis, abscess, or surgical wound is noted. Fungal cultures may be helpful in immunocompromised patients. Among other microbiology investigations, consider diagnostic serologic testing, such as viral culture, polymerase chain reaction, rapid immunoassay antigen test, or direct and immunofluorescent antibody staining to establish the source of infection when herpes simplex virus, enterovirus, or influenza infection is suspected. Viruses are a common cause of sepsis, with high rates of mortality for influenza.23-40 When available, consult an infectious disease team early to help with investigation and antimicrobial therapy.
Lactic Acid. When there is insufficient delivery of oxygen to the tissue, such as with hypoperfusion in sepsis and septic shock, aerobic metabolism will shift to anaerobic to continue the generation of adenosine triphosphate, for cellular survival. This anaerobic mechanism will lead to the generation of a byproduct: lactate. The normal range of lactate in children is 0.5 to 2.2 mmol/L,41 and an elevated lactate level can be an indicator of sepsis. In fact, multiple studies in children with sepsis or septic shock have shown the association between high lactate levels and mortality or poor outcome in sepsis. However, data regarding its use as a diagnostic tool still are sparse in the pediatric population; most studies show its value as a prognostic indicator. One prospective study in children with undifferentiated SIRS showed that a high lactate level of > 4 mmol/L was associated with a relative risk of 5.5 (95% CI, 1.9-16.0) of developing organ dysfunction within 24 hours.42 In another study evaluating the predictive value of blood lactate and in-hospital mortality, the odds for in-hospital mortality increased by 38% for every 1 mmol/L increase in blood lactate (odds ratio [OR], 1.38; 95% CI, 1.30-1.46; P < 0.001).43
In 2017, Sitaraman et al reported that the mean lactate levels were significantly higher in non-survivors than survivors (5.12 ± 3.51 vs. 3.13 ± 1.71 mmol/L; P = 0.0001). Specifically, a lactate level ≥ 4 mmol/L at admission to the PICU was a predictor of mortality (OR, 5.4; 95% CI, 2.45-12.09). If the lactate did not decrease by more than 10%, patients had a greater risk of mortality (likelihood ratio, 2.83; 95% CI, 1.82-4.41).44 Another study showed that serum lactate normalization, but not rate of clearance, was associated with a decrease in organ dysfunction (relative risk [RR], 0.46; 95% CI, 0.29-0.73; adjusted RR, 0.47; 95% CI, 0.29-0.78).45 It is noteworthy that most studies on lactate in children are done outside of the emergency department (ED) in the PICU.
Procalcitonin. Procalcitonin is a polypeptide prohormone of calcitonin. In the healthy population, the serum level is undetectable, but it is increased when there is a bacterial infection, probably as a result of bacterial endotoxins, making procalcitonin not only useful in detecting sepsis, but also in differentiating bacterial from viral infection.46,47, 48 Published data on its clinical use, especially in the emergency department, are promising. Procalcitonin appears to be a better indicator of serious bacterial infections compared to white blood cell count, absolute neutrophil count, and percent neutrophils,49,50 and of better use in children, as it is not age dependent.51 In addition, serum procalcitonin appears to be a better predictor of poorer outcome than C-reactive protein and neutrophil count in septic children. Elevated levels correlate with the presence of multiorgan dysfunction (P = 0.0001) and shock (P = 0.003).51
The radiological evaluation is tailored to the clinical scenario. Providers should consider a chest radiograph for the child with respiratory symptoms, abnormal lung findings, or a white blood cell count > 20,000 cells/mm3.52 Abdominal imaging should be obtained for the child with a concern of an intra-abdominal process, such as appendicitis. Consider a brain computed tomography scan for children with an altered level of consciousness or new-onset seizures; in addition, DIC from sepsis may predispose to intracranial bleeds. Cardiac echocardiography should be considered in children with a new murmur or other signs of endocarditis, such as Osler nodes and splinter hemorrhages, or for those who develop signs of cardiogenic shock (cardiomegaly, hepatomegaly, and respiratory failure). If osteomyelitis or a septic joint is suspected based on physical exam findings of a limp, swollen, or stiff joint, consider radiographs, ultrasound, bone scan, or magnetic resonance imaging.
Although sepsis requires early recognition and treatment, in children some of the SIRS criteria, such as tachycardia and tachypnea, may have other causes. SIRS has a high specificity but a poor sensitivity for sepsis. One series showed an overall sensitivity of 31.2% (95% CI, 27.3-35.4%) and specificity of 95.7% (95% CI, 94.2-97%).53 Benign causes of tachycardia include fear, fever, and pain. Evaluate the child in the parent’s arms, allow the child to calm down, or keep the child on a monitor and leave the room to obtain more accurate vital signs. Tachycardia and tachypnea also typically are associated with fever. If the child is not showing any other signs of sepsis or septic shock, such as poor perfusion, then treat the fever with an antipyretic and reevaluate the child. Finally, tachycardia may be a sign of pain. Something as simple as acute otitis media may be extremely painful in a child. Treat the pain and reevaluate as above.
Tachycardia also may be secondary to dehydration. Carefully assess for indicators of dehydration, especially in children with gastrointestinal losses, such as decreased tears and urine output. Consider an intravenous fluid bolus to rehydrate the patient and reevaluate the tachycardia while closely observing for other signs and symptoms of sepsis and septic shock. Pneumonia also may present with tachypnea and tachycardia. Keep in mind that pneumonia also may be the source of infection in a septic patient.
Furthermore, myocarditis also should be on the differential of a persistently tachycardic child. Frequently reassess the response to fluid and monitor for crackles, hepatomegaly, or other signs of fluid overload. Most importantly, not every state of shock is due to sepsis. There are four types of shock leading to tissue hypoperfusion and end-organ damage: distributive, cardiogenic, hypovolemic, and obstructive.54 (See Table 7.) Sepsis is included in distributive shock. Sometimes, the initial clinical presentation makes it difficult to rapidly differentiate the types of shock in the ED. History, physical exam, and frequent reassessments are key when determining response to treatment.
Finally, while following the septic shock guidelines, consider endocrine causes of persistent shock, such as adrenal insufficiency or hypothyroidism, and other findings, such as pneumothorax, intra-abdominal hypertension, or abdominal compartment syndrome, as a reason for persistent hypotension.27
As in adults, early recognition of sepsis and septic shock is crucial to improving outcomes.55 Even a one-hour delay in the initiation of appropriate resuscitation measures in pediatric patients with sepsis was associated with increased mortality (OR, 2.29; 95% CI, 1.19-4.44).56 However, there are conflicting data, and more research in this area is warranted. For example, in a large longitudinal study, there was a clear benefit of implementing a quality intervention bundle focused on recognition of pediatric sepsis and timely antibiotic and fluid administration.57 In fact, mortality was five times higher in children who did not receive bundle-compliant care (OR, 5.0; 95% CI, 1.9-14.3) compared to those who did (OR, 0.20; 95% CI, 0.07-0.53).57
However, in a recent meta-analysis published in the New England Journal of Medicine, the researchers reported that children with sepsis who received early goal-directed therapy had no improvement in 90-day mortality (OR, 0.97; 95% CI, 0.82-1.14; P = 0.68) and it was associated with increased healthcare costs.58
Currently the American College of Critical Care Medicine Guidelines emphasize early recognition and the implementation of a sepsis recognition bundle exemplified by the “septic shock identification trigger tool” shown in Figure 1. It is recommended that this bundle contain a trigger tool, rapid clinical assessment of the child, and initiation of the therapeutic approach. 27
However, as acceptance and implementation of pathways is site specific, it is recommended to create a home-built bundle, adapted to the structure, staffing, equipment, and metrics of each institution.27
Once a child is identified as being in septic shock, follow the pediatric advanced life support (PALS) resuscitation algorithm shown in Figure 2.27 It is important to initiate IV/intraosseous (IO) access and fluid resuscitation within the first five minutes of recognition. Aim for early antibiotic administration, and tailor the inotropes or vasopressors as the clinical scenario mandates. These specific therapeutic interventions and the evidence behind them are detailed below.
Vascular Access. Initiate IV access within five minutes of recognition of sepsis or septic shock. If possible, place a minimum of two large-bore, free-flowing IV catheters. These depend on the age and size of the child, but aim for at least a 20 G needle if possible (the larger the better). At least two individuals should attempt these at the same time, one on each side. Consider looking at the child’s feet and scalp for veins.
If the IV is not in place after two attempts or 90 seconds in the setting of severe septic shock, insert an IO needle.59 Ultrasound-guided peripheral access also may be helpful in patients for whom IV access is difficult to establish. Do not delay care for central line placement; resuscitation can be done via peripheral or IO access adequately.
Oxygen Therapy. Provide supplemental oxygen immediately via a 100% non-rebreather face mask. If the patient is in respiratory distress, consider high-flow nasal cannula or noninvasive positive pressure ventilation. This will help increase oxygen content in the blood and delivery to the already poorly perfused tissues.11 Thereafter, closely monitor the oxygenation and work of breathing of the child. (See section below on mechanical ventilation.)
A critical aspect of resuscitating a septic child is to replete the patient's intravascular volume. Evidence still is lacking regarding the choice of the proper solution, but crystalloids, such as normal saline and Ringer’s lactate, are equally effective as colloids, yet cheaper than the latter.31-60
While laboratory tests are being drawn and antibiotics prepared, the child requires fluid resuscitation. Infuse up to 60 mL/kg of isotonic fluids in the first 15 to 60 minutes of recognition of shock. Start with a volume of 20 mL/kg within the first five minutes. This can be rapidly pushed in with 60 mL syringes or rapid infusers if available; using IV pumps may be too slow. Using a three-way stop cock to create a push-pull system can allow rapid drawing and pushing of fluid.
It is crucial to monitor the response to fluid therapy after each bolus: Look for an increase in blood pressure, drop in heart rate, improved peripheral pulses and capillary refill, increased urine output, and level of consciousness. If there is no or little improvement, administer another bolus of 20 mL/kg of fluid, until reaching a total of 60 mL/kg over an hour.
It is noteworthy that a 2012 large, multicenter, multinational sub-Saharan study (the FEAST trial) showed a worse outcome with aggressive fluid resuscitation. This was thought to be due to the inability to deal with complications of fluid therapy as a result of a lack of infrastructure and technical support as well as to high rates of anemia and malnutrition.61 However, this study has raised questions about the paradigm of aggressive fluid resuscitation, calling for more studies. In the meantime, in low-resource settings or settings in which mechanical ventilation or pediatric intensive care may be delayed, use caution with fluid resuscitation.
In addition, neonates younger than 30 days of age and children with cardiac or renal disease with septic shock warrant less aggressive therapy, such as 5 to 10 mL/kg boluses. Because of the above data and the differential of septic shock previously discussed, which also includes cardiogenic shock, pay close attention to complications of fluid overload, such as crackles in the lungs or hepatomegaly, by reassessing for these after every bolus.
When a child remains in the state of shock after 60 mL/kg and rapid (over 15 to 60 minutes) fluid resuscitation, the patient is diagnosed with fluid refractory shock (i.e., septic shock). At this point, vasoactive drips should be started.
Understanding the mechanism of action of the different cardiovascular agents and on which receptors they work can help identify which one may be more suitable for the different types of septic shock and end-effect desired.27-62 (See Tables 8 and 9.) For example, norepinephrine has a more direct effect on peripheral vasculature than dopamine, dobutamine, and epinephrine, and, hence, is more potent in reversing hypotension in vasodilatory (warm) shock. Experts also recommend norepinephrine’s use when there is low systemic vascular resistance clinically seen as wide pulse
pressure with diastolic blood pressure < 50% of the systolic pressure.63,64
Ionotropic agents, such as dopamine, dobutamine, and epinephrine, are the drugs of choice when there is depressed cardiac contractility. In addition, dopamine and epinephrine at high dosage (> 15 mcg/kg/min and > 0.3 mcg/kg/min, respectively) exert a sympathomimetic effect and a vasoconstrictive effect as well.
The 2017 guidelines recommend starting with epinephrine for cold shock and norepinephrine for warm shock.27 (See Figure 2.) Dopamine is a second-line agent.27 In fact, two recent publications described a decreased mortality and improved outcomes with the use of epinephrine as a first-line treatment in cold shock.63,64 Ramaswamy et al compared epinephrine to dopamine in pediatric septic shock and showed that epinephrine is better than dopamine for treatment of cold shock, with an odds ratio (OR) of shock resolution in the first hour equal to 4.8 (95% CI, 1.3-17.2; P = 0.019 ).65 In another study, dopamine drip was associated with higher mortality (OR, 6.5; 95% CI, 1.1-37.8; P = 0.037) and healthcare-associated infections (OR, 67.7; 95% CI, 5.0-910.8; P = 0.001) compared to epinephrine.66
Vasopressor support is a dynamic process. The first choice of vasopressor may need to be adjusted as the patient’s response is evaluated.
Finally, some authors suggest the use of vasodilatory agents, such as nitroprusside and type III phosphodiesterase inhibitors (PDEIs), like milrinone and inamrinone, when there is high systemic vascular resistance and low cardiac output, in addition to inotropes. PDEIs have a long half-life (1 to 10 hours) depending on the clearance and preferably are infused via central venous lines. These drips may lower the blood pressure; this typically responds to small boluses of fluids (5 mL/kg) and immediate discontinuation of the drug.27
Guidelines recommend administration of vasoactive agents through a central venous line when possible.27-31 However, if properly diluted, these agents, including epinephrine (e.g., 1 mg/50 mL), can be infused via a peripheral line to avoid delay in care. If extravasation of epinephrine occurs, treat with 1 to 5 mg of phentolamine diluted in 5 mL of normal saline.27
At this point, the patient ideally has been moved to a PICU. However, this often is not the case. At this point in time, central venous access should be started if not yet in place to aim for more specific and objective goal-directed therapy. Consider other causes of shock, such as pneumothorax, pericardial tamponade, or endocrine emergencies, if no improvement is noted and treat as identified.27-31
Add corticosteroids if a suspected or proven absolute adrenal insufficiency is noted, although mortality may not change.27-67 Use a hydrocortisone IV infusion at 50 mg/m2/24 hours.27 Consult the PICU and extracorporeal membrane oxygenation teams if available or start transfer to a hospital that has these resources.
IV Antibiotics. The Surviving Sepsis Guidelines stress the importance of antibiotic administration within one hour of sepsis recognition.11 Early administration of antibiotics is crucial to decrease mortality rates in patients with severe sepsis or septic shock. In one study, the mortality increased significantly with every one-hour delay in administration of antibiotics, but only after three hours delay from the initial dose. Specifically, for patients with more than a three-hour delay to initial and first appropriate antimicrobials, the OR for PICU mortality was 3.92 (95% CI, 1.27-12.06) and 3.59 (95% CI, 1.09-11.76), respectively.68 Therefore, do not delay the administration of antibiotics. Interestingly, however, recent adult data regarding time to antibiotics are mixed. A 2015 meta-analysis of adult patients did not show any benefit to early antibiotic treatment,69 yet a 2017 multicenter study of more than 40,000 adult patients showed that early antibiotic infusion rather than time to fluid resuscitation was associated with lower in-hospital mortality.70 Therefore, although it would be best to have two IV or IO lines for fluids and antibiotics, it may be acceptable to hold the completion of the fluid bolus in order to infuse the antibiotic, if a second access could not be placed. Remember, that many antibiotics also can be given intramuscularly if needed.
Start with a broad-spectrum carbapenem (e.g., meropenem, imipenem/cilastatin, or doripenem) or extended-range penicillin/β-lactamase inhibitor combination (e.g., piperacillin/tazobactam or ticarcillin/clavulanate).11 Several third- or higher-generation cephalosporins also can be used, especially as part of a multidrug regimen. Ceftriaxone plus vancomycin is widely available and easy to use and will provide wide Gram-negative and Gram-positive coverage, respectively. Always keep in mind all possible pathogens and the anticipated local microbial resistance. The following points may help guide the antibiotic choice:
Finally, consult with the infectious disease team early to help with the antibiotic choice. See Table 10 for the dosage of all above listed antibiotics and antivirals.
Mechanical Ventilation. The decision to intubate is based on clinical judgment. Beware of apnea, increased work of breathing, or decreased level of consciousness with inability to protect the airway. A Glasgow Coma Scale score < 8 or one that is rapidly deteriorating is an indication to intubate. Consider the following factors: When a child is anticipated to receive very large volumes of fluid during resuscitation > 60 mL/kg,71 remember that young infants have smaller functional residual capacity in the lungs and may require earlier intubation.72 Also, intubation in severe septic shock decreases the body’s demand on lung perfusion and helps divert perfusion to other organs.
Watch the child closely if intubating. The start of positive pressure ventilation in addition to sedatives will decrease the venous return and preload further and risk precipitating cardiovascular collapse and cardiac arrest. If possible, only intubate when the child already has received adequate fluid resuscitation and is on or starting inotropic support. Otherwise, have these at the bedside for immediate administration if needed.27
Avoid the use of etomidate for sedation. Several studies, including a 2012 meta-analysis, have shown etomidate to be harmful in pediatric patients with septic shock.73 A slow push of ketamine (0.25 to 1 mg/kg)62 unless otherwise contraindicated is a good alternative sedative, especially since it has relatively stable hemodynamics.
Other Therapeutic Options. Another important consideration for fluid therapy is the use of blood products. Guidelines recommend an initial target of 10 g/dL of hemoglobin as in adults, which changes to > 7 g/dL once the patient is stabilized.27
The American College of Critical Care Medicine and PALS emphasize maintaining or restoring good perfusion, adequate heart rate for age, and good respiratory support as in airway, oxygenation, and circulation within the first hour of shock recognition.27
Sepsis and septic shock resuscitation aim to reach specific therapeutic endpoints discussed in the previous sections and listed below.
Noninvasive Methods. Very simple measures can guide the provider’s approach to the septic child. Data have shown that a simple combined assessment of heart rate, CRT, and systolic blood pressure is a reliable indicator of shock in children. 74 Reassess the patient frequently after each treatment. Monitor the heart rate. A decrease in the heart rate suggests an improvement in the intravascular volume status. However, as tachycardia is not specific for shock, assess other clinical parameters also. Specifically, guidelines recommend aiming for the following:31
As for the blood pressure, albeit a useful indicator of shock and macrovascular circulation, when all other clinical parameters are reassuring and improving, some authors recommend against its use as an isolated marker of persistent shock state in children to guide further aggressive therapy.13
Despite a lack of evidence for the value of ultrasound as a tool for assessing the intravascular volume in the pediatric population, its role is very important in the adult requiring fluid resuscitation.75,76 Further studies are required in children.
Invasive Methods: Central Venous Pressure and Central Venous Oxygen Saturation. Central venous pressure (CVP) monitoring is one of the most commonly used methods for early goal-directed therapy. The target CVP recommended is 8 to 12 mmHg in patients with spontaneous breathing, and 12 to 15 mmHg in those who are receiving positive pressure ventilation.57 However, despite the wide use of CVP to guide fluid therapy, caution is recommended with its use as an isolated parameter because a myriad of other factors (diastolic dysfunction, pulmonary hypertension, or increased intrathoracic pressure) can affect it.77
In children, current recommendations are to monitor the central venous oxygen saturation (SCVO2) during resuscitation, aiming for a saturation ≥ 70%.31 de Oliviera et al showed that targeting an SCVO2 > 70% was associated with decreased mortality from 39.2% to 11.8% (P = 0.002) in pediatric septic shock.78 However, other studies have failed to prove the benefit of SCVO2 monitoring over less-invasive strategies, such as lactate serial checks, in terms of predicting in-hospital mortality.79 SCVO2 can be measured either with a catheter tip in the superior vena cava or from a femoral
catheter with its tip in the inferior vena cava.
Admit all children with proven or suspected septic shock for observation. If the hemodynamic abnormalities (e.g., tachycardia and poor perfusion) were reversed in the emergency department, the child should be admitted to the inpatient floor in collaboration with PICU. All children with septic shock should be admitted to a PICU. As soon as possible after recognizing septic shock, inform the PICU team or initiate transfer to a specialized, probably tertiary care, center with a PICU. This should not delay any ED resuscitative measures and care, but will allow the child to reach definitive care faster.
Pediatric septic shock is a high-stakes diagnosis with elevated morbidity and mortality if not recognized and treated appropriately. As in adults, providers should attempt to recognize it early; ED trigger tools will help. Develop local ED pathways to treat rapidly and appropriately while closely monitoring response to treatment. Children may require up to 60 mL/kg of normal saline over one hour. Recognizing the suspected infectious etiology early will help with the choice of antibiotics; however, consider MRSA in all patients. Finally, if the child is not responding as expected, consider an alternative diagnosis.
Keep in mind the following common pitfalls:
Financial Disclosure: To reveal any potential bias in this publication, and in accordance with Accreditation Council for Continuing Medical Education guidelines, we disclose that Dr. Hocum (pharmacist reviewer) reports he is an employee of United Therapeutics. Dr. Dietrich (editor), Dr. Skrainka (CME question reviewer), Dr. Sawaya (author), Dr. Chedid (author), Dr. El Majzoub (author) Dr. Leetch (peer reviewer), Ms. Coplin (executive editor), Ms. Mark (executive editor), and Ms. Hatcher (editorial group manager ) report no relationships with companies related to the field of study covered by this CME activity.