Vasopressors and inotropes in the treatment of human septic shock: effect on innate immunity?

Catecholamines have been suggested to modulate innate immune responses in experimental settings. The significance hereof in the treatment of human septic shock is unknown. We therefore sought if and how vasopressor/inotropic doses relate to pro-inflammatory mediators during treatment of septic shock. We prospectively studied 20 consecutive septic shock patients. For 3 days after admission, hemodynamic variables, lactate and plasma levels of interleukins (IL)-6 and 8, tumor necrosis factor (TNF)-α, and elastase-α(1)-antitrypsin were measured six hourly. Doses of vasoactive drugs were recorded. Of the 20 patients, nine died in the intensive care unit. Dobutamine doses were positively associated and related to TNF-α plasma levels, independently of disease severity, hemodynamics, and outcome, in multivariable models. Dopamine doses were positively associated with IL-6, and norepinephrine was inversely associated with IL-8 and TNF-α levels. Our observations suggest that catecholamines used in the treatment of human septic shock differ in their potential modulation of the innate immune response to sepsis in vivo. Dobutamine treatment may contribute to circulating TNF-α and dopamine to IL-6, independently of activated neutrophils. Conversely, norepinephrine may lack pro-inflammatory actions.

INTRODUCTION

Human septic shock is characterized by release of pro-inflammatory mediators in the host defense against invading microorganisms, which overwhelms anti-inflammatory mediators, following activation of the complement system and neutrophils and production of cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukins [1-5]. Vasopressor and inotropic drugs commonly used in the treatment of the syndrome to augment arterial blood pressure and cardiac function have been suggested to down- or upregulate innate immunity in experimental settings with contradicting results, depending on models, species, challenges, drugs, and adrenergic receptors [6-22]. It has been suggested that the use of drugs in the hemodynamic management of human septic shock may modulate immune responses in vivo and thereby contribute to their effects on outcome, even independently of hemodynamics [8, 20, 23, 24]. In experimental human endotoxemia, for instance, low doses of β-adrenergic dobutamine did not inhibit circulating innate immune responses, while epinephrine did [25]. In contrast, in a single randomized clinical trial, dobutamine was suggested to increase hepatosplanchnic release of TNF-α in septic shock, as compared to treatment by enoximone [26]. The interest for catecholamine-induced modulation of immune responses has recently been revived by the observation that endogenous, neutrophil-derived catecholamines play an important (autocrine) role in the host defense during experimental sepsis [10, 27]. There are no in vivo data to support any action of catecholamine drugs on inflammatory responses.

To further elucidate a potential role in vivo of drug treatment of human septic shock in modulating innate immunity, we measured, at six-hourly intervals, pro-inflammatory mediators and recorded vasopressor/inotropic drug doses in 20 consecutive septic shock patients until 72 h after admission in the intensive care unit (ICU) and studied longitudinal associations and relations between variables in the course of disease.

MATERIALS AND METHODS

Patients

We prospectively studied 20 consecutive patients admitted into the ICU because of septic shock, not receiving corticosteroid treatment. After obtaining informed consent in each eligible patient or closest relative, patients were enrolled within 12 h after admission. The study had been approved by the Institutional Review Board and the Hospital Committee on Ethics. Criteria for septic shock were clinical evidence of infection, temperature above 38.5°C or below 36.0°C, tachycardia (>90 beats/min), and tachypnea (>20/min) or necessity for mechanical ventilation. Shock was defined as a fall in systolic arterial blood pressure below 90 mmHg or by more than 30 mmHg in prior hypertensive patients (in the absence of other causes of hypotension and despite adequate fluid administration), or need for administration of vasoactive therapy, together with at least one sign of inadequate tissue perfusion (oliguria, mental alterations, hyperlactatemia).

Therapeutic Protocol

Patients were monitored with help of an arterial catheter for measurement of mean arterial pressure (MAP; millimeters of mercury) and by a pulmonary artery catheter (n = 14) for measurement of cardiac output (CO; liters per minute), central venous pressure (CVP; millimeters of mercury), mean pulmonary artery pressure (millimeters of mercury), and pulmonary artery occlusion pressure (millimeters of mercury). In the absence of a pulmonary artery catheter, CVP monitoring was done with help of a central venous catheter. The heart rate (beats per minute) was recorded continuously. Patients were treated by attending physicians not involved in the study, with help of antibiotics (after taking appropriate samples for culture), fluids, and vasoactive drugs through continuous infusions, as guided by the clinical and hemodynamic response. Dopamine, dobutamine, and/or norepinephrine were infused if an increase in forward blood flow or pressure, respectively, was considered necessary, on clinical ground. Blood cultures were taken when clinically indicated. Local specimens for culture were collected depending on a suspected focus of infection. Blood cultures were processed using delayed vial entry bottles for aerobic and anaerobic cultures and Bactec 94/9240 automatic analyzers (Becton-Dickinson, Erembodegem, Belgium). Bottles were incubated for a maximum of 7 days. If the analyzers showed growth, Gram stains were prepared and the sensitivity of the organisms for antibiotics was assessed. Local cultures were processed according to standardized procedures. Mechanical ventilation was instituted in all but one patient.

Study Protocol

Patient variables, such as age, gender, underlying disease, source of sepsis, blood, and local culture results, were recorded. Variables necessary to compute the Acute Physiology and Chronic Health Evaluation (APACHE)-II score were recorded and used to estimate severity of disease in critically ill patients. For 3 days (days 0, 1, and 2) after admission, patients entered a six-hourly hemodynamic measurement and blood sampling schedule, at 3.00, 9.00, 15.00, and 21.00 h, as soon as possible after enrollment (beginning at day 0). In our unit, pulmonary artery catheters are removed 72 h after insertion to prevent catheter-related infection. Hemodynamic variables were measured with patients in the supine position, after calibration and zeroing to atmospheric pressure at the mid-chest level (Viggo-Spectramed, Spectramed, Bilthoven, The Netherlands; monitor TramscopeR, Marquette Electronics, Milwaukee, WI, USA), at end-expiration. For CO measurements, the average of triplicate injections of 10 mL of D5W at room temperature, at random in the respiratory cycle, was used. The doses of concomitantly infused vasoactive drugs were recorded. Hemodynamic measurements were performed until the pulmonary artery catheter was taken out by the attending physicians or until death. Heparin-anticoagulated blood was taken six hourly from the arterial catheter to determine plasma lactate levels and daily to determine creatinine plasma levels. Blood samples for the determination of plasma levels of pro-inflammatory mediators that are commonly implicated in the pathogenesis of severe sepsis and shock were obtained at inclusion and every 6 h. The samples were collected in tubes containing soybean trypsin inhibitor (100 μg/mL, final concentration), ethylenediaminetetraacetate (10 mmol/L), and benzamidine (10 mmol/L) to prevent in vitro activation. All tubes were centrifuged for 10 min at 1,300×g, and aliquots of the plasma were stored immediately at −70°C until assayed. The length of stay until discharge from, or death in the ICU, was recorded. Patients were considered to have survived septic shock if alive until discharge from the ICU.

Assays

Lactate concentrations (normal value <1.8 mmol/L) and creatinine (normal value <130 μmol/L) concentrations in plasma were determined with help of an analyzer (Boehringer-Mannheim Hitachi analyzers 911 and 747, Almere, The Netherlands). Plasma interleukin (IL)-6 levels were measured by an enzyme-linked immunosorbent assay using the monoclonal antibody CLB.IL-6 [3]. Results were related to dose–response curves obtained with recombinant IL-6 and expressed as picograms per milliliter. The upper limit of normal is 10 pg/mL. IL-8 was measured by an ELISA in which antibodies to human recombinant IL-8 (rIL-8; British Biotechnology Ltd, Oxford, UK) were used. Plates were coated with a monoclonal antibody against rIL-8 (CLB3.IL-8), and bound IL-8 was detected by a biotinylated monoclonal antibody. The lower detection limit is <5 pg/mL with normal values below 20 pg/mL. The TNF-α plasma concentration was measured by enzyme immunoassay (Innogenetics, Zwijnaarde, Belgium), with an interassay variation of 9% and an intra-assay variation ranging from 0.8% to 8%; the lower limit of detection is 4 pg/mL and normal values are less than 20 pg/mL. Elastase-α1-antitrypsin was measured with help of a radioimmunoassay. Normal values for elastase-α1-antitrypsin are <100 ng/mL. The intra- and interassay variation coefficients for the assays described were <15 and <20%, respectively.

Calculations and Statistical Analysis

Cardiac index (CI) was calculated as CO/body surface area (liters per minute per square meter). If necessary, values were logarithmically transformed to obtain normal distributions (Kolmogorov–Smirnov test P > 0.05). To study doses of vasopressor/inotropic drugs in relation to pro-inflammatory mediators, generalized estimating equations (GEE) were done, to take repeated measurements in the same patients into account; we entered APACHE-II, MAP, CI, and survival as covariates to adjust for disease severity, hemodynamics, and outcome. The standardized regression coefficient was calculated from the regression coefficient multiplied by the ratio of standard deviations. Differences between groups in initial, highest, and final values for hemodynamic and pro-inflammatory mediators were evaluated using the non-parametric Mann–Whitney U test. For dobutamine, the partial correlation coefficient (r), with patient number and time as covariates, was used to evaluate relations for pooled data, taking repeated measurements in the same patients into account, as well as APACHE-II scores and MAP. Exact P values are given if >0.001 and were considered statistically significant if <0.05. Values are median and range in text and tables and mean ± standard error of the mean (SEM) in figures.

RESULTS

Patient Characteristics

Table 1 describes patient characteristics. Nine patients (45%) died in the ICU, four of them within 3 days after admission. On day 1, two patients died and one patient was discharged from the ICU. On day 2, one patient died and one patient was discharged from the ICU. On day 3, one patient died and one patient was discharged from the ICU, leaving 13 patients in the study at 72 h after inclusion.

Table 1

Patient Characteristics

Age (years)	65 (21–83)
Gender (male/female)	12/8
Underlying disease
COPD	3
Diabetes mellitus	1
Ischemic heart disease	3
Liver cirrhosis	6
Malignancy	7
Renal insufficiency	1
Vascular disease	1
Other	4
Source of sepsis
Cholecystitis/cholangitis	2
Diverticulitis	1
Ischemic colitis	1
Mediastinitis	1
Respiratory tract infection	7
Urinary tract infection	4
Genital tract infection	1
Endocarditis	1
Skin	2
APACHE-II score	31 (15–41)
Mechanical ventilation	18
Vasopressor/inotropic treatment	20
Serum creatinine (μmol/L)	177 (49–675)
Renal replacement therapy	6
Duration of observation (h)	72 (6–72)
Length of stay in the ICU (days)	5 (1–29)
Mortality in the ICU	9

Median (range) or number of patients where appropriate

COPD chronic obstructive pulmonary disease, APACHE-II score, Acute Physiology and Chronic Health Evaluation-II score, ICU intensive care unit

Hemodynamics

As seen in Table 2, patients had a hyperdynamic circulation with tachycardia, mild hypotension, and increased CI. Mean arterial pressure was lower and CVP, and lactate plasma levels were higher in non-survivors compared to survivors. Non-survivors had more vasopressor drugs administered compared to survivors (Table 3). Seven patients had received dobutamine at any point of the disease course. Non-survivors had persistent lactic acidosis.

Table 2

Hemodynamic Variables and Vasopressors/Inotropics in the Course of Disease in Outcome Groups

		Survivors	Non-survivors	P
		n = 11	n = 9
HR, beats/min	I	118 (105–150)	126 (97–143)	0.73
	H	120 (105–176)	130 (100–159)	0.91
	L	100 (68–133)	116 (90–130)	0.23
	F	107 (61–133)	130 (90–146)	0.22
MAP, mmHg	I	70 (53–100)	63 (49–82)	0.27
	H	90 (76–100)	80 (49–96)	0.14
	L	58 (46–80)	56 (42–72)	0.34
	F	76 (70–91)	56 (42–91)	0.03
CVP, mmHg	I	8 (4–13)	9 (4–18)	0.30
	H	11 (6–15)	17 (11–21)	0.003
	L	5 (4–8)	7 (2–18)	0.76
	F	7 (5–15)	12 (5–22)	0.03
CI, L/min/m2	I	4.2 (2.1–6.2)	3.4 (1.8–7.2)	0.90
	H	4.6 (3.0–6.6)	3.5 (2.4–7.2)	0.56
	L	1.6 (2.1–5.2)	2.6 (1.5–6.8)	0.52
	F	3.7 (2–6)	3.2 (2.0–6.8)	0.52
Lactate, mmol/L	I	1.7 (1.0–5.1)	2.6 (0.9–10.0)	<0.001
	H	2.0 (1.3–5.1)	3.5 (1.1–11.6)	0.14
	L	1.0 (0.7–2.0)	1.9 (0.7–10.0)	0.05
	F	1.1 (0.9–2.0)	2.4 (1.0–11.6)	0.01

Median (range) and Mann–Whitney U test

HR heart rate (beats per minute), MAP mean arterial pressure, CVP central venous pressure, CI cardiac index. I initial, H highest, L lowest, F final values in the course of time

Table 3

Course of pro-inflammatory mediators and drug doses in outcome groups

	Survivors	Non-survivors	P
	n = 11	n = 9
Inflammatory mediators
IL-6, pg/mL
I	293 (17–60,152)	475 (74–161,787)	0.77
H	320 (31–60,152)	761 (197–161,787)	0.55
F	48 (4–426)	133 (9–161,787)	0.11
IL-8, pg/mL
I	573 (29–10,429)	1,357 (98–12,741)	0.26
H	843 (47–10,458)	1,648 (225–12,741)	0.41
F	85 (7–1,085)	345 (52–12,741)	0.04
TNF-α, pg/mL
I	49 (17–301)	56 (9–79)	0.46
H	66 (39–301)	56 (19–90)	0.30
F	30 (5–82)	26 (5–90)	0.94
Elastase-α1-antitrypsin, ng/mL
I	145 (10–716)	131 (12–707)	0.82
H	200 (18–721)	168 (12–905)	0.77
F	98 (18–570)	160 (9–405)	0.60
Drug doses
Dopamine, μg/kg/min
I	8 (0–19)	17 (8–22)	0.007
H	12 (0–19)	19 (8–27)	0.012
F	2 (0–16)	19 (5–27)	<0.001
Dobutamine, μg/kg/min
I	0 (0–21)	0 (0–22)	0.23
H	0 (0–21)	12 (0–30)	0.11
F	0 (0–5)	5 (0–30)	0.07
Norepinephrine, μg/kg/min
I	0 (0–0.16)	0 (0–0.13)	0.15
H	0.05 (0–0.21)	0.24 (0–0.34)	0.004
F	0 (0–0.16)	0.14 (0–0.34)	0.002

Median (range) and Mann–Whitney U test

IL-6 (8) interleukin-6 (8), TNF-α tumor necrosis factor alpha, I initial, H highest, F final values in the course of time

Pro-inflammatory Mediators

IL-6 and IL-8 plasma levels were elevated above normal in 189 of 195 (97%) and 190 of 195 (97%) measurements, respectively. TNF-α plasma levels were elevated above normal in 125 of 160 (78%) and elastase-α1-antitrypsin in 126 of 195 (65%) measurements. Inflammatory mediators did not differ between survivors and non-survivors, besides final IL-8 levels which were higher in non-survivors (Table 3). The seven patients receiving dobutamine in the disease course had higher TNF-α levels (47 [6-130] pg/mL) than those not receiving dobutamine (30 [5-301] pg/mL), independently of APACHE-II scores, MAP, CI, use of other drugs, and outcome (GEE, P < 0.001).

Associations and Relations Between Vasopressor Doses and Innate Immunity

Figure 1 shows that TNF-α plasma levels fell less in the seven septic shock patients with dobutamine compared to the 13 patients without dobutamine. Table 4 shows that plasma levels of TNF-α were higher in those patients receiving dobutamine than in those not receiving the drug, independent of APACHE-II, MAP, CI, and use of other drugs. In a multivariable analysis including outcome, dobutamine doses were positively associated with TNF-α levels (standardized regression coefficient 0.57, P < 0.001), independently of APACHE-II, hypotension (P = 0.031), CI, and non-survival (P = 0.007). The partial correlation coefficient for the relation between TNF-α and dobutamine, adjusted for repeated measurements and APACHE II score, was 0.38 (P < 0.001). Figure 2 shows the relation between TNF-α levels and dobutamine doses in those patients receiving the drug. Other associations were observed between dopamine doses and IL-6 levels and, inversely, between norepinephrine doses and IL-8 and TNF-α levels, in some multivariable models. In any case, none of the vasopressor/inotropic drugs was associated with elastase-α1-antitrypsin levels.

Fig. 1

Course of TNF-α plasma levels in seven septic shock patients with (filled circles) and 13 patients without (open squares) dobutamine infusion at six-hourly time points for the first 72 h after inclusion. Values are mean ± SEM; P = 0.018 (GEE).

Table 4

Generalized Estimating Equations for Pro-Inflammatory Mediators and Vasopressor/Inotropic Doses

	IL-6 (pg/mL)		IL-8 (pg/mL)		TNF-α (pg/mL)		Elastase-α1-antitrypsin (ng/mL)
	B	P	B	P	B	P	B	P
Univariable:
Dopamine, μg/kg/min	0.33	0.03		0.48		0.85		0.77
Dobutamine, μg/kg/min		0.19		0.89	0.24	0.01		0.26
Norepinephrine, μg/kg/min		0.57		0.10	–0.30	0.03		0.17
Multivariable:
Dopamine, μg/kg/min	0.33	0.02		0.08		0.74		0.53
Dobutamine, μg/kg/min		0.40		0.80	0.36	<0.001		0.24
Norepinephrine, μg/kg/min		0.70	−0.22	0.02	−0.38	0.04		0.15
APACHE-II	−0.35	0.04		0.91		0.06		0.36
Dopamine, μg/kg/min		0.06		0.16		0.85		0.22
Dobutamine, μg/kg/min		0.87		0.69	0.21	0.02		0.27
Norepinephrine, μg/kg/min		0.51	−0.23	0.01		0.10		0.06
MAP	−0.28	0.01		0.06		0.18	0.09	0.004
Dopamine, μg/kg/min	0.40	0.01		0.31		0.82		0.64
Dobutamine, μg/kg/min		0.29		0.77	0.60	<0.001		0.43
Norepinephrine, μg/kg/min		0.84		0.07		0.45		0.42
CI, L/min/m2	0.51	0.002		0.17	0.20	0.02		0.11

Only statistically significant regression coefficients are shown

IL-6 (8) interleukin-6 (8), TNF-α tumor necrosis factor-alpha, APACHE-II Acute Physiology and Chronic Health Evaluation-II score, MAP mean arterial pressure, CI cardiac index, B standardized regression coefficient

Fig. 2

Scatterplot of pooled data of (logarithmic) TNF-α plasma levels against dobutamine doses given in seven patients with septic shock treated with help of dobutamine (any dose), at six-hourly time points for the first 72 h after inclusion for observations when dobutamine was given, partial r = 0.29, P = 0.06 in survivors (filed circles) and r = 0.42, P = 0.001 in non-survivors (open squares).

DISCUSSION

Our observations suggest that, in the treatment of human septic shock, dobutamine increases circulating TNF-α and dopamine increases IL-6, independently of disease severity, hemodynamics, and outcome. Conversely, norepinephrine may lack pro-inflammatory properties. The differences between dobutamine and dopamine suggest that β and dopaminergic actions were involved, respectively.

The immune alterations, hemodynamic abnormalities, and associations with mortality in our patients agree with previous reports [1–5, 28]. The positive association and relation between increases in TNF-α with increasing doses of dobutamine, a β1- and a weak α1- and β2-adrenergic receptor agonist, agrees with the literature suggesting dobutamine- and not enoximone-induced secretion of TNF-α in isolated hepatocytes and the hepatosplanchnic region of septic shock patients [7, 26]. It may not agree with the lack of effect of the drug in the human endotoxemia model [25] and the inhibition of TNF-α and IL-8 secretion in endotoxin-challenged isolated (human) monocytes and whole blood by β-adrenergic receptor actions [9, 13, 15, 20]. Indeed, circulating leukocytes may not be the source of the TNF-α increase by dobutamine in our study, since the drug did not affect levels of neutrophilic elastase-α1-antitrypsin. Nevertheless, our data may also be in line with the pro-inflammatory effect of β-receptor stimulation enhancing IL-6 and IL-8 production in endotoxin-challenged human monocytes, whole blood, or endothelial cells in vitro [11, 14, 18]. Moreover, the inverse association between TNF-α and IL-8 on the one hand and doses of norepinephrine, an α1,2- and weak β1-agonist, on the other further supports involvement of β1-receptors in the potentially pro-inflammatory effect of dobutamine. On the other hand, the data may explain in part the detrimental effects of high-dose dobutamine used in previous studies to increase tissue oxygen delivery to supranormal levels in shock states that may otherwise be beneficial [20].

Alpha- and β-receptor stimulation may have opposing effects on TNF-α production in vitro, since (endogenous) α2-receptor stimulation may stimulate TNF-α production by macrophages and Kupffer cells in some experimental studies [19] but not in others [17], and in vivo reports are scarce [10, 16, 22]. The negative associations between TNF-α and IL-8 levels and norepinephrine dosing, however, suggests an anti-inflammatory effect by norepinephrine via α-receptor stimulation in septic shock, as suggested before to occur in septic patients [9]. In contrast, dopamine treatment was associated with increased IL-6 levels in most models evaluated, suggesting IL-6 release by endothelium or hepatocytes by D2 receptors, as reported [7, 8, 11, 21]. In any case, the effect of dopamine, having β1- and α1-adrenergic properties also [8], may have been different from that of dobutamine and norepinephrine, thereby favoring predominant dopaminergic effects. Stress or catecholamines have also been implicated in the regulation of IL-10 [8, 9, 14, 18], which we did not measure, so we cannot exclude that alterations in the latter did underlie some of the reported associations and relations. Nevertheless, potentially less pro-inflammatory effects of norepinephrine than of dopamine and dobutamine may explain in part a better outcome of use of the former in the treatment of shock in the observational SOAP study [24]. In the study by De Backer, norepinephrine- and dopamine-treated patients had similar mortality, but adverse events were more frequent with the latter [29]. Otherwise, the lack of potential effect of catecholamines used in the treatment of septic shock on neutrophil activation agrees with a previous study in healthy volunteers [30], but contrasts with aggravation and amelioration of endotoxin-induced lung injury in rats by α1- and α2-receptor actions on neutrophils, respectively [6].

The limitations of our study include relatively small number of patients and, by virtue of study design, evidence on the basis of statistical associations and relations only, so that results should be interpreted cautiously. For instance, the predictive value of circulating pro-inflammatory mediators for outcome, reported by others [1-5], could not be confirmed, except for IL-8, by our small study and limited period of observation. On the other hand, analyses were adjusted for disease severity, hemodynamics, and outcome, so that the positive relation between dobutamine doses and TNF-α levels in the early course of disease may reflect cause effect relations, rather than a common origin, i.e., severe shock with TNF-α-induced myocardial depression necessitating dobutamine treatment and being associated with demise [28]. Indeed, this is the first study, to our knowledge, to address the in vivo immune-modulating effect of various catecholamines used early in the management of septic shock, independently of disease severity, hemodynamics, and outcome. Prospective evaluations of drug effects in septic shock may wish to include pro-inflammatory mediator levels. In fact, our observations argue in favor of immunosurveillance in future studies on the hemodynamic management of human septic shock with help of vasopressor/inotropic drugs.

In conclusion, our prospective observations suggest that catecholamines used early in the treatment of human septic shock differ in their potential to modulate the innate immune response to sepsis in vivo, by differing adrenergic and dopaminergic receptor stimulation.