Association between diastolic blood pressure during the first 24 h and 28-day mortality in patients with septic shock: a retrospective observational study

Background Although the mean arterial pressure (MAP) target of 65 mmHg was achieved, diastolic blood pressure (DBP) was still low in some septic shock patients. The effects of DBP on the prognosis and optimal target for patients with septic shock are unclear. We sought to investigate the relationship between DBP and 28-day mortality in septic shock patients. Methods In this retrospective observational study, we obtained data from the Chinese Database in Intensive Care (CDIC). We included patients with an admission diagnosis of septic shock and shock was controlled. DBP was measured every 1 h, and the mean DBP during the first 24 h (mDBP24h) was recorded. The primary outcome was 28-day mortality. Multivariable logistic regression determined the relationship between mDBP24h and 28-day mortality. Results In total, 1251 patients were finally included. The 28-day mortality of included septic shock patients was 28.3%. The mDBP24h, not mSBP24h, was higher among 28-day survivors compared with non-survivors. 28-day mortality was inversely associated with mDBP24h (unadjusted OR 0.814 per 10 mmHg higher mDBP24h, P = 0.003), with a stepwise increase in 28-day mortality at lower mDBP24h. The 28-day mortality of patients with mDBP24h < 59 mmHg had an absolute risk reduction of 9.4% (P = 0.001). And mDBP24h < 59 mmHg was the remaining high risk factor inversely associated with 28-day mortality after multivariable adjustment (adjusted OR 1.915, 95% CI 1.037–3.536, P = 0.038), while mMAP24h and mSBP24h were not. Conclusion In patients with septic shock after initial resuscitation, we observed an inverse association between mDBP24h and 28-day mortality. The poor outcomes in patients with mDBP24h < 59 mmHg provide indirect evidence supporting a further DBP goal of 59 mmHg for patients with septic shock after MAP of 65 mmHg was achieved. Supplementary Information The online version contains supplementary material available at 10.1186/s40001-023-01315-z.


Background
Septic shock is the most common form of circulatory shock in intensive care units [1].And septic shock is considered a leading causes of death for critical patients worldwide [2].A cross-section survey study of fortyfour ICUs in mainland China showed that septic shock accounted for 53.3% of all sepsis patients, while 90-day mortality was up to 51.94% [3].Thus, the surviving sepsis campaign bundle including fluid resuscitation are the most important therapeutic measures to ensure adequate tissue perfusion and prevent poor outcomes in patients with septic shock [4][5][6].Initially, maintaining a mean arterial pressure (MAP) greater than 65 mmHg as part of the early fluid resuscitations has been always recommended by the surviving sepsis campaign guidelines [4,6].However, even then the target of MAP was achieved, the mortality of septic patients was high [7,8], indicating that simply reaching the MAP target value is inadequate.
Although a MAP of 65 mmHg was achieved, some patients with septic shock had low diastolic blood pressure (DBP) [9,10].DBP is a good marker of vascular tone and upstream pressure for the coronary perfusion.It has been confirmed that low level of DBP, not systolic blood pressure and MAP, was the independent predictor of early progression to septic shock [11], associated with the development of acute kidney injury (AKI) [12,13], and significantly associated with in-hospital mortality [14,15].DBP has been recommended as a trigger to start norepinephrine (NE) treatment while cooperated with MAP in the early resuscitation of septic shock [16,17].Considering the clinical relationships between the DBP level and sepsis progression, maintaining a suitable DBP level could be crucial and have immediate effect on prognosis in patients with septic shock.
Given the lack of clinical evidence of specific DBP target levels in septic shock patients, we sought to describe the relationship between DBP and 28-day mortality among patients with septic shock.We hypothesized that 28-day mortality among patients with septic shock would increase as a function of lower DBP and that a threshold DBP may be identified as an optimal DBP range.

Study population
We conducted a retrospective observational study in which the data were extracted from the Chinese Database in Intensive Care (CDIC).The latest CDIC contains about 7,000 admitted to the Department of Crit Care Medicine, Zhongda Hospital, Southeast University, China, from January 2016 to July 2022.Patients in CDIC with septic shock diagnosis within 24 h after ICU admission and shock control were eligible for inclusion.The diagnosis of septic shock was consistent with the third international consensus definitions for sepsis and septic shock (Sepsis-3) [18].Shock control was defined as achievement of sustained mean arterial blood pressure of at least 65 mmHg, together with urine flow at least 0.5 ml/kg/h for two consecutive hours, or decreased serum lactate great than or equal to 10% from baseline by 6 h after septic shock diagnosis [19].We only included the first intensive Care Unit (ICU) admission of each patients and excluded patients younger than 18 years, died in the first 24 h after ICU admission, accompanied by moderate or severe aortic valve insufficiency.
The present study was approved by the Research Ethics Commission of Zhongda Hospital Southeast University which certified that the present study was performed in accordance with all required guidelines and regulations (2023ZDSYLL004-P01).

Data collection and outcome
All demographic data including age, gender, source of infection, chronic comorbidities, vital sign, laboratory, clinical and outcome data were collected.We included the worst values of laboratory test data in the first 24 h after septic shock admission diagnosis.Vital signs containing DBP, systolic blood pressure (SBP), MAP, heart rate (HR), and central venous pressure (CVP) were all recorded every 1 h.Blood pressure of septic shock patients was preferentially recorded from invasive arterial blood pressure monitoring methods, and otherwise from noninvasive methods.The mean DBP during the first 24 h (mDBP 24h ) was calculated as the mean recorded values of the first 24 h after septic shock admission diagnosis.The other vital signs (mMAP 24h , mSBP 24h , mHR 24h , mCVP 24h ) calculation methods are the same as mDBP 24h .
The primary outcome in the CDIC derivation was 28-day mortality.We also recorded other outcome data, such as new mechanical ventilation (MV) and continuous renal replacement therapy (CRRT) during ICU stay, length of ICU and hospital stay, ICU and hospital mortality.

Statistical analysis
Continuous variables are presented as medians [interquartile ranges (IQRs)] and the Mann-Whitney U test was used for comparison in groups.Categorical variables are expressed as number (percentage), and Pearson χ 2 test is used to compare between groups.The number of missing or censoring values are presented in Additional file 1: Table S1.Variables with more than 25% missing ratio were excluded [21].Outliers were censored, and missing data of less than 25% were replaced with the sequence mean value.
Logistic regression was used to find the association between mDBP 24h and 28-day mortality before and after adjusting for age, gender, Acute Physiology and Chronic Health Evaluation II (APACHE II), peak VIS of the first 24 h after ICU admission.We use the area under the receiver-operator characteristic (AUC, c-statistic) value, and use the Youden's J index to define the optimal cutoff value.The 28-day survival was evaluated using the Kaplan-Meier survival analysis and Cox proportionalhazards analysis.Two-tailed P-value < 0.05 was considered as statistical significance.Analyses were performed by IBM SPSS statistic 25.

Study population
The CDIC included 6997 unique ICU patient admissions, and 1548 patients both met septic shock diagnosis and shock control definition, then 297 was excluded due to the exclusion criteria (Fig. 1).The mean age of 1251 patients with septic shock was 68.0 years (55.0-78.0),including 67.5% males.The median Acute Physiology and Chronic Health Evaluation II score (APACHE II) was 19.0 (14.0-25.0).Lung was the leading cause of infection (50.7%).
The 28-day mortality of the septic shock patients enrolled was 28.3%.Compared with septic shock patients in 28-day survival group, the APACHE II and SOFA score were significantly increased in the 28-day non-survival group (P < 0.001).The proportion of patients using vasoactive drugs and VIS was similar between the two groups.However mDBP 24h and mMAP 24h was significantly lower in 28-day non-survival group, while mSBP 24h was similar (Table 1).
The patients were further divided into two groups according to whether the mDBP 24h was less than 59 mmHg.Compared with patients with mDBP 24h ≥ 59 mmHg, patients with mDBP 24h < 59 mmHg had older age, higher APACHE score, higher serum creatinine, lower levels of central venous oxygen saturation, more patients received mechanical ventilation and renal replacement therapy, and had higher ICU and hospital mortality (Additional file 3: Table S3).We analyzed the relationship between mDBP 24h and 28-day mortality in patients with mDBP 24h < 59 mmHg group.There is no correlation between DBP and mortality in the DBP impaired (mDBP 24h < 59 mmHg) group, OR 0.964 (95%CI 0.925-1.003,P = 0.073), which may be related to the small sample size.
The duration of mDBP 24h < 60 mmHg in the first 24 h was divided according to the interquartile range.Patients with septic shock in the first quartile had the lowest 28-day mortality, indicating that the longer duration of mDBP 24h < 60 mmHg, the higher the 28-day mortality was (P = 0.020) (Fig. 5).In contrast, the longer maintained mDBP 24h in 60-70 mmHg during the first 24 h, the lower the 28-day mortality was (P = 0.009)   (Additional file 7: Figure S2).While in other mDBP 24h ranges, there was no significant difference in mortality among different mDBP 24h duration (Additional file 5: Table S5).
The subgroup analysis of relationship between mDBP 24h ≥ 59 mmHg and 28-day mortality showed that among the septic shocks patients who were younger than 65 years, underlying hypertension, APACHE II above 20, and P/F ratio less than or equal to 187 mmHg, mDBP 24h ≥ 59 mmHg was more relevant to 28-day survival (Fig. 6).Similar subgroup results were found in the relationship between mDBP 24h, mMAP 24h and 28-day survival, but not in mSBP 24h subgroup analysis (Additional file 8: Figure S3).

Discussion
In this retrospective study of a large tertiary ICU septic shock controlled patients, we demonstrate that mDBP 24h is inversely associated with 28-day mortality.The septic shock controlled patients who were able to maintain a mDBP 24h great than or equal to 59 mmHg had lower 28-day mortality.Among those patients with a mDBP 24h blow 59 mmHg, they had more severely illness condition and higher 28-day mortality.These data also suggest that mDBP 24h , not mMAP 24h and mSBP 24h , was an independent predictor of 28-day mortality.
Surviving Sepsis Campaign guidelines recommended targeting a MAP of 65 mmHg in the initial resuscitation of septic shock patients [4].However, even if septic shock patients get the MAP target above 65 mmHg, the 90-day mortality was still around 40% [8,22].Numerous studies have confirmed that there are still microcirculation disorders after shock resuscitation [23,24].DBP was the only independent microcirculatory determinant of tissue oxygen saturation resaturation (resStO 2 ) [25], which was measured by Near infrared spectrometry as one of the main studied microcirculation parameters and strongly associated with outcome in sepsis patients [26,27].The findings of our study, which showed a higher DBP target (≥ 59 mmHg) in septic shock controlled patients was associated with lower lactate levels and better prognosis, may indirectly support the view of a correlation between DBP and microcirculation perfusion.
Vasodilation is an important pathophysiological feature and plays a key role in the progression of hypotension and tissue hypoperfusion in septic shock [28].Considering DBP is a good marker of arterial tone, a low DBP in patients with septic shock detected at peripheral vessels should reflect the systemic vasodilation [10].A retrospective cohort study indicated that DBP lower than 52 mmHg of nonsevere sepsis patients at emergence department(ED) triage (OR 4.59; 95% CI 1.57-13.39)was independently predict early progression to severe sepsis or septic shock within 96 h of ED presentation [11].Other trials showed that low DBP was associated with the development of severe AKI [13].And DBP within 24 h admission, not MAP, was a potential important hemodynamic target for preventing AKI in ICU patients [12].Further studies proved that DBP, but not SBP, was one of the independent positive predictive factors of ICU patients' outcome [14,15,29].We also found that the serum creatinine was significantly higher in the low mDBP 24h group and a strong independent association between mDBP 24h and mortality.
Another physiological feature of DBP is a determinant of coronary perfusion.More than 50% of patients with septic shock have evidence of a reduced coronary flow blood reserve, which is a predictor of ICU mortality in septic shock [30].A low DBP may impair the myocardial perfusion, especially in the case of tachycardia [31].Our study showed that myoglobin was significantly higher in the low mDBP 24h group, suggesting that low DBP may be associated with myocardial ischemia.SPRINT data confirmed that a DBP lower than 50 mmHg was significantly associated with increased cardiovascular events in patients with 50 years older and a screening SBP of 130 to 180 mmHg [32].And a DBP lower than 70 mmHg was significantly associated with mortality of patients with coronary artery disease [33].A national cross-sectional survey showed that 39.6% and 17.0% of sepsis patients, respectively, had underlying hypertension and coronary artery disease in Chinese ICUs [3].Therefore, a low DBP level during treatment for septic shock may significantly increase the risk of cardiovascular events.
The possible pathophysiological mechanisms of low DBP and high mortality are as follows: first, low DBP indicates more obvious vasodilation, which will lead to tissue hypoperfusion [10,13]; second, low DBP will lead to reduced coronary blood flow and increase cardiovascular adverse events [30,33]; the last one, low DBP is Fig. 2 28-day mortality as a function of the mDBP 24h of septic shock controlled patients associated with impaired microcirculation [25].Therefore, we need to further correct low DBP even after MAP target is achieved.
European Society of Intensive Care Medicine recommended that the combination of MAP (60-65 mmHg) and DBP (> 40 mmHg) targets should be considered as trigger to start vasopressor treatment in septic shock    gested that we should initiated noradrenaline infusion along with the 30 ml/kg fluid bolus when DBP is lower than 50 mmHg [34].However, these DBP cutoff values were either based of experts practice or the estimated value corresponded with a MAP of 65 mmHg and a SBP of 90 mmHg, and were not supported by clinical studies.Our findings supported that the mDBP 24h should be raised to a higher pressure level (≥ 59 mmHg) in the first 24 h of patients with septic shock controlled after initial resuscitation, showing it was associated with the illness severity and mortality benefit.

Limitations
This retrospective study has a number of inherent limitations we should acknowledge.First, the missing data could bias the results and also other possible residual confounders due to single-center retrospective design, Second, patients were retrospectively enrolled from a single center which may impede the generalization of the results.The results of this single-center retrospective study need further studies to confirm.Third, this observational study could not lead to causal inferences for any associations.Finally, the mDBP 24h may include both noninvasive and invasive arterial pressure, and we could not distinguish the source of DBP measurements.Fig. 6 Subgroup analysis of the association between 28-day mortality and mDBP 24h ≥ 59 mmHg in septic shock patients

Conclusions
There was an inverse correlation between DBP in the first 24 h and 28-day mortality among septic shock controlled patients admitted to the ICU.Patients with a mDBP 24h less than 59 mmHg during the first 24 h after septic shock controlled had an increased risk of 28-day mortality.These findings provide indirect support for a DBP target of 59 mmHg for septic shock controlled patient in ICU.More high quality prospective or randomized controlled studies are needed to further validate the DBP target in septic shock patients.

Fig. 1
Fig. 1 Flow of screening the shock controlled patients after ICU admission of septic shock

Table 1
Baseline data of septic shock patients between 28 days survival and no-survival groups APACHE II Acute Physiology and Chronic Health Evaluation II, SOFA Sequential Organ Failure Assessment, COPD Chronic Obstructive Pulmonary Disease, mSBP 24h mean Systolic Blood Pressure of the first 24 h after septic shock, mDBP 24h mean Diastolic Blood pressure of the first 24 h after septic shock, mMAP 24h mean Mean Artery Pressure of the first 24 h after septic shock, mHR 24h mean Heart Rate of the first 24 h after septic shock, mCVP 24h mean Centre Venous Pressure of the first 24 h after septic shock, IQR Interquartile Range, VIS Vasoactive-Inotropic Score, CRRT Continuous Renal Replacement Therapy

Table 2
Baseline characteristics of the study population according to different mDBP

Table 2 (
continued) APACHE II Acute Physiology and Chronic Health Evaluation II, SOFA Sequential Organ Failure Assessment, COPD Chronic Obstructive Pulmonary Disease, mSBP 24h mean Systolic Blood Pressure of the first 24 h after septic shock, mDBP 24h mean Diastolic Blood pressure of the first 24 h after septic shock, mMAP 24h mean Mean Artery Pressure of the first 24 h after septic shock, mHR 24h mean Heart Rate of the first 24 h after septic shock, mCVP 24h mean Centre Venous Pressure of the first 24 h after septic shock, IQR Interquartile Range, VIS Vasoactive-Inotropic Score, CRRT Continuous Renal Replacement Therapy a Intravenous fluid included crystalloids and colloid in the first 24 h after ICU admission of septic shock

Table 3
Predictors of 28-day mortality on multivariable regressionAPACHE II Acute Physiology and Chronic Health Evaluation II, mDBP 24h mean Diastolic Blood pressure of the first 24 h after septic shock, mSBP 24h mean Systolic Blood Pressure of the first 24 h after septic shock, mMAP 24h mean Mean Artery Pressure of the first 24 h after septic shock, P/F ratio Ratio of arterial partial oxygen pressure to inhaled oxygen concentration VIS Vasoactive-Inotropic Score

Table 4
Cumulative survival analysis of septic shock patients with different mDBP 24h levels