metricas
covid
Buscar en
Enfermedades Infecciosas y Microbiología Clínica (English Edition)
Toda la web
Inicio Enfermedades Infecciosas y Microbiología Clínica (English Edition) Computerised sepsis protocol management. Description of an early warning system
Journal Information
Vol. 36. Issue 2.
Pages 84-90 (February 2018)
Visits
2044
Vol. 36. Issue 2.
Pages 84-90 (February 2018)
Original article
Full text access
Computerised sepsis protocol management. Description of an early warning system
Protocolo informático de manejo integral de la sepsis. Descripción de un sistema de identificación precoz
Visits
2044
Begoña de Diosa,
Corresponding author
begomarsella@hotmail.com

Corresponding author.
, Marcio Borgesa, Timothy D. Smithb, Alberto del Castilloc, Antonia Sociasc, Leticia Gutiérrezc, Jordi Nicolásd, Bartolomé Lladóe, Jose A. Rochef, Maria P. Díazg, Yolanda Lladóa, Equipo de Sepsis
a Unidad Multidisciplinar de Sepsis, Hospital Son Llàtzer, Palma de Mallorca, Spain
b Servicio de Medicina Intensiva, Clínica Juaneda, Palma de Mallorca, Spain
c Servicio Medicina Intensiva, Hospital Son Llàtzer, Palma de Mallorca, Spain
d Servicio de Farmacia, Hospital Son Llàtzer, Palma de Mallorca, Spain
e Servicio de Medicina Interna, Hospital Son Llàtzer, Palma de Mallorca, Spain
f Servicio de Urgencias, Hospital Son Llàtzer, Palma de Mallorca, Spain
g Servicio de Microbiología, Hospital Son Llàtzer, Palma de Mallorca, Spain
This item has received
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (1)
Tables (6)
Table 1. Activation criteria for the protocol for the comprehensive management of sepsis.
Table 2. Recommendations for the management of severe sepsis and septic shock.
Table 3. Score criteria in the Computerized Vital Sign Detection System (CVSDS).
Table 4. Mechanism of consultation and treatment modification per unit.
Table 5. Type of intervention conducted per unit.
Table 6. Type of intervention based on the source of infection.
Show moreShow less
Abstract
Introduction

New strategies need to be developed for the early recognition and rapid response for the management of sepsis. To achieve this purpose, the Multidisciplinary Sepsis Team (MST) developed the Computerized Sepsis Protocol Management (PIMIS). The aim of this study was to evaluate the convenience of using PIMIS, as well as the activity of the MST.

Methods

An analysis was performed on the data collected from solicited MST consultations (direct activation of PIMIS by attending physician or telephone request) and unsolicited ones (by referral from the microbiology laboratory or an automatic referral via the hospital vital signs recording software [SIDCV]), as well as the hospital department, source of infection, treatment recommendation, and acceptance of this.

Results

Of the 1581 first consultations, 65.1% were solicited consultations (84.1% activation of PIMIS and 15.9% by telephone). The majority of unsolicited consultations were generated by the microbiology laboratory (95.2%), and 4.8% from the SIDCV. Referral from solicited consultations were generated sooner (5.63days vs 8.47days; p<0.001) and came from clinical specialties rather than from the surgical ward (73.0% vs 39.1%; p<0.001). A recommendation was made for antimicrobial prescription change in 32% of first consultations. The treating physician accepted 78.1% of recommendations.

Conclusions

The high rate of solicited consultations and acceptance of recommended prescription changes suggest that a MST is seen as a helpful resource, and that PIMIS software is perceived to be useful and convenient to use, as it is the main source of referral.

Keywords:
Sepsis
Computer-assisted sepsis management protocol
Hospital multidisciplinary sepsis team
Resumen
Introducción

Es preciso desarrollar nuevas estrategias que permitan una identificación precoz y una inmediata instauración de medidas efectivas en el abordaje de la sepsis. La unidad multidisciplinar de sepsis (UMS) desarrolló una herramienta: el Protocolo Informático de Manejo Integral de la Sepsis (PIMIS). El objetivo de este estudio es evaluar la intervención de la UMS y la utilidad del PIMIS.

Métodos

Se analizaron las intervenciones según fueran realizadas por consulta directamente solicitada (activación de PIMIS o consulta telefónica) o no solicitada (aislamientos microbiológicos y el Sistema Informático de Detección de Constantes Vitales [SIDCV]), los servicios, el tipo de infección, la recomendación de cambio de antibiótico y el grado de aceptación.

Resultados

De las 1.581 consultas, el 65,1% se solicitaron directamente: un 84,1% por activación del PIMIS por el médico responsable y un 15,9% por contacto telefónico directo. Entre las consultas no solicitadas, el 95,2% procedían de microbiología y el 4,8% del SIDCV. Las consultas directamente solicitadas se realizaron más precozmente que las no solicitadas (5,63días vs. 8,47días; p<0,001) y la frecuencia fue mayor en los servicios médicos frente a los quirúrgicos (73,0% vs. 39,1%; p<0,001). Se recomendó un cambio de antibiótico en el 32% de las primeras consultas y se aceptó en el 78,1% de los casos.

Conclusiones

La elevada proporción de consultas directamente solicitadas y aceptación de las recomendaciones demuestra que la intervención de la UMS es valorada y respetada. El PIMIS es el principal mecanismo de consulta, lo que lo convierte en una herramienta útil y conveniente para la identificación precoz y el abordaje de la sepsis.

Palabras clave:
Sepsis
Protocolo Informático de Manejo Integral de la Sepsis
Unidad multidisciplinar de sepsis
Full Text
Introduction

Sepsis is still one of the leading causes of death among hospitalized patients. In Spain, the latest studies show that there has been an increase in its incidence.1 Thus, it is essential to develop early detection mechanisms and tools in order to prevent the development of complications.

During the last few years, different strategies have been created in order to improve the management of sepsis, some of them originated in the critical care medicine department or in the internal medicine unit.2,3 Also, the essential role played by the nursing team in its detection and follow-up has been stressed out.4,5

In an attempt to improve the comprehensive management of patients with sepsis, back in the year 2006 our center created the very first multidisciplinary unit in sepsis care (MUSC) in Spain. The team included one (1) doctor with specific formation in infectious diseases plus one (1) nurse with exclusive dedication, and one (1) multidisciplinary team with partial dedication including specialists on the following medical fields: intensive medicine; ER; pneumology; internal medicine; pharmacy; microbiology; and general surgery.

The MUSC has a triple goal. In the first place, it is focused on promoting the early detection of severe sepsis. Secondly, on implementing measures for the management and treatment of sepsis based on the guidelines proposed by the Surviving Sepsis Campaing.6 Thirdly, the MUSC aims at optimizing antibiotic treatments.

The involvement of a specialist on infectious diseases has been confirmed to improve the prognosis of these patients.7,8 At some centers, other multidisciplinary teams have been implementing programs to optimize the antibiotic treatment resulting in an improvement of both the prescription process and the use of antibiotics.9,10

In order to guarantee an early intervention, the MUSC created one computerized tool: The Computerized Protocol for the Comprehensive Management of Sepsis (PIMIS, in Spanish). Its goals are: to allow the early identification of sepsis and the immediate implementation of a set of effective measures in order to avoid the development of complications and improve the prognosis of patients.

This study describes the development and implementation of the PIMIS.

Methods

One observational, descriptive and retrospective study was conducted between January 1st 2011 and June 30th, 2012 where the following variables were gathered: the different mechanisms of inclusion of a patient in the PIMIS; the unit the patient had been referred from; the days elapsed between the patient's admission and the medical consultation (DMC); the source of infection; the etiology (nosocomial); the type of recommendation in the change of antibiotic treatment and the degree of acceptance of the adults patients included in the PIMIS and hospitalized in the Hospital Son Llàtzer. This hospital provides healthcare to 225,000 people and has 400 beds.

Four (4) different mechanisms can make a patient enter the PIMIS: (1) through direct computerized activation by his treating physician; (2) through direct telephone consultation with the MUSC; (3) after confirmation of significant microbiological isolation; and (4) once the alert from the Computerized Vital Sign Detection System (CVSDS) has gone off. We talk about direct consultation requests (DCR) whenever a patient enters the PIMIS through direct request by his treating physician or through the phone, while non-requested consultations (NRC) are those when the patient enters the PIMIS after all the microbiological information has been collected or the alert from the CVSDS has gone off (Fig. 1).

Fig. 1.

Mechanisms of inclusion of a patient in the Computerized Protocol for the Comprehensive Management of Sepsis (PIMIS).

(0.26MB).

When a patient is suspicious of suffering from severe sepsis, after selecting the PIMIS tool, one check-list opens with the criteria for systemic inflammatory response syndrome (SIRS); organic dysfunction; and inflammatory markers (C-reactive protein; normal <5mg/l and procalcitonin; normal <0–05ng/ml) (Table 1). When, at least, two (2) criteria for SIRS and one (1) criterion for organic dysfunction are met, or the markers are high, the patient's condition is identified as severe sepsis and after check-list validation, the automatic activation of the protocol is generated. Once the patient has been included in the PIMIS, an automatic alert is sent to the MUSC through the generation of one list that identifies both the patient and his inclusion criteria. From that very moment, the patient is assessed by someone at the MUSC who will make all the necessary recommendations on the management and specific treatment of the patient. The PIMIS can be activated from all hospital units.

Table 1.

Activation criteria for the protocol for the comprehensive management of sepsis.

Systemic inflammatory response syndrome 
Temperature 100.4°F or <96.8°F 
Heart rate >90bpm 
Respiratory rate >20bpm or PCO2 <32mmHg 
Leukocytosis >12,000/μl or <4000/μl or 10 per cent>immature forms 
 
Organic dysfunction 
Altered level of awareness 
SBP <90mmHg or MBP <70mmHg or a reduced SBP >40mmHg or under 2 SD in adults of the same age 
Arterial hypoxemia (PaO2/FiO2<300) or O2 saturation <90 per cent 
Oliguria (<0.5ml/kg/h) during the last 2h yet despite an adequate resuscitation 
Increased creatinine levels >0.5mg/dl or >twice its normal values 
Coagulopathy: INR >1.5 or APTT >60s or thrombocytopenia <100,000/μl 
Oliguria (<0.5ml/kg/h) during the last 2h yet despite an adequate resuscitation 
Hyperbilirubinemia >4mg/dl 
Hyperlactacidemia >3mmol/l 
C reactive protein >twice its normal values 
Procalcitonin >twice its normal values 

SD: standard deviation; FiO2: fraction of inspired oxygen; INR: international normalized ratio; MBP: mean blood pressure; PaO2: partial pressure of oxygen; SBP: systolic blood pressure; PCO2: partial pressure of carbon dioxide; SIRS: systemic inflammatory response syndrome; APTT: activated partial thromboplastin time.

Parallel to the creation of a list of the patients included, recommendations are made on what therapeutic management should be followed: initial resuscitation; hemodynamic support; and individualized associated therapies based on the recommendations from the Surviving Sepsis Campaing11 (Table 2), plus a series of requirements: blood culture extractions; chest x-rays; lactate extractions for monitoring purposes and organic dysfunction parameters; CRP and PCT both 6 and 24h after the inclusion of the patient (always) and the microbiological sample collection (if applicable). The activation of a patient in the PIMIS due to microbiological isolation usually happens after holding the daily meeting with the microbiology unit, and once the results from the most significant samples have been disclosed. With these results, it is time for the clinical assessment of the patient and should he meet the criteria for sepsis, he enters and is activated through the PIMIS.

Table 2.

Recommendations for the management of severe sepsis and septic shock.

Initial resuscitation (grade 1C)  During the first 6h
Guarantee hourly diuresis 0.5ml/kg/h and MBP 65mmHg
Placement of CVC: CVP 8–12cmH2O; CVO2S ≥70 per cent or MVO2S ≥65 per cent 
Fluid therapy (grade 1C)  1000ml crystalloids or 300–500ml colloids in 30min 
Antibiotic therapy (grade 1B)  Early: within the first hour after SSep detection
Choice made based on etiology (community/nosocomial) and local epidemiology
Broad spectrum and good penetration
Association in: SS, suspicion of Pseudomonas aeruginosa, neutropenic 
Controlling the source of infection (grade C)  Assess early surgical intervention
Drainage, debridement
Removal of all intravascular devices, prostheses, foreign bodies 
Vasopressor drugs (grades A-D)  In severe sepsis with high blood pressure or lactate >3mmol/l
Noradrenaline and dopamine (1C)
Dopamine: avoid use of low doses (1A)
Place arterial IV (1D) 
Inotropic drugs (grade 1C)  In SS and low output consider dobutamine 
Steroids (grade B-C)  In SS with low blood pressure despite VAD
Hydrocortisone 200–300mg/24h×7 days (2B)
Assess adding P.O. fludrocortisone 50mg/24h (2C) 
Recombinant activated protein C (grade 2B)  Indicated in septic shock with failure of 2 organs and/or APACHE II>25
Xigris® 24mg/kg/h×96h
See contraindications 
Administration of hematologic products  Hemoglobin target 7–9g/dl (1B)
Transfusion of platelets when <5000/μl or 5000–30,000/μl when risk of bleeding (2D) 
Respiratory failure  Consider ventilator support when: RR>30–35bmp or O2sat<90 per cent or VMK>30 per cent PO2<60mmHg or PaO2/FiO2<200 or pH<7.35/PCO2>45mmHg 
Sedation, analgesia, relaxation (grade B)  According to ICU and resuscitation protocols
Avoid prolonged relaxation 
Glycemic control (grades B-C)  Correcting IV and s.c. insulin 
Renal replacement therapy (grade 2B)  Use of intermittent hemodialysis and continuous veno-venous hemofiltration indiscriminately 
Bicarbonate (grade C)  Not use when pH ≥7.15 
Deep venous thrombosis prophylaxis (grade A)  Consider compression measures
Low molecular weight heparin. Enoxaparin 40mg/24h s.c.; >100kg (without a clear recommendation: 60mg/24h)
IV sodium heparin 5000IU/24
Stress ulcer prophylaxis (grades A-B)  Use of anti-H2 (1A)
Use of PPI (1B) 
Nutritional support (grade E)  IV dextrose until the beginning of the enteral nutrition 

CVC: central venous catheter; VAD: vasoactive drugs; RR: respiratory rate; PPI: proton pump inhibitors; IV: intravenous; MBP: mean blood pressure; PCO2: partial pressure of carbon dioxide; PaO2: partial pressure of oxygen; CVP: central venous pressure; s.c.: subcutaneous; O2sat: oxygen saturation; CVO2S: central venous oxygen saturation; MVO2S: mixed venous oxygen saturation; SSep: severe sepsis; SS: septic shock; ICU: intensive care unit; VMK: ventimask; P.O.: orally.

With the hemodynamic parameters introduced in the nursing computing system together with some predefined laboratory values, one score is generated that categorizes the patient as suspicious of sepsis with scores >6 points (Table 3). The score should always be obtained during the last 24h. The MUSC receives an alert with the list of patients whose score is over 6 points every 24h. This system has been part of a pilot study to assess its internal validity during the last few months of the study.

Table 3.

Score criteria in the Computerized Vital Sign Detection System (CVSDS).

Assigned score 
Prothrombin activity (percentage)  >60  50–60  <50 
Bicarbonate (mmol/l)  18–21  15–17  <15 
Total bilirubin (mg/dl)  2–6  7–11  >12 
Creatinine (mg/dl)  1.2–1.5  1.51–2.49  ≥2.5 
FiO2 (percentage)  24–31  35–49  ≥50 
Heart rate (bmp)  100–125  –  >125 
Plasma lactate (mmol/l)  2–2.9  3–3.9  ≥4 
Leukocytes (×103/μl)  11–14.9  15–19.9  ≥20 
Platelets (×103/μl)  50–100  20–49.9  <20 
Procalcitonin (ng/ml)  0.5–1.99  2–9.99  ≥10 
C reactive protein (mg/l)  50–99  100–200  >200 
Oxygen saturation (percentage)      <90 
Temperature (°F)  38–38.9    ≥39/≤35.5 
Mean blood pressure (mmHg)    60–65  <60 

FiO2: fraction of inspired oxygen.

The members of the MUSC are distributed and proceed with the daily assessment of the patients included in the PIMIS and/or selected by the CVSDS in order to ensure that they meet the clinical criteria for sepsis; if so, follow-up is continued until the end of the process. During the first consultation, certain therapeutic recommendations are made and then communicated directly to the treating physician and shown in an inter-consultation report. The recommendations to change the antibiotic treatment can be of four (4) different types: (a) de-escalation–when the number of antibiotics or the antibiotic spectrum is reduced based on the pattern of resistances; (b) change due to poor progression–when there are clinical and/or analytical criteria for SIRS or organic dysfunction beyond the first 72h; (c) dose adjustment or inadequate treatment–when the antibiotic does not have in vitro activity or cannot adequately treat the source of infection, or its administration can lead to adverse events that exceed all expected benefits; and (d) sequential therapy–when goin from IV administration to oral administration. The optimization of the antibiotic treatment is supervised by a pharmaceutical expert from the MUSC.

The recommendation is accepted when the change of antibiotic treatment matches the recommendation made by the MUSC.

The categorical variables are expressed as relative and absolute frequences. The continuous variables are expressed as mean and standard deviations (SD) and compared using the t-Student t test, or the ANOVA test for the study of variables with normal distribution, and the Mann–Whitney t test for the study of variables with non-normal distribution. The statistical analysis was conducted using the SPSS software version 17.0 (Chicago, IL, USA), and the EPIDAT software version 3.1.

Results

During the study period, 1581 new consultations at the MUSC were reported on 1340 patients – averaging some 89 new consultations/month; 78.5 per cent were community episodes.

Both the referral unit of the patient and the type of consultation made are shown in Table 4. The ER (22.6 per cent) and the ICU (21 per cent) were the units that handled the largest number of consultations.

Table 4.

Mechanism of consultation and treatment modification per unit.

Unit  Patients
n=1581 
PCMSSep n=865  DPC n=164  CVSDS
n=18 
Microb.
n=360 
Other
n=174 
Nosoc.
n=340 
DMC (m, SD)  CR percentage  NRC percentage  ACS n=506  Accept.
n=395 
ER  353  252 (70.6)  4 (1.1)  6 (1.7)  59 (16.5)  32 (9.0)  89 (26.2)  1.3 (1.8)  71.7  16.5  71 (19.9)  38 (53.5) 
ICU  332  237 (66.7)  34 (10.2)  –  25 (7.5)  36 (10.8)  3 (0.9)  9.2 (16.9)  76.9  7.5  139 (41.9)  128 (92.1) 
General surgery  193  46 (23.8)  15 (7.8)  3 (1.6)  100 (51.8)  29 (13.5)  68 (20)  12.5 (19.9)  31.6  51.8  73 (37.8)  55 (75.3) 
Internal medicine  160  107 (66.9)  5 (3.1)  2 (1.3)  34 (21.3)  12 (7.5)  32 (9.4)  6.1 (9.3)  70.0  21.3  34 (21.3)  28 (82.4) 
Oncology  126  37 (29.4)  57 (45.2)  3 (2.4)  20 (15.9)  9 (7.1)  36 (10.6)  7.5 (10.6)  74.6  15.9  54 (42.9)  44 (81.5) 
Pnneumatology  104  89 (85.6)  1 (1.0)  –  8 (7.7)  6 (5.7)  9 (2.6)  3.01 (3.9)  86.6  7.7  20 (19.2)  14 (70.0) 
Digestive system  77  20 (26.0)  18 (23.4)  1 (1.3)  33 (42.9)  5 (6.5)  28 (8.2)  7.7 (8.4)  49.4  42.9  25 (32.5)  17 (68.0) 
Urology  75  19 (25.3)  11 (14.7)  3 (4.0)  27 (36.0)  15 (15.7)  19 (5.6)  6.9 (9.8)  40.0  36.0  28 (37.3)  24 (85.7) 
Anesth. and res.  35  22 (62.9)  6 (17.1)    2 (5.7)  5 (14.3)  6 (1.8)  3.9 (4.3)  80.0  5.7  13 (37.1)  9 (69.2) 
Gyn. and obstr.  26  6 (23.1)  2 (7.7)  –  14 (53.8)  4 (15.3)  4 (1.2)  5.4 (6.5)  30.8  53.8  12 (46.2)  10 (83.3) 
Cardiology  21  4 (19.0)  2 (9.5)  –  13 (61.9)  2 (9.5)  14 (4.1)  11.7 (9.2)  28.5  61.9  8 (38.1)  5 (62.5) 
Nephrology  18  5 (27.8)  5 (27.8)  –  7 (38.9)  1 (5.6)  6 (1.8)  6.2 (7.9)  55.6  38.9  11 (61.1)  10 (90.9) 
Hematology  15  10 (66.7)  1 (6.7)  –  3 (20.0)  1 (6.7)  5 (1.5)  8.9 (12.0)  73.4  20.0  6 (40.0)  4 (66.7) 
Neurology  12  2 (16.7)  2 (16.7)  –  7 (58.3)  1 (8.3)  7 (2.1)  11.2 (13.1)  33.4  58.3  5 (41.7)  4 (80.0) 
Trauma. and ortho.  12  6 (50)  –  –  4 (33.3)  2 (16.7)  10 (2.4)  8.3 (4.5)  50.0  33.3  4 (33.0)  4 (100) 
Other med. specialties  20  3 (15.0)  1 (5.0)    4 (20.0)  12 (60.0)  1 (0.3)  5.5 (2.0)  20.0  20.0  3 (15.0)  1 (5.0) 

Accept.: antibiotic change accepted; Anesth. and res.: anesthesiology and resuscitation; ACS: antibiotic change suggested; CR: consultation requested; DPC: direct phone contact; DMC: days until medical consultation; Gyn. and obstr.: gynecology and obstetrics; Microb.: Microbiological isolation; NRC: non-requested consultation; Nosoc.: nosocomial; PCMSSep: Protocol for the comprehensive management of severe sepsis; CVSDS: Computerized Vital Sign Detection System; Req.: consultation requested; Trauma. and ortho.: traumatology and orthopedics; ICU: intensive care unit; ER: emergency room.

Mechanisms for the activation of the Computerized Protocol for the Comprehensive Management of Sepsis (PIMIS)

The leading mechanism of consultation was direct activation of the PIMIS by the treating physician (54.7 per cent). Basically, the patients were being referred from medical units (91.1 per cent); the ER (29.1 per cent) followed by the ICU (27.4 per cent); the internal medicine unit (12.4 per cent); and the pneumology unit (10.3 per cent), respectively.

The second mechanism of inclusion in the PIMIS followed the microbiological information collected (22.8 per cent). Over half the patients assessed were included through this mechanism in several units: cardiology (61.9 per cent); neurology (58.3 per cent); gynecology and obstetrics (53.8 per cent); and general surgery units (51.8 per cent).

The direct phone contact was responsible for 10.4 per cent of all inclusions in the PIMIS coming these referrals from oncology units (34.7 per cent); the ICU (20.7 per cent); and digestive system units (10.9 per cent). The CVSDS identified only 18 patients with sepsis, which amounts to only 1.1 per cent of all consultations made.

Direct consultation requests (DCR) vs non-requested consultations (NRC)

Most consultations were DCRs (65.1 per cent). Among them, 84.1 per cent were the result of activation of the PIMIS by the treating physician, and 15.9 per cent by activation through direct pone contact. The percentage was significantly higher in the medical units compared to the surgical units (73.0 per cent vs 39.1 per cent; p<0.001). Similarly, The DCRs happened much earlier (5.63days vs 8.47days; p<0.001); 95.2 per cent of all NRCs came from microbiology, and 4.8 per cent from the CVSDS. The time elapsed between the patient's admission and the MUSC medical consultation is shown in Table 4 (days until medical consultation [DMC]). The DCRs made through PIMIS direct activation happened earlier than the DCRs made through direct phone contact (4.93days vs 9.33days; p<0.001).

Source of infection

At the first consultation, the most common infection was of respiratory origin (34.4 per cent), followed by abdominal origin (22.4 per cent); and then urinary origin (18.2 per cent). In 23.9 per cent of the cases the source of infection could not be identified.

Recommendation of antibiotic change

The change of antibiotics was recommended in 506 (32 per cent) of the first consultations, and later accepted in 398 cases (78.1 per cent). The frequency of acceptance was widely variable among the different medical specialties. The percentage of acceptance was significantly higher in the DCRs (80.6 per cent vs 72.4 per cent; p=0.04).

Types of recommendation

The main reason to recommend a change in the antibiotic regime was poor progression (38.5 per cent) followed by inadequate treatment (33.9 per cent) (Table 5). The units where these changed occurred due to poor progression of the patient were mainly the anesthesiology and resuscitation unit (78.6 per cent); the digestive system unit (63.2 per cent) followed by the ER (52.9 per cent) and the ICU (48.6 per cent). Dose adjustment was the most common intervention in the surgical unit (general surgery; gynecology and obstetrics; urology; traumatology), as well as in the cardiology and neurology units. De-escalation was the main intervention in the internal medicine unit (45.8 per cent), while the sequential therapy was the main intervention in the neumology unit (25.6 per cent).

Table 5.

Type of intervention conducted per unit.

Unit  DE
n=121 (22.7 per cent) 
PP
n=205 (38.5 per cent) 
DA
n=181 (33.9 per cent) 
ST
n=26 (4.9 per cent) 
Total
n=533 
ER  10 (14.7)  36 (52.9)  21 (30.9)  1 (1.5)  68 (19.0) 
ICU  36 (24.7)  71 (48.6)  34 (23.3)  5 (3.4)  146 (44.0) 
General surgery  20 (29.0)  18 (26.1)  29 (42.0)  2 (2.9)  69 (35.8) 
Internal medicine  22 (45.8)  9 (18.8)  16 (33.3)  1 (2.1)  48 (30.0) 
Oncology  7 (12.5)  26 (46.4)  20 (35.7)  3 (5.4)  56 (44.4) 
Pneumology  12 (27.9)  4 (9.3)  16 (37.2)  11 (25.6)  43 (41.3) 
Digestive system  1 (5.3)  12 (63.2)  5 (26.3)  1 (5.3)  19 (24.7) 
Urology  5 (17.9)  7 (25.0)  16 (57.1)  –  28 (37.3) 
Anesth. and res.  2 (14.3)  11 (78.6)  1 (7.1)  –  14 (40.0) 
Gyn. and obstr.  1 (7.7)  1 (7.7)  9 (69.2)  2 (15.4)  13 (50.0) 
Cardiology  2 (40.0)  1 (20.0)  2 (40.0)  –  5 (23.8) 
Nephrology  1 (10.0)  4 (40.0)  5 (50.0)  –  10 (55.6) 
Hematology  1 (25.0)  2 (50.0)  1 (25.0)  –  4 (26.7) 
Neurology  1 (25.0)  –  3 (75.0)  –  4 (33.0) 
Trauma. and ortho.  –  2 (50.0)  2 (50.0)  –  4 (33.3) 
Other med. specialties  –  1 (50.0)  1 (50.0)  –  2 (28.6) 

DA: dose adjustment; Anesth. and res.: anesthesiology and resuscitation; DE: de-escalation; Gyn. and obstr.: gynecology and obstetrics; PP: poor progression; Trauma. and ortho.: traumatology and orthopedics; ST: sequential therapy; ICU: intensive care unit; ER: emergency room.

The antibiotic dose adjustment was the most common intervention in the management of infections like urinary tract infections (UTI); catheter-related infections; skin infections; and skin and soft tissue infections (Table 6). Among all infections, it was the UTIs where the antibiotic de-escalation intervention was most significantly implemented. On the contrary, among the abdominal and respiratory infections, it was the antibiotic change intervention due to poor progression the one most widely implemented.

Table 6.

Type of intervention based on the source of infection.

  DE
n=64 
PP
n=117 
DA
n=92 
ST
n=12 
Pulmonary  53 (24.7)  81 (37.7)  65 (30.2)  16 (7.4) 
Abdominal  21 (17.5)  64 (53.3)  33 (27.5)  2 (1.7) 
UTI  20 (26.0)  23 (29.9)  32 (41.6)  2 (2.6) 
Catheter  3 (18.8)  3 (18.8)  10 (62.5)  – 
SSTI  3 (11.5)  8 (30.8)  15 (57.7)  – 
Gynecological  1 (20)  –  3 (60)  1 (20) 
Trauma. and ortho.  1 (16.7)  2 (33.3)  3 (50)  – 
CNS  1 (16.7)  3 (50)  2 (33.3)  – 
Head and neck  –  1 (50)  1 (50)  – 
Unknown  8 (29.6)  10 (37.0)  5 (18.5)  4 (14.8) 

DA: dose adjustment; DE: de-escalation; SSTI: skin and soft tissues infections; UTI: urinary tract infection; PP: poor progression; CNS: central nervous system; Trauma. and ortho.: traumatology and orthopedics; ST: sequential therapy.

Discussion

There are two (2) important aspects that characterize the management of sepsis at our center. On the one hand, the existence of one MUSC including medical and surgical specialists. On the other hand, the existence of one computerized tool for the identification, assessment, and registry of patients with potentially severe sepsis: the PIMIS – a whole new ballgame in Spain.

Different computerized alert systems have been created to promote the identification and implementation of measures for the management of sepsis in units different than the ICU.3,5,12,13 They all share one idea – to allow an early identification and facilitate the comprehensive and intensive management of potentially critical conditions. Unlike the computerized tool developed by Ferreras et al.14 – of ER implementation, our protocol allows the activation from all hospital units.

Our analysis shows the detailed activities of every unit, while former studies only compare the differences between medical and surgical units.15 Thanks to this we know what units need healthcare improvement.

Most consultations that take place at the MUSC happen during the direct activation of the PIMIS, which shows its acceptance and recognition. Also, it is possible that the automatic generation of one set of recommendations is seen as a useful tool for the management of the patient. However, other professionals rather use the direct phone consultations. This may be due to different causes such as a greater trust in direct verbal communication; ignorance or lack of information on the very existence of the PIMIS; or distrust in technology.

Overall, the DCRs are the main mechanism of consultation, which shows that the recommendations made for the management of sepsis by parts of the MUSC are recognized and accepted. One of the main challenges that the members of the MUSC face is for their job to be accepted and recognized by specialists from their own centers. Such a requirement ensures cooperation with different medical specialties and validates the effectiveness of programs like this.

Most patients assessed through NRCs were patients from microbiological isolations. This could delay the detection of sepsis and the prescription of the adequate antibiotic treatment, since the medical assessment occurs 24h after sending the sample without having made any consultations yet on early management or empirical treatment issues. As a matter of fact, in these cases there is a significant difference in the days elapsed between the patient's admission and the assessment by the MUSC. In the future, we think that these efforts should focus on promoting early detection practices and making PIMIS more accessible.

As of today, different institutional strategies have been developed to promote the implementation of programs in an attempt to optimize antibiotic prescription16–18 since it has been reported that up to 50 per cent of all antibiotic prescriptions have been inappropriate.19 In our study, 32 per cent of all initial prescriptions were considered inappropriate. Gómez et al.3 showed that checking with a specialist in infectious diseases increased the number of appropriate treatments in initial prescriptions.

Compared to former studies, the frequency of modification of the antibiotic prescription was higher.20–22 The results are especially relevant in the surgical units.19,23,24 One of the reasons that may explain these results is the integration of the staff from the different surgical units into the MUSC. Also, the fact that the recommendations are communicated directly to the treating physician and not just detailed in the clinical history may have favored the degree of acceptance.

Also, we should stress out the high percentage of changes accepted at the ICU according to former studies.25,26 This may be due to the fact that the MUSC was created in the critical care medicine department, and many of its members come from such unit.

When it comes to the type of change recommendation made, the fact that the most common type of recommendation is due poor progression may suggest that help is wanted as a second option, when the therapeutic management is more complicated and help from a specialist in infectious diseases is deemed necessary.

It is possible that our intervention, on top of optimizing the antibiotic treatment also reduces its use since the intervention promotes antibiotic de-escalation and early sequential therapy, yet this is something that needs to be confirmed in an economic study.

Although our study shows the experience of one single center, we firmly believe that the thorough description of how our intervention works may encourage other groups to define and organize strategies in other centers.

Recently, in the last consensus document on the definitions of sepsis,27 the use of the criteria for SIRS is put into question in its diagnosis, suggesting the use of the qSOFA score as a new tool of clinical assessment. In our study period, previous recommendations were still effective and included the SIRS criteria, however, we believe that this score can facilitate the assessment and identification of severity in patients with sepsis.

One of the limitations of our study is that we did not collect the number of episodes of sepsis they did not ask our unit about. Although there is no way of knowing or comparing the prognosis of both groups, the goal of our study was to stress out the importance of organizing coordinated managements with the simultaneous implementation of measures from one multidisciplinary perspective. Hopefully, we will be able to examine the clinical variables in future studies. On the other hand, all those consultations made for diagnostic assessment purposes or reasons other than antibiotic prescription have not been collected either.

In sum, this study shows that one computerized tool like the PIMIS can be a valid strategy for the detection of sepsis. Also, the high percentage of acceptance of the recommendations made means that the activity from the MUSC is accepted and assessed positively.

Conflicts of interests

The authors declare no conflicts of interest whatsoever.

Acknowledgements

We wish to thank the rest of the team at the multidisciplinary unit in sepsis care: J Tarradas, B Comas, S Pons, J Bauzá, A Liébana, A Villoslada, MC Pérez, C Gallego, V Fernández-Baca, M Aranda, R Morales, O Gutiérrez, J Barceló, A Llompart, R Poyo-Guerrero, D Muñiz. We also wish to thank our hospital computer experts: VM Estrada, A Hernández, F Velasco.

References
[1]
C. Bouza, T. López-Cuadrado, Z. Saz-Parkinson, J.M. Amate-Blanco.
Epidemiology and recent trends of severe sepsis in Spain: a nationwide population-based analysis (2006–2011).
BMC Infect Dis, 14 (2014), pp. 3863
[2]
R.P. Dellinger, M.M. Levy, A. Rhodes, D. Annane, H. Gerlach, S.M. Opal, Surviving Sepsis Campaign Guidelines Committee including The Pediatric Subgroup, et al.
Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock, 2012.
Intensive Care Med, 39 (2013), pp. 165-228
[3]
J. Gomez, S.J. Conde Cavero, J.L. Hernandez Cardona, M.L. Nuñez, J. Ruiz Gomez, M. Cantera, et al.
The influence of the opinion of an infectious disease consultant on the appropriateness of antibiotic treatment in a general hospital.
J Antimicrob Chemother, 38 (1996), pp. 309-314
[4]
D.P. McQuillen, R.M. Petrak, R.B. Wasserman, R.G. Nahass, J.A. Scull, L.P. Martinelli.
The value of infectious diseases specialists: non-patient care activities.
Clin Infect Dis, 47 (2008), pp. 1051-1063
[5]
J.J. Schentag, C.H. Ballow, A.L. Fritz, J.A. Paladino, J.D. Williams, T.J. Cumbo.
Changes in antimicrobial agent usage resulting from interactions among clinical pharmacy, the infectious disease division, and the microbiology laboratory.
Diagn Microbiol Infect Dis, 16 (1993), pp. 255-264
[6]
P. Carling, T. Fung, A. Killion, N. Terrin, M. Barza.
Favorable impact of a multidisciplinary antibiotic management program conducted during 7 years.
Infect Control Hosp Epidemiol, 24 (2003), pp. 699-706
[7]
N.I. Shapiro, M.D. Howell, D. Talmor, D. Lahey, L. Ngo, J. Buras, et al.
Implementation and outcomes of the Multiple Urgent Sepsis Therapies (MUST) protocol.
Crit Care Med, 34 (2006), pp. 1025-1032
[8]
G.E. Schramm, R. Kashyap, J.J. Mullon, O. Gajic, B. Afessa.
Septic shock: a multidisciplinary response team and weekly feedback to physicians improve the process of care and mortality.
Crit Care Med, 39 (2011), pp. 252-258
[9]
K.M. Picard, S.C. O’Donoghue, D.A. Young-Kershaw, K.J. Russell.
Development and implementation of a multidisciplinary sepsis protocol.
Crit Care Nurse, 26 (2006), pp. 43-54
[10]
K.M. Buck.
Developing an early sepsis alert program.
J Nurs Care Qual, 29 (2014), pp. 124-132
[11]
R.P. Dellinger, M.M. Levy, J.M. Carlet, J. Bion, M.M. Parker, R. Jaeschke, International Surviving Sepsis Campaign Guidelines Committee, et al.
Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock: 2008.
Crit Care Med, 36 (2008), pp. 296-327
[12]
K.K. Giuliano, M. Lecardo, L. Staul.
Impact of protocol watch on compliance with the surviving sepsis campaign.
Am J Crit Care, 20 (2011), pp. 313-321
[13]
A.M. Sawyer, E.N. Deal, A.J. Labelle, C. Witt, S.W. Thiel, K. Heard, et al.
Implementation of a real-time computerized sepsis alert in non-intensive care unit patients.
Crit Care Med, 39 (2011), pp. 469-473
[14]
J.M. Ferreras, D. Judez, G. Tirado, C. Aspiroz, R. Martínez-Álvarez, P. Dorado, et al.
Implementación de un sistema de alarmas automático para la detección precoz de los pacientes con sepsis grave.
Enferm Infecc Microbiol Clin, 33 (2015), pp. 508-515
[15]
F. López-Medrano, R. San Juan, O. Serrano, F. Chaves, C. Lumbreras, M. Lizasoain, et al.
Impact of a non-compulsory antibiotic control program (PACTA): cost reductions and decreases in some nosocomial infection.
Enferm Infecc Microbiol Clin, 23 (2005), pp. 186-190
[16]
J. Cobo Reinoso, J. Oliva Domínguez, M. Soler Vigil, J. Martínez-Beltrán, L. Pedraza Cezón, S. Moreno Guillén.
Evaluation of an advisory program in antibiotic therapy.
Rev Clin Esp, 202 (2002), pp. 78-83
[17]
E. Lo, K. Rezai, A.T. Evans, M.G. Madariaga, M. Phillips, W. Brobbey, et al.
Why don’t they listen? Adherence to recommendations of infectious disease consultations.
Clin Infect Dis, 38 (2004), pp. 1212-1218
[18]
B.N. Kim.
Compliance with an infectious disease specialist's advisory consultations on targeted antibiotic usage.
J Infect Chemother, 11 (2005), pp. 84-88
[19]
E. Raineri, A. Pan, P. Mondello, A. Acquarolo, A. Candiani, L. Crema.
Role of the infectious diseases specialist consultant on the appropriateness of antimicrobial therapy prescription in an intensive care unit.
Am J Infect Control, 36 (2008), pp. 283-290
[20]
T.H. Dellit, R.C. Owens, J.E. McGowan Jr., D.N. Gerding, R.A. Weinstein, J.P. Burke, Infectious Diseases Society of America; Society for Healthcare Epidemiology of America, et al.
Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America guidelines for developing an institutional program to enhance antimicrobial stewardship.
Clin Infect Dis, 44 (2007), pp. 159-177
[21]
P. Lesprit, C. Landelle, C. Brun-Buisson.
Unsolicited post-prescription antibiotic review in surgical and medical wards: factors associated with counselling and physicians’ compliance.
Eur J Clin Microbiol Infect Dis, 32 (2013), pp. 227-235
[22]
B. Johannsson, S.E. Beekmann, A. Srinivasan, A.L. Hersh, R. Laxminarayan, P.M. Polgreen.
Improving antimicrobial stewardship: the evolution of programmatic strategies and barriers.
Infect Control Hosp Epidemiol, 32 (2011), pp. 367-374
[23]
J.E. McGowan.
Antimicrobial stewardship — the state of the art in 2011: focus on outcome and methods.
Infect Control Hosp Epidemiol, 33 (2012), pp. 331-337
[24]
J. Rodríguez-Baño, J.R. Paño-Pardo, L. Alvarez-Rocha, A. Asensio, E. Calbo, E. Cercenado, et al.
Programs for optimizing the use of antibiotics (PROA) in Spanish hospitals: GEIH-SEIMC, SEFH and SEMPSPH consensus document.
Enferm Infecc Microbiol Clin, 30 (2012), pp. 22.e1-22.e23
[25]
C. Pulcini, C. Pradier, C. Samat-Long, H. Hyvernat, G. Bernardin, C. Ichai, et al.
Factors associated with adherence to infectious diseases advice in two intensive care units.
J Antimicrob Chemother, 57 (2006), pp. 546-550
[26]
M. Girardis, L. Rinaldi, L. Donno, M. Marietta, M. Codeluppi, P. Marchegiano, Sopravvivere alla Sepsis Group of the Modena-University Hospital, et al.
Effects on management and outcome of severe sepsis and septic shock patients admitted to the intensive care unit after implementation of a sepsis program: a pilot study.
Crit Care, 13 (2009), pp. R143
[27]
M. Singer, C.S. Deutschman, C.W. Seymour, M. Shankar-Hari, D. Annane, M. Bauer, et al.
The third international consensus definitions for sepsis and septic shock (Sepsis-3).
JAMA, 315 (2016), pp. 801-810

Please cite this article as: de Dios B, Borges M, Smith TD, del Castillo A, Socias A, Gutiérrez L, et al. Protocolo informático de manejo integral de la sepsis. Descripción de un sistema de identificación precoz. Enferm Infecc Microbiol Clin. 2018;36:84–90.

Copyright © 2016. Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
Download PDF
Article options
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos

Quizás le interese:
10.1016/j.eimce.2024.01.002
No mostrar más