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Print version ISSN 0104-1169
Rev. Latino-Am. Enfermagem vol.20 no.5 Ribeirão Preto Sept./Oct. 2012
Endotracheal suction in intubated critically ill adult patients undergoing mechanical ventilation: a systematic review1
Débora Oliveira FavrettoI; Renata Cristina de Campos Pereira SilveiraII; Silvia Rita Marin da Silva CaniniII; Livia Maria GarbinIII; Fernanda Titareli Merízio MartinsIV; Maria Célia Barcellos DalriII
IMSc, Assistant Professor, Nursing undergraduate course, Instituto de Ciências Exatas e Naturais, Universidade Federal de Mato Grosso, Campus Universitário de Rondonópolis, Brazil
IIPhD, Professor, Escola de Enfermagem de Ribeirão Preto, Universidade de São Paulo, WHO Collaborating Centre for Nursing Research Development, Brazil
IIIRN, MSc, Escola de Enfermagem de Ribeirão Preto, Universidade de São Paulo, WHO Collaborating Centre for Nursing Research Development, Brazil
IVRN, PhD, Escola de Enfermagem de Ribeirão Preto, Universidade de São Paulo, WHO Collaborating Centre for Nursing Research Development, Brazil
AIM: identify and analyze in the literature the evidence of randomized controlled trials on care related to the suctioning of endotracheal secretions in intubated, critically ill adult patients undergoing mechanical ventilation.
METHOD: the search was conducted in the PubMed, EMBASE, CENTRAL, CINAHL and LILACS databases. From the 631 citations found, 17 studies were selected.
RESULTS: Evidence was identified for six categories of intervention related to endotracheal suctioning, which were analyzed according to outcomes related to hemodynamic and blood gas alterations, microbial colonization, nosocomial infection, and others.
CONCLUSIONS: although the evidence obtained is relevant to the practice of endotracheal aspiration, the risks of bias found in the studies selected compromise the evidence's reliability.
Descriptors: Nursing Care; Critical Care; Suction; Intubation, Intratracheal; Intensive Care Units.
Endotracheal suction is a procedure which aims to keep airways patent by mechanically removing accumulated pulmonary secretions, above all in patients with artificial airways(1).
Despite being a necessary procedure, it can lead to complications, such as lesions in the tracheal mucosa, pain, discomfort, infection, alterations of the hemodynamic parameters and of the arterial gases, bronchoconstriction, atelectasis, increase in intra-cranial pressure, and alterations in cerebral blood flow, among others(1-2).
Considering this procedure's complexity, a prior evaluation of the need for suction is indispensable, as this is an invasive, complex procedure that must be undertaken by judicious indication, as it can cause harm to the patient(1,3). For this procedure, it is important that the nurse has knowledge based on valid scientific evidence concerning the different methods of endotracheal suction and aspects related to it.
Despite there being scientific evidence for the safe and efficient accomplishment of endotracheal suction, many of these recommendations have not been observed in nurses' clinical practice, due above all to poor knowledge about this procedure(4). It is believed that grouping and synthesizing the available evidence can assist clinical nurses, nurse lecturers and student nurses in incorporating it into their care practice, as well as guiding new research.
It was in this context that the present study aimed to identify and analyze the scientific evidence about nursing care related to the suctioning of endotracheal secretions in critically-ill, intubated adult patients undergoing mechanical ventilation.
This is a systematic review of the literature, guided by the recommendations of the Cochrane Collaboration(5).
The review question, devised based in the PICO strategy(6), was: considering the different methods and steps of endotracheal suction, what is the most effective and safest way of accomplishing it in critically-ill, intubated adult patients, undergoing mechanical ventilation, so as to keep the airways unobstructed, while avoiding or minimizing its complications?
The inclusion criteria were studies of randomized controlled trials (RCT), published in full, in English, Portuguese or Spanish, undertaken with adult patients (> 18 years old), who were critically ill, intubated and undergoing mechanical ventilation, and which addressed the effectiveness and safety of endotracheal suction.
The search was carried out in the databases PubMed, EMBASE, CENTRAL, CINAHL and LILACS. The search strategy considered sets of terms related to the study population (P); to the intervention evaluated (I); to the type of study to be included (type of study) and to the exclusion of pediatric and neonatal studies (limits). Descriptors were selected from each database's controlled vocabulary, as well as non-controlled descriptors, which were combined within each set of terms using the Boolean connector OR. The search strategy proposed by the Cochrane Collaboration(5) was adapted for finding the ECCRs (Figure 1).
The search strategy for the databases PubMed, EMBASE and CINAHL was: ((P AND I) AND study design) NOT limits. For the CENTRAL database, which is specific for controlled trials, the strategy adopted was: (P AND I) NOT limits. For the LILACS database, on the other hand, the search strategy which permitted the identification of the most studies was: P AND I. The search was undertaken in April 2010; 631 citations were found.
The selection of the studies (Figure 2) was initially carried out based on a reading of the titles and abstracts, based on the inclusion criteria. 36 publications were considered potentially eligible: 35 contained insufficient information for selection in the titles and abstracts. These 71 studies were selected for reading in full, of which 17 were included in this systematic review's sample.
A data collection form devised for the present study was used for the extraction of the data. It took into consideration the instructions on content and appearance presented by the Cochrane Collaboration(5).
The extraction of the data from each study was undertaken by two reviewers. Initially, the principal reviewer extracted the data from all of the studies selected. Next, the studies were distributed among three reviewers, who acted as independent validators. The studies were also evaluated for risk of bias, taking into account the sequence generation, allocation concealment, blinding of participants, care providers and the evaluators of the outcomes, incomplete data on outcomes, selective reporting and other sources of bias(5,7). It is considered that studies with a low risk of bias are unlikely to have serious alterations in their results. An uncertain level of risk, on the other hand, raises doubts about the reliability of the studies' results, and a high risk of bias seriously weakens the results' reliability(7).
Finally, the data extracted from the studies included in this systematic review was analyzed and presented in a descriptive form.
The 17 RCT included were published between 1987 and 2009, with 11 (64.7%) published after 2000, 2003 standing out, with four articles (23.5%).
The results of the studies allowed the grouping of evidence into six categories of intervention related to endotracheal suction: research-based endotracheal suction compared to normal endotracheal suction, in one study(8); routine endotracheal suction compared to minimally-invasive endotracheal suction, in two studies(9-10); open system endotracheal suctioning compared to closed system endotracheal suctioning, in eight studies(11-18); change of closed system at 24 compared to 48 hours, in two studies(19-20); daily change of the closed system compared to non-routine change, in one study(21); and saline instillation compared to non-saline instillation, in three studies(22-24).
The interventions were undertaken analyzing outcomes referent to hemodynamic alterations, alterations in blood gases, microbial colonization and nosocomial infection, quantity of secretion suctioned, pulmonary alterations, memory of the experience of endotracheal suction on the part of the patient, and discomfort related to the suction.
The results of the outcomes analyzed for the intervention categories in the studies selected are presented in Figure 3.
In relation to the risk of bias in the studies selected (Figure 4), it may be observed that in 94.12% of the studies, the reliability of the results may be questioned, due both to uncertain levels of risk of bias and to high risk of bias. The uncertain level of risk of bias was visible in the following areas: generation of random sequence (47.06%), allocation concealment (58.82%), blinding of participants and care providers (41.18%) and blinding of the evaluator of the outcome (52.94%). The high risk of bias stood out in the following areas: blinding of the participants and care providers (47.06%), blinding of the evaluator of the outcome (17.65%) and other sources of bias (35.29%).
Only one study(23) reported a low risk of bias in all the areas analyzed; it's results, therefore, were considered highly reliable. In general, the areas in which a low risk of bias was predominant were: incomplete data about outcome (94.12%), selective reporting (94.12%) and other sources of bias (52.94%).
In relation to the interventions studied and to the outcomes evaluated, it may be observed that on comparing research-based endotracheal suction with normal endotracheal suction, for the majority of outcomes evaluated, the results obtained were better for Groups which received interventions based on research. The study selected which covered this category of intervention(8) shows various methodological limitations, as shown in the analysis of risk of bias. A low risk of bias was observed in only one of the areas analyzed. Due to this, the study results may be questioned.
Regarding minimally-invasive endotracheal suctioning(9-10), the results obtained evidence that this intervention is responsible for the lowest occurrence of adverse effects (hemodynamic alterations, O2 saturation, and presence of blood in the mucous), compared to normal endotracheal suctioning. This also applied to the memory of undergoing suctioning, which contributes to reducing the number of people who experience discomfort with the intervention. Despite the minimally-invasive suction producing the best results, a high number of protocol deviations were observed, in which patients allocated to the minimally-invasive suctioning group were, at some point, aspirated in the usual way(9). This led to a high risk of bias in the area "other sources of bias" and suggests that, depending on the patient's condition, this form of aspiration may not be the most appropriate. The study in question(9) reports that, probably, such an intervention would not be able to aspirate all the secretions present in the airways, causing its accumulation.
Regarding the studies which compared the open system of endotracheal suction with the closed system(11-18), it was observed that few presented a low risk of bias in relation to the allocation of subjects, allocation concealment and blinding. Prominent among the outcomes analyzed is the occurrence of ventilation-associated pneumonia (VAP). The criteria used for its diagnosis varied between the studies, however, there was no difference in the occurrence of VAP when the two systems of aspiration were compared.
In relation to cardiac frequency, arterial pressure and O2 saturation, the results found are in line with another review(25), which included crossover studies, in addition to randomized controlled trials, with the best results occurring with the use of the closed system when compared to the open.
On analyzing the time interval for changing the closed suction system, the selected studies(19-21) presented a low risk of bias for the majority of their areas. Differences were not identified between the Groups where the systems were changed every 24 hours compared to every 48 hours, or with daily changing compared to non-routine changing, for any of the outcomes analyzed.
Regarding the instillation of normal saline before the endotracheal suction, compared to non-instillation, the selected studies(22-24) present differences concerning how the suction was accomplished. Thus, different outcomes were observed, which made it impossible to undertake comparison between the studies. In relation to the results obtained for the outcomes analyzed, only oxygen saturation levels presented a result which was unfavorable to the saline instillation. Differences were not found between the Groups studied for cardiac frequency, arterial pressure, partial pressure of oxygen and atelectasis. The Group with saline instillation presented the best results regarding quantity of secretion aspirated. These results are questionable, however, as the quantity of normal saline instilled was not discounted from the measurement of the quantity of secretion collected. Further, in the case of this intervention, the study with the lowest risk of bias and the largest sample(24) reported results favorable to saline instillation in the prevention of VAP.
Results of the analysis of these outcomes for the same intervention were found in other literature reviews(26-27). One narrative review on the issue(26) showed that despite including predominantly non-randomized studies, and not evaluating the quality and risk of bias in said studies, the results obtained are similar to those found in the present review, in relation to cardiac frequency, arterial pressure and O2 saturation levels. Regarding the partial pressure of oxygen, results were found which contra-indicated the instillation of normal saline; differences were not found in relation to the quantity of secretion aspirated among the Groups studied. Further, evidence was found that the saline instillation increases the displacement of micro-organisms from the endotracheal cannula to the lower airways, which would increase the risk of nosocomial pneumonia.
Another systematic review(27) on instillation of normal saline, which included other methodological designs and studies with pediatric and neonatal patients, found results similar to those of the present review for cardiac frequency, arterial pressure and partial pressure of oxygen, O2 saturation, and quantity of secretion aspirated. In relation to the occurrence of VAP, this review identified one study which did not find differences between the Groups analyzed.
It may be observed, therefore, that the evidence on instillation of normal saline remains contradictory. However, other studies(1-2,4), which reviewed the practices of endotracheal suction, including studies with diverse methodological designs and populations (adult, pediatric, neonatal), submit recommendations which contra-indicate the instillation of normal saline.
From this review's findings, one may observe the lack of randomized controlled trials which cover the diverse aspects of endotracheal suction and outcomes. Due to this, guidelines put forward recommendations based in studies with lower levels of evidence, such as non-randomized, observational, quasi-experimental studies(1).
An ongoing controversy was also observed in the studies selected concerning the results of the outcomes analyzed for the interventions studied, due to there being few studies on specific interventions or outcomes, or due to differing results being found among the studies.
Another aspect observed was the lack of methodological information in the studies selected, compromising the analysis of risk of bias and, consequently, the evaluation of the results' reliability and validity. The importance can be seen, therefore, of publishing the RCT in line with the CONSORT recommendations (Consolidated Standards of Reporting Trials)(28), describing the methodological steps with enough detail for the studies' reliable comprehension, as well as making it possible to identify possible limitations.
Endotracheal suction is an intervention which requires specific knowledge about the patient's clinical condition, physio-pathological aspects, mechanical ventilation and respiratory therapy; therefore, studies for obtaining evidence upon which the practice is based are crucial. Based on the results obtained and the considerations made, it may be noted that although important evidence on endotracheal aspiration exists, this intervention still needs extensive investigation, principally through RCT.
Based on the results obtained from this systematic review, the following evidence on endotracheal suction was found:
- Research-based endotracheal suction produced the best results for mean arterial pressure, cardiac frequency, partial pressure of oxygen and partial pressure of carbon dioxide, when compared to usual aspiration;
- Minimally-invasive endotracheal suction, compared to routine endotracheal aspiration, results in fewer side effects (increase in systolic arterial pressure, increase in pulse pressure and drop in oxygen saturation levels) and less memories, in the patient, of having been suctioned;
- The closed system of endotracheal suction had better results related to cardiac frequency, arterial pressure, cardiac rhythm, oxygen saturation levels and cross-contamination between the bronchial system and gastric juice, when compared to the open system. However, there was no difference between the two suction systems concerning the occurrence of VAP and microbial colonization of the endotracheal secretions and tubing of the ventilator;
- The changing of the closed suction system every 48 hours or non-routinely, and its changing every 24 hours do not differ in terms of the occurrence of VAP. Neither was there any difference in microbial colonization of the endotracheal secretions and suction catheter, when the system was changed every 24 or 48 hours.
- Saline instillation and non-saline instillation do not differ in terms of cardiac frequency, arterial pressure, partial pressure of oxygen and the occurrence of atelectasis. Regarding the quantity of secretion aspirated, although results were identified which were favorable to the instillation of 05mL of normal saline (compared to the instillation of 10mL and non-saline instillation), conclusive evidence was not found about this outcome, due to the study's methodological limitations. In addition, the saline instillation was associated with lower occurrence of VAP, compared to non-saline instillation.
The methodological limitations and risks of bias found in the studies selected reduce the reliability of the evidence found, demonstrating the need for further studies.
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Maria Célia Barcellos Dalri
Universidade de São Paulo. Escola de Enfermagem de Ribeirão Preto
Departamento de Enfermagem Geral e Especializada
Av. dos Bandeirantes, 3900
Bairro: Monte Alegre
CEP: 14040-902, Ribeirão Preto, SP, Brasil
Received: Apr. 3rd 2012
Accepted: Sept. 4th 2012
1 Paper extracted from Master's Dissertation "Aspiração endotraqueal em pacientes críticos adultos intubados sob ventilação mecânica: revisão sistemática", presented to Escola de Enfermagem de Ribeirão Preto, Universidade de São Paulo, WHO Collaborating Centre for Nursing Research Development, Brazil. Supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Process # 2009/06693-2.