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3.
Respir Care ; 69(5): 575-585, 2024 Apr 22.
Article in English | MEDLINE | ID: mdl-38307525

ABSTRACT

BACKGROUND: Open respiratory secretion suctioning with a catheter causes pain and tracheobronchial mucosal injury in intubated patients. The goal of mechanical insufflation-exsufflation (MI-E) is to move secretions proximally and noninvasively by generating a high peak expiratory air flow. Nebulized hypertonic saline with hyaluronic acid (HS-HA) may facilitate suctioning by hydration. We assessed the safety and tolerance of a single session of airway clearance with MI-E and HS-HA in critically ill intubated patients. METHODS: Adults with a cuffed artificial airway were randomized to (1) open suctioning, (2) open suctioning after HS-HA, (3) MI-E, or (4) MI-E with HS-HA. Adverse events, pain and sedation/agitation scores, and respiratory and hemodynamic variables were collected before, during, and 5-min and 60-min post intervention. RESULTS: One-hundred twenty subjects were enrolled and completed the study. Median (interquartile range [IQR]) Acute Physiology and Chronic Health Evaluation II (APACHE II) score was 22 (16-28); median (IQR) age was 69.0 (57.0-75.7) y, and 90 (75%) were male. Baseline respiratory and hemodynamic variables were comparable. Adverse events occurred in 30 subjects (25%), with no between-group differences. Behavioral pain equivalents and Richmond Agitation-Sedation Scale were higher during suctioning in groups 1 (P < .001) and 2 (P < .001). Independent predictive variables for higher pain and agitation/sedation scores were study groups 1 and 2 and simultaneous analgosedation, respectively. Noradrenaline infusion rates were lower at 60 min in groups 2 and 4. PaO2 /FIO2 had decreased at 5 min after open suctioning in group 1 and increased at 60 min in group 3. CONCLUSIONS: We observed no difference in adverse events. MI-E avoids pain and agitation.

4.
J Intensive Care Med ; 37(12): 1606-1613, 2022 Dec.
Article in English | MEDLINE | ID: mdl-35642279

ABSTRACT

Objective: There exists controversy about the pathophysiology and lung mechanics of COVID-19 associated acute respiratory distress syndrome (ARDS), because some report severe hypoxemia with preserved respiratory system mechanics, contrasting with "classic" ARDS. We performed a detailed hourly analysis of the characteristics and time course of lung mechanics and biochemical analysis of patients requiring invasive mechanical ventilation (IMV) for COVID-19-associated ARDS, comparing survivors and non-survivors. Methods: Retrospective analysis of the data stored in the ICU information system of patients admitted in our hospital ICU that required IMV due to confirmed SARS-CoV-2 pneumonia between March 5th and April 30th, 2020. We compare respiratory system mechanics and gas exchange during the first ten days of IMV, discriminating volume and pressure controlled modes, between ICU survivors and non-survivors. Results: 140 patients were included, analyzing 11 138 respiratory mechanics recordings. Global mortality was 38.6%. Multivariate analysis showed that age (OR 1.092, 95% (CI 1.014-1.176)) and need of renal replacement therapies (OR 10.15, (95% CI 1.58-65.11)) were associated with higher mortality. Previous use of Angiotensin Converting Enzyme inhibitor (ACEI)/angiotensin-receptor blockers (ARBs) also seemed to show an increased mortality (OR 4.612, (95% CI 1.19-17.84)) although this significance was lost when stratifying by age. Respiratory variables start to diverge significantly between survivors and non-survivors after the 96 to 120 hours (hs) from mechanical ventilation initiation, particularly respiratory system compliance. In non survivors, mechanical power at 24 and 96 hs was higher regardless ventilatory mode. Conclusions: In patients admitted for SARS-CoV-2 pneumonia and requiring mechanical ventilation, non survivors have different respiratory system mechanics than survivors in the first 10 days of ICU admission. We propose a checkpoint at 96-120 hs to assess patients improvement or worsening in order to consider escalating to extracorporeal therapies.


Subject(s)
COVID-19 , Pneumonia , Respiratory Distress Syndrome , Adult , Humans , COVID-19/therapy , Respiration, Artificial , SARS-CoV-2 , Critical Illness/therapy , Retrospective Studies , Angiotensin Receptor Antagonists , Angiotensin-Converting Enzyme Inhibitors
5.
Rev. esp. quimioter ; 31(supl.1): 43-46, sept. 2018. graf
Article in English | IBECS | ID: ibc-179449

ABSTRACT

Infectious diseases are disorders caused by many different microorganisms that produce clinical conditions with a wide variation in patient-rated symptoms and severity. Therefore, different diagnostic and prognostic tools are needed to help make the most accurate decisions at each moment of patient's care with suspected infection. This mini review will analyse how some biomarkers reduce the level of uncertainty in the making decision process at some phases of sepsis, including prompt identification of septic patients, early initiation of empiric broad-spectrum antimicrobials, regimen and duration


La patología infecciosa puede ser debida a microorganismos muy diferentes que producen cuadros clínicos con una expresividad muy variada tanto en los síntomas como en la gravedad. Por ello, se necesitan diferentes herramientas diagnósticas y pronósticas que ayuden a tomar las decisiones más adecuadas en cada momento de la atención a un paciente con sospecha de infección. En esta mini revisión se analizará cómo algunos biomarcadores disminuyen el nivel de incertidumbre en la toma de decisiones clínicas en algunas fases de la atención a la sepsis, como puede ser la propia identificación del paciente séptico, la necesidad de iniciar tratamiento antimicrobiano, el tipo y su duración


Subject(s)
Humans , Sepsis/diagnosis , Communicable Diseases/diagnosis , Anti-Infective Agents/therapeutic use , Biomarkers/analysis , Sepsis/physiopathology , Communicable Diseases/physiopathology , Lactic Acid/analysis , Calcitonin Gene-Related Peptide/analysis , Severity of Illness Index
6.
Clin Case Rep ; 5(6): 809-811, 2017 06.
Article in English | MEDLINE | ID: mdl-28588816

ABSTRACT

Sodium-glucose cotransporter 2 (SGLT2) inhibitors are able to provoke diabetic ketoacidosis (DKA) with absence or low levels of ketone bodies in urine and slightly elevated blood glucose levels, which could delay the diagnosis; however, the presence of high urine output, due to the excretion of glucose, can help to identify the true cause.

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