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1.
Jpn J Nurs Sci ; : e12601, 2024 May 02.
Article in English | MEDLINE | ID: mdl-38698302

ABSTRACT

AIM: The study aimed to ascertain a framework of nursing practices to elicit consent from lightly sedated ventilated patients. METHODS: Study participants were nurses working in intensive care and critical care wards, whose observations and semi-structured interviews were assessed using a modified grounded theory approach. RESULTS: A total of 15 concepts were generated, from which three categories and three subcategories were generated. Category 1: Nurses taking the lead in providing assistance by sharing signs of change while continuing the invasive treatment, working to maintain the patient's life, alleviation of pain, promotion of awareness of the current situation, and acclimating them to the treatment environment as the basis for building a relationship between patients and nurses. Category 2: Searching for points of agreement and reaching a compromise involves the nurse drawing out the patient's thoughts, hopes, and expectations, and transforming the relationship into a patient-centered one by sharing goals with the patient in order to achieve them. Category 3: Organizing collaboration within care supported the patient's ability to move safely while maintaining the patient's pace to achieve shared goals, and guided the patient's independent actions. CONCLUSIONS: Even when patients recover from an acute life-threatening situation, their physical sensations remain vague and their functional decline continues. Rather than simply eliciting consent from patients, the structure of nursing practice to elicit such response from patients involves drawing out the patient's thoughts, hopes, and expectations, as well as guiding the patient toward goals that they have created together with the nurse and utilizing the patient's strengths to achieve these goals.

2.
Intensive Crit Care Nurs ; 68: 103118, 2022 Feb.
Article in English | MEDLINE | ID: mdl-34393008

ABSTRACT

OBJECTIVES: To elucidate how patients' illness severity, respiratory status, or haemodynamics are associated with the pain score of critically ill patients. METHODS: This was an observational study of patients on mechanical ventilation after surgeries. At rest and on turning, patient pain was evaluated using the Behavioural Pain Scale (BPS) and the Critical-Care Pain Observation Tool (CPOT). Related factors were collected from medical records and analysed. FINDINGS: Multiple logistic regression analysis was performed using data on 127 scenarios. An increase of >2 in BPS score on turning was affected by the Acute Physiology and Chronic Health Evaluation (APACHE) II score (odds ratio [OR] = 0.864), systolic blood pressure at rest (OR = 1.032), BPS at rest (OR = 0.638), heart rate difference (OR = 1.124), and tidal volume difference (OR = 0.548). An increase of >2 in CPOT on turning score was associated with the APACHE II score (OR = 0.894), Sequential Organ Failure Assessment score (OR = 1.248), systolic blood pressure at rest (OR = 1.025), heart rate difference (OR = 1.096), and tidal volume difference (OR = 0.578). CONCLUSION: The Behavioural Pain Scale and the Critical-Care Pain Observation Tools were associated with illness severity and haemodynamics. A reduction in tidal volume may be useful in assessing pain.


Subject(s)
Critical Illness , Respiration, Artificial , Critical Care , Humans , Intensive Care Units , Pain , Pain Measurement , Respiration, Artificial/adverse effects
3.
Intensive Crit Care Nurs ; 42: 75-79, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28347628

ABSTRACT

OBJECTIVE: To determine how respiratory status and other aspects of the patients' condition affect pain assessments. METHODS:  Pain was assessed in 20 patients aged ≥20 years who underwent cardiovascular surgery, and required postoperative mechanical ventilation in an intensive care unit using the Behavioral Pain Scale (BPS). A BPS score of ≥6 (pain) versus <6 (no pain) was the dependent variable for determining the effect on pain. RESULTS:  Multiple logistic regression analysis showed that in 99 observations made at rest, pre- and post-turning and pre- and post-tracheal suctioning, the BPS score was significantly affected by gender, the Acute Physiology and Chronic Health Evaluation (APACHE) II score, Richmond Agitation-Sedation Scale score, PaCO2, and HCO3-. The associations between BPS scores and APACHE II scores and HCO3- demonstrated that pain results from biological responses to invasion. Increases in PaCO2 affecting only the total BPS score suggests that PaCO2 is associated with other pain responses, regardless of respiratory status. CONCLUSION:  The BPS score was significantly associated with disease severity and ventilatory capacity, demonstrating a need to examine pain assessment methods tailored to the severity of underlying disease, degree of respiratory failure and other aspects of individual patient's condition for effective pain management.


Subject(s)
Communication Barriers , Pain Measurement/standards , Respiration, Artificial/adverse effects , APACHE , Aged , Aged, 80 and over , Female , Humans , Intensive Care Units/organization & administration , Logistic Models , Male , Middle Aged , Pain/nursing , Pain Measurement/methods , Tokyo
4.
Mol Immunol ; 46(5): 858-65, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18977535

ABSTRACT

Mx, an interferon-inducible protein, is found in various vertebrates and confers resistance to several RNA viruses. At least two Mx proteins occur in vertebrates, and these proteins are key components of innate defense against viral infection. In mice and humans, the two Mx genes have different antiviral activities. Both Mx1 and Mx2 have also been detected in pigs, although only a partial sequence of porcine Mx2 has been reported, and there is no information on its antiviral activity. Here, we report the structure of the intact porcine Mx2 gene having an open reading frame of 2136 bp. We also determined the sequence of the genomic region containing the entire porcine Mx2 gene in addition to Mx1 gene. A weak constitutive expression of porcine Mx2 mRNA and endogenous Mx2 protein was observed in interferon-untreated cells. Porcine endogenous Mx2 protein showed nuclear localization. Furthermore, assays using NIH3T3 cells transfected with Mx genes showed that porcine Mx2 possessed antiviral activity against influenza, although this activity was lower than that of human MxA. This report is the first to describe the intact porcine Mx2 gene, which is a functional gene that may play a key role in the clearance of viruses in pigs.


Subject(s)
GTP-Binding Proteins/genetics , GTP-Binding Proteins/immunology , Influenza A virus/immunology , Orthomyxoviridae Infections/immunology , Swine/genetics , Swine/immunology , Animals , Cloning, Molecular , Dogs , GTP-Binding Proteins/biosynthesis , Gene Expression Regulation/immunology , Influenza A virus/genetics , Influenza A virus/metabolism , Mice , Myxovirus Resistance Proteins , NIH 3T3 Cells , Organ Specificity/immunology , Orthomyxoviridae Infections/genetics , Orthomyxoviridae Infections/metabolism , Orthomyxoviridae Infections/veterinary , Swine Diseases/genetics , Swine Diseases/immunology , Swine Diseases/metabolism
5.
Biochem Genet ; 45(1-2): 11-24, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17203407

ABSTRACT

Mx1 has been implicated in resistance to the influenza virus. We have now identified four alleles of the Mxl gene in domesticated breeds of pigs. Two of the alleles encode deletion variants (a 3-bp deletion in exon 13 and an 11-bp deletion in exon 14), which might be expected to interfere with Mx activity. The porcine Mxl genes corresponding to wild type, the 3-bp deletion mutant, and the 11-bp deletion mutant were cloned and expressed in NIH3T3 cells, and the antiviral activity for influenza virus was assayed. Virus yield was observed to be 10-100-fold greater with the 11-bp deletion allele than that for wild type and the 3-bp deletion alleles. The results suggest that the 11-bp deletion type is lacking antiviral activity able to contribute to the interference of influenza virus replication.


Subject(s)
GTP-Binding Proteins/genetics , Influenza A Virus, H3N2 Subtype , Orthomyxoviridae Infections/genetics , Polymorphism, Genetic , Swine/genetics , Amino Acid Sequence , Animals , Antibodies, Monoclonal/pharmacology , Base Sequence , Breeding , GTP-Binding Proteins/metabolism , Genetic Predisposition to Disease , Influenza A Virus, H3N2 Subtype/growth & development , Interferons/immunology , Mice , Molecular Sequence Data , Myxovirus Resistance Proteins , NIH 3T3 Cells , Orthomyxoviridae Infections/virology , Sequence Homology, Nucleic Acid , Transfection , Virus Replication/drug effects
6.
Nucleic Acids Res ; 30(22): 4830-5, 2002 Nov 15.
Article in English | MEDLINE | ID: mdl-12433985

ABSTRACT

The RNA interference (RNAi) phenomenon is a recently observed process in which the introduction of a double-stranded RNA (dsRNA) into a cell causes the specific degradation of a mRNA containing the same sequence. The 21-23 nt guide RNAs, generated by RNase III cleavage from longer dsRNAs, are associated with sequence-specific mRNA degradation. Here, we show that dsRNA specifically suppresses the expression of HIV-1 genes. To study dsRNA-mediated gene interference in HIV-1-infected cells, we have designed six long dsRNAs containing the HIV-1 gag and env genes. HIV-1 replication was totally suppressed in a sequence-specific manner by the dsRNAs in HIV-1-infected cells. Especially, E2 dsRNA containing the major CD4-binding domain sequence of gp120, as the target of the HIV-1 env gene, dramatically inhibited the expression of the HIV-1 p24 antigen in PBMCs for a relatively long time. The dsRNA interference method seems to be a promising new strategy for anti-HIV-1 gene therapeutics.


Subject(s)
Anti-HIV Agents/pharmacology , HIV-1 , Leukocytes, Mononuclear/virology , RNA, Double-Stranded/pharmacology , Animals , COS Cells , Cell Line , Cells, Cultured , Dose-Response Relationship, Drug , Gene Expression Regulation, Viral/drug effects , Genes, env , Genes, gag , HIV Core Protein p24/biosynthesis , HIV Core Protein p24/genetics , HIV Infections/prevention & control , HIV-1/genetics , HIV-1/metabolism , HeLa Cells , Humans , RNA Interference , RNA, Antisense/pharmacology , RNA, Viral/biosynthesis , Virus Replication/drug effects
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