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1.
J Clin Anesth ; 88: 111137, 2023 09.
Article in English | MEDLINE | ID: mdl-37182398

ABSTRACT

STUDY OBJECTIVES: To assess the prevalence of preoperative acidosis and lactatemia in elderly patients having hip fracture surgery and their association with post-operative mortality. DESIGN: Retrospective cohort study. SETTING: Single tertiary medical center. PATIENTS: Patients ≥65 years having first traumatic hip fracture surgery between 2018 and 2021. MEASUREMENTS: 90-day postoperative mortality. MAIN RESULTS: In total, 1267 patients were included in the primary analysis (mean (SD) age 83(8) years; 802 (69%) females; median [Interquartile Range (IQR)] American Society of Anesthesiologists (ASA) physical score 3 [2,3]). Of these, 1227 were available for the multivariable analyses. Median [IQR] time from hospitalization to surgery was 28 [20, 42] hours. All-cause 90-day mortality rate was 9% (N = 114). The incidence of preoperative acidosis (pH < 7.35) and lactatemia (>1.2 mmol/L) was significantly higher among non-survivors. Mortality was highest in patients with both acidosis and lactatemia (19.1% compared to 4.4% among patients with neither). In a multivariable model, pH <7.35 and lactate >1.2 mmol/L remained independent predictors of 90-day mortality, with adjusted odds ratio (aOR) (95%CI) of 1.99 (1.31 to 3.04) and 2.32 (1.44 to 3.74), respectively, p = 0.001 for both. Time from hospitalization to surgery was not associated with mortality after adjustment for metabolic indices, aOR 1.00 (0.99, 1.00). CONCLUSIONS: Preoperative acidosis and lactatemia are common among patients ≥65 years having hip fracture surgery and are associated with 90-day all-cause mortality. Time from hospital admission to surgery is not an independent risk factor, once adjusted for metabolic indices. Future studies should evaluate whether the increased risk associated with preoperative metabolic disturbances is modifiable.


Subject(s)
Hip Fractures , Female , Humans , Aged , Aged, 80 and over , Male , Retrospective Studies , Prevalence , Hip Fractures/surgery , Risk Factors , Hospitalization
2.
JAMA ; 321(23): 2292-2305, 2019 06 18.
Article in English | MEDLINE | ID: mdl-31157366

ABSTRACT

Importance: An intraoperative higher level of positive end-expiratory positive pressure (PEEP) with alveolar recruitment maneuvers improves respiratory function in obese patients undergoing surgery, but the effect on clinical outcomes is uncertain. Objective: To determine whether a higher level of PEEP with alveolar recruitment maneuvers decreases postoperative pulmonary complications in obese patients undergoing surgery compared with a lower level of PEEP. Design, Setting, and Participants: Randomized clinical trial of 2013 adults with body mass indices of 35 or greater and substantial risk for postoperative pulmonary complications who were undergoing noncardiac, nonneurological surgery under general anesthesia. The trial was conducted at 77 sites in 23 countries from July 2014-February 2018; final follow-up: May 2018. Interventions: Patients were randomized to the high level of PEEP group (n = 989), consisting of a PEEP level of 12 cm H2O with alveolar recruitment maneuvers (a stepwise increase of tidal volume and eventually PEEP) or to the low level of PEEP group (n = 987), consisting of a PEEP level of 4 cm H2O. All patients received volume-controlled ventilation with a tidal volume of 7 mL/kg of predicted body weight. Main Outcomes and Measures: The primary outcome was a composite of pulmonary complications within the first 5 postoperative days, including respiratory failure, acute respiratory distress syndrome, bronchospasm, new pulmonary infiltrates, pulmonary infection, aspiration pneumonitis, pleural effusion, atelectasis, cardiopulmonary edema, and pneumothorax. Among the 9 prespecified secondary outcomes, 3 were intraoperative complications, including hypoxemia (oxygen desaturation with Spo2 ≤92% for >1 minute). Results: Among 2013 adults who were randomized, 1976 (98.2%) completed the trial (mean age, 48.8 years; 1381 [69.9%] women; 1778 [90.1%] underwent abdominal operations). In the intention-to-treat analysis, the primary outcome occurred in 211 of 989 patients (21.3%) in the high level of PEEP group compared with 233 of 987 patients (23.6%) in the low level of PEEP group (difference, -2.3% [95% CI, -5.9% to 1.4%]; risk ratio, 0.93 [95% CI, 0.83 to 1.04]; P = .23). Among the 9 prespecified secondary outcomes, 6 were not significantly different between the high and low level of PEEP groups, and 3 were significantly different, including fewer patients with hypoxemia (5.0% in the high level of PEEP group vs 13.6% in the low level of PEEP group; difference, -8.6% [95% CI, -11.1% to 6.1%]; P < .001). Conclusions and Relevance: Among obese patients undergoing surgery under general anesthesia, an intraoperative mechanical ventilation strategy with a higher level of PEEP and alveolar recruitment maneuvers, compared with a strategy with a lower level of PEEP, did not reduce postoperative pulmonary complications. Trial Registration: ClinicalTrials.gov Identifier: NCT02148692.


Subject(s)
Intraoperative Care , Lung Diseases/prevention & control , Obesity/complications , Positive-Pressure Respiration/methods , Postoperative Complications/prevention & control , Surgical Procedures, Operative/adverse effects , Adult , Anesthesia, General , Body Mass Index , Female , Humans , Lung Diseases/etiology , Male , Middle Aged , Pleural Diseases/etiology , Pleural Diseases/prevention & control , Pulmonary Atelectasis/therapy , Respiratory Insufficiency/etiology , Respiratory Insufficiency/prevention & control , Tidal Volume , Treatment Outcome
3.
Int J Obstet Anesth ; 40: 39-44, 2019 11.
Article in English | MEDLINE | ID: mdl-31230990

ABSTRACT

BACKGROUND: We investigated the correlation between lumbar epidural analgesia onset time and pain intensity at 60 and 120 min after initiation. METHODS: We conducted a prospective observational study of nulliparous women receiving lumbar epidural analgesia (initial bolus 15 mL bupivacaine 0.1% with fentanyl 3.33 µg/mL), followed by patient-controlled epidural analgesia (PCEA). The measured variable was lumbar epidural analgesia onset time (time to pain numerical rating score ≤3). Secondary outcomes were pain score at 60 and 120 min and at full dilatation; and analgesic requirements through the labor. RESULTS: One-hundred-and-five women were eligible for analysis. There was a significant correlation between lumbar epidural analgesia onset time and pain intensity at 60 min (Spearman's R2=0.286, P=0.003), but not at 120 min (R2=0.030, P=0.76). Women who requested more PCEA boluses during the first 120 min had a longer lumbar epidural analgesia onset time (R2=0.321, P=0.001) and reported higher pain scores at 60 min (R2=0.588, P <0.001) and at 120 min (R2=0.539, P <0.001). Women who reported higher pain scores at 60 min had more pain at 120 min (R2=0.47, P <0.001) and higher analgesic consumption during labor (R2=0.403, P <0.001). Women who were at a greater cervical dilatation at 60 and 120 min had higher pain scores at the same time point (R2=0.259, P=0.008 and R2=0.243, P=0.013 respectively). CONCLUSION: There was a correlation between the onset time of lumbar epidural analgesia during labor and the pain score 60 min later but this had disappeared by 120 min.


Subject(s)
Analgesia, Epidural/methods , Analgesia, Obstetrical/methods , Analgesia, Patient-Controlled/statistics & numerical data , Adult , Analgesia, Patient-Controlled/methods , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/therapeutic use , Anesthetics, Local/administration & dosage , Anesthetics, Local/therapeutic use , Bupivacaine/administration & dosage , Bupivacaine/therapeutic use , Cohort Studies , Female , Fentanyl/administration & dosage , Fentanyl/therapeutic use , Humans , Labor, Obstetric , Pregnancy , Prospective Studies , Time Factors , Treatment Outcome
5.
Int J Obstet Anesth ; 35: 4-9, 2018 08.
Article in English | MEDLINE | ID: mdl-29502991

ABSTRACT

BACKGROUND: Laboring women with low platelet counts may be denied neuraxial block due to concerns about causing a spinal-epidural hematoma. AIMS: To assess the anesthetic management, complications and outcome variables of women with low platelet counts, and to expand the existing data regarding the safety of neuraxial blocks in this patient population. METHODS: This is a retrospective analysis of anesthetic and obstetric data from women with platelet counts <100 000/µL, who were admitted to a single referral center during 2011-2014. The rate of neuraxial block and related complications were examined in relation to the platelet count and the results combined with published data to assess the risk of spinal-epidural hematoma. RESULTS: During the study period, 471 of 45 462 women (1%) had a low platelet count (<100 000/µL). The rate of neuraxial block was significantly higher in women with platelet counts of 70-99 000/µL (280/394, 71.1%) when compared to women with platelet counts of 50-69 000/µL and 0 to 49 000/µL (23/59, 38.9% and 5/18, 27.8%, respectively, P <0.0001). Women in the lower platelet count ranges had a higher risk of cesarean delivery under general anesthesia and longer hospital stay. No neuraxial hematoma were reported. CONCLUSIONS: This study contributes a substantial series of neuraxial blocks among women with low platelet counts. The findings support that the risk of hematoma is low if the platelet count is <100 000/µL, specifically between 70 and 99 000/µL. Risk assessment in the lower count ranges requires a much larger sample.


Subject(s)
Anesthesia, Obstetrical/methods , Nerve Block/methods , Platelet Count , Adult , Female , Hematoma/etiology , Humans , Nerve Block/adverse effects , Pregnancy , Retrospective Studies , Thrombelastography
7.
Trials ; 18(1): 202, 2017 04 28.
Article in English | MEDLINE | ID: mdl-28454590

ABSTRACT

BACKGROUND: Postoperative pulmonary complications (PPCs) increase the morbidity and mortality of surgery in obese patients. High levels of positive end-expiratory pressure (PEEP) with lung recruitment maneuvers may improve intraoperative respiratory function, but they can also compromise hemodynamics, and the effects on PPCs are uncertain. We hypothesized that intraoperative mechanical ventilation using high PEEP with periodic recruitment maneuvers, as compared with low PEEP without recruitment maneuvers, prevents PPCs in obese patients. METHODS/DESIGN: The PRotective Ventilation with Higher versus Lower PEEP during General Anesthesia for Surgery in OBESE Patients (PROBESE) study is a multicenter, two-arm, international randomized controlled trial. In total, 2013 obese patients with body mass index ≥35 kg/m2 scheduled for at least 2 h of surgery under general anesthesia and at intermediate to high risk for PPCs will be included. Patients are ventilated intraoperatively with a low tidal volume of 7 ml/kg (predicted body weight) and randomly assigned to PEEP of 12 cmH2O with lung recruitment maneuvers (high PEEP) or PEEP of 4 cmH2O without recruitment maneuvers (low PEEP). The occurrence of PPCs will be recorded as collapsed composite of single adverse pulmonary events and represents the primary endpoint. DISCUSSION: To our knowledge, the PROBESE trial is the first multicenter, international randomized controlled trial to compare the effects of two different levels of intraoperative PEEP during protective low tidal volume ventilation on PPCs in obese patients. The results of the PROBESE trial will support anesthesiologists in their decision to choose a certain PEEP level during general anesthesia for surgery in obese patients in an attempt to prevent PPCs. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT02148692. Registered on 23 May 2014; last updated 7 June 2016.


Subject(s)
Anesthesia, General , Intraoperative Care/methods , Lung Diseases/prevention & control , Lung/physiopathology , Obesity/complications , Positive-Pressure Respiration/methods , Surgical Procedures, Operative , Anesthesia, General/adverse effects , Body Mass Index , Clinical Protocols , Female , Humans , Intraoperative Care/adverse effects , Lung Diseases/diagnosis , Lung Diseases/etiology , Lung Diseases/physiopathology , Male , Obesity/diagnosis , Obesity/physiopathology , Positive-Pressure Respiration/adverse effects , Protective Factors , Research Design , Risk Factors , Surgical Procedures, Operative/adverse effects , Time Factors , Treatment Outcome
8.
Br J Anaesth ; 116(2): 255-61, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26787795

ABSTRACT

BACKGROUND: Transfusion of allogeneic blood influences outcome after surgery. Despite widespread availability of transfusion guidelines, transfusion practices might vary among physicians, departments, hospitals and countries. Our aim was to determine the amount of packed red blood cells (pRBC) and blood products transfused intraoperatively, and to describe factors determining transfusion throughout Europe. METHODS: We did a prospective observational cohort study enrolling 5803 patients in 126 European centres that received at least one pRBC unit intraoperatively, during a continuous three month period in 2013. RESULTS: The overall intraoperative transfusion rate was 1.8%; 59% of transfusions were at least partially initiated as a result of a physiological transfusion trigger- mostly because of hypotension (55.4%) and/or tachycardia (30.7%). Haemoglobin (Hb)- based transfusion trigger alone initiated only 8.5% of transfusions. The Hb concentration [mean (sd)] just before transfusion was 8.1 (1.7) g dl(-1) and increased to 9.8 (1.8) g dl(-1) after transfusion. The mean number of intraoperatively transfused pRBC units was 2.5 (2.7) units (median 2). CONCLUSION: Although European Society of Anaesthesiology transfusion guidelines are moderately implemented in Europe with respect to Hb threshold for transfusion (7-9 g dl(-1)), there is still an urgent need for further educational efforts that focus on the number of pRBC units to be transfused at this threshold. CLINICAL TRIAL REGISTRATION: NCT 01604083.


Subject(s)
Blood Transfusion/methods , Blood Transfusion/statistics & numerical data , Intraoperative Care/methods , Intraoperative Care/statistics & numerical data , Cohort Studies , Europe , Female , Hospitals/statistics & numerical data , Humans , Male , Middle Aged , Prospective Studies
9.
Br J Anaesth ; 115 Suppl 2: ii3-14, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26658199

ABSTRACT

Perioperative acute kidney injury (AKI) is not uncommon and is associated with considerable morbidity and mortality. Recently, several definition systems for AKI were proposed, incorporating both small changes of serum creatinine and urinary output reduction as diagnostic criteria. Novel biomarkers are under investigation as fast and accurate predictors of AKI. Several special considerations regarding the risk of AKI are of note in the surgical patient. Co-morbidities are important risk factors for AKI. The surgery in itself, especially emergency and major surgery in the critically ill, is associated with a high incidence of AKI. Certain types of surgeries, such as cardiac and transplantation surgeries, require special attention because they carry higher risk of AKI. Nephrotoxic drugs, contrast dye, and diuretics are commonly used in the perioperative period and are responsible for a significant amount of in-hospital AKI. Before surgery, the anaesthetist is required to identify patients at risk of AKI, optimize anaemia, and treat hypovolaemia. During surgery, normovolaemia is of utmost importance. Additionally, the surgical and anaesthesia team is advised to use measures to reduce blood loss and avoid unnecessary blood transfusion. Hypotension should be avoided because even short periods of mean arterial pressure <55-60 mm Hg carry a risk of postoperative AKI. Higher blood pressures are probably required for hypertensive patients. Urine output can be reduced significantly during surgery and is unrelated to perioperative renal function. Thus, fluids should not be given in excess for the sole purpose of avoiding or treating oliguria. Use of hydroxyethyl starch needs to be reconsidered. Recent evidence indicates a beneficial effect of administering low-chloride solutions.


Subject(s)
Acute Kidney Injury/diagnosis , Intraoperative Complications/diagnosis , Postoperative Complications/diagnosis , Acute Kidney Injury/etiology , Acute Kidney Injury/therapy , Biomarkers/metabolism , Comorbidity , Humans , Perioperative Care/methods , Risk Factors
10.
Br J Anaesth ; 111 Suppl 1: i62-70, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24335400

ABSTRACT

Blood transfusion saves many lives but carries significant risk of injury. Currently, red blood cell (RBC) concentrates can be stored up to 42 days. Concerns have recently been raised about the safety and efficacy of transfusing stored RBCs. Refrigerated storage results in a 'storage lesion' that is reflected by metabolic derangements, RBC shape modification, rheological changes, oxidative injury to lipids and proteins, alterations in oxygen affinity and delivery, increased adhesion of RBCs to endothelial cells, and accumulation of bioactive substances in storage media. In animal models, transfusion of aged, but not fresh, RBCs induces organ injury, inflammation, coagulopathy, and impaired oxygen delivery. A number of clinical studies, mostly observational or retrospective and from a single centre, have reported an association between transfusion of older RBCs and increased clinically significant outcomes, such as increased morbidity and mortality in certain patient populations, including trauma, critical care, and cardiac surgery. Others, however, have failed to indicate an influence of RBC age on outcome. The quality of evidence is currently too poor to make recommendations to change current transfusion practice; however, the transfusion community looks forward to the results of randomized trials currently addressing the long-standing question regarding the effects of RBC storage on clinically significant outcomes.


Subject(s)
Blood Preservation , Erythrocyte Transfusion/adverse effects , Erythrocytes/physiology , Clinical Trials as Topic , Humans
11.
J Clin Pediatr Dent ; 34(4): 287-9, 2010.
Article in English | MEDLINE | ID: mdl-20831127

ABSTRACT

The purpose of this pilot study was to investigate the prevalence of trauma to incisor teeth in children with normal overjet and lip competence, treated with methylphenidate (Ritalin) for attention deficit hyperactivity disorder (ADHD). The study group consisted of 24 children (19 boys, 5 girls) aged 5-12 years (mean 8.45 +/- 2.25), diagnosed with ADHD and treated with methylphenidate at a minimal dosage of 10 mg per day. The control group consisted of 22 healthy children (13 boys, 9 girls) aged 5-12 years (mean 9.15 +/- 2.28). The dental examination included incisor relation measurements in the anterior segment (overjet), which was recorded using an orthodontic ruler. Lip competence was clinically determined, and anterior teeth were examined for dental trauma. The prevalence of dental trauma was significantly higher in the study group than in the control group (29.1% vs. 4.5% P = 0.02, t-test one tail). In conclusion, children with ADHD treated with methylphenidate have a high-risk for dental trauma. We believe that preventing dental trauma in this high risk group is possible. Consequently, the pediatrician and all medical staff attending to these children should encourage parents to consult frequently with a pediatric dentist to diagnose dental trauma and provide early treatment when needed.


Subject(s)
Attention Deficit Disorder with Hyperactivity/drug therapy , Central Nervous System Stimulants/therapeutic use , Incisor/injuries , Methylphenidate/therapeutic use , Central Nervous System Stimulants/administration & dosage , Cephalometry , Child , Child, Preschool , Dental Enamel/injuries , Dental Occlusion , Dentin/injuries , Female , Humans , Lip/anatomy & histology , Male , Methylphenidate/administration & dosage , Pilot Projects
12.
Acta Anaesthesiol Scand ; 53(5): 665-72, 2009 May.
Article in English | MEDLINE | ID: mdl-19419362

ABSTRACT

BACKGROUND: The post-void residual volume is higher among parturients who received epidural analgesia than those who received no or alternative analgesia. METHODS: This prospective, randomized, controlled, non-blinded study was performed in a tertiary referral center labor suite. The post-void residual volume was measured by a transabdominal ultrasound following a voiding attempt. Healthy parturients with low-dose epidural analgesia in active labor were randomized either to walk to the toilet or to use a bedpan for voiding. The primary outcome measure (post-void residual volume in labor) was compared between the study groups. RESULTS: The toilet group (n=34) and the bedpan group (n=28) demonstrated similar post-void residual volumes (212 +/- 100 vs. 168 +/- 93 ml, P=0.289). Twenty patients (59%) randomized to the toilet group were unable to walk and actually voided in a bedpan. A secondary analysis was performed analyzing the groups as treated. The post-void residual volume was significantly lower in the actual toilet group (n=14, 63 +/- 24 ml) vs. the bedpan group (n=48, 229 +/- 200 ml), P=0.0052. Thirteen (93%) women who walked to the toilet managed to void before the ultrasound measurement vs. 20/48 (42%) using the bedpan, P=0.001. Fewer women who managed to walk to the toilet required urinary bladder catheterization during the labor than women who used the bedpan (6/14, 43% vs. 36/48, 75%) P=0.028. CONCLUSION: Women who were randomized to walk to the bathroom with epidural analgesia and were able to do so during labor had a significantly reduced post-void residual volume and a reduced requirement for urinary catheterization.


Subject(s)
Analgesia, Epidural , Analgesia, Obstetrical , Urodynamics/physiology , Walking/physiology , Adult , Double-Blind Method , Endpoint Determination , Female , Humans , Pregnancy , Prospective Studies , Treatment Outcome , Ultrasonography , Urinary Bladder/diagnostic imaging , Urinary Bladder/physiology , Urination/physiology
13.
Int J Obstet Anesth ; 17(3): 238-42, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18501587

ABSTRACT

BACKGROUND: Guidelines for the management of cardiac arrest during pregnancy exist but they are based on little research. The study hypothesis was that experienced medical clinicians who specialise in obstetric care would not follow current International Liaison Committee on Resuscitation/American Heart Association recommendations in this situation. METHODS: Following waiver of informed consent by the institutional review board, an anonymous structured scenario questionnaire survey was conducted among relevant hospital clinicians. Demographic details included field of expertise and resuscitation experience. A single case vignette of maternal cardiac arrest was presented, followed by nine questions to examine knowledge of existing recommendations for maternal cardiopulmonary resuscitation. Statistical analyses were performed using SPSS version 12 software (SPSS Inc, Chicago, IL). RESULTS: The overall response rate was 67% (30/45 questionnaires). Specialist obstetricians, midwives and anaesthetists from 17 hospitals participated. Forty-three percent (n=13) claimed broad experience, 50% (n=15) claimed some experience and 6.7% (n=2) claimed no experience in adult resuscitation. Participants were divided in their opinions regarding every choice of action: positioning, need to administer cricoid pressure during mask ventilation, timing of intubation, location of external chest compression, location of paddle placement for delivery of shock during ventricular fibrillation, the timing of defibrillation versus fetal delivery, medication doses and the need to rupture the membranes at an early phase of the resuscitation. CONCLUSION: Specialist clinicians who treat pregnant women in hospital on a daily basis possess a limited knowledge of the recommendations for treating maternal cardiac arrest.


Subject(s)
Anesthesiology/standards , Cardiopulmonary Resuscitation/standards , Clinical Competence/standards , Heart Arrest/therapy , Adult , Aged , Female , Health Care Surveys , Humans , Male , Middle Aged , Midwifery/standards , Obstetrics/standards , Practice Guidelines as Topic
14.
Med Hypotheses ; 68(3): 484-92, 2007.
Article in English | MEDLINE | ID: mdl-17141964

ABSTRACT

Elderly surgical patients constitute a unique surgical group. They require special consideration in order to preempt the long term adverse effects of anesthesia. This paper examines the proposition that general anesthesia causes harm to elderly patients with its impact being felt long after the anesthetic agents are cleared from the body. One complication, Postoperative Cognitive Decline (POCD), is associated with the administration of anesthesia and deep sedation. Its' occurrence may herald an increase in morbidity and mortality. Based on both human and animal data, this paper outlines a unitary theoretical framework to explain these phenomena. If this hypothesis proves to be correct, anesthesiologist should consider regional rather than general anesthesia for equivalent surgical procedures to reduce POCD and consequently achieving superior patient outcome.


Subject(s)
Anesthesia, General/adverse effects , Anesthesia, General/mortality , Cognition Disorders/etiology , Aged , Central Nervous System/physiopathology , Central Nervous System Diseases/etiology , Cognition Disorders/classification , Humans , Postoperative Complications/epidemiology
15.
Acta Anaesthesiol Scand ; 50(10): 1297-303, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16978160

ABSTRACT

BACKGROUND: This prospective, non-randomized study compared post-void residual volume in laboring and postpartum women with or without epidural analgesia. METHODS: The study was conducted over 1 year with institutional review board approval. Parturients were recruited in early labor and self-selected to either the study (with epidural) or control (without epidural) group. Post-void residual volume was compared between groups, using transabdominal ultrasound during labor, and on postpartum day 1 and 2. Main outcome measure was intrapartum residual bladder volume. RESULTS: Thirty patients were recruited to each group. During labor, residual bladder volume was significantly larger in the epidural group compared with the non-epidural group [median (range)] 240 (12-640), ml vs. 45 (13-250) ml, respectively, P < 0.001], but was similar on postpartum day 1 and 2. Twenty-five (83%) women with epidural analgesia required bladder catheterization during labor vs. one (3.3%) without (P < 0.0001). CONCLUSION: The greater post-void residual volume and increased inability to void in parturients with epidurals suggests that epidural analgesia plays a role in intrapartum urinary retention.


Subject(s)
Anesthesia, Epidural , Labor, Obstetric/physiology , Parturition/physiology , Urinary Bladder/anatomy & histology , Urination/physiology , Urine , Choice Behavior , Female , Humans , Parturition/drug effects , Patient Selection , Pregnancy , Ultrasonography , Urinary Bladder/diagnostic imaging , Urinary Catheterization/statistics & numerical data
16.
Br J Anaesth ; 97(4): 468-72, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16873385

ABSTRACT

We report the case of a Child class C cirrhotic patient who was diagnosed with coronary artery disease in the course of his pretransplantation evaluation. He underwent off-pump coronary artery bypass grafting (OPCAB), which was complicated with acute renal failure. The morbidity and mortality associated with cardiac operation in patients with cirrhosis is discussed, and the potential advantage of OPCAB in this patient population is emphasized.


Subject(s)
Coronary Artery Bypass, Off-Pump/methods , Coronary Disease/complications , Liver Cirrhosis/complications , Liver Transplantation , Coronary Disease/surgery , Hospital Mortality , Humans , Liver Cirrhosis/surgery , Male , Middle Aged , Treatment Outcome
17.
Int J Obstet Anesth ; 15(2): 145-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16488141

ABSTRACT

A parturient (grand multipara) developed arrested labour complicated by severe fetal heart rate decelerations. Senior physicians explained the need for a caesarean section, but she chose to deliver vaginally since rabbinical blessing could not be obtained. Forcing the mother to have a cesarean section without consent is considered "civil battery." The dilemma faced by medical staff and the implications of her refusal for the treating medical staff are described.


Subject(s)
Cesarean Section , Emergency Medical Services , Obstetric Labor Complications/therapy , Religion , Treatment Refusal , Adult , Female , Heart Rate, Fetal/physiology , Humans , Infant, Newborn , Israel , Obstetric Labor Complications/surgery , Oligohydramnios/physiopathology , Pregnancy , Pregnancy Outcome
18.
Childs Nerv Syst ; 17(8): 478-82, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11508537

ABSTRACT

OBJECTS: The relationship between increased central venous pressure (CVP) and development of hydrocephalus has been extensively discussed in the neuropediatric literature. However, the possibility of a direct connection has not been systematically examined. The purpose of this prospective study was to examine whether there was a correlation between elevated CVP and hydrocephalus in children undergoing cardiac catheterization. METHODS: We used cardiac catheterization to measure the right atrial and superior vena caval pressure in 37 children (mean age 30 months) with congenital heart malformations. The children had CVP higher than normal (mean 10.2+/-3.1 mmHg, range 4-18). To evaluate the size of the lateral and fourth ventricles, we performed CT scans of the brain on each child. Abnormal scans were found in 15/37 children, showing brain atrophy (12/37), ventriculomegaly (3/37), and focal infarction (1/37). Cerebral atrophy was more likely to occur in young children (P<0.001). The average head circumference among these children was less than 2SD below the mean for healthy children of comparable ages. Using a correlation coefficient regression model, no relationship was found between CVP and ventricular diameters or head circumference. CONCLUSIONS: These results argue against the hypothesis that mild to moderately elevated venous pressure is involved in the mechanism and development of pediatric hydrocephalus.


Subject(s)
Cardiac Catheterization , Central Venous Pressure , Cerebral Ventricles/pathology , Heart Defects, Congenital/complications , Hydrocephalus/etiology , Cerebral Ventricles/physiopathology , Child , Child, Preschool , Female , Heart Defects, Congenital/diagnosis , Heart Defects, Congenital/physiopathology , Humans , Hydrocephalus/pathology , Hydrocephalus/physiopathology , Infant , Intracranial Pressure , Male , Prospective Studies , Tomography, X-Ray Computed
19.
J Clin Anesth ; 13(5): 383-6, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11498322

ABSTRACT

Airway problems are easiest to manage when they are anticipated. Difficult intubation might, however, occur in patients with no obvious signs or symptoms suggesting airway difficulty. We describe a case where laryngeal inlet was obscured by a large vallecular cyst that was discovered during rapid-sequence induction of general anesthesia, causing difficulty in tracheal intubation. Once the patient was allowed to recover from general anesthesia, the trachea could be safely intubated using a fiberoptic bronchoscope.


Subject(s)
Cysts/complications , Intubation, Intratracheal , Adult , Appendectomy , Bronchoscopy , Cysts/surgery , Fiber Optic Technology , Humans , Male
20.
J Surg Oncol ; 78(1): 17-21, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11519063

ABSTRACT

BACKGROUND AND OBJECTIVES: The surgical strategy for the treatment of resectable synchronous hepatic metastases of colorectal cancer remains controversial. This study was performed to assess the outcome of combined resection of colorectal cancer and liver metastases. METHODS: The perioperative data, morbidity, and survival of the patients who underwent combined colon and liver resections for synchronous colorectal liver metastases from 1988 to 1999 were compared to the parameters of the patients who underwent colon resection followed by resection of liver metastases in a staged setting. RESULTS: 198 hepatic resections were performed, of which 112 procedures in 103 patients were done for metastatic colorectal carcinoma. Twenty six patients (25%) had combined hepatic and colon resection and were compared to 86 patients with metachronous metastases who underwent colon and hepatic resection in the staging setting. Postoperative morbidity was 27 and 35%, respectively. There was no hospital mortality in the combined group vs. 2.3% in the staged group. Blood loss, intensive care unit (ICU) stay and length of postoperative stay (LOS) were similar in both groups. The 5 years cumulative survival of the group after combined surgery was 28% vs. 27% of the group after isolated hepatic resections (P = 0.21). CONCLUSION: Combined colon and hepatic resection is a safe and efficient procedure for the treatment of synchronous colorectal liver metastases. It can be performed with acceptable morbidity and no perioperative mortality. The survival after combined procedure is comparable to the one achieved after staged procedure of colon resection followed by liver resection.


Subject(s)
Colectomy/methods , Colonic Neoplasms/surgery , Hepatectomy/methods , Liver Neoplasms/surgery , Rectal Neoplasms/surgery , Adult , Aged , Aged, 80 and over , Colectomy/mortality , Colonic Neoplasms/pathology , Digestive System Surgical Procedures/methods , Female , Hepatectomy/mortality , Humans , Liver Neoplasms/secondary , Male , Middle Aged , Rectal Neoplasms/pathology , Retrospective Studies , Survival Rate
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