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1.
Arch Psychiatr Nurs ; 36: 78-84, 2022 02.
Article in English | MEDLINE | ID: mdl-35094830

ABSTRACT

AIM: This study aimed to determine the relationship between pregnant women's anxiety levels related to concerns about the effect of coronavirus on prenatal attachment. DESIGN AND METHOD: This a descriptive and correlational design study was conducted from September 2020 to January 2021; it included 101 pregnant women who were more than 20 weeks pregnant. Introductory questionnaire, the Coronavirus Anxiety Scale and the Prenatal Attachment Inventory were used as data collection tools. RESULTS: Of the participants, 80.2% were 35 years old or younger. The participants' mean Coronavirus Anxiety Scale score was 8.85 ± 5.02 (min: 0, max: 17), which was close to the scale's cut-off value. Of the participants, 68.3% had high levels of perceived anxiety about coronavirus. The participants' mean Prenatal Attachment Inventory score was 60.08 ± 21.26 (min: 21, max: 84). Of the participants, 54.3% had high levels of Prenatal Attachment Inventory. Correlation analysis found a negative, but significant relationship between the participants' scores on the Coronavirus Anxiety Scale and the Prenatal Attachment Inventory (r = -244, p = 0.014). CONCLUSION: The participants' prenatal attachment levels increased as their perceived anxiety scores about coronavirus decreased.


Subject(s)
Coronavirus Infections , Coronavirus , Adult , Anxiety , Female , Humans , Pregnancy , Pregnant Women , Surveys and Questionnaires
2.
Midwifery ; 99: 103013, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33957520

ABSTRACT

OBJECTIVE: Evaluation of the mental health of pregnant women during the early and peak stages of the Covid-19 outbreak DESIGN: Online survey PARTICIPANTS: Pregnant women over the age of 18 years with no mental disorder during the pre-pregnancy period (N = 729). MEASUREMENTS AND FINDINGS: Mental disorders were assessed using the "Depression Anxiety Stress Scale" and social support was determined using the "Multidimensional Perceived Social Support Scale." Pregnant women had moderate levels of anxiety and depression and mild levels of stress. Anxiety, depression, and stress of moderate or high severity was reported in 62.2%, 44.6%, and 32.2% of the women, respectively. Pregnant women who lost their jobs during the pandemic period showed a 3-fold increase in the risk of anxiety, a 6-fold increase in the risk of depression, and a 4.8-fold increase in the risk of stress. An increase in the perception of social support has protective effects against all three mental disorders during pregnancy. In pregnant women with at least one obstetric risk, the risk of antenatal anxiety is 2 times higher than that in women with no risk. Similarly, women with a chronic physical illness before pregnancy have a higher risk of anxiety during pregnancy than healthy women. Financial strain has predictive value for anxiety and depression, and advanced age is a predictor for depression. KEY CONCLUSIONS: The incidence of mental disorders in pregnant women during the pandemic period was much higher than that during the pre-pandemic period. The high frequency of antenatal mental disorders can lead to an increase in the frequency of obstetric and maternal complications in the short and long term. IMPLICATIONS FOR PRACTICE: Early detection of inadequate social support and economic difficulties of pregnant women during the pandemic period is recommended for protecting their mental health. Pregnant women should have easy access to psychosocial support, and they should be provided obstetric counseling during the pandemic conditions.


Subject(s)
Anxiety , COVID-19 , Depression , Pregnancy Complications , Stress, Psychological , Unemployment/psychology , Adult , Anxiety/diagnosis , Anxiety/epidemiology , Anxiety/prevention & control , COVID-19/epidemiology , COVID-19/psychology , Depression/diagnosis , Depression/epidemiology , Depression/prevention & control , Female , Health Surveys , Humans , Maternal Health , Mental Health/trends , Pregnancy , Pregnancy Complications/diagnosis , Pregnancy Complications/epidemiology , Pregnancy Complications/prevention & control , Pregnancy Complications/psychology , Prenatal Care/methods , Prenatal Care/statistics & numerical data , SARS-CoV-2 , Social Support , Stress, Psychological/diagnosis , Stress, Psychological/epidemiology , Stress, Psychological/prevention & control , Turkey/epidemiology
3.
Complement Med Res ; 28(4): 336-343, 2021.
Article in English | MEDLINE | ID: mdl-33477165

ABSTRACT

AIM: The research was conducted as a randomized controlled pilot study to evaluate the effects of reflexology on lactation in mothers who delivered by cesarean section (CS). METHODS: A single-blind randomized controlled experimental study was conducted with a total of 60 postpartum women in the reflexology application (n = 30) and control groups (n = 30). After the CS, the mothers in the control group were given approximately 3-h routine nursing care after recovering from the effects of anesthesia; the introductory information form was applied, and the Breastfeeding Charting System and Documentation Tool (LATCH) and visual analog scale (VAS) for the signs of the onset of lactation were implemented on the first and second days. Reflexology was applied to the women in the intervention group after an average of 3 h following the mother's condition had become stable and she had recovered from the effects of anesthesia. Reflexology was applied a total of 20 min - 10 min for the right foot, 10 min for the left foot - twice a day with 8-h intervals on the first and second days after CS. After the last reflexology application, the LATCH and VAS for the signs of the onset of lactation were applied. RESULTS: Of the women, 70% breastfed their babies within 60 min after delivery; 46.7% of the mothers received breastfeeding training and 81.7% needed support for breastfeeding after the CS. The LATCH breastfeeding scores of the women in the intervention group on both days were significantly higher compared to those of the women in the control group (p < 0.001). On the first day after the CS, apart from breast pain, there was no significant difference between the two groups in terms of breast heat and breast tension (p > 0.05). On the second day after the CS, apart from breast tension, there was no significant difference between the groups in terms of breast heat and breast pain (p < 0.05). In the study, women in the intervention group were found to have higher scores in terms of all three symptoms compared to the control group (p < 0.05). CONCLUSIONS: In the study, it was determined that LATCH scores and signs of the onset of breastfeeding increased in the mothers who received reflexology after CS.


Subject(s)
Breast Feeding , Musculoskeletal Manipulations , Cesarean Section , Female , Humans , Infant , Lactation , Pilot Projects , Pregnancy , Single-Blind Method
4.
Perspect Psychiatr Care ; 57(1): 179-188, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32441811

ABSTRACT

PURPOSE: This study aims to determine the effect of individualized care provided based on Swanson's Caring Theory on the grief, depression, anxiety, and stress levels of women who had a miscarriage. DESIGN AND METHODS: A total of 104 women who experienced a miscarriage were randomized as study (n = 52) and control (n = 52) groups. FINDINGS: The women's physical, emotional, behavioral, and cognitive grief symptoms decreased after receiving Swanson's care (P < .001). Negative feelings about the future, level of depression, and anxiety levels diminished after receiving Swanson's Care (P < .001). PRACTICE IMPLICATIONS: Supportive care and counseling provided after miscarriage were found to contribute to women's psychosocial well-being and to improve their ability to cope with psychological symptoms.


Subject(s)
Abortion, Spontaneous , Counseling , Grief , Abortion, Spontaneous/psychology , Adaptation, Psychological , Anxiety , Depression , Female , Health Status , Humans , Pregnancy , Social Support , Stress, Psychological
5.
Ann Endocrinol (Paris) ; 74(1): 49-52, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23337021

ABSTRACT

We report on a 30-year-old female acromegalic patient treated with the growth hormone (GH) receptor antagonist pegvisomant at a low dose after the failure of long-acting lanreotide, neurosurgery and radiotherapy treatment to restore IGF-1 levels. The combination treatment was well tolerated and produced a dramatic improvement in the patient's condition (reduction in visual field defects, relief of headache and excessive perspiration), normalization of IGF-I levels and a considerable decrease in tumor size, enabling a dramatic decrease in lanreotide dosage and, ultimately, its withdrawal.


Subject(s)
Acromegaly/drug therapy , Adenoma/drug therapy , Drug Resistance, Neoplasm , Growth Hormone-Secreting Pituitary Adenoma/drug therapy , Human Growth Hormone/analogs & derivatives , Peptides, Cyclic/therapeutic use , Somatostatin/analogs & derivatives , Acromegaly/etiology , Acromegaly/pathology , Adenoma/complications , Adenoma/pathology , Adult , Antineoplastic Agents/therapeutic use , Chemotherapy, Adjuvant , Female , Growth Hormone-Secreting Pituitary Adenoma/complications , Growth Hormone-Secreting Pituitary Adenoma/pathology , Human Growth Hormone/therapeutic use , Humans , Remission Induction , Somatostatin/therapeutic use , Tumor Burden/drug effects
6.
Tex Heart Inst J ; 35(2): 147-51, 2008.
Article in English | MEDLINE | ID: mdl-18612443

ABSTRACT

We analyzed the postoperative short- and mid-term outcomes of a series of patients with annuloaortic ectasia who underwent a modified Bentall operation in our clinic from September 2000 through March 2006. The study included 44 patients. Their average age was 53.4 +/- 14.1 years. The underlying disease was degenerative aortic aneurysm in 42 patients (95.5%) and acute aortic dissection in 2 patients (4.5%). Six patients (13.6%) had Marfan phenotype. Aortic insufficiency was moderate in 30 patients (68.2%) and severe in 14 patients (31.8%). In our modification of the Bentall technique, we completed the resection of the aortic root while leaving 5 to 10 mm of native aortic wall tissue to support the anastomosis. A long piece of Teflon felt (width, 0.5-1 cm) was laid on the annulus, and nonpledgeted 2-0 polyester sutures were passed in turn through the Teflon felt, the preserved aortic tissue, and the aortic annulus. A thin piece of Teflon felt was also used in the coronary artery reimplantation sites. Fibrin glue was routinely applied to all anastomoses. There were no intraoperative deaths. One patient died in the hospital after surgery for acute type I aortic dissection. Another patient died 1 year after the operation from prosthetic-valve endocarditis. No patient required surgical correction of excessive postoperative bleeding. Kaplan-Meier curves showed overall survival of 0.94 (95% confidence intervals, 0.9-0.99). We consider our approach an easy, effective way to minimize bleeding from the anastomoses and at the aortic root--a common challenge in aortic surgery.


Subject(s)
Aortic Aneurysm, Thoracic/surgery , Aortic Dissection/surgery , Biocompatible Materials/therapeutic use , Hemostasis, Surgical/methods , Polytetrafluoroethylene/therapeutic use , Postoperative Hemorrhage/prevention & control , Adult , Aged , Cohort Studies , Female , Humans , Male , Middle Aged , Postoperative Hemorrhage/etiology , Retrospective Studies , Suture Techniques , Treatment Outcome
8.
Anadolu Kardiyol Derg ; 6(4): 347-51, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17162282

ABSTRACT

OBJECTIVE: The aim of this study was to compare the effects of two different cardioplegic solutions on nitric oxide (NO) release from coronary vasculature in patients with type II diabetes mellitus undergoing coronary artery bypass grafting (CABG) surgery. METHODS: Forty patients undergoing elective CABG surgery were randomized to be given crystalloid (Group 1) or blood (Group 2) cardioplegia. Aortic and coronary sinus blood samples were taken at three different time periods and the release of NO from the coronary vasculature was determined by measuring its stable end-products, nitrite and nitrate. The difference between the aortic and coronary sinus concentrations of nitrite and nitrate represents the amount of NO released by coronary vascular bed. RESULTS: Before application of aortic cross-clamp, at T1 period, the levels of nitrite/nitrate from the coronary vasculature were similar in both groups (6.53+/-1.21 microM vs 6.07+/-1.24 microM , p>0.05). However after the removal of cross-clamp, a significant decrease in NO was observed in Group 1 as compared with Group 2 (4.21+/-0.73 microM vs 4.92+/-1.02 microM, p<0.01) . This decrease persisted at T3 period, after 30 minutes of reperfusion in group 1 being significantly different from group 2 (3.86+/-0.49 vs 4.37+/-0.72 microM, p<0.05). CONCLUSION: This study has shown that in patients with type II diabetes mellitus crystalloid cardioplegia causes a decrease in the release of NO from coronary vascular bed during aortic cross-clamp and reperfusion period whereas more physiologic blood cardioplegia did not. Our findings indicate that blood cardioplegia protects endothelial function better than crystalloid cardioplegia in diabetic patients.


Subject(s)
Cardioplegic Solutions/therapeutic use , Coronary Artery Bypass , Coronary Artery Disease/drug therapy , Coronary Artery Disease/surgery , Diabetes Mellitus, Type 2 , Nitric Oxide/metabolism , Aged , Cardioplegic Solutions/administration & dosage , Coronary Artery Disease/blood , Coronary Vessels/metabolism , Endothelium, Vascular/metabolism , Female , Humans , Male , Middle Aged , Nitric Oxide/blood , Treatment Outcome
9.
Ann Thorac Cardiovasc Surg ; 12(5): 319-23, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17095973

ABSTRACT

BACKGROUND: Since the presence of pulmonary hypertension (PHT) affects the prognosis of the patients, it is important to manage and evaluate PHT. The aim of this study was to compare the hemodynamic effects of inhaled nitroglycerin and iloprost during early postoperative period, in patients with PHT undergoing mitral valve replacement surgery. MATERIALS AND METHODS: One hundred patients with PHT (mean pulmonary artery pressure (MPAP) >25 mmHg at rest), were randomized to receive either inhalation of nitroglycerin (group I; n=50) or iloprost (group II; n=50) in the postoperative period. In both groups, baseline hemodynamic parameters were recorded before the treatment (T(0)). Then, patients in group I received 20 microg.kg(-1) nitroglycerin and those in group II received 2.5 microg.kg(-1) iloprost. The same parameters were recorded immediately after the end of the treatment (T(1)). RESULTS: In both study groups MPAP and pulmonary vascular resistance (PVR) were found to be significantly lower at T(1) when compared to that of T(0) period (p<0.05). MPAP and PVR were significantly lower and mean arterial pressure (MAP) was significantly higher in group II when compared to group I at T(1) period (p<0.05). In addition to decreases in PVR and MPAP, iloprost also increased cardiac output (CO)(4.9+/-1.3 vs 5.1+/-0.9, p<0.05) and stroke volume (SV)(48+/-13 vs 56+/-13, p<0.05). CONCLUSION: Inhaled iloprost and nitroglycerin, both effectively reduce MPAP and PVR without affecting MAP, systemic vascular resistance (SVR) and CO. However, iloprost seems to be a more powerful pulmonary vasodilator, therefore we suggest iloprost inhalation in patients with severe PHT.


Subject(s)
Heart Valve Diseases/surgery , Heart Valve Prosthesis Implantation , Hypertension, Pulmonary/drug therapy , Iloprost/administration & dosage , Mitral Valve , Nitroglycerin/administration & dosage , Pulmonary Wedge Pressure/drug effects , Drug Therapy, Combination , Female , Follow-Up Studies , Heart Valve Diseases/complications , Humans , Hypertension, Pulmonary/etiology , Hypertension, Pulmonary/physiopathology , Male , Middle Aged , Preoperative Care/methods , Prospective Studies , Treatment Outcome , Vasodilator Agents/administration & dosage
10.
Circ J ; 70(11): 1432-6, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17062966

ABSTRACT

BACKGROUND: Aprotinin is a serine protease inhibitor used extensively in cardiac operations to reduce postoperative bleeding. It also has cardioprotective effects in ischemia/reperfusion injury. In this study, the effects of aprotinin on the release of cardiac markers were evaluated in patients who had good ventricular function and were undergoing coronary artery bypass grafting with cardiopulmonary bypass (CPB). METHODS AND RESULTS: Eighty male patients with an ejection fraction >or=40%, were randomized into either an aprotinin (Group-I; n=40) or control (Group-II; n=40) group. Patients in the aprotinin group received the full Hammersmith doses of aprotinin (2 x 10(6) KIU pre-CPB, 2 x 10(6) KIU at pump prime, 500,000 KIU/h during CPB), whereas the patients in the control group received only saline solutions. Cardiac troponin-I (cTnI) levels were measured before surgery, immediately after surgery, and at postoperative 6(th), 12(th), 24(th) h and 5(th) day. Creatine kinase (CK)-MB measurements were performed at the same time except for the postoperative 5(th) day. Cardiac index (CI), mixed venous oxygen saturation and lactate dehydrogenase (LDH) measurements were also performed. CONCLUSION: Although all patients were in reasonable condition, less myocardial enzyme leakage occurred on the aprotinin group, suggesting that aprotinin has a protective effect on the myocardium beyond that achieved with blood cardioplegia and systemic hypothermia. Because of aprotinin's effects on multiple targets of metabolism, its protective value might increase in more complicated cases.


Subject(s)
Aprotinin/therapeutic use , Cardiopulmonary Bypass/methods , Reperfusion Injury/drug therapy , Serine Proteinase Inhibitors/therapeutic use , Adult , Aged , Aprotinin/pharmacology , Coronary Artery Disease/surgery , Creatine Kinase, MB Form/blood , Double-Blind Method , Heart/drug effects , Heart/physiopathology , Heart Arrest, Induced/adverse effects , Humans , Hypothermia/physiopathology , L-Lactate Dehydrogenase/blood , Male , Middle Aged , Prospective Studies , Reperfusion Injury/blood , Reperfusion Injury/physiopathology , Reperfusion Injury/prevention & control , Serine Proteinase Inhibitors/pharmacology , Troponin T/blood
11.
Can J Anaesth ; 53(9): 919-25, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16960270

ABSTRACT

PURPOSE: Despite the well-documented impairment of pulmonary function after cardiopulmonary bypass, effective precautions and ideal management strategies for this problem are still under debate. This study aimed to evaluate the effects of continuous positive airway pressure (CPAP) applied during cardiopulmonary bypass on respiratory and hemodynamic variables. METHODS: In this randomized, prospective, controlled trial, 120 male patients, aged 45 to 70 yr undergoing first-time elective bypass surgery, were randomly assigned to receive either 10 cm H2O of CPAP (Group I; n = 60) during cardiopulmonary bypass, or serve as control (Group II; n = 60), where the patient's lungs were vented to atmosphere during the bypass period. RESULTS: Alveolar-arterial oxygen partial pressure difference and shunt fraction were significantly higher in the control group compared with the CPAP group after cardiopulmonary bypass (T2) and after closure of sternum (T3), (P < 0.05). No differences between groups with respect to hemodynamic variables were observed at any time. Postoperative pulmonary function variables were lower in both groups compared to baseline values. CONCLUSIONS: Continuous positive airway pressure administered during cardiopulmonary bypass decreased shunt fraction and alveolar-arterial oxygen partial pressure difference during surgery, but had no sustained effect on either variable postoperatively. We conclude that, in patients with normal preoperative pulmonary function, application of 10 cm H2O CPAP does not improve lung function after cardiac surgery.


Subject(s)
Continuous Positive Airway Pressure , Coronary Artery Bypass , Lung/physiopathology , Aged , Carbon Dioxide/blood , Cardiopulmonary Bypass , Humans , Male , Middle Aged , Oxygen/blood , Prospective Studies
12.
Heart Vessels ; 21(3): 152-6, 2006 May.
Article in English | MEDLINE | ID: mdl-16715189

ABSTRACT

The purpose of this study was to evaluate the acute cardioprotective effect of high-dose methylprednisolone (25 mg/kg) in the controlled in vivo model of myocardial ischemia-reperfusion injury occurring during cardiopulmonary bypass. Forty nondiabetic male patients with three-vessel disease undergoing first-time bypass surgery were enrolled for this double-blind prospective study. Patients were randomized to be given 25 mg/kg methylprednisolone (Group I) and saline (Group II) 1 h before cardiopulmonary bypass. The levels of cardiac troponin-I (cTnI) were used as a marker of myocardial tissue damage in myocardial ischemia-reperfusion injury. The cTnI levels were measured before surgery, at the second hour after cardiopulmonary bypass, at the 6th and 24th hours, and 5th day postoperatively. There was no significant difference between the two groups in respect to the duration of ischemia and reperfusion. The preoperative cTnI levels were 0.22+/-0.29 ng/ml in Group I and 0.23+/-0.28 ng/ml in Group II. cTnI levels increased to 2.40+/-1.0 ng/ml in Group I and 3.19+/-0.88 ng/ml in Group II at the 2nd hour after cardiopulmonary bypass. When the differences between T1 and T0 level that showed the amount of troponin release occurring due to ischemia-repefusion injury was calculated and then compared, there was a significant difference between Groups I and II (P=0.024). The cTnI levels measured at 6 h after CPB were 1.98+/-0.63 ng/ml in Group I and 2.75+/-1.15 ng/ml in Group II (P=0.049). cTnI levels decreased to 0.22+/-0.10 ng/ml in Group I and 0.49+/-0.25 ng/ml in Group II on the postoperative day 5 (P=0.0001). Univalent regression analysis showed that preoperative high-dose corticosteroid usage decreased the troponin release in about 12% and this effect was statistically significant (R2=0.12, P<0.05). A single dose of intravenous methylpredisolone (25 mg/kg) given 1 h before ischemia reduced myocardial ischemia-reperfusion injury. These results demonstrated that the acute cardioprotective effect of corticosteroids has much potential in the future for reducing ischemia-reperfusion injury occurring during cardiopulmonary bypass when it is inevitable.


Subject(s)
Cardiopulmonary Bypass , Coronary Artery Bypass , Coronary Disease/surgery , Glucocorticoids/administration & dosage , Methylprednisolone/administration & dosage , Myocardial Reperfusion Injury/prevention & control , Aged , Coronary Disease/blood , Double-Blind Method , Glucocorticoids/pharmacology , Humans , Male , Methylprednisolone/pharmacology , Middle Aged , Prospective Studies , Troponin I/blood
13.
Anesth Analg ; 102(4): 1076-81, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16551902

ABSTRACT

Inguinal herniorrhaphy is commonly performed on an outpatient basis under nerve blocks or local or general anesthesia (GA). Our hypothesis is that use of paravertebral blocks (PVB) as the sole anesthetic technique will result in shorter time to achieve home readiness and improved same-day recovery over a 'fast-track' GA. Fifty patients were randomly assigned to receive either PVB or GA under standardized protocols (PVB = 0.75% ropivacaine, followed by propofol sedation; GA = dolasetron 12.5 mg, propofol induction, rocuronium, endotracheal intubation; desflurane; bupivacaine 0.25% for field block). Eligibility for postanesthetic care unit (PACU) bypass and data on time-to-postoperative pain, ambulation, home readiness, and incidence of adverse events were collected. More patients in the PVB group (71%) met the criteria to bypass the postanesthetic care unit compared with patients in the GA group (8%; P < 0.001). Only 3 (13%) of patients in the PVB group requested treatment for pain while in the hospital, compared with 12 (50%) patients in the GA group, despite infiltration with local anesthetic (P = 0.005). Patients in the PVB group were able to ambulate earlier (102 +/- 55 minutes) than those in the GA group (213 +/- 108 minutes; P < 0.001). Time-to-home readiness and discharge times were shorter for patients in the PVB group (156 +/- 60 and 253 +/- 37 minutes) compared with those in the GA group (203 +/- 91 and 218 +/- 93 minutes) (P < 0.001). Adverse events (e.g., nausea, vomiting, sore throat) and pain requiring treatment in the first 24 hours occurred less frequently in patients who had received PVB than in those who had received GA. In outpatients undergoing inguinal herniorrhaphy, PVB resulted in faster time to home readiness and was associated with fewer adverse events and better analgesia before discharge than GA.


Subject(s)
Anesthesia Recovery Period , Anesthesia, General/methods , Autonomic Nerve Block/methods , Hernia, Inguinal/surgery , Adult , Aged , Amides/therapeutic use , Chi-Square Distribution , Confidence Intervals , Female , Follow-Up Studies , Hernia, Inguinal/drug therapy , Humans , Male , Middle Aged , Pain, Postoperative/drug therapy , Pain, Postoperative/prevention & control , Ropivacaine , Single-Blind Method
14.
Anesthesiology ; 102(5): 1001-7, 2005 May.
Article in English | MEDLINE | ID: mdl-15851888

ABSTRACT

BACKGROUND: Both general and nerve block anesthesia are effective for shoulder surgery. For outpatient surgery, it is important to determine which technique provides more efficient recovery. The authors' goal was to compare nerve block with general anesthesia with respect to recovery profile and patient satisfaction after rotator cuff surgery. METHODS: In this clinical trial, 50 consenting outpatients (aged 18-70 yr) were randomly assigned to receive either fast-track general anesthesia followed by bupivacaine (0.25%) wound infiltration or interscalene brachial plexus block (0.75% ropivacaine), each under standardized protocols. Blinded recovery room nurses assessed the need for pain treatment and rated patient eligibility for bypass of the phase 1 postanesthesia care unit and for discharge home. Patients were followed up for 2 weeks postoperatively. The primary outcome measures were postanesthesia care unit bypass and same-day discharge. Other same-day recovery outcomes included severity of and treatment for pain and time to ambulation. Postoperative outcomes at home included satisfaction with the anesthesia technique and absence of complications (at 2 weeks). RESULTS: Patients who received nerve block (vs. general anesthesia) bypassed the postanesthesia care unit more frequently (76 vs. 16%; P < 0.001), reported less pain, ambulated earlier, were ready for home discharge sooner (123 vs. 286 min; P < 0.001), had no unplanned hospital admissions (vs. 4 of 25 patients who underwent general anesthesia; P = 0.05), and were more satisfied with their care. No complications were reported in either treatment group. CONCLUSIONS: Nerve block anesthesia for outpatient rotator cuff surgery provides several same-day recovery advantages over general anesthesia.


Subject(s)
Ambulatory Surgical Procedures , Anesthesia, General , Nerve Block , Orthopedic Procedures , Rotator Cuff/surgery , Adolescent , Adult , Aged , Anesthesia Recovery Period , Brachial Plexus , Female , Humans , Male , Middle Aged , Pain, Postoperative/drug therapy , Pain, Postoperative/epidemiology , Postoperative Period , Prospective Studies , Treatment Outcome
15.
Anesth Analg ; 100(4): 976-981, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15781509

ABSTRACT

It has been suggested that use of peripheral nerve blocks (PNBs) may have some potential benefits in the outpatient setting. There have been no studies specifically comparing PNBs performed with short-acting local anesthetics with general anesthesia (GA) in patients undergoing outpatient knee surgery. We hypothesized that a combination of lumbar plexus and sciatic blocks using a short-acting local anesthetic will result in shorter time-to-discharge-home as compared with GA. Patients scheduled to undergo knee arthroscopy were randomized to receive a GA (midazolam, fentanyl, propofol, N(2)O/O(2)/desflurane via laryngeal mask airway) or lumbar plexus/sciatic block (PNBs; 2-chloroprocaine). Patients given GA also received an intraarticular injection of 20 mL 0.25% bupivacaine for postoperative pain control. Patients in the PNB group were given midazolam (up to 4 mg) and alfentanil (500-750 microg) before block placement and propofol 30-50 microg . kg(-1) . min(-1) for intraoperative sedation. Relevant perioperative times, postanesthesia care unit bypass rate, severity of pain, and incidence of complications were compared between the two groups. Fifty patients were enrolled in the study; 25 patients each received GA or PNBs. Total operating room time did not differ significantly between the 2 groups (97 +/- 37 versus 91 +/- 42 min). Seventy-two percent of patients receiving PNB met criteria enabling them to bypass Phase I postanesthesia care unit compared with only 24% of those receiving GA (P < 0.002). Time to meet criteria for discharge home (home readiness) and time to actual discharge were significantly shorter for patients given PNBs than for patients given GA (131 +/- 62 versus 205 +/- 94 and 162 +/- 71 versus 226 +/- 96, respectively). Under the conditions of our study, the combination of lumbar plexus and sciatic blocks with 2-chloroprocaine 3% was associated with a superior recovery profile compared with GA in patients having outpatient knee arthroscopy.


Subject(s)
Anesthesia Recovery Period , Anesthesia, General , Arthroscopy , Knee/surgery , Nerve Block , Peripheral Nerves , Adolescent , Adult , Aged , Female , Humans , Length of Stay , Male , Middle Aged , Pain Measurement , Pain, Postoperative/drug therapy , Pain, Postoperative/epidemiology , Treatment Outcome
16.
Anesthesiology ; 101(1): 127-32, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15220781

ABSTRACT

BACKGROUND: General anesthesia (GA) and brachial plexus block have been used successfully for surgery on the upper extremities. Controversy exists as to which method is more suitable in outpatients undergoing hand and wrist surgery. The authors hypothesized that infraclavicular brachial plexus block (INB) performed with a short-acting local anesthetic would result in shorter time to discharge home as compared with "fast-track" GA. METHODS: After obtaining written informed consent, 52 patients (aged 18-65 yr, American Society of Anesthesiologists physical status I-III) were randomly assigned to receive either an INB or GA under standardized protocols (INB = 3% 2-chloroprocaine + HCO3 + epinephrine 1:300000, followed by propofol sedation; GA = 12.5 mg dolasetron, propofol induction, followed by laryngeal mask airway insertion and desflurane for maintenance; 0.25% bupivacaine for wound infiltration). At the conclusion of the procedure, nurses blinded to the study goals and the anesthetic technique used a modified Aldrete score to decide whether patients could bypass the postanesthesia care unit. Additional data were collected regarding time to postoperative pain, ambulation, home readiness, and incidence of adverse events. RESULTS: More patients in the INB group (79%) met the criteria to bypass the postanesthesia care unit compared with patients in the GA group (25%; P < 0.001). Compared with patients in the GA group, fewer patients in the INB group had pain (visual analog scale score > 3) on arrival to the postanesthesia care unit (3% vs. 43%; P < 0.001). None of the patients in the INB group requested treatment for pain while in the hospital, compared with 48% of patients in the GA group (P < 0.001). Patients in the INB group were able to ambulate earlier (82 +/- 41 min) compared with those in the GA group (145 +/- 70 min; P < 0.001). Time to home readiness and discharge times were shorter for patients in the INB group (100 +/- 44 and 121 +/- 37 min) compared with those in the GA group (203 +/- 91 and 218 +/- 93 min; P < 0.001). Adverse events (e.g., nausea, vomiting, sore throat) occurred less frequently in patients undergoing INB as compared with those undergoing GA. CONCLUSION: Infraclavicular brachial plexus block with a short-acting local anesthetic was associated with time-efficient anesthesia, faster recovery, fewer adverse events, better analgesia, and greater patient acceptance than GA followed by wound infiltration with a local anesthetic in outpatients undergoing hand and wrist surgery.


Subject(s)
Ambulatory Surgical Procedures , Anesthesia, General , Hand/surgery , Nerve Block , Orthopedic Procedures , Wrist/surgery , Adolescent , Adult , Aged , Analgesics/administration & dosage , Analgesics/therapeutic use , Anesthesia Recovery Period , Anesthesia, General/adverse effects , Anesthetics, Local , Brachial Plexus , Female , Humans , Male , Middle Aged , Nerve Block/adverse effects , Pain, Postoperative/drug therapy , Pain, Postoperative/epidemiology , Patient Discharge , Patient Satisfaction , Postoperative Complications/epidemiology , Time Factors
17.
Reg Anesth Pain Med ; 28(5): 380-3, 2003.
Article in English | MEDLINE | ID: mdl-14556125

ABSTRACT

BACKGROUND: Considerable controversy exists over the relationship of paresthesia to nerve stimulation. The purpose of this study was to determine the frequency with which patients report paresthesia at the point that an acceptable motor response is obtained to low-intensity current electrical stimulation. METHODS: Low-intensity current nerve stimulation (0.6 mA, 200 microseconds, 2 Hz) was used to identify the brachial plexus in 64 consecutive patients having shoulder or arm surgery with an interscalene block. During nerve localization and while maintaining a motor response (0.20 mA-0.40 mA), the patients were queried regarding any radiating sensation or pain (paresthesia) in the shoulder or extremity on the side of the blockade. Sensory distribution of the block, motor strength of the arm muscles, and adequacy of anesthesia were used to assess the extent of blockade. RESULTS: Ninety-five percent of patients had satisfactory surgical anesthesia. None of the patients spontaneously reported having a paresthesia during nerve stimulation. However, on careful questioning, half of the patients (55%) reported electrical paresthesia, defined as dull tingling sensation traveling down to their hands and coinciding with the motor response. In addition, most patients (71%) spontaneously reported having a mild, radiating paresthesia on initial injection of local anesthetic. CONCLUSIONS: Painful paresthesiae should be infrequent when a low-stimulating current is used to identify the neural components of the brachial plexus and when the block needle is advanced slowly. Low-current intensity nerve stimulation can be used to achieve successful interscalene block with minimal discomfort to the patient.


Subject(s)
Brachial Plexus , Paresthesia/etiology , Peripheral Nerves/physiology , Adult , Arm/surgery , Electric Stimulation , Humans , Motor Neurons/physiology , Nerve Block/methods , Shoulder/surgery
18.
Anesthesiology ; 99(4): 855-8, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14508317

ABSTRACT

BACKGROUND: The aim of this study was to investigate the postoperative hemodynamic effects of nitroglycerin inhalation on patients with pulmonary hypertension undergoing mitral valve replacement surgery. METHODS: Twenty patients who underwent mitral valve replacement surgery were included in the study. In the surgical intensive care unit, at T0 (before the inhalation of nitroglycerin), basal systemic and pulmonary hemodynamics were recorded. Then, 2.5 microg x kg-1 x min-1 nitroglycerin liquid nebulized by a 2-l gas flow of 40% oxygen and air mixture was administered to the patients who were diagnosed as having pulmonary hypertension (mean pulmonary arterial pressures > 25 mmHg). The same parameters were measured at the first (T1), third (T2), and fifth (T3) hours after the beginning of this treatment and 1 h after the end of nitroglycerin inhalation (T4). RESULTS: There were no statistically significant differences at T0, T1, T2, T3, or T4 with respect to heart rate, mean arterial pressure, systemic vascular resistance, cardiac index, mixed venous oxygen saturation, arteriovenous oxygen content difference, or arterial carbon dioxide tension. However, mean pulmonary artery pressure, pulmonary vascular resistance, and intrapulmonary shunt fraction were significantly lower, and the arterial oxygen tension/fraction of inspired oxygen ratio was higher at T1, T2, and T3 when compared to that of T0 and T4. CONCLUSION: The results suggest that nitroglycerin inhalation produces a significant reduction in both mean pulmonary artery pressure and pulmonary vascular resistance in patients after mitral valve operations without reducing mean arterial pressure and systemic vascular resistance. Therefore, it might be a safe and useful therapeutic intervention during the postoperative course.


Subject(s)
Hypertension, Pulmonary/drug therapy , Mitral Valve Insufficiency/surgery , Mitral Valve Stenosis/surgery , Nitroglycerin/administration & dosage , Administration, Inhalation , Adult , Female , Hemodynamics/drug effects , Hemodynamics/physiology , Humans , Hypertension, Pulmonary/physiopathology , Male , Middle Aged , Mitral Valve Insufficiency/drug therapy , Mitral Valve Stenosis/drug therapy , Vascular Resistance/drug effects , Vascular Resistance/physiology
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