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1.
S Afr J Surg ; 62(2): 70, 2024 May.
Article in English | MEDLINE | ID: mdl-38838127

ABSTRACT

SUMMARY: We present a previously healthy 13-year-old male, who sustained a handlebar injury after falling from his bicycle. The computerised tomography (CT) scan indicated a probable pancreatic neoplasm associated with a retroperitoneal haematoma which was, following resection, confirmed histologically to be a solid pseudopapillary neoplasm of the pancreas. These are rare tumours of the pancreas, especially in young males. The rarity of this neoplasm and the mechanism that led to its presentation make this an interesting and unique case.


Subject(s)
Abdominal Injuries , Pancreatic Neoplasms , Tomography, X-Ray Computed , Wounds, Nonpenetrating , Humans , Male , Pancreatic Neoplasms/diagnostic imaging , Pancreatic Neoplasms/surgery , Tomography, X-Ray Computed/methods , Wounds, Nonpenetrating/diagnostic imaging , Wounds, Nonpenetrating/complications , Wounds, Nonpenetrating/surgery , Adolescent , Abdominal Injuries/diagnostic imaging , Abdominal Injuries/surgery , Abdominal Injuries/complications , Hematoma/diagnostic imaging , Hematoma/etiology , Hematoma/surgery , Bicycling/injuries
2.
J Feline Med Surg ; 11(8): 683-91, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19539509

ABSTRACT

Glycaemic control and remission probabilities were compared in 24 newly diagnosed diabetic cats treated twice daily with either glargine, protamine zinc (PZI) or lente insulin and fed a low carbohydrate diet. After day 17, the probability of remission was substantially higher for cats with lower mean 12h blood glucose concentrations on day 17, irrespective of insulin type. Glargine-treated cats had lower mean 12h blood glucose concentrations on day 17 than PZI- or lente-treated cats, and all eight glargine-treated cats achieved remission compared to three PZI- and two lente-treated cats. The probability of remission was greater for cats treated with glargine than cats treated with PZI or lente insulin. In newly diagnosed diabetic cats, twice daily treatment with glargine provides better glycaemic control and higher probability of remission compared to twice daily treatment with PZI or lente insulin. Good glycaemic control soon after diagnosis is associated with increased probability of remission and should be the goal of insulin therapy.


Subject(s)
Cat Diseases/drug therapy , Diabetes Mellitus/veterinary , Hypoglycemic Agents/administration & dosage , Insulin, Long-Acting/administration & dosage , Insulin/analogs & derivatives , Protamines/administration & dosage , Analysis of Variance , Animals , Blood Glucose , Cat Diseases/blood , Cat Diseases/diet therapy , Cats , Diabetes Mellitus/blood , Diabetes Mellitus/diet therapy , Diabetes Mellitus/drug therapy , Dietary Carbohydrates/administration & dosage , Female , Insulin/administration & dosage , Insulin Glargine , Male , Remission Induction/methods , Treatment Outcome
3.
J Vet Pharmacol Ther ; 31(3): 205-12, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18471141

ABSTRACT

The pharmacological effects of glargine, protamine zinc (PZI), and lente insulins were evaluated in nine healthy cats. A 3-way crossover study was performed and plasma concentrations of insulin and glucose were determined for 24 h after a single subcutaneous injection of each insulin at 3-day intervals. Time to onset of action did not differ between insulins. Mean time to first nadir glucose was longer for glargine (14 h) relative to PZI (4 h) and lente (5 h). PZI was biphasic in action with nadirs at 4 and 14 h with the second nadir occurring at a similar time to glargine. Nadir glucose did not differ significantly between insulin types. The duration of action was similar for glargine and PZI and was longer than that for lente insulin. Mean daily glucose after glargine and PZI were also similar and were lower than after lente insulin. Time to reach peak insulin did not differ between insulin types. Time to return to baseline insulin level for PZI was longer than glargine but did not differ significantly from lente. In conclusion, healthy cats injected subcutaneously with glargine, compared to those injected with lente insulin, have a later glucose nadir and longer duration of action. Glargine and PZI had similar durations of action in study cats but a larger study is required to obtain precise comparisons of duration of action.


Subject(s)
Blood Glucose/drug effects , Hypoglycemic Agents/pharmacology , Insulin, Long-Acting/pharmacology , Insulin/analogs & derivatives , Animals , Area Under Curve , Cats , Female , Hypoglycemic Agents/pharmacokinetics , Insulin/pharmacokinetics , Insulin/pharmacology , Insulin Glargine , Insulin, Long-Acting/pharmacokinetics , Kaplan-Meier Estimate , Male , Time Factors
4.
Am J Psychiatry ; 158(12): 1982-8, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11729013

ABSTRACT

OBJECTIVE: This study evaluated the efficacy and safety of paroxetine for the treatment of patients with chronic posttraumatic stress disorder (PTSD). METHOD: Outpatients with chronic PTSD according to DSM-IV criteria and a score of 50 or more on the Clinician-Administered PTSD Scale, part 2, were randomly assigned to take placebo (N=186), 20 mg/day of paroxetine (N=183), or 40 mg/day of paroxetine (N=182) for 12 weeks. Efficacy was assessed by examining the change in total score from baseline to endpoint on the Clinician-Administered PTSD Scale, part 2, and rates of response ("very much improved" or "much improved") for global improvement on the Clinical Global Impression scale. RESULTS: Paroxetine-treated patients in both dose groups demonstrated significantly greater improvement on primary outcome measures compared to placebo-treated patients in the intent-to-treat analysis. Moreover, paroxetine treatment resulted in statistically significant improvement compared to placebo on all three PTSD symptom clusters (reexperiencing, avoidance/numbing, and hyperarousal), social and occupational impairment, and comorbid depression. Paroxetine was effective for both men and women. Treatment response did not vary by trauma type, time since trauma, or severity of baseline PTSD or depressive symptoms. Both doses were well tolerated. CONCLUSIONS: Doses of 20 and 40 mg/day of paroxetine are effective and well tolerated in the treatment of adults with chronic PTSD.


Subject(s)
Paroxetine/administration & dosage , Stress Disorders, Post-Traumatic/drug therapy , Adult , Chronic Disease , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Follow-Up Studies , Humans , Male , Middle Aged , Paroxetine/adverse effects , Personality Assessment , Sex Factors , Stress Disorders, Post-Traumatic/diagnosis , Stress Disorders, Post-Traumatic/psychology , Treatment Outcome
5.
Psychiatr Clin North Am ; 24(4): 817-29, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11723635

ABSTRACT

Alternative therapies and therapy modalities for SAD are needed because: Established treatments (CBT and pharmacologic) do not help everyone who seeks help. Established treatments provide only partial decrease in symptoms for many patients. Patients may experience recurrence of symptoms in long-term follow-up. CBT does not reach enough patients in need. Alternative treatment approaches and modalities may also be needed to address the successful outcomes of CBT. Success in overcoming social anxiety symptoms can generate a whole new set of challenges. For example, a 31-year-old man who overcomes his fear of dating and begins his first romantic relationship may need a less symptomatically focused therapy to deal with issues that arise in this relationship. Likewise, a woman whose decreased social anxiety enables her to get a long-awaited promotion may need to deal with the stress of adjusting to her new responsibilities. An individual who overcomes phobia of public speaking and still has mild anxiety may need to graduate to a forum such as Toastmasters to provide continued exposure to further develop confidence and skills in public speaking.


Subject(s)
Complementary Therapies/methods , Phobic Disorders/therapy , Psychotherapy/methods , Adjustment Disorders/therapy , Adult , Anxiety Disorders/therapy , Desensitization, Psychologic , Eye Movements , Humans , Hypnosis , Male , Psychoanalysis , Psychotherapy, Brief , Self-Help Groups , Therapy, Computer-Assisted
6.
Am J Psychiatry ; 158(9): 1467-73, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11532733

ABSTRACT

OBJECTIVE: Reliance on the categorical model of psychiatric disorders has led to neglected study of posttraumatic sequelae that fall short of full criteria for posttraumatic stress disorder (PTSD). Substantial disability and suicidal risk is associated with subthreshold PTSD, but this association has not been well studied. In addition, no studies have examined the role of comorbidity in explaining disability and impairment in subthreshold PTSD. METHOD: On National Anxiety Disorders Screening Day 1997, 2,608 out of 9,358 individuals screened for affective and anxiety disorders at 1,521 sites across the United States reported at least one PTSD symptom of at least 1 month's duration. Impairment, comorbid anxiety disorders, major depressive disorder, and rates of suicidality were determined and compared for individuals with no, one, two, three, or four (full PTSD) symptoms on a screening questionnaire. Regression analyses examined the relative contribution of subthreshold PTSD and comorbid disorders to impairment and suicidal ideation. RESULTS: Impairment, number of comorbid disorders, rates of comorbid major depressive disorder, and current suicidal ideation increased linearly and significantly with each increasing number of subthreshold PTSD symptoms. Individuals with subthreshold PTSD were at greater risk for suicidal ideation even after the authors controlled for the presence of comorbid major depressive disorder. CONCLUSIONS: Higher numbers of subthreshold PTSD symptoms were associated with greater impairment, comorbidity, and suicidal ideation. Disability and impairment found in previous studies of subthreshold PTSD symptoms may be related in part to the presence of comorbid disorders. However, the presence of subthreshold PTSD symptoms significantly raised the risk for suicidal ideation even after the authors controlled for major depressive disorder. Given the broad public health implications of these findings, more efforts are needed to identify subthreshold PTSD symptoms in clinical populations, epidemiologic surveys, and treatment studies.


Subject(s)
Stress Disorders, Post-Traumatic/diagnosis , Suicide/psychology , Adolescent , Adult , Aged , Aged, 80 and over , Anxiety Disorders/diagnosis , Anxiety Disorders/epidemiology , Comorbidity , Depressive Disorder/diagnosis , Depressive Disorder/epidemiology , Female , Health Surveys , Humans , Life Change Events , Linear Models , Male , Middle Aged , Severity of Illness Index , Stress Disorders, Post-Traumatic/epidemiology , Stress Disorders, Post-Traumatic/psychology , Suicide/statistics & numerical data , Surveys and Questionnaires , United States/epidemiology
7.
Curr Psychiatry Rep ; 2(4): 335-40, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11122978

ABSTRACT

There are no systematic data available on combining medication and psychotherapy in the treatment of individuals with post-traumatic stress disorder (PTSD), despite its widespread practice. Careful review of the acute trials literature reveals that psychosocial and pharmacologic treatments each leave a substantial proportion of individuals with residual symptoms. This paper discusses a treatment model involving a phase- oriented treatment approach that begins with pharmacotherapy and continues with trauma-focused psychotherapy. Other combined approaches also are discussed. A rationale supporting the need for psychosocial treatment in the majority of patients who receive pharmacotherapy for chronic PTSD is presented.


Subject(s)
Psychotherapy , Selective Serotonin Reuptake Inhibitors/therapeutic use , Stress Disorders, Post-Traumatic/drug therapy , Clinical Trials as Topic , Combined Modality Therapy , Humans , Patient Care Planning , Prognosis , Treatment Outcome , Wounds and Injuries/psychology
8.
Int J Psychoanal ; 81 ( Pt 3): 513-27, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10967773

ABSTRACT

Despite the widespread use of long-term psychodynamic treatments, methodologically rigorous outcome studies have not been conducted. The authors describe the results of a feasibility study designed to (1) investigate whether patients in psychodynamic treatment, including psychoanalysis, could be recruited and retained as research subjects, (2) determine patient and therapist compliance with self-report measures, rater-administered structured interviews and session audiotaping and (3) obtain pilot data on changes in these measures after one year of treatment. Nine patients entering psychoanalysis and fifteen entering psychodynamic psychotherapy were studied at baseline, six months and one year. Major findings were as follows: (1) recruitment rates were 27% (psychoanalysis) and 83% (psychotherapy), (2) all patients who remained in treatment remained in the research protocol, (3) drop-out rates among research participants and non-participants were equivalent, (4) current Axis I (usually affective or anxiety) disorders were found in over 60% of patients, (5) Axis II disorders in the absence of current Axis I disorders were rare, (6) despite a small number (N) of participants, significant positive change was demonstrated on a variety of measures after one year. Results suggest that it is possible to demonstrate a therapeutic effect of psychodynamic treatments, including psychoanalysis, but changing negative clinical perceptions of research is necessary if methodologically rigorous outcome studies are to be possible in the future.


Subject(s)
Outcome Assessment, Health Care , Patient Selection , Psychotherapy , Adult , Feasibility Studies , Female , Humans , Male , Mental Disorders/therapy , Patient Compliance , Pilot Projects , Treatment Outcome
10.
Am J Psychiatry ; 157(3): 451-3, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10698824

ABSTRACT

OBJECTIVE: Childhood trauma has been associated with increased risk for both panic disorder and dissociative symptoms in adulthood. The authors hypothesized that among individuals with a primary diagnosis of panic disorder, those experiencing depersonalization/derealization during panic attacks would be more likely to have a history of childhood trauma. METHOD: Rates of traumatic events were compared between panic disorder patients with (N=34) and without (N=40) prominent depersonalization/derealization during panic attacks. Symptom severity in the two groups was also examined. RESULTS: Contrary to the authors' hypothesis, no evidence was found that depersonalization/derealization during panic attacks was associated with childhood trauma. Minimal differences in severity of illness were found between patients with dissociative symptoms and those without such symptoms. CONCLUSIONS: This finding is consistent with a multifactorial model of dissociation. Factors other than childhood trauma and general psychopathology may underlie vulnerability to dissociative symptoms in panic disorder.


Subject(s)
Child Abuse/statistics & numerical data , Dissociative Disorders/diagnosis , Life Change Events , Panic Disorder/diagnosis , Adolescent , Adult , Aged , Ambulatory Care , Child Abuse/diagnosis , Child Abuse, Sexual/diagnosis , Child Abuse, Sexual/statistics & numerical data , Comorbidity , Depersonalization/diagnosis , Depersonalization/epidemiology , Depersonalization/psychology , Diagnosis, Differential , Dissociative Disorders/epidemiology , Dissociative Disorders/psychology , Humans , Middle Aged , Panic Disorder/epidemiology , Panic Disorder/psychology , Severity of Illness Index
11.
Harv Rev Psychiatry ; 7(5): 247-56, 2000.
Article in English | MEDLINE | ID: mdl-10689590

ABSTRACT

Recent evidence suggests that an etiologic model of posttraumatic stress disorder (PTSD) must include both vulnerability factors (presumably related to dysregulation of stress responses and/or failure of normal restitutive mechanisms following trauma) and factors related to trauma severity. The fact that rates of PTSD increase with the severity of trauma suggests that normal adaptive mechanisms may become overwhelmed even in the absence of vulnerability factors. Consistent with this view, efforts to demarcate normative from disordered reactions to severe trauma, such as the new diagnosis of acute stress disorder, have had limited success. Debate over the moral and scientific implications of receiving a trauma-related diagnosis has further complicated the issue and perpetuated a false dichotomy concerning normative responses. The literature on clinical trials in PTSD is reviewed. The range of treatment responses, and the categorical breadth of compounds studied, requires interpretation before the literature as a whole can be understood. One of the many limitations of this new literature is the absence of treatment-outcomes research on individuals with the common comorbidity of substance abuse. The most recent findings with selective serotonin-reuptake inhibitors and related compounds indicate a more optimistic outlook for pharmacological treatment of PTSD than was suggested by earlier trials. Given these observations, investigators will hopefully be encouraged to pursue study and development of treatment models that include both pharmacological and psychosocial interventions.


Subject(s)
Psychotherapy/methods , Selective Serotonin Reuptake Inhibitors/therapeutic use , Stress Disorders, Post-Traumatic/etiology , Stress Disorders, Post-Traumatic/therapy , Acute Disease , Clinical Trials as Topic , Combined Modality Therapy , Humans , Severity of Illness Index , Stress Disorders, Post-Traumatic/diagnosis , Stress, Psychological/diagnosis , Stress, Psychological/psychology
12.
Depress Anxiety ; 10(3): 89-98, 1999.
Article in English | MEDLINE | ID: mdl-10604081

ABSTRACT

UNLABELLED: To evaluate the effects of maintenance treatment and durability of gains after treatment discontinuation, responders to either phenelzine (PZ) or cognitive-behavioral group therapy (CBGT) from an acute trial comparing these two treatments as well as pill placebo and a psychotherapy control (educational supportive group therapy) were enrolled into maintenance and treatment-free follow-up phases. EXPERIMENTAL DESIGN: Responders to an acute trial contrasting PZ and CBGT entered a six-month maintenance phase. Patients who continued to respond through the maintenance phase entered a six-month treatment free phase. Patients receiving pill placebo or educational supportive group therapy in the acute trial did not enter the long term study. PRINCIPAL OBSERVATIONS: PZ patients entered maintenance more improved than CBGT patients, and nonrelapsing PZ patients maintained their superior gains throughout the study. Relapse during maintenance did not differ between treatments. However, PZ patients showed a trend toward greater relapse during treatment-free follow-up. There was a greater relapse among patients with generalized social phobia with phenelzine. CONCLUSIONS: PZ and cognitive-behavioral group therapy may differ in their long term effects. The superiority seen with PZ on some measures in the acute study persisted in patients who maintained their gains over the course of maintenance and treatment-free follow-up. However, CBGT may lead to a greater likelihood of maintaining response after treatment has terminated. Replication with larger samples is needed, as is a study of the acute and long-term efficacy of combined PZ and CBGT.


Subject(s)
Cognitive Behavioral Therapy , Monoamine Oxidase Inhibitors/therapeutic use , Phenelzine/therapeutic use , Phobic Disorders/therapy , Psychotherapy, Group , Adult , Analysis of Variance , Chi-Square Distribution , Confounding Factors, Epidemiologic , Female , Follow-Up Studies , Humans , Male , Patient Dropouts , Phobic Disorders/drug therapy , Prognosis , Recurrence
13.
Am J Psychiatry ; 156(11): 1677-85, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10553729

ABSTRACT

OBJECTIVE: A new diagnosis can greatly influence scientific research, access to resources, and treatment selection in clinical practice. The authors review the historical evolution, rationale, empirical foundation, and clinical utility to date of the recently introduced diagnosis of acute stress disorder. METHOD: The conceptual basis and relevant methods for identifying a psychiatric syndrome are reviewed with respect to acute stress disorder, including selection of criteria for core symptoms; considerations of sensitivity and specificity of a syndrome definition; longitudinal course; and distinctions between normative and pathological phenomena. Particular attention is devoted to two major issues: the implications of the core feature requirement of three of five dissociative symptoms, and the question of whether there should be two separate diagnoses (acute stress disorder and post-traumatic stress disorder [PTSD]) describing posttraumatic syndromes. The widely divergent approaches in DSM-IV and ICD-10 are also reviewed. RESULTS: The diagnosis of acute stress disorder does not appear to achieve the important objective of providing adequate clinical coverage for individuals with acute posttraumatic symptoms. The validity and utility of requiring peritraumatic dissociative symptoms as a core feature are questionable, as is the separation of essentially continuous clinical phenomena into two disorders with different criteria sets (acute stress disorder and PTSD) based on persistence of symptoms for 30 or more days. CONCLUSIONS: Longitudinal studies using acute stress disorder criteria, as well as broader considerations of the clinical and scientific functions that posttraumatic diagnoses should serve, suggest a need to reevaluate the current DSM-IV approach to posttraumatic syndromes.


Subject(s)
Anxiety Disorders/diagnosis , Dissociative Disorders/diagnosis , Stress Disorders, Post-Traumatic/diagnosis , Terminology as Topic , Acute Disease , Adult , Anxiety Disorders/classification , Anxiety Disorders/psychology , Diagnosis, Differential , Dissociative Disorders/classification , Dissociative Disorders/psychology , Female , Humans , Life Change Events , Longitudinal Studies , Male , Psychiatric Status Rating Scales/statistics & numerical data , Reproducibility of Results , Sensitivity and Specificity , Stress Disorders, Post-Traumatic/classification , Survivors/psychology
16.
Ann Thorac Surg ; 65(4): 1020-4, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9564921

ABSTRACT

BACKGROUND: The ulnar artery has been used as a coronary bypass graft in 8 patients when it was deemed unsafe to harvest the radial artery after evaluation of the arterial circulation in the forearm and hand. METHODS: The ulnar artery was removed from the lower three quarters of the forearm, along with its satellite veins. Dissection was commenced distally near the wrist and extended proximally to where the ulnar artery passed between the two heads of origin of the flexor digitorum superficialis. The artery was divided distally above the wrist joint and proximally at a point immediately below the origin of the common interosseus artery. RESULTS: Ten ulnar arteries were removed for use as coronary artery bypass grafts; two were rejected, one because of severe calcification and the other because of atherosclerotic occlusion. The remaining eight ulnar arteries were grafted successfully to coronary arteries other than the left anterior descending. No early hand or cardiac complications were observed. CONCLUSIONS: The ulnar artery is an alternative coronary artery bypass graft that may be used when the radial artery is dominant and cannot be removed without risk. The ulnar artery is in close proximity to the ulnar nerve and harvesting has the potential to injure the nerve. Therefore, until the use of the ulnar artery has been more fully evaluated it should be used only when other options have been exhausted.


Subject(s)
Coronary Artery Bypass , Ulnar Artery/transplantation , Aged , Aged, 80 and over , Arterial Occlusive Diseases/pathology , Arteriosclerosis/pathology , Calcinosis/pathology , Coronary Artery Bypass/methods , Dissection , Follow-Up Studies , Forearm/blood supply , Graft Survival , Hand/blood supply , Humans , Male , Middle Aged , Muscle, Skeletal/blood supply , Radial Artery/transplantation , Regional Blood Flow/physiology , Risk Factors , Treatment Outcome , Ulnar Artery/innervation , Ulnar Artery/pathology , Ulnar Artery/surgery , Ulnar Nerve/anatomy & histology , Wrist/blood supply , Wrist Joint/blood supply
17.
J Clin Psychopharmacol ; 18(2): 132-5, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9555598

ABSTRACT

We report the results of an 8-week open trial of imipramine in 15 patients with social phobia. Nine patients completed the trial; six dropped out early because of adverse effects. The mean reduction in the Liebowitz Social Anxiety Scale was 15% and 18% for the intent-to-treat and completer groups, respectively; the overall response rate (based on the Clinical Global Impression Scale of 1 or 2, very much or much improved) was 20% (3/15) and 22% (2/9), respectively. The results from this open trial do not support the efficacy of imipramine as a treatment for social phobia.


Subject(s)
Antidepressive Agents, Tricyclic/therapeutic use , Imipramine/therapeutic use , Phobic Disorders/drug therapy , Adult , Antidepressive Agents, Tricyclic/adverse effects , Female , Humans , Imipramine/adverse effects , Male , Middle Aged , Phobic Disorders/psychology , Psychiatric Status Rating Scales , Single-Blind Method
18.
J Clin Psychopharmacol ; 18(1): 10-8, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9472837

ABSTRACT

The symptom overlap between posttraumatic stress disorder (PTSD) and other pharmacotherapy-responsive disorders suggests that pharmacotherapy might be effective. Nevertheless, of the eight published placebo-controlled trials investigating the pharmacotherapy of PTSD, only four found statistically significant efficacy for the treatment being studied. This literature possesses a number of methodologic limitations, including the fact that most studies have been conducted with war veterans, who may constitute a more treatment-refractory population. Several open trials and one controlled trial with selective serotonin reuptake inhibitors have reported improvement in some or all core PTSD symptoms (reexperiencing, avoidance, numbing, and hyperarousal). The authors hypothesized that paroxetine might be effective in PTSD, based on findings of its particular efficacy for anxiety and agitation in studies of depressed patients. The study presented here summarizes a 12-week, open-label trial of paroxetine among patients with noncombat-related, chronic PTSD. Outcome was assessed by an independent evaluator, the treating physician, and the patient, with the use of established rating scales for depression, anxiety, general symptoms, and PTSD core symptoms. A repeated-measures analysis of variance revealed highly significant improvement in all three symptom clusters, as well as in associated anxiety, depressive, and dissociative symptoms, with 11 of 17 (65%) patients rated as much or very much improved. The mean reduction in PTSD symptom scores was 48%. Exploratory analyses revealed that cumulative childhood trauma was negatively correlated with pharmacotherapy response (r = -0.52, p = 0.03). There was also significant variation in the time course of response across symptom clusters, which is suggestive of multiple mechanisms of response. Because paroxetine seems a highly promising treatment for all three symptom clusters of PTSD, a placebo-controlled clinical trial is warranted.


Subject(s)
Antidepressive Agents, Second-Generation/therapeutic use , Paroxetine/therapeutic use , Selective Serotonin Reuptake Inhibitors/therapeutic use , Stress Disorders, Post-Traumatic/drug therapy , Adult , Female , Humans , Male , Stress Disorders, Post-Traumatic/pathology
19.
Aust Fam Physician ; 25(7): 1101-3, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8768277

ABSTRACT

Morbid obesity is a very difficult condition to treat. Any operation intended to help the patient Jose weight is no more than a beginning, and must be combined with rigorous postoperative care or it will surely fail.


Subject(s)
Gastroplasty , Obesity, Morbid/surgery , Humans , Postoperative Care , Treatment Outcome
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