Monday, January 27, 2020
Refractory Monosymptomatic Nocturnal Enuresis Treatment
Refractory Monosymptomatic Nocturnal Enuresis Treatment    Role of Posterior Tibial Nerve Stimulation in the Treatment ofà  Refractory Monosymptomatic Nocturnal Enuresis: A Pilot Study  Ali Abdel Raheem,* Yasser Farahat, Osama El-Gamal, Maged Ragab,à  Mohamed Radwan, Abdel Hamid El-Bahnasy, Abdel Naser El-Gamasyà  and Mohamed Rasheed  Purpose: We evaluated the early clinical and urodynamic results of posterior tibialà  nerve stimulation in patients with refractory monosymptomatic nocturnal enuresis.  Materials and Methods: We randomly assigned 28 patients with refractoryà  monosymptomatic nocturnal enuresis to 2 equal groups. Group 1 received aà  weekly session of posterior tibial nerve stimulation for 12 weeks and group 2 wasà  the placebo group. Evaluation was performed in each group at baseline and afterà  posterior tibial nerve stimulation to compare clinical and urodynamic findings.  Another clinical assessment was done 3 months after the first followup.  Results: The 2 groups were comparable in baseline clinical and urodynamic data.  Overall, 13 patients (46.4%) had detrusor overactivity and 14 (50%) had decreasedà  bladder capacity. After treatment 11 group 1 patients (78.6%) had a partial or fullà  response to posterior tibial nerve stimulation but only 2 (14.3%) in group 2 had aà  partial response (p 0.002). Also, the average number of wet nights in group 1 wasà  significantly lower than at baseline (p 0.002). All urodynamic parameters significantlyà  improved in group 1. In contrast, the number of wet nights and urodynamicà  parameters did not change significantly in group 2. At 3-month followup the numberà  of patients with a partial or full response in group 1 had decreased from 11 (78.6%)à  to 6 (42.9%). No change was evident in group 2.  Conclusions: Posterior tibial nerve stimulation can be a viable treatment optionà  in some patients with refractory monosymptomatic nocturnal enuresis. However,à  deterioration in some responders with time suggests the need for maintenanceà  protocols.  Key Words: urinary bladder, nocturnal enuresis, transcutaneous electricà  nerve stimulation, urodynamics, treatment outcomeà  NOCTURNAL enuresis is usually associatedà  with severe psychological and socialà  distress to children and their families.  1 In recent years several treatmentà  modalities emerged to treat NE, suchà  as behavioral therapy,2 alarm treatment,à  3 medical therapy with desmopressin,à  oxybutynin and imipramine,à  and combination therapy.4ââ¬â6 However,à  none has been completely successful andà  the relapse rate of all of them is significant.  7ââ¬â9 Therefore, there is a great needà  to find other treatments that could beà  more effective and durable than currentà  therapy.à  The pathogenesis of refractory NEà  was discussed in many studies and attributedà  to decreased bladder capacityà  and/or PTNS was introduced with earlyà  promising results as neuromodulativeà  therapy for diseases that involve theà  lower urinary tract and for refractory conditions inà  adults and children.15ââ¬â19 These beneficial effects ofà  PTNS for controlling various bladder disorders ledà  us to try it in patients with refractory primary MNE.à    MATERIALS AND METHODS  A total of 28 patients were included in this prospective,à  randomized, placebo controlled, single blind study fromà  January 2010 to March 2012 at the urology department atà  Tanta University Hospital. The study protocol was reviewedà  and approved by the Tanta University institutionalà  review board. Informed consent was obtained fromà  all participants or from parents if the patient was youngerà  than 18 years.  We recruited patients with severe (3 or more wet nightsà  per week) primary MNE at least 6 months in duration inà  whom available conventional and combination therapiesà  had failed, including desmopressin, anticholinergics andà  an alarm. We excluded those with secondary NE, nonMNE,à  nocturnal polyuria and any neurological abnormality.  All patients provided a detailed history and underwentà  complete physical examination, urinalysis, x-ray of theà  lumbo-sacral spine and ultrasound of the urinary system.à    All patients were asked to keep a nocturnal enuresis diaryà  for 2 weeks, which included the time of sleep and arousal,à  and whether they had a dry or wet bed in the morning.  Nocturnal urinary output was measured as the total urineà  volume collected in the diaper after voiding during the lastà  night (assessed by weighing the diaper in the morning)à  plus the first morning urine volume. Nocturnal polyuriaà  was defined as nocturnal urine output 130% or greater ofà   EBC for age.20  The Arabic version of a 2-day frequency-volume chartà  (adapted from the Pan Arab Continence Society, www.pacsoffice.com) was obtained from all patients to confirmà  that the problem was MNE. Daytime functional bladder  capacity was considered the recorded MVV. EBC for ageà  was calculated by the formula, 30 _ (age in years _ 30).  Children with MVV less than 65% of EBC for age wereà  considered to have a small bladder.20  All patients also underwent urodynamic tests, as performedà  by the same urodynamicist using a Delphis-KTà  device (Laborie, Toronto, Ontario, Canada), includingà  1) uroflowmetry with PVR estimation by ultrasound for atà  least 2 voids and 2) cystometrogram, including 1 fillingà  cycle using an 8Fr double lumen urethral catheter withà  the patient supine and a slow filling rate of 10 ml perà  minute.  Patients were randomly divided into 2 equal groups byà  method. Randomization was done blindly by having anà  independent nurse randomly take a card from an envelopeà  containing 14 cards for group 1 and 14 for group 2. Groupà  1 received active PTNS treatment sessions using theà  Urgentà ® PC Neuromodulation System, while group 2 underwentà  a sham procedure.  Treatment Protocol  We applied the technique described by Stoller.21 The patientà  lay supine with the soles of the feet together, and theà  knees abducted and flexed (frog position). A 34 gaugeà  needle was inserted percutaneously approximately 2à  inches (5 cm) cephalad to the medial malleolus and 1 cmà  from the posterior margin of the tibia at an angle of 60à  degrees from the skin surface and the lead wire attachedà  to it. The surface electrode was placed on the same legà  near the arch of the foot over the calcaneus bone. Theà  device was turned on and amplitude was slowly increasedà  until the largest toe of the patient began to curl, the digitsà  fanned or the entire foot extended, indicating proximity toà  the nerve bundle (see figure). If this response was notà  achieved or pain occurred near the insertion site, theà  device was turned off and the procedure was repeated.  When the needle was inserted in the correct position, theà  current was set at a tolerable level (pain threshold) andà  the session continued for 30 minutes.  For the sham procedure we tested only the foot responseà  to the electrical impulse and then turned off theà  apparatus during the whole session. To avoid patientà  identification of the type of procedure all participantsà  were informed that they may or may not feel a sensoryà  stimulus in the lower extremities during the treatmentà  sessions.  Groups 1 and 2 underwent 12 weekly outpatient treatmentà  sessions. All participants were advised to stop allà  medical treatment for NE at least 1 month before startingà  PTNS but to continue behavioral therapy, including fluidà  A, neuromodulation system. B, system in use with flexion of left largest toe.à    restriction at night, complete bladder emptying beforeà  sleep and awakening 2 hours after sleep to void.  Patient Assessment  The first patient evaluation was done in the first 2 weeksà  after the last session. This evaluation involved repeatingà  the clinical and urodynamic assessments. The clinical partà  included a nocturnal enuresis diary for 2 weeks in whichà  the number of wet nights/week was reported as well as aà  2-day frequency-volume chart.  The clinical response to treatment was assessed asà  outlined by the International Childrenââ¬â¢s Continence Society,à  including no responseââ¬âless than a 50% decrease inà  the total number of wet nights, partial responseââ¬â50% toà  89% decrease, responseââ¬â90% or greater decrease and fullà  responseââ¬â100% decrease.20 Urodynamic assessment includedà  uroflowmetry, PVR measurement and cystometry.  The second evaluation was done 3 months after the lastà  session. It involved clinical evaluation using nocturnalà  and voiding diaries only.  Statistical Analysis  All statistical analysis was performed using SPSSà ® 17.à    Data are shown as the mean SD unless otherwise specified.  The Student t and paired sample t tests were usedà  for comparison between groups and in the same group,à  respectively. Nonparametric data were compared by theà  Wilcoxon signed ranks or Mann-Whitney U test. Statisticalà  significance was considered at p 0.05.  RESULTS  Recruited for this study were 28 patients with refractoryà  NE who met inclusion criteria. Initial assessmentà  and baseline characteristics of each groupà  showed no significant difference in clinical and urodynamicà  parameters (table 1). Overall, in the 2à  groups DO was present in 13 patients (46.4%) andà  14 (50%) had decreased bladder capacity.à    The procedure was performed easily with no adverseà  effects in all cases. No patient discontinuedà  the planned sessions.  At the end of the PTNS sessions clinical assessmentà  revealed significant improvement in the average numberà  of wet nights per week in group 1 (decrease fromà  4.7 to 2.6, p 0.002, table 2). Compared to the placeboà  group, the number of wet nights after treatment wasà  significantly lower in group 1 (p 0.041, table 2). Atà  that time 4 group 1 patients (28.6%) had a completeà  response to PTNS, 7 (50%) had a partial response andà  3 were nonresponders. However, in group 2 there wereà  2 patients (14.3%) with a partial response, while theà  remainder did not respond. When we compared the 2à  groups, the difference in this response rate was statisticallyà  significant (p 0.002, table 2).  At first evaluation after the end of treatment, theà  active group showed significant improvement in allà  urodynamic parameters compared to baseline, includingà  first and strong desire to void, and MCCà  (p 0.002, 0.01 and 0.000, respectively, table 2). Inà  group 2 these parameters did not significantly differà  compared to baseline (table 2). Also, DO disappearedà  in 2 of 7 group 1 patients but this improvement wasà  not noted in the sham treated group (table 2). Statisticalà  analysis revealed that the difference be-  Table 1. Patient characteristics  Active Placebo p Value  No. boys/girls 8/6 9/5 1  Mean SD age (yrs) 13.7 2.8 14 2.8 0.8  Mean SD body mass index  (kg/m2)  24.95 4.40 26.27 4.23 0.43  Mean SD max urine flow  (ml/sec)  26.85 6.74 23.28 5.49 0.13  Mean SD PVR (ml) 6.21 7.11 5.86 5.48 0.9  Mean SD daytime frequency 3.9 0.67 4.29 0.64 0.07  Mean SD MVV (ml) 266.57 82 288.93 106.29 0.27  Mean SD No. wet nights/wk 4.7 1.3 5.1 1.4 0.42  No. detrusor overactivity:  Present 7 6 1  Absent 7 8 ââ¬â  Mean SD void desire (ml):  1st 148.46 25.89 153.50 21.65 0.59  Strong 260.43 84.18 271.79 75.43 0.71  Mean SD MCC (ml) 291.21 86.82 322.21 76.04 0.32  Table 2. Intragroup and intergroup comparisons of clinical and urodynamic findings after PTNS at first evaluation  Active Placebo  Baseline After Treatment p Value Baseline After Treatment p Value Posttreatment p Value  Mean SD void desire (ml):  1st 148.46 25.89 177.71 35.48 0.002 153.50 21.65 154.14 20.71 0.59 0.041  Strong 260.43 84.18 283.64 72.03 0.01 271.79 75.43 271.6 72.8 0.94 0.67  Mean SD MCC (ml) 291.21 86.82 322.5 65.89 0.000 322.21 76.04 323.57 77.44 0.57 0.97  No. detrusor overactivity:  Present 7 5 0.44 6 6 1 0.7  Absent 7 9 8 8  Mean SD MVV (ml) 266.57 82 280.14 71.81 0.022 288.93 106.29 291.07 96.84 0.73 0.6  Mean SD No. wet nights/wk 4.7 1.3 2.6 2.2 0.002 5.1 1.4 4.7 2.1 0.08 0.041  No. response: ââ¬â ââ¬â ââ¬â ââ¬â  Full 4 0 0.002  Partial 7 2  None 3 12  1516 POSTERIOR TIBIAL NERVE STIMULATION FOR REFRACTORY NOCTURNAL ENURESIS  tween the 2 groups in this regard was not statisticallyà  significant (p 0.7, table 2). Furthermore, inà  this evaluation urodynamic parameters showed thatà  bladder volume at first desire to void was significantlyà  higher in group 1 than in group 2 (p 0.041).  On the other hand, bladder volume at strong desireà  to void and MCC did not significantly differ betweenà  the groups (p 0.67 and 0.97, respectively, table 2).  Five of the 8 group 1 patients with decreased EBCà  showed improved capacity. MVV also significantlyà  increased after treatment from a mean of 266.57à  82 to 280.14 71.81 cc (p 0.022, table 2).  When we studied the relationship between the responseà  to PTNS and initial urodynamic findings, weà  noted that all 10 group 1 patients with small bladderà  capacity and/or DO showed a good response to treatment,à  including 4 and 6 with a full and partial response,à  respectively. However, when we compared the type ofà  response in those with normal vs abnormal urodynamicà  results, the 4 patients with normal urodynamic findingsà  in this group had a poor response to the sessions, includingà  3 with no response and 1 with only a partial response.  This difference was significant (p 0.007).  Clinical results at 3 months after the last sessionà  showed some deterioration in early results in theà  active group. In this group the number of patientsà   à  ith a full response decreased from 4 to 2 and theà  number of those with a partial response decreasedà  from 7 to 4. No change was detected in the otherà  group. However, when we compared the responseà  rate in the 2 groups at this time, we detected noà  significant difference (p 0.13). In addition, theà  average number of wet nights per week at that timeà  was 2.9 in group 1 and 4.2 in group 2, which did notà  significantly differ (p 0.07).  DISCUSSION  This study demonstrates that PTNS could be of valueà  in some patients with primaryMNEin whom previousà  conventional therapies failed. To our knowledge thisà  treatment modality has not been tried before in suchà  cases but it has been successfully used for overactiveà  bladder syndrome,22,23 lower urinary tract dysfunctionà  in adults and children,15,18 refractory overactive bladder,à  16 refractory vesical dysfunction19 and refractoryà  nonneurogenic bladder sphincter dysfunction.17à    Absent daytime lower urinary tract symptoms inà  patients with NE does not necessarily mean that theà  bladder functions well because DO and/or decreasedà  bladder capacity was previously reported in suchà  patients.10,11 The clinical response to desmopressinà  therapy is less satisfactory when NE is associatedà  with decreased bladder capacity and/or DO.12ââ¬â14 Inà  our study we detected DO and decreased bladderà  capacity in 46.4% and 50% of patients, respectively,à  although patients with MNE only were included inà  analysis. These values agree with previous reportsà  showing bladder overactivity24 and small bladderà  capacity25 in 49% and 50% of children with MNE,à  respectively. These findings may partially explainà  the mechanism of resistance to the previous treatmentà  trials in our patients.  Our results and those of others reveal that PTNSà  can be applied easily and safely in children.18,19à  After the 12 PTNS sessions in our series, patientsà  showed a significant increase in MVV and urodynamicà  parameters, including first and strong desireà  to void, and MCC, compared to the placebo group.  These results agree with those in previous reportsà  demonstrating that PTNS increased cystometric capacityà  from 197 to 252 cc26 and from 243 to 340 cc,27à  and increased MVV by 39 cc, which was statisticallyà  significant.23  However, at 3-month followup we detected someà  deterioration in the response rate compared to earlyà  results. The overall number of full and partial respondersà  decreased from 11 (78.6%) to 6 (42.9%) inà  group 1. This deterioration during followup suggestsà  that PTNS may have temporary efficacy and its effectà  decreases gradually with time. This finding was alsoà  noted in patients with overactive bladder treated withà  PTNS. van der Pal reported that 7 of 11 patients withà  an initially good response had evidence of subjectiveà  and objective deterioration after PTNS.28 They suggestedà  the need for maintenance treatment.  The early promising results of this study encouragedà  us to suggest that PTNS might be effectiveà  in patients with refractory primary MNE inà  whom nocturnal polyuria is not an etiological factorà  but in whom the main underlying pathologicalà  condition is decreased bladder capacity and/or DO.  However, the exact mechanism that could explainà  the mode of action of this treatment modality isà  still unknown. PTNS may induce some inhibitoryà  effects on DO. The existence of this functionalà  abnormality in the bladder implies that the detrusorà  is not completely relaxed between voids.à    Therefore, the capacity of the overactive bladder isà  usually smaller than that of the bladder with aà  normal detrusor. Consequently, the clinical responseà  usually occurs when bladder capacity increasesà  and DO improves after PTNS. This explanationà  may be supported by the improvement inà  bladder capacity (functional and cystometric) andà  the disappearance of DO in patients who respondedà  to PTNS in our study.  The main limitations of this study are the smallà  sample size and the short 3-month followup. Inà  addition, we did not repeat urodynamic tests atà  the second followup at 3 months to avoid patientà  discomfort but depended only on the patient clinicalà  response. However, this information could be important for assessing the cause of the deterioration in PTNS efficacy after treatment wasà  stopped.  CONCLUSIONS  PTNS appears to be a viable treatment option inà  some patients with refractory primary MNE. However,à  deterioration in the response rate with timeà  raises important questions about the long-termà  efficacy of this therapy and the need for furtherà  maintenance sessions. More studies are needed toà  support our findings and select patients whoà  would be good candidates for this therapy.    
Sunday, January 19, 2020
Management Of Pacific Douglas-Fir Stands To Maintain Black-Tailed Deer Populations :: Environment Animals Environmental Essays
Management Of Pacific Douglas-Fir Stands To Maintain Black-Tailed Deer Populations      Introduction    Within the Pacific Northwest region of the United States, intensive, even-aged silviculture has simplified the structure and species composition of native forest stands. Within the range of the coastal Pacific Douglas-fir (Pseudotsuga menziesii), old-growth forests presently cover only 13 percent of the region; 60 percent of these remnants occur in patches less than 40 hectares in size. In this region, total land area consisting of old-growth forest before extensive logging has been estimated at 60-90 percent (Williams and Marcot 1991). As a result of intense clearcutting practices, early successional stages have become predominant and later stages have declined. Shifts in age classes of forests have been accompanied by changes in composition and abundance of fauna. Declines in population numbers, changes in conception dates, and an increase to 27 percent annual mortality (vs 5% in higher elevation old-growth stands) are a cause for implementing appropriate silvicultural practices in    Douglas-fir stands managed for both timber production and a stable black-tailed deer (Odocoileus hemionus columbianus) population (McNay and Voller 1995, Brown 1992). This report will attempt to describe a fairly new and promising silvicultural method that can potentially be able to satisfy both of these criteria.     Coastal Douglas-Fir Characteristics    The habitat type that this report is concerned with is the Tsuga heterophylla zone which contains a large geographical area west of the crest of the Cascade Mountains. Much of the central portion of this zone is occupied by subclimax forests dominated by coastal Douglas-fir (Williamson 1983, Scott 1980). The rest is dominated by western hemlock (Tsuga heterophylla). The original old-growth forest, whose origin was primarily periodic, catastrophic fire, frequently had understory components of western hemlock and western redcedar (Thuja plicata). On very xeric soils, Douglas-fir may be the major species of the climax stand.     Douglas-fir is a species of medium tolerance, long life, large size, and rapid juvenile height growth. It does not sprout, but after 25 years of age bears good seed crops every 5 to 7 years. The seed disseminates well to about six tree lengths and up to one-half mile. Unmanaged stands vary between 81 and 190 cubic feet mean-annual increment at age sixty. Scott (1980) suggests that average yields of about 300 cubic feet per acre are possible in managed stands. For maximum yield, Douglas-fir is commonly grown on rotations of 40 to 60 years, depending on the site and the landowners' objectives.  					    
Saturday, January 11, 2020
Harry Harlow Essay
Harlow was researching the primates at the Henry Vilas Zoo, to study learning and memory in monkeys. While doing this Harlow discovered something very interesting, the monkeys were starting to develop strategies for Harlowââ¬â¢s tests that he set up. They were known as ââ¬Ëlearning setsââ¬â¢ but then later to be said as ââ¬ËLearning to learnââ¬â¢. To further this development, Harlow was in need of regular access to infant primates. He then thought breeding his own colony of Rhesus monkeys in the year 1932. To help the studies Harlow decided to hand rear the infants in a nursery setting, where he would separate the infants from their mothers 12 hours after birth and place them in wire cages on their own with a cloth on the floor. While caring for the infant monkeys, Harlow was intrigued as to why every time they took the cloth away to give them a clean one, they would cry and through a fit. In human infants we would call this behaviour a tantrum.  They often cling on to the cloth with their little hands as hard as they could and while sleeping they would cuddle up to it. Most scientists didnââ¬â¢t pay much attention to this, they would say that itââ¬â¢s because of reduction of food, that if they could feed like they would of a mother, the infant would be satisfied. Harlow did not accept this answer and was rather intrigued with what he could find about this matter. The scientist learned to hand rear the infants properly, but when they were with other infants, they huddled in a corner while clinging to the cloth, the infants were unable to socialise. With this as inspiration, Harlow wanted to test the ââ¬Ëbonds between mother and childââ¬â¢. In those days scientists were to believe that if you fussed over your child to much that it would become spoilt. It was a big thing to neglect your Childââ¬â¢s cries unless for feeding or changing. With the infant monkeys, Harlow wanted to prove this theory wrong, that babies    do need nurturing to develop better in life, that they need the bond between mother and child. To begin the tests Harlow invented what he called a surrogate mother. Separated from their mother about 12 hours after birth, the infant monkeys were raised with a surrogate mother.  Harlow tried 2 different types of ââ¬Ëmotherââ¬â¢; Wire mother who was made completely out of wire with a nipple so the infant monkeys can feed, the other was a ââ¬Ëcloth motherââ¬â¢ made with wood wrapped with cloth. Both surrogate mothers were equipped with a light bulb to keep the infants warm by imitating the warmth from a real mother. Eventually the infant ran and clung to the ââ¬Ëcloth motherââ¬â¢. Thinking that the infant would let go when it is hungry, the scientists observed the infant for hours to notice that when the infant became hungry it would hang on to the ââ¬Ëcloth motherââ¬â¢ and reach over to the ââ¬Ëwire motherââ¬â¢ to feed. It would repeat this actions several times.  While Harlow was undergoing all this research, he noticed that the infants who were being raised by a wire mothers were having difficulties in digesting the milk. Although the cloth surrogate infant was gaining the same weight as the wire surrogate infant, the wire mother infants were having constant diarrhea. Harlowââ¬â¢s interpretation on this particular behavior was that the lack of contact and comfort was psychologically impacting on their stress levels which was effecting their digestive system.    
Friday, January 3, 2020
Why Physician Assisted Suicide Should Be An Available And...
  Dying On Your Own Terms  Jenell Mote  Mohave Community College  Nursing I  NUR 121  Ms. Goss  March 30, 2016 Dying On Your Own Terms  Dying on your own terms is a very controversial topic. It seems that both sides of the argument feel very strongly about their position. In this paper, I will argue that physician assisted suicide should be an available and accessible option for patients that are opting to end their lives on their own terms. Choosing to utilize physician assisted suicide can decrease pain and suffering, allow a person to die with dignity and independence by not feeling that they are becoming a burden on their family, and prevent a person from dying alone. Some of the reasons people are against physician assisted suicide include their personal religious beliefs and the fear that it may get out of hand and target certain people in society, including being used on people with disabilities or certain races.   In my opinion, the biggest reason to legalize physician assisted suicide is decreasing pain and suffering in terminally ill patients. I can imagine that knowing you are dying is hard enough. Pain and suffering should not be added to that. Palliative care, defined by the World Health Organization (WHO), is an approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatmentShow MoreRelatedAssess the Intent and Impact of Publicity-Oriented Legal Challenges to Physician-Assisted Suicide3908 Words à  |à  16 PagesHS542ON Section A Nov 2011  Health Rights and Responsibilities  Professor A. 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