<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	>
<channel>
	<title>Comments on: Response by Cantor Sherman</title>
	<atom:link href="http://smokeythemagnificent.com/2009/04/20/response-by-cantor-sherman/feed/" rel="self" type="application/rss+xml" />
	<link>http://smokeythemagnificent.com/2009/04/20/response-by-cantor-sherman/</link>
	<description>Failing the Turing Test since 1986</description>
	<pubDate>Sat, 19 May 2012 11:22:07 +0000</pubDate>
	<generator>http://wordpress.org/?v=2.7.1</generator>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
		<item>
		<title>By: myrick</title>
		<link>http://smokeythemagnificent.com/2009/04/20/response-by-cantor-sherman/#comment-4338</link>
		<dc:creator>myrick</dc:creator>
		<pubDate>Mon, 23 Jan 2012 17:36:34 +0000</pubDate>
		<guid isPermaLink="false">http://smokeythemagnificent.com/?p=92#comment-4338</guid>
		<description>If a man conducts his sex life according to traditional Jewish ethics, he cannot contract HIV. A man can contract HIV only by engaging in behaviour that, in light of Jewish ethics, is irresponsible and immoral. Why alter the male body merely to reduce the cost of his bad behaviour? Why make the pessimistic assumption, immediately after a boy is born, that he will grow up to be a horndog and manwhore, who will not only engage in casual sex but also disdain condoms? 

Cantor Sherman, no one claims that circumcision "prevents" HIV and you should know better than to make that claim. The claim is that it lowers the probability that a healthy man will contract HIV from a single unprotected sexual encounter with an infected woman. This alleged fact is useless if circumcised men engage in more risky sex. The African clinical trials were terminated after 6 months, meaning that we cannot rule out the possibility that circumcision does no more than delay the inevitable. The African trials, about which I have many grave reservations (as per Boyle and Hill in the December 2011 Journal of Law and Medecine), should have been allowed to run for at least 10 years.</description>
		<content:encoded><![CDATA[<p>If a man conducts his sex life according to traditional Jewish ethics, he cannot contract HIV. A man can contract HIV only by engaging in behaviour that, in light of Jewish ethics, is irresponsible and immoral. Why alter the male body merely to reduce the cost of his bad behaviour? Why make the pessimistic assumption, immediately after a boy is born, that he will grow up to be a horndog and manwhore, who will not only engage in casual sex but also disdain condoms? </p>
<p>Cantor Sherman, no one claims that circumcision &#8220;prevents&#8221; HIV and you should know better than to make that claim. The claim is that it lowers the probability that a healthy man will contract HIV from a single unprotected sexual encounter with an infected woman. This alleged fact is useless if circumcised men engage in more risky sex. The African clinical trials were terminated after 6 months, meaning that we cannot rule out the possibility that circumcision does no more than delay the inevitable. The African trials, about which I have many grave reservations (as per Boyle and Hill in the December 2011 Journal of Law and Medecine), should have been allowed to run for at least 10 years.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Cindy</title>
		<link>http://smokeythemagnificent.com/2009/04/20/response-by-cantor-sherman/#comment-86</link>
		<dc:creator>Cindy</dc:creator>
		<pubDate>Sun, 10 May 2009 01:26:31 +0000</pubDate>
		<guid isPermaLink="false">http://smokeythemagnificent.com/?p=92#comment-86</guid>
		<description>Is Neonatal Circumcision Clinically Beneficial? Argument Against


Robert S. Van Howe 

Nat Clin Pract Urol.  2009;6(2):74-75.  ©2009 Nature Publishing Group
Posted 03/26/2009
 
Clinical benefit is only one facet of clinical decision making; medical risks and financial costs also need to be considered. For example, many of the benefits espoused by advocates of circumcision would be more effectively achieved by penectomy, which has the additional benefit of preventing unwanted pregnancies. Of course, penectomy is too invasive, and is not a practical solution. Many of the "clinical benefits" lauded by advocates of circumcision include reduced risk of phimosis, balanitis, urinary tract infections (UTIs), genital cancer and sexually transmitted infections (STIs); however, evidence for these benefits are weak or nonexistent, and several alternatives to circumcision are available that are more effective, less invasive, and less expensive.

Phimosis is as common in circumcised newborns as it is in boys who are not circumcised. Topical steroids are effective in approximately 85% of patients,[1] and could eliminate the need for newborn circumcision to avoid phimosis. Balanitis is more common in circumcised than uncircumcised boys under age 3 years, but may be more common in uncircumcised older boys. The only published adult study of balanitis showed that a referral bias occurred among circumcised men: the control group had a 47.8% circumcision rate,[2] but the participants were from the UK, where the circumcision rate is around 21%. Balanitis can typically be treated with topical antimicrobials.

Newborn boys are more likely to have urinary tract abnormalities compared with girls, particularly in the first 6 months of life; however, many boys later outgrow these abnormalities. Observational studies have found that uncircumcised boys are at increased risk of UTIs during the first 6 months, but this finding might be a result of differential rates of prematurity, urine collection, false-positive urine specimens, and the frequency at which health care is sought.[3] In the absence of anatomic defects, UTIs do not require surgery and can be treated with oral antibiotics. The risk of UTI resulting in chronic renal disease is remote.

Of the 16 studies that assessed whether an association exists between circumcision status and the risk of cervical cancer in female partners, only 1 study found a significant association: a positive association in 1 study out of 16 studies is what would be expected by chance alone. Furthermore, a newly available vaccine against human papillomavirus (HPV) could prevent most cases of cervical cancer. With regard to a reduced prostate cancer risk after circumcision, the medical evidence that supports this association is weak.[4] The incidence of penile cancer is rare (0.8 cases per 100,000); two case–control studies in the US found that, when adjusted for phimosis, newborn circumcision was not associated with penile cancer.[5,6] The association between phimosis and penile cancer might explain why only half of patients with penile cancers are positive for HPV DNA, whereas nearly all patients with cervical cancer have HPV DNA. The other half of patients with penile cancer are probably associated with balanitis xerotica obliterans, the leading cause of true phimosis. Countries with very low circumcision rates, such as Japan, Norway, Finland and Denmark, have a lower age-adjusted incidence of penile cancer than the US. Low-risk sexual practices combined with screening and treatment of HPV infection and phimosis may be more effective and less invasive than universal circumcision.

The effect of circumcision on STIs is varied. Circumcision status has no consistent association with herpes simplex virus 2, HPV, gonorrhea, or chlamydia.[7-9] Men who are not circumcised, particularly in Africa, are at a slightly greater risk of syphilis and genital ulcerative disease, but have a lower risk of genital discharge syndrome compared with circumcised men.[7-9] As genital discharge syndrome is more common than genital ulcers, the overall rate of STIs is greater in circumcised men. STIs can be prevented and/or treated more effectively, less invasively, and less expensively with condoms and antibiotics than with circumcision.

Randomized controlled trials in Africa have shown some efficacy for circumcision in preventing HIV infection; however, these trials have bias for both participants and researchers (e.g. selection, lead time, expectation, attrition, intervention and length), improper randomization and early study termination, which amplified the lead-time bias. Each type of bias contributed towards overestimating the treatment effect. Advocates for circumcision believe that data from these randomized controlled trials, which recruited motivated, self-selected, well-compensated, high-risk adults, can be extrapolated to the general population in Africa and to infants; however, no studies have shown an association between HIV and neonatal circumcision. On the contrary, in a study of 52,143 heterosexual men attending a sexual health clinic, circumcised men had a greater risk of HIV infection than uncircumcised men.[10] Among developed nations, the US has the highest rates of heterosexually transmitted HIV and newborn circumcision. Condoms, when used consistently, provide 99% protection. HIV infections can also be prevented by choosing sexual partners responsibly and by treating STIs. For the cost of every circumcision performed in Africa, 3,500 condoms can be purchased. As condoms can provide nearly complete protection from HIV infection, circumcision adds little value.

Circumcision removes a complex, pentilaminar, specialized, junctional structure that contains nearly all the penis' fine-touch neuroreceptors. Not surprisingly, the foreskin is the most sensitive portion of the penis. Circumcision can reduce the sensitivity of the glans to fine-touch and vibration.[11,12] No wonder adults who undergo circumcision report less-satisfying sex, reduced sensitivity and erectile function, difficulty with intromission, and increased premature ejaculation.[13] Other commonly reported complications of circumcision include infection (1–3%), excessive bleeding (1–9%), meatitis (20%), meatal stenosis (5–8%), subcutaneous granuloma (5%), balanitis (16%), coronal adhesions (30%), skin bridges (2%), and phimosis (1–2%). Parents also request a repeat circumcision for cosmetic reasons in 2% of cases. Furthermore, circumcised newborn boys are 12 times more likely to acquire community-associated methicillin-resistant Staphylococcus aureus infections than uncircumcised newborns.[14] Other less-common complications of circumcision include septicemia, meningitis, Fournier gangrene, staphylococcal scalded skin syndrome, osteomyelitis, septic arthritis, tetanus, herpes simplex infection, empyema, pubic hair strangulation, denudation of the penis, glans amputation, urethral fistula, penile edema, pyogenic granulomas, acute urinary retention with acute renal failure, ruptured bladder, UTI or urine advancing in subcutaneous fascial plains, penile ischemia, pneumothorax, pseudoparaphimosis, pulmonary embolism, unilateral leg cyanosis, gastric rupture, myocardial injury and erythema multiforme.

Circumcision has no medical indication during the newborn period, and it is not the first-line preventive for any illness. Very few adult men choose to be circumcised, full disclosure is a rarity, and parental proxy consent for newborn circumcision is not valid.[15] No reason exists that can justify why circumcision cannot wait until the infant is old enough to choose for himself. As a public health measure, newborn circumcision in the US has failed to show a benefit in protecting against cervical cancer, penile cancer, STIs, and HIV.


References
Ashfield JE et al. (2003) Treatment of phimosis with topical steroids in 194 children. J Urol 169: 1106–1108 
Mallon E et al. (2000) Circumcision and genital dermatoses. Arch Dermatol 136: 350–354 
Van Howe RS (2005) Effect of confounding in the association between circumcision status and urinary tract infection. J Infect 51: 59–68 
Van Howe RS (2007) Case number and the financial impact of circumcision in reducing prostate cancer. BJU Int 100: 1193–1194 
Daling JR et al. (2005) Penile cancer: importance of circumcision, human papillomavirus and smoking in in situ and invasive disease. Int J Cancer 116: 606–616 
Tseng HF et al. (2001) Risk factors for penile cancer: results of a population-based case–control study in Los Angeles County (United States). Cancer Causes Control 12: 267–277 
Weiss HA et al. (2006) Male circumcision and risk of syphilis, chancroid, and genital herpes: a systematic review and meta-analysis. Sex Transm Infect 82: 101–109 
Van Howe RS (2007) Genital ulcerative disease and sexually transmitted urethritis and circumcision: a meta-analysis. Int J STD AIDS 18: 799–809 
Van Howe RS (2007) Human papillomavirus and circumcision: a meta-analysis. J Infect 54: 490–496 
Mor Z et al. (2007) Declining rates in male circumcision amidst increasing evidence of its public health benefit. PLoS ONE 2: e861 
Sorrells ML et al. (2007) Fine-touch pressure thresholds in the adult penis. BJU Int 99: 864–869 
Yang DM et al. (2008) Circumcision affects glans penis vibration perception threshold [Chinese]. Zhonghua Nan Ke Xue 14: 328–330 
Fink KS et al. (2002) Adult circumcision outcomes study: effect on erectile function, penile sensitivity, sexual activity and satisfaction. J Urol 167: 2113–2116 
Nguyen DM et al. (2007) Risk factors for neonatal methicillin-resistant Staphylococcus aureus infection in a well-infant nursery. Infect Control Hosp Epidemiol 28: 406–411 
Svoboda JS et al. (2000) Informed consent for neonatal circumcision: an ethical and legal conundrum. J Contemp Health Law Policy 17: 61–133
 

Reprint Address

Department of Pediatrics and Human Development Michigan State University College of Human Medicine, 1414 West Fair Avenue Suite 226, Marquette, MI 49855, USA; E-mail: rsvanhowe@mgh.org



Robert S. Van Howe, Clinical Professor in the Department of Pediatrics and Human Development, Michigan State University College of Human Medicine, Marquette, MI, USA.


Disclosure: The author declared no competing interests</description>
		<content:encoded><![CDATA[<p>Is Neonatal Circumcision Clinically Beneficial? Argument Against</p>
<p>Robert S. Van Howe </p>
<p>Nat Clin Pract Urol.  2009;6(2):74-75.  ©2009 Nature Publishing Group<br />
Posted 03/26/2009</p>
<p>Clinical benefit is only one facet of clinical decision making; medical risks and financial costs also need to be considered. For example, many of the benefits espoused by advocates of circumcision would be more effectively achieved by penectomy, which has the additional benefit of preventing unwanted pregnancies. Of course, penectomy is too invasive, and is not a practical solution. Many of the &#8220;clinical benefits&#8221; lauded by advocates of circumcision include reduced risk of phimosis, balanitis, urinary tract infections (UTIs), genital cancer and sexually transmitted infections (STIs); however, evidence for these benefits are weak or nonexistent, and several alternatives to circumcision are available that are more effective, less invasive, and less expensive.</p>
<p>Phimosis is as common in circumcised newborns as it is in boys who are not circumcised. Topical steroids are effective in approximately 85% of patients,[1] and could eliminate the need for newborn circumcision to avoid phimosis. Balanitis is more common in circumcised than uncircumcised boys under age 3 years, but may be more common in uncircumcised older boys. The only published adult study of balanitis showed that a referral bias occurred among circumcised men: the control group had a 47.8% circumcision rate,[2] but the participants were from the UK, where the circumcision rate is around 21%. Balanitis can typically be treated with topical antimicrobials.</p>
<p>Newborn boys are more likely to have urinary tract abnormalities compared with girls, particularly in the first 6 months of life; however, many boys later outgrow these abnormalities. Observational studies have found that uncircumcised boys are at increased risk of UTIs during the first 6 months, but this finding might be a result of differential rates of prematurity, urine collection, false-positive urine specimens, and the frequency at which health care is sought.[3] In the absence of anatomic defects, UTIs do not require surgery and can be treated with oral antibiotics. The risk of UTI resulting in chronic renal disease is remote.</p>
<p>Of the 16 studies that assessed whether an association exists between circumcision status and the risk of cervical cancer in female partners, only 1 study found a significant association: a positive association in 1 study out of 16 studies is what would be expected by chance alone. Furthermore, a newly available vaccine against human papillomavirus (HPV) could prevent most cases of cervical cancer. With regard to a reduced prostate cancer risk after circumcision, the medical evidence that supports this association is weak.[4] The incidence of penile cancer is rare (0.8 cases per 100,000); two case–control studies in the US found that, when adjusted for phimosis, newborn circumcision was not associated with penile cancer.[5,6] The association between phimosis and penile cancer might explain why only half of patients with penile cancers are positive for HPV DNA, whereas nearly all patients with cervical cancer have HPV DNA. The other half of patients with penile cancer are probably associated with balanitis xerotica obliterans, the leading cause of true phimosis. Countries with very low circumcision rates, such as Japan, Norway, Finland and Denmark, have a lower age-adjusted incidence of penile cancer than the US. Low-risk sexual practices combined with screening and treatment of HPV infection and phimosis may be more effective and less invasive than universal circumcision.</p>
<p>The effect of circumcision on STIs is varied. Circumcision status has no consistent association with herpes simplex virus 2, HPV, gonorrhea, or chlamydia.[7-9] Men who are not circumcised, particularly in Africa, are at a slightly greater risk of syphilis and genital ulcerative disease, but have a lower risk of genital discharge syndrome compared with circumcised men.[7-9] As genital discharge syndrome is more common than genital ulcers, the overall rate of STIs is greater in circumcised men. STIs can be prevented and/or treated more effectively, less invasively, and less expensively with condoms and antibiotics than with circumcision.</p>
<p>Randomized controlled trials in Africa have shown some efficacy for circumcision in preventing HIV infection; however, these trials have bias for both participants and researchers (e.g. selection, lead time, expectation, attrition, intervention and length), improper randomization and early study termination, which amplified the lead-time bias. Each type of bias contributed towards overestimating the treatment effect. Advocates for circumcision believe that data from these randomized controlled trials, which recruited motivated, self-selected, well-compensated, high-risk adults, can be extrapolated to the general population in Africa and to infants; however, no studies have shown an association between HIV and neonatal circumcision. On the contrary, in a study of 52,143 heterosexual men attending a sexual health clinic, circumcised men had a greater risk of HIV infection than uncircumcised men.[10] Among developed nations, the US has the highest rates of heterosexually transmitted HIV and newborn circumcision. Condoms, when used consistently, provide 99% protection. HIV infections can also be prevented by choosing sexual partners responsibly and by treating STIs. For the cost of every circumcision performed in Africa, 3,500 condoms can be purchased. As condoms can provide nearly complete protection from HIV infection, circumcision adds little value.</p>
<p>Circumcision removes a complex, pentilaminar, specialized, junctional structure that contains nearly all the penis&#8217; fine-touch neuroreceptors. Not surprisingly, the foreskin is the most sensitive portion of the penis. Circumcision can reduce the sensitivity of the glans to fine-touch and vibration.[11,12] No wonder adults who undergo circumcision report less-satisfying sex, reduced sensitivity and erectile function, difficulty with intromission, and increased premature ejaculation.[13] Other commonly reported complications of circumcision include infection (1–3%), excessive bleeding (1–9%), meatitis (20%), meatal stenosis (5–8%), subcutaneous granuloma (5%), balanitis (16%), coronal adhesions (30%), skin bridges (2%), and phimosis (1–2%). Parents also request a repeat circumcision for cosmetic reasons in 2% of cases. Furthermore, circumcised newborn boys are 12 times more likely to acquire community-associated methicillin-resistant Staphylococcus aureus infections than uncircumcised newborns.[14] Other less-common complications of circumcision include septicemia, meningitis, Fournier gangrene, staphylococcal scalded skin syndrome, osteomyelitis, septic arthritis, tetanus, herpes simplex infection, empyema, pubic hair strangulation, denudation of the penis, glans amputation, urethral fistula, penile edema, pyogenic granulomas, acute urinary retention with acute renal failure, ruptured bladder, UTI or urine advancing in subcutaneous fascial plains, penile ischemia, pneumothorax, pseudoparaphimosis, pulmonary embolism, unilateral leg cyanosis, gastric rupture, myocardial injury and erythema multiforme.</p>
<p>Circumcision has no medical indication during the newborn period, and it is not the first-line preventive for any illness. Very few adult men choose to be circumcised, full disclosure is a rarity, and parental proxy consent for newborn circumcision is not valid.[15] No reason exists that can justify why circumcision cannot wait until the infant is old enough to choose for himself. As a public health measure, newborn circumcision in the US has failed to show a benefit in protecting against cervical cancer, penile cancer, STIs, and HIV.</p>
<p>References<br />
Ashfield JE et al. (2003) Treatment of phimosis with topical steroids in 194 children. J Urol 169: 1106–1108<br />
Mallon E et al. (2000) Circumcision and genital dermatoses. Arch Dermatol 136: 350–354<br />
Van Howe RS (2005) Effect of confounding in the association between circumcision status and urinary tract infection. J Infect 51: 59–68<br />
Van Howe RS (2007) Case number and the financial impact of circumcision in reducing prostate cancer. BJU Int 100: 1193–1194<br />
Daling JR et al. (2005) Penile cancer: importance of circumcision, human papillomavirus and smoking in in situ and invasive disease. Int J Cancer 116: 606–616<br />
Tseng HF et al. (2001) Risk factors for penile cancer: results of a population-based case–control study in Los Angeles County (United States). Cancer Causes Control 12: 267–277<br />
Weiss HA et al. (2006) Male circumcision and risk of syphilis, chancroid, and genital herpes: a systematic review and meta-analysis. Sex Transm Infect 82: 101–109<br />
Van Howe RS (2007) Genital ulcerative disease and sexually transmitted urethritis and circumcision: a meta-analysis. Int J STD AIDS 18: 799–809<br />
Van Howe RS (2007) Human papillomavirus and circumcision: a meta-analysis. J Infect 54: 490–496<br />
Mor Z et al. (2007) Declining rates in male circumcision amidst increasing evidence of its public health benefit. PLoS ONE 2: e861<br />
Sorrells ML et al. (2007) Fine-touch pressure thresholds in the adult penis. BJU Int 99: 864–869<br />
Yang DM et al. (2008) Circumcision affects glans penis vibration perception threshold [Chinese]. Zhonghua Nan Ke Xue 14: 328–330<br />
Fink KS et al. (2002) Adult circumcision outcomes study: effect on erectile function, penile sensitivity, sexual activity and satisfaction. J Urol 167: 2113–2116<br />
Nguyen DM et al. (2007) Risk factors for neonatal methicillin-resistant Staphylococcus aureus infection in a well-infant nursery. Infect Control Hosp Epidemiol 28: 406–411<br />
Svoboda JS et al. (2000) Informed consent for neonatal circumcision: an ethical and legal conundrum. J Contemp Health Law Policy 17: 61–133</p>
<p>Reprint Address</p>
<p>Department of Pediatrics and Human Development Michigan State University College of Human Medicine, 1414 West Fair Avenue Suite 226, Marquette, MI 49855, USA; E-mail: <a href="mailto:rsvanhowe@mgh.org">rsvanhowe@mgh.org</a></p>
<p>Robert S. Van Howe, Clinical Professor in the Department of Pediatrics and Human Development, Michigan State University College of Human Medicine, Marquette, MI, USA.</p>
<p>Disclosure: The author declared no competing interests</p>
]]></content:encoded>
	</item>
</channel>
</rss>

