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Chronic Medical Illnesses and 
Sex in Aging 
MARC EVANS M. ABAT, MD, FPCP, FPCGM 
Head, Center for Healthy Aging, The Medical City 
Consultant, Philippine General Hospital, Manila Doctors Hospital, 
Cardinal Santos Medical Center
The Sexual Response Cycle
Cardiovascular disease 
• Hypertension, Dyslipidemia and 
Atherosclerosis 
• Coronary artery disease 
• Cardiomyopathy 
• Valvular heart disease 
• Cardiac dysrrhythmia 
• Heart failure 
• Peripheral arterial disease
Considerations 
• Reduction in the cardiovascular endurance to perform 
the sexual act 
• Concerns about triggering an acute cardiac event 
during the sexual act 
– Angina and Acute myocardial infarction 
– Arrhythmia 
– Acute cardiac failure/congestion 
• Circulatory problems leading to 
– Poor erection 
– Claudication/limb ischemia 
• Anxiety and depression accompanying above concerns 
effects on libido, erection, ability to orgasm
• Medication concerns 
Medications Effects on Sexual Act 
digoxin Decreased desire, erection, and frequency of sexual 
relations 
Beta blockers Small increased risk of fatigue and sexual dysfunction 
Nitrates Preclude the use of PDE-5 inhibitors (e.g. sildenafil) to 
improve erection 
diuretics Loss of libido, difficulty initiating and sustaining 
erection, and difficulty with orgasm 
ACEi/ARBs Neutral to positive effects 
CCB Poor erection, sexual dysfunction 
Central agents 
(clonidine, 
methyldopa) 
Poor erection. Loss of libido, impaired ejaculation
Recommendations for Care
General Considerations 
• Sexual activity is reasonable in 
– Low risk patients (Class IIa; Level of Evidence B) 
– Can exercise >3 to 5 METS without angina, 
excessive dyspnea, ischemic ST-segment changes, 
cyanosis, hypotension, or arrhythmia (Class IIa; 
Level of Evidence C) 
• Cardiac rehabilitation and regular exercise 
– useful to reduce the risk of cardiovascular 
complications (Class IIa; Level of Evidence B). 
Circulation. 2012;125:00-00.)
Coronary Artery Disease 
• Sexual activity is reasonable for 
– patients with no or mild angina (Class IIa; Level of 
Evidence B). 
– 1 or more weeks after uncomplicated MI if the patient 
is without cardiac symptoms during mild to moderate 
physical activity (Class IIa; Level of Evidence C) 
– undergone complete coronary revascularization (Class 
IIa; Level of Evidence B) 
– undergone non-coronary open heart surgery (Class 
IIa; Level of Evidence C). 
Circulation. 2012;125:00-00.)
• For patients with incomplete coronary 
revascularization 
– exercise stress testing can be considered to assess 
the extent and severity of residual ischemia (Class 
IIb; Level of Evidence C). 
Circulation. 2012;125:00-00.)
Heart Failure 
• Sexual activity is reasonable for patients with 
compensated and/or mild (NYHA class I or II) 
heart failure (Class IIa; Level of Evidence B) 
Circulation. 2012;125:00-00.)
Valvular Heart Disease 
• Sexual activity is reasonable 
– mild or moderate valvular heart disease and no or 
mild symptoms (Class IIa; Level of Evidence C). 
– Normally functioning prosthetic valves, 
successfully repaired valves, and successful 
transcatheter valve interventions (Class IIa; Level 
of Evidence C). 
Circulation. 2012;125:00-00.)
Arrhythmias, Pacemakers, and ICDs 
• Sexual activity is reasonable for patients with 
– atrial fibrillation or atrial flutter and well-controlled 
ventricular rate (Class IIa; Level of Evidence C). 
– history of atrioventricular nodal reentry tachycardia, 
atrioventricular reentry tachycardia, or atrial tachycardia 
with controlled arrhythmias (Class IIa; Level of Evidence C). 
– pacemakers (Class IIa; Level of Evidence C). 
– ICD implanted for primary prevention (Class IIa; Level of 
Evidence C). 
– ICD used for secondary prevention in whom moderate 
physical activity (>3–5 METS) does not precipitate 
ventricular tachycardia or fibrillation and who do not 
receive frequent multiple appropriate shocks (Level of 
Evidence C). 
Circulation. 2012;125:00-00.)
Hypertrophic Cardiomyopathy 
• Sexual activity is reasonable (Class IIa; Level of 
Evidence C). 
Circulation. 2012;125:00-00.)
Cardiovascular drugs that can improve 
symptoms and survival 
• should not be withheld because of concerns 
about the potential impact on sexual function 
(Class III: Harm; Level of Evidence C). 
Circulation. 2012;125:00-00.)
PDE5 inhibitors (e.g. sildenafil, vardenafil, 
tadalafil) 
• useful for the treatment of ED in patients with 
stable CVD (Class I; Level of Evidence A) 
• Safety unknown in patient with severe aortic 
stenosis or HCM (Class IIb; Level of Evidence C). 
• should not be used in patients receiving nitrate 
therapy (Class III; Level of Evidence B) 
• Nitrates should not be administered (Class III; 
Level of Evidence B) 
– within 24 hours of sildenafil or vardenafil 
administration 
– or within 48 hours of tadalafil administration 
Circulation. 2012;125:00-00.)
Other Concerns 
• Nonsystemic (local or topical) estrogen use for 
the treatment of dyspareunia in women with CVD 
is reasonable (Class IIa; Level of Evidence C) 
• caution patients with CVD regarding the potential 
for adverse events with the use of herbal 
medications with unknown ingredients that are 
taken for treatment of sexual dysfunction (Class 
IIb; Level of Evidence C) 
Circulation. 2012;125:00-00.)
General Management 
• Accurate risk stratification and Optimal 
management of cardiovascular conditions 
– Sexual dysfunction may have to be a tolerated 
medication side effect in certain situations 
• Use of comfortable sexual positions 
• Use of non-penetrative sexual 
activities/prolonging foreplay (e.g. 
fellatio/cunnilingus/masturbation) 
• Use of non-sexual activities to enhance physical 
closeness, affection 
• Judicious use of the PDE5 inhibitors
Respiratory Diseases 
• Chronic obstructive 
pulmonary disease 
• Chronic respiratory 
failure from other causes 
(e.g. bronchiectasis, or 
pulmonary fibrosis) 
• Bronchial asthma 
• Lung cancer
Concerns 
• Shortness of breath and hypoxemia during 
increased physical activity 
– Leading to difficulty sustaining sexual activity 
• Fatigue affecting desire 
• Resulting asthenia contributing to difficulty in 
participation and performance 
• Unexpected pulmonary symptoms during 
intercourse (e.g. excessive phlegm production, 
sudden hemoptysis)
• Resulting anxiety and depressioneffects on 
libido, erection, ability to orgasm 
• Medication concerns (although generally less 
due to localized pulmonary effects) 
– Anticholinergic agents (e.g. ipratropium, 
tiotropium)—decreased libido, vaginal dryness, 
difficulty reaching orgasm 
– Beta agonists (e.g. salbutamol)
Case Report 
• 63-yr-old man, affected by severe (stage GOLD IV) 
stable COPD, treated with long-term oxygen therapy 
for 2 years 
• evaluation performed 3x under stable conditions with 
the patient breathing room air; no change in his 
medications 
• Most comfortable position used (standing or woman 
on top) 
• Oxygen saturation measured at 
– 5 min before sex 
– Duration of sex (from excitement to ejaculation) 
– Up to 10 mins after sex 
– More than 10-min after sex 
Respiratory Medicine. June 2008. 102(6 ),927-931.
• Baseline evaluation using 6- 
minute-walk 
– Sudden and deep fall in 
oxygen saturation during the 
test 
• Evaluation during sex (3 
separate occasions) 
– Increased in dyspnea 
sensation 
– Higher baseline heart rate 
– Increase in heart rate during 
sex 
– Slower but steady increase in 
oxygen saturation during and 
within 10 minutes after sex 
Respiratory Medicine. June 2008. 102(6 ),927-931.
• Attributed to increased ventilation and 
perfusion relative to amount of muscles used 
during sex
General Management 
• Optimal management of respiratory condition 
• Respiratory premedication prior to sexual activity 
• Pulmonary toilette prior to sexual act 
• Use of comfortable sexual positions 
• Use of non-penetrative sexual 
activities/prolonging foreplay (e.g. 
fellatio/cunnilingus/masturbation) 
• Use of non-sexual activities to enhance physical 
closeness, affection 
• Use of lubricants
Chronic Liver Disease 
• Changes in circulating sex hormones 
• Fatigue 
• Medication effects (e.g. diuretics, beta 
blockers) 
• Water retention 
• Autonomic dysfunction
Chronic Kidney Disease 
• Co-morbidities related to vascular and 
neuropathic complications of underlying cause 
(e.g. diabetes mellitus) 
• Effects of uremia 
– Fatigue 
– Decreased energy/endurance 
– Uremic appearance and smell
Endocrine disorders 
• Diabetes mellitus 
– Microvascular complications (particularly 
neuropathy) 
– Macrovascular complications (e.g. heart disease, 
stroke, kidney disease) 
• Thyroid disorders 
– Both hypo- and hyperthyroidism lead to decreases 
in sexual desire, arousal, lubrication and orgasm
• Use of hormonal treatments or medication 
effects 
– Antiandrogens (e.g. bicalutamide) 
– GnRH analogs (e.g. leuprolide) 
– Increased prolactin (e.g. from use of 
antidepressants)
Musculoskeletal Disorders 
• Osteoarthritis 
• Gout 
• Rheumatoid Arthritis 
• Disc disease 
• Osteoporosis 
• Spondylisthesis 
• Radiculopathies
• Musculoskeletal pain or joint ROM limitation 
may affect activities related to sexual 
performance 
• Neurogenic effects of structural disorders 
• Vascular effects of long-term NSAID/COX-2 
inhibitor use
This is a LAMP…….not a woman in 
lithotomy position
The most powerful sex 
organ is….. 
THE BRAIN
Dementing disorders 
• Impaired partner 
recognition and relation 
• Increased interest 
hypersexuality 
• Decreased or loss of 
interest 
• Decreased ability to 
perform 
• Aberrant sexual behavior 
• Disinhibition 
• Sexual abuse 
• Alzheimer’s disease 
• Vascular dementia 
• Lewy Body dementia 
• Frontal lobe dementia
• Medication effects 
– Cholinesterase inhibitors (e.g. donepezil, 
rivastigmine)increased libido 
– NMDA receptor antagonist (e.g. 
memantine)decreased libido 
– Antipsychotics 
• Better sexual performance (with relief of psychosis) 
• Case reports of retrograde ejaculation, priapism with 
risperidone and olanzapine
Cerebrovascular disease 
• Motor and sensory 
deficits 
• Autonomic dysfunction 
• Concerns about further 
stroke episodes and 
other neurologic 
symptoms (e.g. 
seizures) 
• Psychologic issues 
• Decreased libido 
• Problems with arousal 
– Erectile dysfunction 
– Problems with vaginal 
tone and lubrication 
– Orgasm problems 
• General difficulties with 
participation due to 
residual deficits
Parkinsonism 
• Postural instability 
• Rigidity 
• Bradykinesia 
• Autonomic 
dysfunction 
• Difficulties in 
positioning and 
performance 
• Erection problems 
• Orgasm difficulties 
• Vaginal dryness 
• Hypersexuality (side 
effect of dopamine 
agonists)
General Management 
• Optimal management of the underlying condition 
– Some medication effects may have to be tolerated 
• Medication rationalization 
• Appropriate timing of activities 
• Use of comfortable sexual positions 
• Use of non-penetrative sexual activities/prolonging 
foreplay (e.g. fellatio/cunnilingus/masturbation) 
• Use of non-sexual activities to enhance physical 
closeness, affection 
• Treatment
Chronic medical illnesses and sex in aging

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Chronic medical illnesses and sex in aging

  • 1. Chronic Medical Illnesses and Sex in Aging MARC EVANS M. ABAT, MD, FPCP, FPCGM Head, Center for Healthy Aging, The Medical City Consultant, Philippine General Hospital, Manila Doctors Hospital, Cardinal Santos Medical Center
  • 3. Cardiovascular disease • Hypertension, Dyslipidemia and Atherosclerosis • Coronary artery disease • Cardiomyopathy • Valvular heart disease • Cardiac dysrrhythmia • Heart failure • Peripheral arterial disease
  • 4. Considerations • Reduction in the cardiovascular endurance to perform the sexual act • Concerns about triggering an acute cardiac event during the sexual act – Angina and Acute myocardial infarction – Arrhythmia – Acute cardiac failure/congestion • Circulatory problems leading to – Poor erection – Claudication/limb ischemia • Anxiety and depression accompanying above concerns effects on libido, erection, ability to orgasm
  • 5. • Medication concerns Medications Effects on Sexual Act digoxin Decreased desire, erection, and frequency of sexual relations Beta blockers Small increased risk of fatigue and sexual dysfunction Nitrates Preclude the use of PDE-5 inhibitors (e.g. sildenafil) to improve erection diuretics Loss of libido, difficulty initiating and sustaining erection, and difficulty with orgasm ACEi/ARBs Neutral to positive effects CCB Poor erection, sexual dysfunction Central agents (clonidine, methyldopa) Poor erection. Loss of libido, impaired ejaculation
  • 6.
  • 8. General Considerations • Sexual activity is reasonable in – Low risk patients (Class IIa; Level of Evidence B) – Can exercise >3 to 5 METS without angina, excessive dyspnea, ischemic ST-segment changes, cyanosis, hypotension, or arrhythmia (Class IIa; Level of Evidence C) • Cardiac rehabilitation and regular exercise – useful to reduce the risk of cardiovascular complications (Class IIa; Level of Evidence B). Circulation. 2012;125:00-00.)
  • 9. Coronary Artery Disease • Sexual activity is reasonable for – patients with no or mild angina (Class IIa; Level of Evidence B). – 1 or more weeks after uncomplicated MI if the patient is without cardiac symptoms during mild to moderate physical activity (Class IIa; Level of Evidence C) – undergone complete coronary revascularization (Class IIa; Level of Evidence B) – undergone non-coronary open heart surgery (Class IIa; Level of Evidence C). Circulation. 2012;125:00-00.)
  • 10. • For patients with incomplete coronary revascularization – exercise stress testing can be considered to assess the extent and severity of residual ischemia (Class IIb; Level of Evidence C). Circulation. 2012;125:00-00.)
  • 11. Heart Failure • Sexual activity is reasonable for patients with compensated and/or mild (NYHA class I or II) heart failure (Class IIa; Level of Evidence B) Circulation. 2012;125:00-00.)
  • 12. Valvular Heart Disease • Sexual activity is reasonable – mild or moderate valvular heart disease and no or mild symptoms (Class IIa; Level of Evidence C). – Normally functioning prosthetic valves, successfully repaired valves, and successful transcatheter valve interventions (Class IIa; Level of Evidence C). Circulation. 2012;125:00-00.)
  • 13. Arrhythmias, Pacemakers, and ICDs • Sexual activity is reasonable for patients with – atrial fibrillation or atrial flutter and well-controlled ventricular rate (Class IIa; Level of Evidence C). – history of atrioventricular nodal reentry tachycardia, atrioventricular reentry tachycardia, or atrial tachycardia with controlled arrhythmias (Class IIa; Level of Evidence C). – pacemakers (Class IIa; Level of Evidence C). – ICD implanted for primary prevention (Class IIa; Level of Evidence C). – ICD used for secondary prevention in whom moderate physical activity (>3–5 METS) does not precipitate ventricular tachycardia or fibrillation and who do not receive frequent multiple appropriate shocks (Level of Evidence C). Circulation. 2012;125:00-00.)
  • 14. Hypertrophic Cardiomyopathy • Sexual activity is reasonable (Class IIa; Level of Evidence C). Circulation. 2012;125:00-00.)
  • 15. Cardiovascular drugs that can improve symptoms and survival • should not be withheld because of concerns about the potential impact on sexual function (Class III: Harm; Level of Evidence C). Circulation. 2012;125:00-00.)
  • 16. PDE5 inhibitors (e.g. sildenafil, vardenafil, tadalafil) • useful for the treatment of ED in patients with stable CVD (Class I; Level of Evidence A) • Safety unknown in patient with severe aortic stenosis or HCM (Class IIb; Level of Evidence C). • should not be used in patients receiving nitrate therapy (Class III; Level of Evidence B) • Nitrates should not be administered (Class III; Level of Evidence B) – within 24 hours of sildenafil or vardenafil administration – or within 48 hours of tadalafil administration Circulation. 2012;125:00-00.)
  • 17. Other Concerns • Nonsystemic (local or topical) estrogen use for the treatment of dyspareunia in women with CVD is reasonable (Class IIa; Level of Evidence C) • caution patients with CVD regarding the potential for adverse events with the use of herbal medications with unknown ingredients that are taken for treatment of sexual dysfunction (Class IIb; Level of Evidence C) Circulation. 2012;125:00-00.)
  • 18. General Management • Accurate risk stratification and Optimal management of cardiovascular conditions – Sexual dysfunction may have to be a tolerated medication side effect in certain situations • Use of comfortable sexual positions • Use of non-penetrative sexual activities/prolonging foreplay (e.g. fellatio/cunnilingus/masturbation) • Use of non-sexual activities to enhance physical closeness, affection • Judicious use of the PDE5 inhibitors
  • 19. Respiratory Diseases • Chronic obstructive pulmonary disease • Chronic respiratory failure from other causes (e.g. bronchiectasis, or pulmonary fibrosis) • Bronchial asthma • Lung cancer
  • 20. Concerns • Shortness of breath and hypoxemia during increased physical activity – Leading to difficulty sustaining sexual activity • Fatigue affecting desire • Resulting asthenia contributing to difficulty in participation and performance • Unexpected pulmonary symptoms during intercourse (e.g. excessive phlegm production, sudden hemoptysis)
  • 21. • Resulting anxiety and depressioneffects on libido, erection, ability to orgasm • Medication concerns (although generally less due to localized pulmonary effects) – Anticholinergic agents (e.g. ipratropium, tiotropium)—decreased libido, vaginal dryness, difficulty reaching orgasm – Beta agonists (e.g. salbutamol)
  • 22. Case Report • 63-yr-old man, affected by severe (stage GOLD IV) stable COPD, treated with long-term oxygen therapy for 2 years • evaluation performed 3x under stable conditions with the patient breathing room air; no change in his medications • Most comfortable position used (standing or woman on top) • Oxygen saturation measured at – 5 min before sex – Duration of sex (from excitement to ejaculation) – Up to 10 mins after sex – More than 10-min after sex Respiratory Medicine. June 2008. 102(6 ),927-931.
  • 23. • Baseline evaluation using 6- minute-walk – Sudden and deep fall in oxygen saturation during the test • Evaluation during sex (3 separate occasions) – Increased in dyspnea sensation – Higher baseline heart rate – Increase in heart rate during sex – Slower but steady increase in oxygen saturation during and within 10 minutes after sex Respiratory Medicine. June 2008. 102(6 ),927-931.
  • 24. • Attributed to increased ventilation and perfusion relative to amount of muscles used during sex
  • 25. General Management • Optimal management of respiratory condition • Respiratory premedication prior to sexual activity • Pulmonary toilette prior to sexual act • Use of comfortable sexual positions • Use of non-penetrative sexual activities/prolonging foreplay (e.g. fellatio/cunnilingus/masturbation) • Use of non-sexual activities to enhance physical closeness, affection • Use of lubricants
  • 26. Chronic Liver Disease • Changes in circulating sex hormones • Fatigue • Medication effects (e.g. diuretics, beta blockers) • Water retention • Autonomic dysfunction
  • 27. Chronic Kidney Disease • Co-morbidities related to vascular and neuropathic complications of underlying cause (e.g. diabetes mellitus) • Effects of uremia – Fatigue – Decreased energy/endurance – Uremic appearance and smell
  • 28. Endocrine disorders • Diabetes mellitus – Microvascular complications (particularly neuropathy) – Macrovascular complications (e.g. heart disease, stroke, kidney disease) • Thyroid disorders – Both hypo- and hyperthyroidism lead to decreases in sexual desire, arousal, lubrication and orgasm
  • 29. • Use of hormonal treatments or medication effects – Antiandrogens (e.g. bicalutamide) – GnRH analogs (e.g. leuprolide) – Increased prolactin (e.g. from use of antidepressants)
  • 30. Musculoskeletal Disorders • Osteoarthritis • Gout • Rheumatoid Arthritis • Disc disease • Osteoporosis • Spondylisthesis • Radiculopathies
  • 31. • Musculoskeletal pain or joint ROM limitation may affect activities related to sexual performance • Neurogenic effects of structural disorders • Vascular effects of long-term NSAID/COX-2 inhibitor use
  • 32. This is a LAMP…….not a woman in lithotomy position
  • 33. The most powerful sex organ is….. THE BRAIN
  • 34. Dementing disorders • Impaired partner recognition and relation • Increased interest hypersexuality • Decreased or loss of interest • Decreased ability to perform • Aberrant sexual behavior • Disinhibition • Sexual abuse • Alzheimer’s disease • Vascular dementia • Lewy Body dementia • Frontal lobe dementia
  • 35. • Medication effects – Cholinesterase inhibitors (e.g. donepezil, rivastigmine)increased libido – NMDA receptor antagonist (e.g. memantine)decreased libido – Antipsychotics • Better sexual performance (with relief of psychosis) • Case reports of retrograde ejaculation, priapism with risperidone and olanzapine
  • 36. Cerebrovascular disease • Motor and sensory deficits • Autonomic dysfunction • Concerns about further stroke episodes and other neurologic symptoms (e.g. seizures) • Psychologic issues • Decreased libido • Problems with arousal – Erectile dysfunction – Problems with vaginal tone and lubrication – Orgasm problems • General difficulties with participation due to residual deficits
  • 37. Parkinsonism • Postural instability • Rigidity • Bradykinesia • Autonomic dysfunction • Difficulties in positioning and performance • Erection problems • Orgasm difficulties • Vaginal dryness • Hypersexuality (side effect of dopamine agonists)
  • 38. General Management • Optimal management of the underlying condition – Some medication effects may have to be tolerated • Medication rationalization • Appropriate timing of activities • Use of comfortable sexual positions • Use of non-penetrative sexual activities/prolonging foreplay (e.g. fellatio/cunnilingus/masturbation) • Use of non-sexual activities to enhance physical closeness, affection • Treatment

Notes de l'éditeur

  1. May be electrolyte related or hormonal mediated ARBs—may actually increase sexual frequency
  2. may be resumed (a) several days after percutaneous coronary intervention (PCI) if the vascular access site is without complications (Class IIa; Level of Evidence C) or (b) 6 to 8 weeks after standard coronary artery bypass graft surgery (CABG), provided the sternotomy