American Journal of Internal Medicine 2018; 6(1): 10-19 http://www.sciencepublishinggroup.com/j/ajim doi: 10.11648/j.ajim.20180601.12 ISSN: 2330-4316 (Print); ISSN: 2330-4324 (Online) Autonomic Dysfunction in Iraqi Patients with Chronic Inflammatory Demyelinating Polyneuropathy Mohammed Majeed Kamil 1 , HaiderAli Mohammed 2 , Bahaa Hassan 3 , Basim Hanoon 3 , Hassan Naji 2 1 Neurology Department, Baquba Teaching Hospital, Dyiala, Iraq 2 Neurology Department, Neurosurgery Teaching Hospital, Baghdad, Iraq 3 Neurology Department, Neurosciences Teaching Hospital, Baghdad, Iraq Email address: To cite this article: Mohammed Majeed Kamil, Haidr Ali Mohammed, Bahaa Hassan, Basim Hanoon, Hassan Naji. Autonomic Dysfunction in Iraqi Patients with Chronic Inflammatory Demyelinating Polyneuropathy. American Journal of Internal Medicine. Vol. 6, No. 1, 2018, pp. 10-19. doi: 10.11648/j.ajim.20180601.12 Received: December 6, 2017; Accepted: December 18, 2017; Published: January 29, 2018 Abstract: Objective:The purpose of this study is to evaluate the autonomic disturbance in patients with chronic inflammatory demyelinating polyneuropathy.Methods:Thirty-eight patients who fit into the AAN criteria of diagnosis of CIDP were studied. Five standard cardiovascular autonomic Ewing tests were performed for every patient in addition to the assessment of autonomic symptoms.Results: The study includes 32 males and 6 females their age ranged from 10 to 69 years. In this study we have seen one child with CIDP whose age was ten years and he had PST impairment. Sexual disturbance was the majorautonomic symptom seen in the males [40.6%], while urinary disturbance 2was the major autonomic disturbance encountered in females [66.6%]. Autonomic function tests [AFT] showed that one quarter of males and half of the females had abnormal AFT. In patients aged between 50-59 years, [40%] having normal autonomic function test, [40%] had PST impairment, while the others have mixed impairment [20%]. None of the patients had pure sympathetic impairment. Regarding the types of CIDP the largest percent [84.2%] of patients have classic type of CIDP while 7.8%, 5.2% and 2.6% had DADS, MADSAM and MMN respectively.Conclusions: Autonomic dysfunction was common in Iraqi CIDP patients. PST impairment is a major pattern of dysautonomia in CIDP. Sexual disturbance in males while urinary disturbance in females were the most common autonomic symptoms encountered. VM, HR response to standing allow an early detection of autonomic dysfunction even in asymptomatic individuals. Keywords: Autonomic Dysfunction, CIDP, Iraqi Patients 1. Introduction 1.1. Definition The term chronic inflammatory demyelinating polyradiculoneuropathy [CIDP] has been used to identify patients with a chronically progressive or relapsing symmetric sensorimotor disorder with cytoalbuminologic dissociation and interstitial and perivascular endoneurial infiltration by lymphocytes and macrophages. In many ways, CIDP can be considered the chronic equivalent of acute inflammatory demyelinating polyradiculoneuropathy [AIDP], the most common form of Guillain-Barré syndrome [GBS]. [1] 1.2. Classification 1- Classic CIDP: Classic chronic inflammatory demyelinating polyradiculoneuropathy [CIDP] is characterized by the occurrence of symmetrical weakness in both proximal and distal muscles that progressively increases for more than two months. The condition is associated with impaired sensation, absent or diminished tendon reflexes, an elevated cerebrospinal fluid protein level, demyelinating nerve- conduction studies, and signs of demyelination in nerve-